Evidence map›Paper›PMID 42464303›Full record

ArticleNutrition & metabolism2026

Low vitamin D status and cardiometabolic trait clustering in a primary-care adult cohort: association analysis and exploratory explainable machine-learning classification.

Boshra Mozaffar, Saleh A Alsanie, Fauzia Ashfaq, Nahlah Jaber Madkhali, Bayan F Alshahrani, Mohd Faheem Khan, Mohammad Idreesh Khan

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Article in Nutrition & metabolism, 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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5 · Who and what money

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7 authors.

Boshra Mozaffar *Department of Clinical Nutrition, College of Nursing and Health Sciences, Jazan University, Jazan, 45142, Saudi Arabia.
Saleh A AlsanieDepartment of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, P.O. Box 6666, Buraydah, 51452, Saudi Arabia.
Fauzia AshfaqDepartment of Clinical Nutrition, College of Nursing and Health Sciences, Jazan University, Jazan, 45142, Saudi Arabia.
Nahlah Jaber MadkhaliDepartment of Clinical Nutrition, College of Nursing and Health Sciences, Jazan University, Jazan, 45142, Saudi Arabia.
Bayan F AlshahraniClinical Nutrition, Medical Cities Program, MOI, Buraydah, Saudi Arabia.
Mohd Faheem Khan *Department of Biotechnology, K.C.M.T, M.J.P. Rohilkhand University, Bareilly, 243003, India.
Mohammad Idreesh KhanDepartment of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, P.O. Box 6666, Buraydah, 51452, Saudi Arabia. moi.khan@qu.edu.sa.ORCID https://orcid.org/0000-0001-9325-6491

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLow serum 25-hydroxyvitamin D (25(OH)D) commonly co-exists with obesity and adverse cardiometabolic traits. However, its cross-sectional association with dyslipidaemia, body composition and glycaemic markers in primary-care adults remains incompletely characterised. This study examined these associations as the primary objective and, as a secondary exploratory objective, assessed whether routine clinical variables could classify concurrent vitamin D deficiency using interpretable machine-learning models.

methodsIn this cross-sectional study, adults attending routine health check-up services underwent anthropometric and body-composition assessment (BMI, body fat mass, body fat percentage and lean mass), metabolic-profile screening and vitamin-status assessment. Vitamin D status was classified as deficient (< 20 ng/mL), insufficient (20-29.9 ng/mL) or sufficient (≥ 30 ng/mL). Group comparisons, correlation analyses and multivariable regression models were performed. In a secondary exploratory analysis, logistic-regression and random-forest models were used to classify vitamin D deficiency from routine clinical variables after internal cross-validation.

resultsIn the overall analytic sample, the mean serum 25(OH)D level was 20.3 ± 8.0 ng/mL, and 50.3% of participants were obese. Vitamin D deficiency was associated with significantly higher BMI, body fat mass, body fat percentage, fasting blood glucose, HbA1c, total cholesterol (TC), low-density lipoprotein cholesterol (LDL-c), triglycerides (TG) and TG-derived very-low-density lipoprotein cholesterol (VLDL-c) and with significantly lower high-density lipoprotein cholesterol (HDL-c) (all p < 0.05). Serum 25(OH)D was inversely correlated with adiposity indices and TG and positively correlated with HDL-c. In the secondary exploratory classification analysis, the dimension-reduced random-forest model showed higher internal discrimination than logistic regression for classifying vitamin D deficiency in this dataset.

conclusionsPrimary-care cohort with a high obesity burden, lower vitamin D status was associated with greater adiposity, less favourable glycaemic indices and a more atherogenic lipid profile. The exploratory machine-learning analysis suggests that routine nutritional, body-composition and biochemical variables may help classify concurrent vitamin D deficiency. However, these findings require external validation and should not be interpreted as evidence of causality or immediate clinical utility.

Indexed as

Body compositionDyslipidaemiaExplainable artificial intelligence (XAI)Feature importanceMachine learningObesityRandom forestVitamin D deficiency

Identifiers

PMID42464303
PMCPMC13660006

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