Evidence mapPaperPMID 42210161Full record

ArticleBMC cardiovascular disorders2026

Serum free fatty acids and progression of coronary artery calcification: sex specific findings from a large U.S. cohort study.

Azra Ramezankhani, Farzad Hadaegh, Farzad Esmaeili

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Article in BMC cardiovascular disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Azra RamezankhaniPrevention of Metabolic Disorders Research Center, Research Institute for Metabolic and Obesity Disorders, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Floor 3th, Number 24, Yemen Street, Shahid Chamran Highway, P.O. Box: 19395-4763, Tehran, Iran.ORCID http://orcid.org/0000-0002-0850-7258
Farzad HadaeghPrevention of Metabolic Disorders Research Center, Research Institute for Metabolic and Obesity Disorders, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Floor 3th, Number 24, Yemen Street, Shahid Chamran Highway, P.O. Box: 19395-4763, Tehran, Iran. fzhadaegh@endocrine.ac.ir.ORCID http://orcid.org/0000-0002-8935-2744
Farzad EsmaeiliPrevention of Metabolic Disorders Research Center, Research Institute for Metabolic and Obesity Disorders, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Floor 3th, Number 24, Yemen Street, Shahid Chamran Highway, P.O. Box: 19395-4763, Tehran, Iran.ORCID http://orcid.org/0000-0002-2265-9995

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudies evaluating the longitudinal relationship between plasma free fatty acids (FFAs) and subclinical atherosclerosis remain limited. We investigated the prospective association between serum FFA levels and the progression of coronary artery calcification (CAC) in a generally healthy, age-, sex-, and racially/ethnically diverse population.

methodsThis study utilized baseline data from the Multi-Ethnic Study of Atherosclerosis cohort, collected from 2000 to 2002, including 2988 women and 2696 men, with outcome data extending to 2012. CAC progression was defined as either the new onset of detectable CAC among participants with a baseline score of zero or a clinically meaningful increase in CAC severity among those with pre-existing CAC, based on established cut-offs. We employed Cox proportional hazards regression to calculate hazard ratios (HR) and 95% confidence intervals (95%CI) for the associations between FFAs and the CAC progression, stratified by sex. We evaluated potential non-linear relationships using restricted cubic splines.

resultsDuring the 9-year follow-up, we identified 1302 cases of CAC progression in women and 1480 cases in men. Serum FFAs were linearly associated with CAC progression in men, with a multivariable-adjusted HR of 1.41 (95% CI: 1.03-1.93) for each mmol/L increase in FFAs. Moreover, men in the highest relative to the lowest quintile of FFAs had a 20% higher risk (1.20; 1.02-1.43). Among women, we found evidence of a potential nonlinear association between FFAs and CAC progression, suggesting a threshold effect in their relationship (P non-linearity: 0.050). We observed no significant effect modification by age, body mass index, diabetes status, or hypertension in the relationship between FFAs and CAC progression.

conclusionsThis study highlights a significant association between FFAs and CAC progression in both men and women, though the nature of this association differs by gender.

Indexed as

Coronary Artery DiseaseFatty Acids, NonesterifiedVascular CalcificationAgedBiomarkersCoronary AngiographyDisease ProgressionFemaleHumansMaleMiddle AgedProportional Hazards ModelsProspective StudiesRisk FactorsSeverity of Illness IndexSex FactorsBiomarkersFatty Acids, NonesterifiedAtherosclerosisCoronary artery calcificationFree fatty acidsSexSubclinical

Identifiers

PMID42210161
PMCPMC13404333

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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 Socratic graph.