AI Article Synopsis

  • Anti-VEGF treatment for neovascular age-related macular degeneration has been effective since its FDA approval in 2004, helping many patients maintain their vision, but responses vary widely, highlighting a need for genetic biomarkers to differentiate treatment outcomes.
  • A study involving 179 treatment-naïve patients showed that while traditional measures like visual acuity could classify many as responders or non-responders, some non-responders still exhibited changes in retinal thickness, indicating potential treatment response that isn't captured by current criteria.
  • Genome-wide association studies aimed at identifying genetic factors influencing treatment response yielded no significant results, pointing to the necessity for larger studies (over 15,000 patients) to better understand anti-VEGF treatment efficacy in n

Article Abstract

Anti-VEGF treatment for neovascular age-related macular degeneration (nAMD) has been FDA-approved in 2004, and since then has helped tens of thousands of patients worldwide to preserve vision. Still, treatment responses vary widely, emphasizing the need for genetic biomarkers to robustly separate responders from non-responders. Here, we report the findings of an observational study compromising 179 treatment-naïve nAMD patients and their reaction to treatment after three monthly doses of anti-VEGF antibodies. We show that established criteria of treatment response such as visual acuity and central retinal thickness successfully divides our cohort into 128 responders and 51 non-responders. Nevertheless, retinal thickness around the fovea revealed significant reaction to treatment even in the formally categorized non-responders. To elucidate genetic effects underlying our criteria, we conducted an undirected genome-wide association study followed by a directed replication study of 30 previously reported genetic variants. Remarkably, both approaches failed to result in significant findings, suggesting study-specific effects were confounding the present and previous discovery studies. Of note, all studies so far are greatly underpowered, hampering interpretation of genetic findings. In consequence, we highlight the need for an extensive phenotyping study with sample sizes exceeding at least 15,000 to reliably assess anti-VEGF treatment responses in nAMD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9181567PMC
http://dx.doi.org/10.3390/ijms23116094DOI Listing

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