Evidence map›Paper›PMID 40225410›Full record

ArticleOphthalmology science

Exploring the Causal Relationships between Lipid Biomarkers and Anti-VEGF Treatment Response in Patients with Neovascular Age-related Macular Degeneration.

Feixiang He, Qifang Chen, Peilin Gu, Xuemei Liu, Yinglian Chen, Ting Liu, Chongyi Li

Abstract read
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Article in Ophthalmology science. 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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2 · The registry

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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

7 authors.

Feixiang HeDepartment of Ophthalmology, Daping Hospital, Third Military Medical University, Chongqing, China.
Qifang ChenDepartment of Ophthalmology, Daping Hospital, Third Military Medical University, Chongqing, China.
Peilin GuDepartment of Ophthalmology, Daping Hospital, Third Military Medical University, Chongqing, China.
Xuemei LiuDepartment of Ophthalmology, Daping Hospital, Third Military Medical University, Chongqing, China.
Yinglian ChenWestern Institution of Health Data Science, Chongqing, China.
Ting LiuDepartment of Ophthalmology, Daping Hospital, Third Military Medical University, Chongqing, China.
Chongyi LiDepartment of Ophthalmology, Daping Hospital, Third Military Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To identify the connections between lipid biomarkers and the anti-VEGF therapy response in patients with neovascular age-related macular degeneration (nAMD). Design: A bidirectional and multivariable Mendelian randomization study. Participants: The summary statistics for anti-VEGF nAMD treatment response included a total of 128 responders, 51 nonresponders, and 6 908 005 genetic variants available for analysis. The sample size of lipid biomarkers is 441 016 and 12 321 875 genetic variants available for analysis. Methods: Two-sample Mendelian randomization (MR) method was conducted to exhaustively appraise the causalities among 13 lipid biomarkers and the risk of different anti-VEGF treatment responses (including visual acuity [VA] and central retinal thickness [CRT]) for nAMD subtypes. Main Outcome Measures: Thirteen lipid biomarkers, VA, and CRT. Results: A positive causal relationship was identified between triglycerides (TGs), apolipoproteins (Apos) E2, ApoE3, total cholesterol (TC), and VA response to anti-VEGF therapy in patients with nAMD, as confirmed by MR-Egger, weighted median, and weighted mode models. The MR-Egger model yielded statistically significant results for TC, ApoA-I, ApoB, and ApoA-V in relation to the CRT response to anti-VEGF treatment in patients with nAMD. In the reverse MR, the MR-Egger model identified significant causal relationships between ApoA-I, low-density lipoprotein cholesterol (LDL-c), ApoE3, and ApoF and the VA response. However, this was not the case in the weighted median and weighted mode models. In the MR-Egger model, ApoB, LDL-c, ApoE3, and ApoM were identified as significantly influencing the CRT response. In the multisample MR analysis, TC, high-density lipoprotein cholesterol, LDL-c, and TG were found to be causally related to VA response, and TC was also identified as being causally related to the CRT response to anti-VEGF therapy in patients with nAMD. Conclusions: This MR study suggests unidirectional causality between TG and ApoE3 and the response to anti-VEGF treatment in patients with nAMD. Financial Disclosures: The author(s) have no proprietary or commercial interest in any materials discussed in this article.

Indexed as

Cause-and-effectLipid biomarkersMendelian randomizationNeovascular age-related macular degeneration

Identifiers

PMID40225410
PMCPMC11986618

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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.