Evidence map›Paper›PMID 29032853›Full record

Trial reportOphthalmology2018

Genetic Polymorphisms of CFH and ARMS2 Do Not Predict Response to Antioxidants and Zinc in Patients with Age-Related Macular Degeneration: Independent Statistical Evaluations of Data from the Age-Related Eye Disease Study.

Melissa J Assel, Fan Li, Ying Wang, Andrew S Allen, Keith A Baggerly, Andrew J Vickers

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Ophthalmology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Proceedings of the National Academy of Sciences of the United States of America · 2018
    Trial
  4. Review
  5. Review
  6. Review
  7. Current Management of Age-Related Macular Degeneration.Advances in experimental medicine and biology · 2021
    Article
  8. Current Management of Age-Related Macular Degeneration.Advances in experimental medicine and biology · 2021
    Article
  9. Article
  10. Zinc and Autophagy in Age-Related Macular Degeneration.International journal of molecular sciences · 2020
    Review
  11. Article
  12. Reply.Ophthalmology · 2020
    Article
  13. Review
  14. Article
  15. Article
  16. Pharmacogenomics of antioxidant supplementation to prevent age-related macular degeneration.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Melissa J AsselDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Fan LiDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.
Ying WangDepartment of Bioinformatics and Computational Biology, MD Anderson Cancer Center, Houston, Texas.
Andrew S AllenDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.
Keith A BaggerlyDepartment of Bioinformatics and Computational Biology, MD Anderson Cancer Center, Houston, Texas.
Andrew J VickersDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: vickersa@mskcc.org.
Duke University · USMemorial Sloan Kettering Cancer Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeConsiderable controversy has erupted in recent years regarding whether genotyping should be part of standard care for patients with age-related macular degeneration (AMD) who are being considered for treatment with antioxidants and zinc. We aimed to determine whether genotype predicts response to supplements in AMD.

designThree separate statistical teams reanalyzed data derived from the Age-Related Eye Disease Study (AREDS), receiving data prepared by the AREDS investigators and, separately, data from investigators reporting findings that support the use of genotyping.

participantsThe population of interest was AREDS participants with AMD worse than category 1 and genotyping data available. Data from the 2 groups overlap imperfectly with respect to measurements made: the largest common set involved 879 participants for whom the same CFH and ARMS2 single nucleotide polymorphisms were measured by both groups.

methodsEach team took a separate but complementary approach. One team focused on data concordance between conflicting studies. A second team focused on replicating the key claim of an interaction between genotype and treatment. The third team took a blank slate approach in attempting to find baseline predictors of treatment response.

main outcome measuresProgression to advanced AMD.

resultsWe found errors in the data used to support the initial claim of genotype-treatment interaction. Although we found evidence that high-risk patients had more to gain from treatment, we were unable to replicate any genotype-treatment interactions after adjusting for multiple testing. We tested 1 genotype claim on an independent set of data, with negative results. Even if we assumed that interactions in fact did exist, we did not find evidence to support the claim that supplementation leads to a large increase in the risk of advanced AMD in some genotype subgroups.

conclusionsPatients who meet criteria for supplements to prevent AMD progression should be offered zinc and antioxidants without consideration of genotype.

Indexed as

Polymorphism, Single NucleotideAgedAllelesAntioxidantsComplement Factor HDietary SupplementsDisease ProgressionDNAFemaleGenotypeHumansMacular DegenerationMalePrognosisProteinsZincAntioxidantsARMS2 protein, humanComplement Factor HDNAProteinsZinc

Identifiers

PMID29032853
PMCPMC5820191
OpenAlexW2763231046

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.