Evidence map›Paper›PMID 41141273›Full record

ArticleFrontiers in nutrition2025

Sexual dimorphism in LC-MS/MS-based vitamin D metabolite profiling and nutrition-acquired biochemical osteomalacia among adolescents.

Shaun Sabico, Nasser M Al-Daghri, Amal Alenad, Yousef Al-Saleh, Malak N K Khattak, Kaiser Wani, Abdullah M Alnaami, Jean-Yves Reginster, Majed S Alokail, Etienne Cavalier

Abstract read
In one paragraph

Article in Frontiers in nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Vitamin D Metabolite Ratios and Association with Type 2 Diabetes Mellitus in a Youth Saudi Population.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Article
  2. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Shaun SabicoChair for Biomarkers of Chronic Diseases, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Nasser M Al-DaghriChair for Biomarkers of Chronic Diseases, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Amal AlenadDepartment of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Yousef Al-SalehDepartment of Medicine, Health Oasis Hospital, Riyadh, Saudi Arabia.
Malak N K KhattakChair for Biomarkers of Chronic Diseases, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Kaiser WaniChair for Biomarkers of Chronic Diseases, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Abdullah M AlnaamiChair for Biomarkers of Chronic Diseases, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Jean-Yves ReginsterProtein Research Chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Majed S AlokailProtein Research Chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Etienne CavalierDepartment of Clinical Chemistry, University of Liège, CIRM, CHU de Liège, Liège, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: We previously reported a high prevalence of biochemical osteomalacia among apparently healthy Arab adolescents using combined mineralization markers. This study examined whether advanced LC-MS/MS-based vitamin D metabolite profiling, including the vitamin D metabolite ratio (VMR), can serve as indicators of biochemical osteomalacia in Arab adolescents. Methods: A total of 976 age- and body mass index-matched adolescents (522 girls, mean age 14.9 ± 1.8 years, body mass index, BMI 23.0 ± 5.9; 454 boys, mean age 14.9 ± 1.7 years, BMI 23.7 ± 5.8) were included in this cross-sectional study. Anthropometrics and biochemical parameters [glucose, lipid profile, calcium (Ca), inorganic phosphorus (Pi), alkaline phosphatase (ALP)] were measured using routine assays. Circulating vitamin D metabolites [24,25(OH)₂D (24, 25 VD), VD2, VD3, total VD] were quantified using LC-MS/MS, and VMR calculated as [24,25 VD/VD] × 100. Deficiency cut-offs were: VD <30 nmol/L, 24,25 VD <3.0 nmol/L, VMR <4%. Biochemical osteomalacia was defined as ≥ 2 abnormal markers (low VD, high ALP, low Ca, or low Pi). Results: All vitamin D metabolites were significantly lower in the biochemical osteomalacia group. Overall, VD showed the highest predictive value (AUC 0.71, Youden index 0.40). Stratified analyses revealed VMR as a modest marker in girls (AUC 0.60), while VD3 performed best in boys (AUC 0.77, Youden index 0.60). Conclusion: VD metabolites as a single test are modest predictors of biochemical osteomalacia in adolescents and differ in accuracy according to sex. Findings in this study should be interpreted as exploratory rather than diagnostic, serving to generate hypotheses and lay groundwork for future clinical and public health applications.

Indexed as

25-hydroxyvitamin DArab adolescentsosteomalaciavitamin D metabolite ratiovitamin D metabolitesVMR

Identifiers

PMID41141273
PMCPMC12545115

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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.