Evidence map›Paper›PMID 39371179›Full record

ArticlemedRxiv : the preprint server for health sciences2024

No Increased Risk of Major Adverse Cardiovascular Events following Nicotinamide Exposure.

Lee Wheless, Ranya Guennoun, Basia Michalski-McNeely, Katlyn M Gonzalez, Rachel Weiss, Siwei Zhang, Lydia Yao, Chris Madden, Hua-Chang Chen, Jefferson L Triozzi and 8 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Lee WhelessTennessee Valley Healthcare System VA Medical Center, Vanderbilt University Medical Center.ORCID 0000-0002-8162-5971
Ranya GuennounWashington University in St. Louis, Department of Medicine, Division of Dermatology.
Basia Michalski-McNeelyWashington University in St. Louis, Department of Medicine, Division of Dermatology.
Katlyn M GonzalezVanderbilt University School of Medicine.
Rachel WeissDepartments of Dermatology.
Siwei ZhangVanderbilt University Medical Center Department of Biostatistics.
Lydia YaoVanderbilt University Medical Center Department of Biostatistics.
Chris MaddenState University of New York Downstate College of Medicine.
Hua-Chang ChenVanderbilt University Medical Center Department of Biostatistics.
Jefferson L TriozziVanderbilt University Medical Center Department of Medicine, Division of Nephrology and Hypertension.
Ran TaoVanderbilt University Medical Center Department of Biostatistics.
Otis WilsonTennessee Valley Healthcare System VA Medical Center, Vanderbilt University Medical Center.
Quinn S WellsVanderbilt University Medical Center Department of Medicine, Division of Cardiovascular Medicine.
Adriana HungTennessee Valley Healthcare System VA Medical Center, Vanderbilt University Medical Center.
Kristin BibeeUniversity of Virginia School of Medicine Department of Dermatology.
Rebecca I HartmanVA Boston Healthcare System.
Yaomin XuVanderbilt University Medical Center Department of Biostatistics.ORCID 0000-0002-3752-4006
VA Million Veteran Program

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Identifying clinical and genetic factors for risk of multiple skin cancers in organ transplant recipientsIK2CX002452 · VA · VETERANS HEALTH ADMINISTRATION · PI LEE E WHELESS · 2023 to 2026
–
Risk Factors for Clinically Aggressive Melanoma in VeteransIK2CX002531 · VA · VA BOSTON HEALTH CARE SYSTEM · PI Rebecca Ivy Hartman · 2024 to 2026
–
CSRD VA I01 CX001897CSRD VA IK2 CX002452CSRD VA IK2 CX002531NCATS NIH HHS UL1 TR002243
6 · The paper itself

Abstract

importanceNicotinamide metabolites have recently been implicated in increased risk of major cardiovascular events (MACE). Supportive data about clinical risk of MACE for nicotinamide users is lacking.

objectiveTo determine whether nicotinamide use results in an increase of MACE. DESIGN SETTING

participantsRetrospective cohort study of two patient cohorts, Vanderbilt University Medical Center (VUMC) and Military Veteran Program (MVP). The risk of MACE in patients exposed to nicotinamide was compared to the risk of MACE in unexposed patients. In the VUMC cohort, 1228 patients were exposed to nicotinamide based on keyword entry for "nicotinamide" or "niacinamide" and hand-review of charts, while 253 were unexposed but had documented recommendation for use. In the MVP cohort, there were 1594 with exposure to nicotinamide propensity score matched to 2694 without exposure. EXPOSURES: The primary exposure for the VUMC cohort was a confirmed exposure to nicotinamide in chart review. The primary exposure for the MVP cohort was medication entry for "nicotinamide" or "niacinamide". MAIN OUTCOMES AND MEASURES: The primary outcome was development of MACE based on a validated phenotype.

resultsBetween both cohorts, 6039 patients were included, of whom 5125 were male with a mean age of 63.2 years. Neither cohort had significant differences in mean age, sex, race and ethnicity between the nicotinamide exposed and unexposed groups. In the VUMC cohort, there was no significant association between nicotinamide exposure and the primary outcome of MACE (HR 0.76, 95% CI 0.46 - 1.25, p = 0.28). MACE prior to nicotinamide exposure was strongly associated with subsequent MACE (HR 9.01, 95% CI 5.90 - 13.70, p < 0.001). In the MVP cohort, we adjusted for MACE risk factors as potential confounding variables and saw no significant association between nicotinamide exposure and MACE (HR 1.00 95% CI 0.75 - 1.32), while history of prior MACE remained strongly associated with subsequent MACE (HR 9.50, 95% CI 6.38 - 14.1). CONCLUSIONS AND RELEVANCE: In this retrospective cohort study of 6039 adults from two different patient populations, we found no increased risk of MACE in patients with nicotinamide exposure.

Indexed as

cohort studyepidemiologymajor adverse cardiovascular eventsnicotinamideskin cancer

Identifiers

PMID39371179
PMCPMC11451707

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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.