Evidence map›Paper›PMID 24921653›Full record

ArticleThe Journal of clinical endocrinology and metabolism2014

Differing effects of metformin on glycemic control by race-ethnicity.

L Keoki Williams, Badri Padhukasahasram, Brian K Ahmedani, Edward L Peterson, Karen E Wells, Esteban González Burchard, David E Lanfear

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Genetic Variants inDiabetes · 2018
    Trial
  5. Trial
  6. Trial
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Breaking down silos: the multifaceted nature of obesity and the future of weight management.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Precision Medicine in Diabetes.Handbook of experimental pharmacology · 2023
    Article
  18. Updates of precision medicine in type 2 diabetes.Cambridge prisms. Precision medicine · 2023
    Review
  19. "The obesity pandemic" in the COVID-19 pandemic - new treatment for an old problem.Pediatric endocrinology, diabetes, and metabolism · 2023
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

L Keoki WilliamsCenter for Health Policy and Health Services Research (L.K.W., B.P., B.K.A., D.E.L.), Department of Internal Medicine (L.K.W., D.E.L.), Department of Public Health Sciences (E.L.P., K.E.W.), Henry Ford Health System, Detroit, Michigan 48202; and Departments of Medicine (E.G.B.) and Bioengineering and Therapeutic Sciences (E.G.B.), University of California, San Francisco, San Francisco, California 94143.
Badri Padhukasahasram
Brian K Ahmedani
Edward L Peterson
Karen E Wells
Esteban González Burchard
David E Lanfear
Henry Ford Health System · USUniversity of California, San Francisco · US

Funding

PHARMACOGENOMICS OF INHALED CORTICOSTEROID RESPONSIVENESS IN PATIENTS WITH ASTHMAR01AI079139 · NIAID · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2009 to 2013
$3.9M
Impact of Race and Genetic Factors on Beta-blocker Effectiveness in Heart FailureR01HL103871 · NHLBI · HENRY FORD HEALTH SYSTEM · PI LANFEAR, DAVID E · 2011 to 2015
$3.5M
Leveraging electronic medical records to perform large-scale diabetes pharmacogenomics among ancestrally diverse patient populationsR01DK113003 · NIDDK · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2017 to 2021
$3.2M
Combined Transcriptomics and Genomics to Find Asthma Genes in Admixed PopulationsR01HL118267 · NHLBI · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2014 to 2017
$2.9M
VALIDATION OF ADHERENCE DATA--USE IN CLINICAL PRACTICER01DK064695 · NIDDK · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2003 to 2010
$2.7M
USING INFORMATION TECHNOLOGY TO IMPROVE ASTHMA ADHERENCER01HL079055 · NHLBI · HENRY FORD HEALTH SYSTEM · PI WILLIAMS, KEOKI · 2005 to 2008
$1.4M
Pharmacogenetics of the B-type Natriuretic Peptide PathwayK23HL085124 · NHLBI · HENRY FORD HEALTH SYSTEM · PI LANFEAR, DAVID E · 2008 to 2012
$632k
NHLBI NIH HHS K23 HL085124NHLBI NIH HHS K23HL085124NHLBI NIH HHS R01 HL079055NHLBI NIH HHS R01HL079055NHLBI NIH HHS R01 HL103871NHLBI NIH HHS R01HL103871NHLBI NIH HHS R01 HL118267NHLBI NIH HHS R01HL118267NIAID NIH HHS R01 AI079139NIAID NIH HHS R01AI079139NIDDK NIH HHS R01 DK064695NIDDK NIH HHS R01DK064695NIDDK NIH HHS R01 DK113003
6 · The paper itself

Abstract

contextMetformin is considered first-line treatment for type 2 diabetes mellitus. However, little is known about its effects in African American individuals.

objectiveThe objective of the study was to assess whether metformin's effect on glycemic control differs by race-ethnicity Design: Electronic health records were used to identify adults who had a diagnosis of diabetes, two or more fills of metformin, and two or more glycated hemoglobin (HbA1c) measurements. Pharmacy claims were used to estimate metformin exposure based on fill frequency and dose dispensed. Regression analyses modeled the relationship between metformin exposure and HbA1c levels. Analyses were stratified by race-ethnicity and baseline HbA1c values.

settingThe study was conducted at a large health system in southeast Michigan.

main outcome measureDifferences in HbA1c levels while on metformin were measured.

resultsWe identified 19 672 patients with diabetes taking metformin; 7429 were African American and 8783 were European American. Baseline HbA1c values in these two groups were 7.81% (61.8 mmol/mol) and 7.38% (57.1 mmol/mol), respectively. Compared with no use, metformin was associated with a 0.62% (6.8 mmol/mol) reduction in HbA1c; however, there was a significant difference by race-ethnicity (P < .001). Among African American individuals, metformin use was associated with a 0.90% (9.8 mmol/mol) reduction in HbA1c levels, whereas among European Americans, metformin was associated with a 0.42% (4.6 mmol/mol) reduction. Irrespective of baseline HbA1c, metformin use was associated with lower HbA1c levels in African American individuals.

conclusionsAfrican American individuals appear to have a better glycemic response to metformin when compared with European Americans. Further studies are needed to determine whether this translates to commensurate reductions in diabetes complications.

Indexed as

Black or African AmericanAdultAgedDiabetes Mellitus, Type 2Electronic Health RecordsFemaleGlycated HemoglobinGlycemic IndexHumansHyperglycemiaHypoglycemic AgentsMaleMetforminMiddle AgedWhite PeopleGlycated Hemoglobinhemoglobin A1c protein, humanHypoglycemic AgentsMetformin

Identifiers

PMID24921653
PMCPMC4154100
OpenAlexW2152817207

What OpenQuestion holds

Texttitle and abstract
Read underepoch 390

Registered trials

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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.