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Amine oxidase copper-containing 3 (AOC3) inhibition: a potential novel target for the management of diabetic retinopathy

International Journal of Retina and Vitreous volume 7, Article number: 30 (2021) Cite this article

Abstract

Background

Diabetic retinopathy (DR), a microvascular complication of diabetes, is the leading cause of visual impairment in people aged 20–65 years and can go undetected until vision is irreversibly lost. There is a need for treatments for non-proliferative diabetic retinopathy (NPDR) which, in comparison with current intravitreal (IVT) injections, offer an improved risk–benefit ratio and are suitable for the treatment of early stages of disease, during which there is no major visual impairment. Efficacious systemic therapy for NPDR, including oral treatment, would be an important and convenient therapeutic approach for patients and physicians and would reduce treatment burden. In this article, we review the rationale for the investigation of amine oxidase copper-containing 3 (AOC3), also known as semicarbazide-sensitive amine oxidase and vascular adhesion protein 1 (VAP1), as a novel target for the early treatment of moderate to severe NPDR. AOC3 is a membrane-bound adhesion protein that facilitates the binding of leukocytes to the retinal endothelium. Adherent leukocytes reduce blood flow and in turn rupture blood vessels, leading to ischemia and edema. AOC3 inhibition reduces leukocyte recruitment and is predicted to decrease the production of reactive oxygen species, thereby correcting the underlying hypoxia, ischemia, and edema seen in DR, as well as improving vascular function.

Conclusion

There is substantial unmet need for convenient, non-invasive treatments targeting moderately severe and severe NPDR to reduce progression and preserve vision. The existing pharmacotherapies (IVT corticosteroids and IVT anti-vascular endothelial growth factor-A) target inflammation and angiogenesis, respectively. Unlike these treatments, AOC3 inhibition is predicted to address the underlying hypoxia and ischemia seen in DR. AOC3 inhibitors represent a promising therapeutic strategy for treating patients with DR and could offer greater choice and reduce treatment burden, with the potential to improve patient compliance.

Background

Diabetic retinopathy (DR) is a highly specific neurovascular complication affecting patients with type 1 and type 2 diabetes mellitus (DM) [1]. DR frequently affects both eyes, but may be asymptomatic during its early stages [1, 2]. As the disease progresses, an individual’s vision may become blurred and their visual field restricted [2]. Ultimately, DR can progress to sight-threatening stages, the leading cause of new blindness among people of working age in developed countries [1]. Both tissue injury and vascular events contribute to vision loss in DR [1, 3], and neurodegeneration due to diabetes itself is an early event in the pathogenesis of DR [4].

Increased vascular permeability and/or capillary non-perfusion in DR leads to diabetic macular edema (DME) and macular ischemia, impairing the individual’s central vision [3, 5]. However, while the pathophysiology of DME and DR are highly interconnected, they may also develop independently [6]. Pre-retinal or vitreous hemorrhage stemming from angiogenesis is associated with damage to retinal neurons in the proliferative phase [3]. Moreover, vitreous contraction creates retinal distortion and tractional detachments, which can be severe and irreversible [1, 3].

Although the optimization of glycemic control, blood pressure, and serum lipid control is recommended to slow the progression of DR and decrease the risk of vision loss, many patients still develop proliferative diabetic retinopathy (PDR) [1]. While blindness in DR is largely preventable and moderate ocular abnormalities may even be reversible with systemic control (HbA1c) [7], treatment for DR is not usually administered until vision loss becomes apparent. Unfortunately, in the USA, only around 35–60% of patients with DM receive adequate DR screening [8, 9], and only 30–49% obtain appropriate follow-up care [10]. International guidelines advise that non-proliferative diabetic retinopathy (NPDR) should not be treated unless clinically significant macular edema is present [11]. PDR is characterized by pathologic vitreoretinal neovascularization, while NPDR comprises hallmark features of intraretinal hemorrhages, microaneurysms, lipid exudates, and capillary nonperfusion [12, 13]. DR severity is frequently graded in clinical studies using the Diabetic Retinopathy Severity Scale (DRSS); DRSS is derived from the ETDRS (Early Treatment Diabetic Retinopathy Study) and classifies mild, moderate, moderately severe, and severe NPDR as levels 35, 43, 47, and 53, respectively [14, 15] (Table 1).

Table 1 Correlation between disease severity levels according to the DRSS and ETDRS classification of DR
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Current treatment options for moderately severe and severe NPDR

While most patients with moderately severe or severe NPDR (DRSS level 47–53) do not receive treatment, these are not benign conditions and therapeutic intervention before the development of PDR, vitreous hemorrhage, or DME could reduce visual loss. The early detection of moderately severe to severe NPDR is especially important as the risk of vision loss increases with disease progression. The risk of developing early PDR after 1 year is 26.3% and 50.2% in patients with DRSS levels of 47 and 53, respectively [16]. Thus, regular screening can help to identify those patients at high risk of rapid progression who would benefit from treatment [1]. In the Phase 3 PANORAMA trial, 53% of patients with severe NPDR and 36% with moderately severe NPDR in the untreated control group developed vision-threatening events, compared with 15% of patients with severe NPDR and 8–10% of patients with moderately severe NPDR in the groups given intravitreal (IVT) treatment with the vascular endothelial growth factor A (VEGF-A) inhibitor aflibercept [18]. Treatment delays in patients who received a sham control before crossing over to ranibizumab in the extension phase of the RISE and RIDE studies also gained fewer ETDRS letters in best-corrected visual acuity score at Month 36 compared with baseline versus those who received ranibizumab throughout the studies [19].

Direct ophthalmic treatment options for NPDR are limited to pan-retinal photocoagulation (PRP), IVT corticosteroids, and IVT VEGF inhibitors. A Cochrane database systematic review of four trials of PRP and one trial of selective photocoagulation of non‐perfusion areas concluded that laser photocoagulation is beneficial for PDR, but the authors noted the paucity of high-quality evidence confirming this conclusion [20]. However, the recent Diabetic Retinopathy Clinical Research Network (DRCR.net) Protocol S study showed that more patients with PDR treated with PRP had vitreous hemorrhages compared with patients receiving ranibizumab [21]. There is some evidence to show that PRP may reduce visual acuity in severe NPDR [22], and a systematic review and economic evaluation found insufficient evidence to recommend PRP in this patient group [23]. PRP sessions are uncomfortable and macular edema may develop or worsen after treatment [23, 24]. In addition, patients who undergo PRP treatment may experience a constricted visual field, reduced night vision, and macular or lens damage [24].

IVT implants of corticosteroids are licensed for the treatment of DME, but their use in DR remains limited as it may be associated with an increase in intraocular pressure and cataract development or worsening [25,26,27,28,29].

The VEGF inhibitors ranibizumab and aflibercept are approved by the US Food and Drug Administration (FDA) for the treatment of DR [30], and bevacizumab is widely used off-label for DME [25]. Brolucizumab, which is FDA approved for neovascular age-related macular degeneration [31], is also under investigation in PDR and DME [32, 33]. IVT VEGF inhibitor injections are invasive, expensive, and can be inconvenient to patients and their caregivers; at times, it may be necessary to treat each eye at a separate visit, thereby doubling treatment, travel, and recovery times, all of which contribute to patient, caregiver, and healthcare system burden [34, 35]. In addition, VEGF inhibitors do not improve ischemia or inflammation, do not provide neuroprotection, and continued VEGF inhibitor treatment is required to sustain any benefit to ischemia-related diabetic retinal dysfunction [35,36,37,38]. Furthermore, not all patients respond meaningfully to VEGF inhibitors [39,40,41]. In a study of DME among patients with NPDR, approximately three-quarters of eyes did not fully respond to aflibercept (108/141), bevacizumab (106/131), or ranibizumab (111/151) at 2 years [41]. If appointments for VEGF inhibitor administration are missed (non-compliance), e.g. due to illness, DR could progress to more severe disease and may result in irreversible sight loss [37].

There is evidence that treatment with an additional drug with a different mode of action may reduce the effects of DR [42]. There are several barriers to compliance to IVT DR therapy and follow up, including lack of DR knowledge, DM end-organ damage, economic burden (both DR and DM), long appointment waiting times, and inability to attend appointments due to work or illness [43,44,45]. Given that compliance to IVT VEGF inhibitor therapy is suboptimal even in patients with age-related macular degeneration and those with DME [46], compliance is likely to be even worse in less symptomatic patients with NPDR.

There is substantial unmet need for treatments that target moderately severe and severe NPDR before sight is compromised. If DR progresses to center-involving diabetic macular edema (CI-DME), patients will need long-term, invasive treatment to prevent further disease progression, which may not restore visual acuity [47]. The DRCR.net Protocol S study of 305 patients with PDR treated with PRP or VEGF inhibitor demonstrated that, at 6 months, the VEGF inhibitor ranibizumab failed to prevent neovascularization in 45% of eyes; however, a reduction in hemorrhage and vitrectomy were also identified in the anti-VEGF-treated patients compared with the PRP-treated patients [21]. The related DRCR.net Protocol V study showed that at 2 years, among 702 patients with CI-DME and good visual acuity (20/25 or better), there was no difference in visual acuity loss among those who received aflibercept, laser photocoagulation, or observation (no intervention) [48].

Encouraging patients to become more active in managing their disease is increasingly important, particularly in DM [49]. Although oral treatments for DR may be more convenient for patients than an IVT injection, they are not without possible drawbacks as patients may forget to take oral agents. In addition, compliance can be tracked more readily by physicians with an IVT injection, as the injection is administered in a clinic compared with self-administration of oral medication at home. Furthermore, with an oral agent for NPDR, the potential for systemic effects, both good and bad, must be considered. Nevertheless, efficacious systemic therapy for NPDR, including oral treatment, may provide a convenient therapeutic approach for patients and physicians, and would reduce the treatment burden for patients and their caregivers.

The role of inflammation in DR

The neurovascular unit describes the interplay between blood vessel endothelial cells and pericytes, astrocytes, Müller cells, and neurons to establish the blood–retinal barrier (BRB), which controls nutrient flow to–and the removal of metabolic waste products from–the neural retina [3]. Müller glial cells are a significant source of inflammatory modulators, suggesting that retinal glial cell activation may play an early role in the onset of inflammatory processes that damage the retina as the disease progresses [50]. Elevated levels of inflammatory cytokines such as interleukin (IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-8, interferon γ (IFNγ), and tumor necrosis factor α (TNFα) are found in the sera or vitreous or aqueous humor of patients with DR [51, 52]. Levels of IL-8 and TNFα are even higher among patients with NPDR compared with PDR [51]. Progressive retinal injury may reduce the integrity of the BRB leading to an accumulation of inflammatory and angiogenic mediators within the vitreous cavity [3]. The build-up of IL-1β and TNFα induces the expression of intracellular adhesion molecule 1 (ICAM1) and vascular cell adhesion molecule 1 (VCAM1), which attract leukocytes leading to leukostasis [53]. A further consequence of BRB impairment is the migration of macrophages into the neurosensory retina and/or an increased adherence to the vasculature [3].

The potential role of corticosteroids in DR

The importance of inflammation in the pathogenesis of DR provides a rationale for using corticosteroids as a treatment strategy–targeting the synthesis of key proinflammatory mediators such as IL-6, IL-8, TNFα, ICAM1, and VEGF [54]. Several corticosteroids have been extensively studied in the treatment of DME, including triamcinolone acetonide (TA), the fluocinolone acetonide (FA) implant, and the dexamethasone (DEX) implant [26,27,28,29, 55, 56]. However, their clinical impact has been less thoroughly assessed in DR.

In an exploratory analysis of data from a DRCR.net Phase 3 trial in DME, IVT TA appeared to reduce the risk of DR progression compared with focal/grid photocoagulation alone [57]. A subsequent exploratory analysis in eyes without PDR at baseline suggested that the 3-year cumulative probability of retinopathy worsening may be higher in TA-treated eyes compared with those treated with the VEGF inhibitor ranibizumab [58]. However, in patients with PDR both treatments were associated with a reduced risk of PDR worsening compared with sham therapy [58]. More recently, a post hoc analysis of data from two Phase 3 DME trials suggested that another corticosteroid treatment, the FA implant, can delay the development of PDR and slow DR progression compared with sham control [59]. Finally, a retrospective cohort study of 60 patients with NPDR and DME found that treatment with the DEX implant could delay DR progression and improve DR severity over 24 months [60].

However, although these data are promising, prospective, randomized trials are lacking. In particular, studies comparing corticosteroid treatment with a VEGF inhibitor in patients with NPDR would be valuable. Furthermore, it is not known whether the current data on patients with DR and DME are applicable to those without DME. Known adverse events of corticosteroids, such as increased interocular pressure, glaucoma, and cataracts [28, 57, 60], could be limiting their widespread use and restricting their use in patients with severe DR and/or those who are pseudophakic.

The role of AOC3 protein in retinal inflammation and neovascularization

Amine oxidase copper-containing 3 (AOC3), also known as semicarbazide-sensitive amine oxidase and vascular adhesion protein 1 (VAP1), is a membrane-bound adhesion protein that facilitates the binding of leukocytes to endothelial cells and their subsequent transmigration to sites of inflammation (Figs. 1 and 2) [61]. AOC3 is abundant in the activated endothelium of vascularized tissues, including the retina, kidney, and liver [62, 63], and is associated with vascular diseases and inflammatory conditions such as chronic kidney disease, chronic liver disease, and DM [61, 64,65,66,67,68,69]. AOC3 has previously been targeted for therapeutic intervention in autoimmune and inflammatory diseases, and several inhibitory compounds have been investigated over the past two decades [70,71,72,73]. Furthermore, AOC3 has been implicated as a possible candidate protein for mediating inflammation and oxidative stress in PDR [74], and may be important in the activation of early events in NPDR [68, 74, 75]. AOC3 is stored in intracellular vesicles and rapidly translocates to the luminal surface of endothelial cells during inflammation [76]. A soluble form of AOC3, which retains enzymatic activity, may also be released by shedding from the endothelial cell membrane following cleavage with matrix metalloproteinases (MMPs) (Fig. 1) [74]. AOC3 on the retinal endothelial cells mediates slow rolling, firm adhesion, and transmigration of leukocytes, triggering leukostasis [61, 77]. Aldehydes, ammonia, and reactive oxygen species are released as a result of the interaction between AOC3 and its substrates, which contribute to inflammation and the accumulation of leukocytes, which rupture the blood vessel leading to ischemia [76]. Although soluble AOC3 does not mediate leukostasis, it contributes to the release of ammonia and reactive oxygen species (Fig. 2). Elevated levels of soluble AOC3 are found in type 1 and type 2 DM, correlating with complications such as end-stage renal disease, cardiovascular mortality, and DR [76, 78]. Furthermore, high levels of soluble AOC3 are predictive of cancer risk in patients with type 2 DM [79].

Fig. 1
figure 1

Amine oxidase copper-containing 3 (AOC3) is stored in intracellular vesicles and rapidly translocates to the luminal surface of endothelial cells during inflammation. Matrix metalloproteinases (MMPs) release a proportion of membrane-bound AOC3 resulting in a soluble, truncated form. Both membrane-bound and soluble AOC3 are enzymatically active. RBC red blood cell

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Fig. 2
figure 2

When amine oxidase copper-containing 3 (AOC3) on the retinal endothelium binds to the AOC3 counter receptor on the leukocyte, aldehydes, ammonia, and reactive oxygen species are released, which contribute to inflammation. Leukostasis is triggered and leukocytes rupture the blood vessel leading to ischemia. Soluble AOC3 does not mediate leukostasis but contributes to the release of ammonia and reactive oxygen species. RBC red blood cell

Full size image

Inhibition and blocking of membrane-bound AOC3 were shown in preclinical models to reduce leukocyte recruitment and thereby transmigration [61, 80, 81]. A further consequence of reduced AOC3 enzymatic activity (of both full length and soluble forms) is a decrease in the oxidative deamination of primary amines, thus reducing the production of aldehydes, ammonia, and hydrogen peroxide [82], and ultimately reactive oxygen species (Fig. 3). Because the neurovascular unit of the retina is highly susceptible to hyperglycemic stress, inflammation, and reactive oxygen species, AOC3 inhibition may improve vascular function and lead to improved DRSS grading. Furthermore, leukocytes secrete proinflammatory cytokines, and therefore AOC3 blockade is predicted to reduce cytokine expression, macrophage recruitment, and choroidal neovascularization [81].

Fig. 3
figure 3

Amine oxidase copper-containing 3 (AOC3) inhibition of membrane-bound form reduces leukocyte recruitment and thereby transmigration. A further consequence of reduced AOC3 enzymatic activity via inhibition of the membrane-bound and soluble forms is likely to be a decrease in the oxidative deamination of primary amines, thus reducing the production of aldehydes, ammonia, and hydrogen peroxide, and ultimately reducing reactive oxygen species. Vascular endothelial growth factor (VEGF) inhibitors bind to the receptor-binding site on VEGF-A, which inhibits interaction with, and activation of, VEGF receptor 2 (VEGFR-2) on the surface of endothelial cells, thereby reducing angiogenesis. RBC red blood cell

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In addition, tissue ischemia and the resulting hypoxia in DR drive expression of VEGF-A [83]. VEGF-A promotes vascular permeability resulting in leakage of plasma through the blood-retinal barrier (BRB) and tissue edema through its interactions with VEGF receptor 2 (VEGFR-2) on vascular endothelial cells (Fig. 4) [83]. All currently available VEGF inhibitors bind to the receptor-binding site on VEGF-A, which inhibits interaction with, and activation of, VEGFR-2 on the surface of endothelial cells and, in turn, reduces angiogenesis, ultimately preventing progression and improving DRSS/ETDRS grading [84, 85]. Aflibercept and conbercept also act to scavenge placental growth factor (PIGF) [85, 86], which may lead to an increase in efficacy because PIGF can indirectly stimulate angiogenesis by binding to VEGFR-1, thus increasing the availability of VEGF-A to activate VEGFR-2 [84]. However, VEGF inhibitors do not reduce inflammation or reactive oxygen species (Fig. 3). Instead, they act on the consequence of the disease–elevated secretion of VEGF–without addressing the actual cause of the disease. Consequently, such treatments are unlikely to result in sustained improvements in DR as they are not expected to ameliorate the underlying hypoxia or ischemia.

Fig. 4
figure 4

Capillary obstruction due to leukostasis and capillary dropout due to death of vascular pericytes and endothelial cells lead to tissue ischemia. Resulting hypoxia may drive expression of vascular endothelial growth factor-A (VEGF-A). VEGF-A promotes vascular permeability resulting in leakage of plasma through the blood–retinal barrier (BRB) and tissue edema through its interactions with VEGF receptor 2 (VEGFR-2) on vascular endothelial cells. RBC red blood cell

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Therapeutic targeting of AOC3 in DR

To date, three orally administered AOC3 inhibitors have been investigated in DR and related conditions: ASP8232, RTU-1096, and BI 1467335 (formerly PXS-4728A) (Table 2) [87,88,89,90,91]. Given that DR shares aspects of its pathogenesis with related conditions, such as DME, success in these related indications may support potential efficacy in DR.

Table 2 Summary of AOC3 inhibitor preclinical and clinical findings in DR and DME
Full size table

Initial findings with ASP8232 were promising: pre-clinical studies demonstrated improved retinal and ocular hyperpermeability and reductions in surrogate markers of disease progression were observed in patients with type 2 DM [87, 88]. However, in the VIDI (VAP1 inhibition in DME) study, ASP8232 failed to reduce central subfield thickness in patients with CI-DME when administered alone, and no additional benefit was observed when combined with ranibizumab [87]. The trial investigators postulated that the presence of significant CI-DME may require inhibition of VEGF for clinical benefit, whereas DR could be reduced by AOC3 inhibition alone; they also suggested that alternative delivery modes may warrant further investigation [87]. It should be noted that, based on non-linear mixed effects exposure–response pharmacodynamic modeling, the effects of ASP8232 are reversible, and acute effects at clinical doses in other indications (i.e. diabetic kidney disease) may have been artefactual [92].

In a mouse model of retinal inflammation, systemic administration of RTU-1096 reduced upregulation of ICAM1, an adhesion molecule for leukocytes, in the retina [91]. In Phase 1 trials that completed in 2015, once-daily oral RTU-1096 was well tolerated at all tested doses and produced a sustained reduction in serum AOC3 in healthy male volunteers [93]. However, no trials of RTU-1096 in DR or any other indication are currently registered on ClinicalTrials.gov, and it is unclear why further development was halted.

BI 1467335 inhibits tethering and rolling of neutrophils and reduces inflammation in animal models [89, 90]. The Phase 2a ‘Randomized, double-masked, placebo-controlled exploratory study to evaluate safety, tolerability, pharmacodynamics, and pharmacokinetics of Orally administered BI 1467335 for 12 weeks with a 12 week follow up period in patients with Non-proliferative diabetic retinopathy without center-involved diabetic macular edema’ (ROBIN) study of BI 1467335 completed in May 2020 [94]. The study met its primary endpoint in ocular safety (proportion of patients with any ocular adverse event up to 24 weeks) and BI 1467335 was well tolerated [95]. However, the study was unable to demonstrate a clear efficacy signal (proportion of patients with a  ≥ 2-step improvement in DRSS [from baseline to Week 12]) [95]; this may have been because the trial’s duration (3 months) was too short to demonstrate a clear efficacy benefit. In addition, taking into account recent findings that suggest venous beading (VB) does not respond to treatment with anti-VEGF therapy in patients with NPDR [96], and that VB may differentiate ETDRS level 53 (severe NPDR) from ETDRS level 47 (moderately severe NPDR) in some patients [15], excluding patients with VB may have improved the efficacy signal in the ROBIN study. BI 1467335 was also being investigated in non-alcoholic steatohepatitis (NASH) [97]; the Phase 2a study met pre-specified targets for inhibiting plasma AOC3 activity compared with placebo and clinically relevant changes in NASH biomarkers [98]. However, based on the risk of drug–drug interactions with the compound in patients with NPDR and NASH, which were identified in another Phase 1 study [99], Boehringer Ingelheim announced that the development of BI 1467335 has been discontinued in both indications [95, 98].

Conclusion

There is substantial unmet need for convenient, non-invasive treatments targeting moderately severe and severe NPDR. By treating the underlying cause of DR rather than its manifestations, resulting improvements may be more sustained. Unlike existing therapies that only target inflammation or angiogenesis, AOC3 inhibition is predicted to reduce leukostasis and reactive oxygen species, ultimately addressing the underlying hypoxia and ischemia seen in DR. Despite recent setbacks in clinical trials, AOC3 inhibition remains an attractive target due to the strength of preclinical data supporting the mechanism of action. The levels of AOC3 inhibition in these trials are likely to have varied among the different agents, and alternative AOC3 inhibitors may be more successful in the future. An orally administered treatment based on either an established or novel mechanism may still be a promising therapeutic strategy for treating patients with DR, with the aim of reducing treatment burden and improving patient compliance.

Availability of data and materials

Not applicable.

Abbreviations

AOC3:

Amine oxidase copper-containing 3

BRB:

Blood–retinal barrier

CI-DME:

Center-involving diabetic macular edema

CKD:

Chronic kidney disease

CST:

Central subfield thickness

DDI:

Drug–drug interaction

DEX:

Dexamethasone

DM:

Diabetes mellitus

DME:

Diabetic macular edema

DR:

Diabetic retinopathy

DRSS:

Diabetic Retinopathy Severity Scale

ETDRS:

Early Treatment Diabetic Retinopathy Study

FA:

Fluocinolone acetonide

FDA:

Food and Drug Administration

ICAM1:

Intracellular adhesion molecule 1

IFN:

Interferon

IL:

Interleukin

IRMA:

Intraretinal microvascular abnormalities

IVT:

Intravitreal

MMP:

Matrix metalloproteinase

NASH:

Non-alcoholic steatohepatitis

NPDR:

Non-proliferative diabetic retinopathy

PDR:

Proliferative diabetic retinopathy

PIGF:

Placental growth factor

PRP:

Pan-retinal photocoagulation

RBC:

Red blood cell

TA:

Triamcinolone acetonide

TNF:

Tumor necrosis factor

VAP1:

Vascular adhesion protein 1

VB:

Venous beading

VCAM1:

Vascular cell adhesion molecule 1

VEGF:

Vascular endothelial growth factor

VEGFR:

Vascular endothelial growth factor receptor

References

  1. Solomon SD, Chew E, Duh EJ, Sobrin L, Sun JK, VanderBeek BL, et al. Diabetic retinopathy: A position statement by the American Diabetes Association. Diabetes Care. 2017;40:412–8.

    Article  PubMed  PubMed Central  Google Scholar 

  2. American Academy of Ophthalmology. What is diabetic retinopathy? 2020. https://www.aao.org/eye-health/diseases/what-is-diabetic-retinopathy. Accessed 25 Jan 2021.

  3. Antonetti DA, Klein R, Gardner TW. Diabetic retinopathy. N Engl J Med. 2012;366:1227–39.

    Article  CAS  PubMed  Google Scholar 

  4. Simo R, Stitt AW, Gardner TW. Neurodegeneration in diabetic retinopathy: Does it really matter? Diabetologia. 2018;61:1902–12.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Sun JK, Radwan SH, Soliman AZ, Lammer J, Lin MM, Prager SG, et al. Neural retinal disorganization as a robust marker of visual acuity in current and resolved diabetic macular edema. Diabetes. 2015;64:2560–70.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Schmidt-Erfurth U, Garcia-Arumi J, Bandello F, Berg K, Chakravarthy U, Gerendas BS, et al. Guidelines for the management of diabetic macular edema by the European Society of Retina Specialists (EURETINA). Ophthalmologica. 2017;237:185–222.

    Article  PubMed  Google Scholar 

  7. White NH, Waltman SR, Krupin T, Santiago JV. Reversal of abnormalities in ocular fluorophotometry in insulin-dependent diabetes after five to nine months of improved metabolic control. Diabetes. 1982;31:80–5.

    Article  CAS  PubMed  Google Scholar 

  8. Lee PP, Feldman ZW, Ostermann J, Brown DS, Sloan FA. Longitudinal rates of annual eye examinations of persons with diabetes and chronic eye diseases. Ophthalmology. 2003;110:1952–9.

    Article  PubMed  Google Scholar 

  9. Paz SH, Varma R, Klein R, Wu J, Azen SP. Noncompliance with vision care guidelines in Latinos with type 2 diabetes mellitus: The Los Angeles Latino Eye Study. Ophthalmology. 2006;113:1372–7.

    Article  PubMed  Google Scholar 

  10. Keenum Z, McGwin G Jr, Witherspoon CD, Haller JA, Clark ME, Owsley C. Patients’ adherence to recommended follow-up eye care after diabetic retinopathy screening in a publicly funded county clinic and factors associated with follow-up eye care use. JAMA Ophthalmol. 2016;134:1221–8.

    Article  PubMed  Google Scholar 

  11. American Academy of Ophthalmology Preferred Practice Pattern Retina/Vitreous Committee. Diabetic Retinopathy PPP 2019. 2019. https://www.aao.org/preferred-practice-pattern/diabetic-retinopathy-ppp. Accessed 25 Jan 2021.

  12. Ishibazawa A, Nagaoka T, Yokota H, Takahashi A, Omae T, Song YS, et al. Characteristics of retinal neovascularization in proliferative diabetic retinopathy imaged by optical coherence tomography angiography. Invest Ophthalmol Vis Sci. 2016;57:6247–55.

    Article  PubMed  Google Scholar 

  13. Duh EJ, Sun JK, Stitt AW. Diabetic retinopathy: current understanding, mechanisms, and treatment strategies. JCI Insight. 2017;2.

  14. Fundus photographic risk factors for progression of diabetic retinopathy. ETDRS report number 12. Early Treatment Diabetic Retinopathy Study Research Group. Ophthalmology. 1991;98:823–33.

  15. Wilkinson CP, Ferris FL 3rd, Klein RE, Lee PP, Agardh CD, Davis M, et al. Proposed international clinical diabetic retinopathy and diabetic macular edema disease severity scales. Ophthalmology. 2003;110:1677–82.

    Article  CAS  PubMed  Google Scholar 

  16. American Academy of Ophthalmology. International clinical diabetic retinopathy disease severity scale detailed table. 2002. http://www.icoph.org/dynamic/attachments/resources/diabetic-retinopathy-detail.pdf. Accessed 25 Jan 2021.

  17. Willis JR, Doan QV, Gleeson M, Haskova Z, Ramulu P, Morse L, et al. Vision-related functional burden of diabetic retinopathy across severity levels in the United States. JAMA Ophthalmol. 2017;135:926–32.

    Article  PubMed  PubMed Central  Google Scholar 

  18. PR Newswire. One-year results from positive phase 3 EYLEA trial in diabetic retinopathy presented at Angiogenesis Symposium. 2019. https://www.prnewswire.com/news-releases/one-year-results-from-positive-phase-3-eylea-trial-in-diabetic-retinopathy-presented-at-angiogenesis-symposium-300792822.html. Accessed 25 Jan 2021.

  19. Brown DM, Nguyen QD, Marcus DM, Boyer DS, Patel S, Feiner L, et al. Long-term outcomes of ranibizumab therapy for diabetic macular edema: The 36-month results from two phase III trials: RISE and RIDE. Ophthalmology. 2013;120:2013–22.

    Article  PubMed  Google Scholar 

  20. Evans JR, Michelessi M, Virgili G. Laser photocoagulation for proliferative diabetic retinopathy. Cochrane Database Syst Rev. 2014:Cd011234.

  21. Sun JK, Glassman AR, Beaulieu WT, Stockdale CR, Bressler NM, Flaxel C, et al. Rationale and application of the Protocol S anti-vascular endothelial growth factor algorithm for proliferative diabetic retinopathy. Ophthalmology. 2019;126:87–95.

    Article  PubMed  Google Scholar 

  22. Iwase T, Kobayashi M, Yamamoto K, Ra E, Terasaki H. Effects of photocoagulation on ocular blood flow in patients with severe non-proliferative diabetic retinopathy. PLoS ONE. 2017;12:e0174427.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. Royle P, Mistry H, Auguste P, Shyangdan D, Freeman K, Lois N, et al. Pan-retinal photocoagulation and other forms of laser treatment and drug therapies for non-proliferative diabetic retinopathy: Systematic review and economic evaluation. Health Technol Assess. 2015;19:v-xxviii, 1–247.

  24. Deschler EK, Sun JK, Silva PS. Side-effects and complications of laser treatment in diabetic retinal disease. Semin Ophthalmol. 2014;29:290–300.

    Article  PubMed  Google Scholar 

  25. Vaziri K, Schwartz SG, Relhan N, Kishor KS, Flynn HW Jr. New therapeutic approaches in diabetic retinopathy. Rev Diabet Stud. 2015;12:196–210.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Urbancic M, Gardasevic TI. Dexamethasone implant in the management of diabetic macular edema from clinician’s perspective. Clin Ophthalmol. 2019;13:829–40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Zur D, Iglicki M, Loewenstein A. The role of steroids in the management of diabetic macular edema. Ophthalmic Res. 2019:1–6.

  28. Campochiaro PA, Brown DM, Pearson A, Chen S, Boyer D, Ruiz-Moreno J, et al. Sustained delivery fluocinolone acetonide vitreous inserts provide benefit for at least 3 years in patients with diabetic macular edema. Ophthalmology. 2012;119:2125–32.

    Article  PubMed  Google Scholar 

  29. Boyer DS, Yoon YH, Belfort R Jr, Bandello F, Maturi RK, Augustin AJ, et al. Three-year, randomized, sham-controlled trial of dexamethasone intravitreal implant in patients with diabetic macular edema. Ophthalmology. 2014;121:1904–14.

    Article  PubMed  Google Scholar 

  30. Sassalos TM, Paulus YM. Prefilled syringes for intravitreal drug delivery. Clin Ophthalmol. 2019;13:701–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Brolucizumab MA. First approval. Drugs. 2019;79:1997–2000.

    Article  Google Scholar 

  32. NCT04278417. A 96-week, two-arm, randomized, single-masked, multi-center, phase III study assessing the efficacy and safety of brolucizumab 6 mg compared to panretinal photocoagulation laser in patients with proliferative diabetic retinopathy. https://clinicaltrials.gov/ct2/show/NCT04278417. Accessed 25 Jan 2021.

  33. NCT04079231. A comparative double masked, two-arm, randomized, multicenter, phase IIIb study analyzing the efficacy and safety of brolucizumab versus aflibercept in patients with visual impairment due to diabetic macular edema (BUZZARD). https://clinicaltrials.gov/ct2/show/NCT04079231. Accessed 25 Jan 2021.

  34. Bolinger MT, Antonetti DA. Moving past anti-VEGF: Novel therapies for treating diabetic retinopathy. Int J Mol Sci. 2016;17:pii: E1498.

  35. Zhao Y, Singh RP. The role of anti-vascular endothelial growth factor (anti-VEGF) in the management of proliferative diabetic retinopathy. Drugs Context. 2018;7:212532.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Sang DN, D’Amore PA. Is blockade of vascular endothelial growth factor beneficial for all types of diabetic retinopathy? Diabetologia. 2008;51:1570–3.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Wubben TJ, Johnson MW. Anti-VEGF therapy for diabetic retinopathy: Consequences of inadvertent treatment interruptions. Am J Ophthalmol. 2019;204:13–8.

    Article  CAS  PubMed  Google Scholar 

  38. Mirshahi A, Roohipoor R, Lashay A, Mohammadi SF, Abdoallahi A, Faghihi H. Bevacizumab-augmented retinal laser photocoagulation in proliferative diabetic retinopathy: A randomized double-masked clinical trial. Eur J Ophthalmol. 2008;18:263–9.

    Article  CAS  PubMed  Google Scholar 

  39. Dabir SS, Das D, Nallathambi J, Mangalesh S, Yadav NK, Schouten JS. Differential systemic gene expression profile in patients with diabetic macular edema: Responders versus nonresponders to standard treatment. Indian J Ophthalmol. 2014;62:66–73.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Kumluang S, Ingsrisawang L, Sangroongruangsri S, Chaikledkaew U, Ratanapakorn T, Ruamviboonsuk P, et al. A real-world study of effectiveness of intravitreal bevacizumab and ranibizumab injection for treating retinal diseases in Thailand. BMC Ophthalmol. 2019;19:82.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Bressler SB, Liu D, Glassman AR, Blodi BA, Castellarin AA, Jampol LM, et al. Change in diabetic retinopathy through 2 years: Secondary analysis of a randomized clinical trial comparing aflibercept, bevacizumab, and ranibizumab. JAMA Ophthalmol. 2017;135:558–68.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Whitehead M, Osborne A, Widdowson PS, Yu-Wai-Man P, Martin KR. Angiopoietins in diabetic retinopathy: Current understanding and therapeutic potential. J Diabetes Res. 2019;2019:5140521.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  43. Duan F, Liu Y, Chen X, Congdon N, Zhang J, Chen Q, et al. Influencing factors on compliance of timely visits among patients with proliferative diabetic retinopathy in southern China: A qualitative study. BMJ Open. 2017;7:e013578.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Chen AJ, Hwang V, Law PY, Stewart JM, Chao DL. Factors associated with non-compliance for diabetic retinopathy follow-up in an urban safety-net hospital. Ophthalmic Epidemiol. 2018;25:443–50.

    Article  PubMed  Google Scholar 

  45. Lu AJ, Chen AJ, Hwang V, Law PY, Stewart JM, Chao DL. Analysis of patient-reported barriers to diabetic retinopathy follow-up. Ophthalmic Surg Lasers Imaging Retina. 2019;50:99–105.

    Article  PubMed  Google Scholar 

  46. Weiss M, Sim DA, Herold T, Schumann RG, Liegl R, Kern C, et al. Compliance and adherence of patients with diabetic macular edema to intravitreal anti-vascular endothelial growth factor therapy in daily practice. Retina. 2018;38:2293–300.

    Article  CAS  PubMed  Google Scholar 

  47. Abu El-Asrar AM. Evolving strategies in the management of diabetic retinopathy. Middle East Afr J Ophthalmol. 2013;20:273–82.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Baker CW, Glassman AR, Beaulieu WT, Antoszyk AN, Browning DJ, Chalam KV, et al. Effect of initial management with aflibercept vs laser photocoagulation vs observation on vision loss among patients with diabetic macular edema involving the center of the macula and good visual acuity: A randomized clinical trial. JAMA. 2019;321:1880–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. American Diabetes Association. 5. Lifestyle management: Standards of medical care in diabetes—2019. Diabetes Care. 2019;42 Suppl 1:S46–60.

  50. Rubsam A, Parikh S, Fort PE. Role of inflammation in diabetic retinopathy. Int J Mol Sci. 2018;19.

  51. Boss JD, Singh PK, Pandya HK, Tosi J, Kim C, Tewari A, et al. Assessment of neurotrophins and inflammatory mediators in vitreous of patients with diabetic retinopathy. Invest Ophthalmol Vis Sci. 2017;58:5594–603.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Wu H, Hwang DK, Song X, Tao Y. Association between aqueous cytokines and diabetic retinopathy stage. J Ophthalmol. 2017;2017:9402198.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Chen W, Esselman WJ, Jump DB, Busik JV. Anti-inflammatory effect of docosahexaenoic acid on cytokine-induced adhesion molecule expression in human retinal vascular endothelial cells. Invest Ophthalmol Vis Sci. 2005;46:4342–7.

    Article  PubMed  Google Scholar 

  54. Whitcup SM, Cidlowski JA, Csaky KG, Ambati J. Pharmacology of corticosteroids for diabetic macular edema. Invest Ophthalmol Vis Sci. 2018;59:1–12.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Campochiaro PA, Hafiz G, Shah SM, Bloom S, Brown DM, Busquets M, et al. Sustained ocular delivery of fluocinolone acetonide by an intravitreal insert. Ophthalmology. 2010;117(1393–9):e3.

    Google Scholar 

  56. Pearson PA, Comstock TL, Ip M, Callanan D, Morse LS, Ashton P, et al. Fluocinolone acetonide intravitreal implant for diabetic macular edema: A 3-year multicenter, randomized, controlled clinical trial. Ophthalmology. 2011;118:1580–7.

    Article  PubMed  Google Scholar 

  57. Bressler NM, Edwards AR, Beck RW, Flaxel CJ, Glassman AR, Ip MS, et al. Exploratory analysis of diabetic retinopathy progression through 3 years in a randomized clinical trial that compares intravitreal triamcinolone acetonide with focal/grid photocoagulation. Arch Ophthalmol. 2009;127:1566–71.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Bressler SB, Qin H, Melia M, Bressler NM, Beck RW, Chan CK, et al. Exploratory analysis of the effect of intravitreal ranibizumab or triamcinolone on worsening of diabetic retinopathy in a randomized clinical trial. JAMA Ophthalmol. 2013;131:1033–40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Wykoff CC, Chakravarthy U, Campochiaro PA, Bailey C, Green K, Cunha-Vaz J. Long-term effects of intravitreal 0.19 mg fluocinolone acetonide implant on progression and regression of diabetic retinopathy. Ophthalmology. 2017;124:440–9.

    Article  PubMed  Google Scholar 

  60. Iglicki M, Zur D, Busch C, Okada M, Loewenstein A. Progression of diabetic retinopathy severity after treatment with dexamethasone implant: A 24-month cohort study the “DR-Pro-DEX Study.” Acta Diabetol. 2018;55:541–7.

    Article  CAS  PubMed  Google Scholar 

  61. Noda K, Nakao S, Zandi S, Engelstadter V, Mashima Y, Hafezi-Moghadam A. Vascular adhesion protein-1 regulates leukocyte transmigration rate in the retina during diabetes. Exp Eye Res. 2009;89:774–81.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Almulki L, Noda K, Nakao S, Hisatomi T, Thomas KL, Hafezi-Moghadam A. Localization of vascular adhesion protein-1 (VAP-1) in the human eye. Exp Eye Res. 2010;90:26–32.

    Article  CAS  PubMed  Google Scholar 

  63. Salmi M, Kalimo K, Jalkanen S. Induction and function of vascular adhesion protein-1 at sites of inflammation. J Exp Med. 1993;178:2255–60.

    Article  CAS  PubMed  Google Scholar 

  64. Boomsma F, van den Meiracker AH, Winkel S, Aanstoot HJ, Batstra MR, Man in 't Veld AJ, et al. Circulating semicarbazide-sensitive amine oxidase is raised both in type I (insulin-dependent), in type II (non-insulin-dependent) diabetes mellitus and even in childhood type I diabetes at first clinical diagnosis. Diabetologia. 1999;42:233–7.

  65. Boomsma F, Pedersen-Bjergaard U, Agerholm-Larsen B, Hut H, Dhamrait SS, Thorsteinsson B, et al. Association between plasma activities of semicarbazide-sensitive amine oxidase and angiotensin-converting enzyme in patients with type 1 diabetes mellitus. Diabetologia. 2005;48:1002–7.

    Article  CAS  PubMed  Google Scholar 

  66. Aalto K, Maksimow M, Juonala M, Viikari J, Jula A, Kahonen M, et al. Soluble vascular adhesion protein-1 correlates with cardiovascular risk factors and early atherosclerotic manifestations. Arterioscler Thromb Vasc Biol. 2012;32:523–32.

    Article  CAS  PubMed  Google Scholar 

  67. Garpenstrand H, Ekblom J, Backlund LB, Oreland L, Rosenqvist U. Elevated plasma semicarbazide-sensitive amine oxidase (SSAO) activity in type 2 diabetes mellitus complicated by retinopathy. Diabet Med. 1999;16:514–21.

    Article  CAS  PubMed  Google Scholar 

  68. Gronvall-Nordquist JL, Backlund LB, Garpenstrand H, Ekblom J, Landin B, Yu PH, et al. Follow-up of plasma semicarbazide-sensitive amine oxidase activity and retinopathy in type 2 diabetes mellitus. J Diabetes Complications. 2001;15:250–6.

    Article  CAS  PubMed  Google Scholar 

  69. Li HY, Lin HA, Nien FJ, Wu VC, Jiang YD, Chang TJ, et al. Serum vascular adhesion protein-1 predicts end-stage renal disease in patients with type 2 diabetes. PLoS ONE. 2016;11:e0147981.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  70. Dunkel P, Gelain A, Barlocco D, Haider N, Gyires K, Sperlagh B, et al. Semicarbazide-sensitive amine oxidase/vascular adhesion protein 1: Recent developments concerning substrates and inhibitors of a promising therapeutic target. Curr Med Chem. 2008;15:1827–39.

    Article  CAS  PubMed  Google Scholar 

  71. Smith DJ, Vainio PJ. Targeting vascular adhesion protein-1 to treat autoimmune and inflammatory diseases. Ann N Y Acad Sci. 2007;1110:382–8.

    Article  CAS  PubMed  Google Scholar 

  72. Bligt-Linden E, Pihlavisto M, Szatmari I, Otwinowski Z, Smith DJ, Lazar L, et al. Novel pyridazinone inhibitors for vascular adhesion protein-1 (VAP-1): Old target-new inhibition mode. J Med Chem. 2013;56:9837–48.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  73. Inoue T, Morita M, Tojo T, Nagashima A, Moritomo A, Imai K, et al. Synthesis and SAR study of new thiazole derivatives as vascular adhesion protein-1 (VAP-1) inhibitors for the treatment of diabetic macular edema: Part 2. Bioorg Med Chem. 2013;21:2478–94.

    Article  CAS  PubMed  Google Scholar 

  74. Murata M, Noda K, Fukuhara J, Kanda A, Kase S, Saito W, et al. Soluble vascular adhesion protein-1 accumulates in proliferative diabetic retinopathy. Invest Ophthalmol Vis Sci. 2012;53:4055–62.

    Article  CAS  PubMed  Google Scholar 

  75. O’Sullivan J, Unzeta M, Healy J, O’Sullivan MI, Davey G, Tipton KF. Semicarbazide-sensitive amine oxidases: Enzymes with quite a lot to do. Neurotoxicology. 2004;25:303–15.

    Article  CAS  PubMed  Google Scholar 

  76. Salmi M, Jalkanen S. Vascular adhesion protein-1: A cell surface amine oxidase in translation. Antioxid Redox Signal. 2019;30:314–32.

    Article  CAS  PubMed  Google Scholar 

  77. Stolen CM, Marttila-Ichihara F, Koskinen K, Yegutkin GG, Turja R, Bono P, et al. Absence of the endothelial oxidase AOC3 leads to abnormal leukocyte traffic in vivo. Immunity. 2005;22:105–15.

    Article  CAS  PubMed  Google Scholar 

  78. Yoshikawa N, Noda K, Shinoda H, Uchida A, Ozawa Y, Tsubota K, et al. Serum vascular adhesion protein-1 correlates with vascular endothelial growth factor in patients with type II diabetes. J Diabetes Complications. 2013;27:162–6.

    Article  PubMed  Google Scholar 

  79. Yu TY, Li HY, Jiang YD, Chang TJ, Wei JN, Lin CM, et al. Serum vascular adhesion protein-1 level predicts risk of incident cancers in subjects with type II diabetes. Cancer Epidemiol Biomarkers Prev. 2014;23:1366–73.

    Article  CAS  PubMed  Google Scholar 

  80. Merinen M, Irjala H, Salmi M, Jaakkola I, Hanninen A, Jalkanen S. Vascular adhesion protein-1 is involved in both acute and chronic inflammation in the mouse. Am J Pathol. 2005;166:793–800.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  81. Noda K, She H, Nakazawa T, Hisatomi T, Nakao S, Almulki L, et al. Vascular adhesion protein-1 blockade suppresses choroidal neovascularization. FASEB J. 2008;22:2928–35.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Murata M, Noda K, Kawasaki A, Yoshida S, Dong Y, Saito M, et al. Soluble vascular adhesion protein-1 mediates spermine oxidation as semicarbazide-sensitive amine oxidase: Possible role in proliferative diabetic retinopathy. Curr Eye Res. 2017;42:1674–83.

    Article  CAS  PubMed  Google Scholar 

  83. Penn JS, Madan A, Caldwell RB, Bartoli M, Caldwell RW, Hartnett ME. Vascular endothelial growth factor in eye disease. Prog Retin Eye Res. 2008;27:331–71.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. Nguyen QD, De Falco S, Behar-Cohen F, Lam WC, Li X, Reichhart N, et al. Placental growth factor and its potential role in diabetic retinopathy and other ocular neovascular diseases. Acta Ophthalmol. 2018;96:e1–9.

    Article  PubMed  Google Scholar 

  85. Papadopoulos N, Martin J, Ruan Q, Rafique A, Rosconi MP, Shi E, et al. Binding and neutralization of vascular endothelial growth factor (VEGF) and related ligands by VEGF Trap, ranibizumab and bevacizumab. Angiogenesis. 2012;15:171–85.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  86. Zhou AY, Bai YJ, Zhao M, Yu WZ, Li XX. KH902, a recombinant human VEGF receptor fusion protein, reduced the level of placental growth factor in alkali burn induced-corneal neovascularization. Ophthalmic Res. 2013;50:180–6.

    Article  CAS  PubMed  Google Scholar 

  87. Nguyen QD, Sepah YJ, Berger B, Brown D, Do DV, Garcia-Hernandez A, et al. Primary outcomes of the VIDI study: Phase 2, double-masked, randomized, active-controlled study of ASP8232 for diabetic macular edema. Int J Retina Vitreous. 2019;5:28.

    Article  PubMed  PubMed Central  Google Scholar 

  88. de Zeeuw D, Renfurm RW, Bakris G, Rossing P, Perkovic V, Hou FF, et al. Efficacy of a novel inhibitor of vascular adhesion protein-1 in reducing albuminuria in patients with diabetic kidney disease (ALBUM): A randomised, placebo-controlled, phase 2 trial. Lancet Diabetes Endocrinol. 2018;6:925–33.

    Article  PubMed  Google Scholar 

  89. Schilter HC, Collison A, Russo RC, Foot JS, Yow TT, Vieira AT, et al. Effects of an anti-inflammatory VAP-1/SSAO inhibitor, PXS-4728A, on pulmonary neutrophil migration. Respir Res. 2015;16:42.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  90. Jarnicki AG, Schilter H, Liu G, Wheeldon K, Essilfie AT, Foot JS, et al. The inhibitor of semicarbazide-sensitive amine oxidase, PXS-4728A, ameliorates key features of chronic obstructive pulmonary disease in a mouse model. Br J Pharmacol. 2016;173:3161–75.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  91. Matsuda T, Noda K, Murata M, Kawasaki A, Kanda A, Mashima Y, et al. Vascular adhesion protein-1 blockade suppresses ocular inflammation after retinal laser photocoagulation in mice. Invest Ophthalmol Vis Sci. 2017;58:3254–61.

    Article  CAS  PubMed  Google Scholar 

  92. Hoefman S, Snelder N, van Noort M, Garcia-Hernandez A, Onkels H, Larsson TE, et al. Mechanism-based modeling of the effect of a novel inhibitor of vascular adhesion protein-1 on albuminuria and renal function markers in patients with diabetic kidney disease. J Pharmacokinet Pharmacodyn. 2020. https://doi.org/10.1007/s10928-020-09716-x

    Article  PubMed  PubMed Central  Google Scholar 

  93. Business Wire. R-Tech Ueno: Announcement on completion of the phase I single-dose clinical trial for the novel VAP-1 inhibitor RTU-1096. 2015. https://www.businesswire.com/news/home/20150524005057/en/R-Tech-Ueno-Announcement-Completion-Phase-Single-Dose-Clinical. Accessed 25 Jan 2021.

  94. NCT03238963. A randomized, double-masked, placebo-controlled exploratory study to evaluate safety, tolerability, pharmacodynamics and pharmacokinetics of orally administered BI 1467335 for 12 weeks with a 12 week follow up period in patients with non-proliferative diabetic retinopathy without center-involved diabetic macular edema (ROBIN Study). https://clinicaltrials.gov/ct2/show/NCT03238963. Accessed 25 Jan 2021.

  95. Boehringer Ingelheim. Boehringer Ingelheim discontinues development of BI 1467335 for Diabetic Retinopathy. 2020. https://www.boehringer-ingelheim.com/press-release/discontinuation-bi-1467335-diabetic-retinopathy. Accessed 25 Jan 2021.

  96. Pearce E, Chong V, Sivaprasad S. Aflibercept reduces retinal hemorrhages and intravitreal microvascular abnormalities but not venous beading: secondary analysis of the CLARITY study. Ophthalmol Retina. 2020;4:689–94.

    Article  PubMed  Google Scholar 

  97. NCT03166735. A multi-centre, double-blind, parallel-group, randomised, placebo controlled phase II a study to investigate safety, tolerability, pharmacodynamics, and pharmacokinetics of different doses of orally administered BI 1467335 during a 12-week treatment period compared to placebo in patients with clinical evidence of NASH. https://clinicaltrials.gov/ct2/show/NCT03166735. Accessed 25 Jan 2021.

  98. Boehringer Ingelheim. Boehringer Ingelheim discontinues development of BI 1467335 for NASH. 2019. https://www.boehringer-ingelheim.us/press-release/boehringer-ingelheim-discontinues-development-bi-1467335-nash. Accessed 25 Jan 2021.

  99. NCT03927209. A phase I, open-label, positron emission tomography study in healthy male subjects to explore the inhibition of monoamine oxidase B in the brain after multiple oral doses of BI 1467335 (non-randomized, open-label, parallel-group study). https://clinicaltrials.gov/ct2/show/NCT03927209. Accessed 25 Jan 2021.

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Acknowledgements

The authors wish to acknowledge the contribution of Jochen Huber and Rolf Herrmann. Medical writing support was provided by Tom Priddle, DPhil, of OPEN Health Communications, funded by Boehringer Ingelheim.

Funding

Medical writing support was funded by Boehringer Ingelheim.

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Authors and Affiliations

  1. Retina-Vitreous Associates Medical Group, Los Angeles, CA, USA

    David S. Boyer

  2. CardioMetabolic Diseases Research, Boehringer Ingelheim Pharma, Biberach an der Riss, Germany

    Joerg F. Rippmann & Remko A. Bakker

  3. Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, USA

    Michael S. Ehrlich

  4. Boehringer Ingelheim International GmbH, Ingelheim Am Rhein, Germany

    Victor Chong

  5. Byers Eye Institute, Stanford University, Palo Alto, CA, USA

    Quan Dong Nguyen

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  1. David S. Boyer
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All authors were involved in planning, drafting, and reviewing the manuscript. All authors approved the final published version and take responsibility for the content of the manuscript. All authors read and approved the final manuscript.

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Competing interests

DB is a consultant with Acucela, Alimera Sciences, Allegro, Bayer, EyePoint Pharmaceuticals, ONL Therapeutics, Oxurion, and Takeda; is a consultant and researcher with Adverum, Aerpio Pharmaceuticals, Allergan, Apellis, Boehringer Ingelheim, Chengdu Kanghong, Clearside Biomedical, Genentech/Roche, Kodiak, Novartis, Regeneron, REGENXBIO, Roche, and Santen; and is a researcher with Aerie Pharmaceuticals, Gemini Therapeutics, Graybug Vision, IONIS Pharmaceuticals, Neurotech, Opthea, and Outlook Therapeutics. QDN serves on Scientific Advisory Boards for Aerie Pharmaceuticals, AsclepiX Therapeutics, EyePoint Pharmaceuticals, Bayer, Boehringer Ingelheim, Genentech/Roche, Regeneron, and Santen. QDN is also the Coordinating Investigator of the ROBIN Study. RAB, VC, MSE, and JFR are employees of Boehringer Ingelheim.

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Boyer, D.S., Rippmann, J.F., Ehrlich, M.S. et al. Amine oxidase copper-containing 3 (AOC3) inhibition: a potential novel target for the management of diabetic retinopathy. Int J Retin Vitr 7, 30 (2021). https://doi.org/10.1186/s40942-021-00288-7

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International Journal of Retina and Vitreous

ISSN: 2056-9920

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