Association of plasma metabolites with treatment response after intravitreal anti-vascular endothelial growth factor injections in treatment-naïve neovascular age-related macular degeneration.

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Tác giả: Rodrigo A Alvarez, Augustine Bannerman, Roshni Bhat, Hanna Choi, Deeba Husain, Hae Min Kang, Raviv Katz, Ivana K Kim, Georgiy Kozak, Inês Laíns, Jessica Lasky-Su, Liming Liang, Kevin M Mendez, Joan W Miller, John B Miller, Archana Nigalye, Krupa Sourirajan, Demetrios G Vavvas, David Wu

Ngôn ngữ: eng

Ký hiệu phân loại: 629.13334 Aerospace engineering

Thông tin xuất bản: England : BMJ open ophthalmology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 718818

BACKGROUND/AIMS: To investigate the association between plasma metabolomic profiles and treatment response after intravitreal anti-vascular endothelial growth factor (VEGF) injections in treatment-naïve neovascular age-related macular degeneration (nAMD). METHODS: This is part of a prospective longitudinal study that included patients with treatment-naïve nAMD who have undergone three loading intravitreal anti-VEGF injections. All patients underwent ophthalmological examinations including spectral domain optical coherence tomography (SD OCT). Fasting blood samples were collected at the time of study enrolment (not to first anti-VEGF injection) and metabolomic profiling was conducted using ultra-performance liquid chromatography-mass spectrometry. Treatment response was defined as no evidence of any subretinal and intraretinal fluid on SD OCT 4-6 weeks after the third injection. Multilevel mixed-effects linear modelling was used to assess associations between plasma metabolites and treatment response. Multiple comparisons were accounted for using the effective number of tests to explain 80% of the variance (ENT80), with a p value threshold of 0.0017. RESULTS: We included 131 eyes of 101 patients, and 69 patients (68.3%) were female. 51 eyes (38.9%) were treatment responders. Taurodeoxycholate (TDCA) was the only plasma metabolite significantly associated with treatment response (β=1.6, ENT80=0.001). CONCLUSION: In our study, TDCA was the most significant plasma metabolite associated with treatment response after three-loading dose of anti-VEGF therapy in patients with nAMD. Bile acids may have a beneficial impact on treatment response in nAMD through their neuroprotective property. Plasma metabolites may be used as biomarkers to predict responses to initial anti-VEGF therapy in patients with nAMD, providing a more individualised treatment plan.
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