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METformin for the MINimization of Geographic Atrophy Progression (METforMIN): A Randomized Trial.
Shen, Liangbo Linus; Keenan, Jeremy D; Chahal, Noor; Taha, Abu Tahir; Saroya, Jasmeet; Ma, Chu Jian; Sun, Mengyuan; Yang, Daphne; Psaras, Catherine; Callander, Jacquelyn; Flaxel, Christina; Fawzi, Amani A; Schlesinger, Thomas K; Wong, Robert W; Bryan Leung, Loh-Shan; Eaton, Alexander M; Steinle, Nathan C; Telander, David G; Afshar, Armin R; Neuwelt, Melissa D; Lim, Jennifer I; Yiu, Glenn C; Stewart, Jay M.
Afiliação
  • Shen LL; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Keenan JD; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Chahal N; Francis I. Proctor Foundation for Research in Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Taha AT; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Saroya J; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Ma CJ; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Sun M; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Yang D; Institute of Cardiovascular Diseases, Gladstone Institute, San Francisco, California.
  • Psaras C; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Callander J; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Flaxel C; Department of Otolaryngology-Head and Neck Surgery, University of California, San Francisco, San Francisco, California.
  • Fawzi AA; Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University, Portland, Oregon.
  • Schlesinger TK; Department of Ophthalmology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
  • Wong RW; North Bay Vitreoretinal Consultants, Santa Rosa, California.
  • Bryan Leung LS; Austin Retina Associates, Austin, Texas.
  • Eaton AM; Department of Ophthalmology, Stanford University School of Medicine, Palo Alto, California.
  • Steinle NC; Retina Health Center, Fort Myers, Florida.
  • Telander DG; California Retina Consultants, Santa Barbara, California.
  • Afshar AR; Retinal Consultants Medical Group, Sacramento, California.
  • Neuwelt MD; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Lim JI; Department of Ophthalmology, University of California, San Francisco, San Francisco, California.
  • Yiu GC; Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois.
  • Stewart JM; Department of Ophthalmology & Visual Sciences, UC Davis Medical Center, Sacramento, California.
Ophthalmol Sci ; 4(3): 100440, 2024.
Article em En | MEDLINE | ID: mdl-38284098
ABSTRACT

Purpose:

Metformin use has been associated with a decreased risk of age-related macular degeneration (AMD) progression in observational studies. We aimed to evaluate the efficacy of oral metformin for slowing geographic atrophy (GA) progression.

Design:

Parallel-group, multicenter, randomized phase II clinical trial.

Participants:

Participants aged ≥ 55 years without diabetes who had GA from atrophic AMD in ≥ 1 eye.

Methods:

We enrolled participants across 12 clinical centers and randomized participants in a 11 ratio to receive oral metformin (2000 mg daily) or observation for 18 months. Fundus autofluorescence imaging was obtained at baseline and every 6 months. Main Outcome

Measures:

The primary efficacy endpoint was the annualized enlargement rate of the square root-transformed GA area. Secondary endpoints included best-corrected visual acuity (BCVA) and low luminance visual acuity (LLVA) at each visit.

Results:

Of 66 enrolled participants, 34 (57 eyes) were randomized to the observation group and 32 (53 eyes) were randomized to the treatment group. The median follow-up duration was 13.9 and 12.6 months in the observation and metformin groups, respectively. The mean ± standard error annualized enlargement rate of square root transformed GA area was 0.35 ± 0.04 mm/year in the observation group and 0.42 ± 0.04 mm/year in the treatment group (risk difference = 0.07 mm/year, 95% confidence interval = -0.05 to 0.18 mm/year; P = 0.26). The mean ± standard error decline in BCVA was 4.8 ± 1.7 letters/year in the observation group and 3.4 ± 1.1 letters/year in the treatment group (P = 0.56). The mean ± standard error decline in LLVA was 7.3 ± 2.5 letters/year in the observation group and 0.8 ± 2.2 letters/year in the treatment group (P = 0.06). Fourteen participants in the metformin group experienced nonserious adverse events related to metformin, with gastrointestinal side effects as the most common. No serious adverse events were attributed to metformin.

Conclusions:

The results of this trial as conducted do not support oral metformin having effects on reducing the progression of GA. Additional placebo-controlled trials are needed to explore the role of metformin for AMD, especially for earlier stages of the disease. Financial Disclosures Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies Idioma: En Revista: Ophthalmol Sci Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies Idioma: En Revista: Ophthalmol Sci Ano de publicação: 2024 Tipo de documento: Article