Evidence map›Paper›PMID 42553109›Full record

ArticleFrontiers in endocrinology2026

Systemic factors associated with poor anatomical response to anti-VEGF therapy in patients with diabetic macular edema: evidence from a large clinical cohort.

Xinru Jia, Yan Shi, Mengxiang He, Dongwei Yao, Chengfei Lin

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Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xinru JiaDepartment of Ophthalmology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Yan ShiDepartment of Ophthalmology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Mengxiang HeNingbo Haishu Taixue Eye Clinic, Ningbo, Zhejiang, China.
Dongwei YaoDepartment of Ophthalmology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Chengfei LinDepartment of Ophthalmology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Diabetic macular edema (DME) is a leading cause of vision impairment in the working-age population worldwide. Although intravitreal anti-vascular endothelial growth factor (anti-VEGF) therapy represents the established first-line treatment, a substantial proportion of patients exhibit inadequate anatomical responses. This retrospective cohort study aimed to identify independent systemic factors associated with poor anatomical response to intravitreal Conbercept in patients with DME. Methods: In this retrospective cohort study, 1,039 eyes from 691 patients with DME were analyzed. All patients underwent a standardized loading phase of intravitreal Conbercept (0.5 mg) administered monthly for three consecutive months. The primary outcome was the absolute and percentage change in central macular thickness (CMT) from baseline to one month after the third injection. Eyes achieving a percentage reduction in CMT exceeding 10% from baseline were classified as "responders." Generalized Estimating Equation (GEE) models were employed to identify independent factors while accounting for the intra-subject correlation between bilateral eyes. Results: Following the three-month Conbercept loading phase, the median CMT decreased significantly from 325.00 μm (IQR: 281.00-448.00 μm) at baseline to 291.00 μm (IQR: 268.00-334.00 μm) at the three-month follow-up, representing a median absolute reduction of 17.00 μm (P < 0.001). Concurrently, median best-corrected visual acuity (BCVA) improved from 0.30 (IQR: 0.15-0.50) to 0.40 (IQR: 0.25-0.50) (P < 0.001). Based on the responder criterion, 431 eyes (41.48%) were classified as responders and 608 eyes (58.52%) as non-responders. In the multivariable linear GEE model, baseline CMT, baseline BCVA, LDL-C, fasting blood glucose, and HbA1c were independently associated with degree of CMT reduction. In the multivariable logistic GEE model, lower baseline CMT (Estimate = -0.008, P < 0.001), higher baseline BCVA (Estimate = 5.274, P < 0.001), elevated fasting blood glucose (Estimate = 0.048, P = 0.030), and elevated HbA1c (Estimate = 0.192, P < 0.001) were independently associated with poor anatomical response. Conclusion: Systemic metabolic status-particularly HbA1c and fasting glucose levels-and baseline ocular morphology are independently associated with of anatomical response to intravitreal Conbercept in DME. These findings highlight the clinical imperative for integrating systemic metabolic optimization into the management strategy for DME patients prior to and during anti-VEGF loading therapy.

Indexed as

Angiogenesis InhibitorsDiabetic RetinopathyMacular EdemaRecombinant Fusion ProteinsVascular Endothelial Growth Factor AAgedFemaleFollow-Up StudiesHumansIntravitreal InjectionsMaleMiddle AgedRetrospective StudiesTreatment OutcomeVisual AcuityAngiogenesis InhibitorsKH902 fusion proteinRecombinant Fusion ProteinsVascular Endothelial Growth Factor Aanti-VEGFcentral macular thicknessconberceptdiabetic macular edemageneralized estimating equationHbA1c

Identifiers

PMID42553109
PMCPMC13433187

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.