# Vitamin D Sufficiency Revisited: Evidence of a Dose–Response Effect for MASLD in Adults at Risk

**Authors:** Gediz Dogay Us, Francesco Innocenti, Ozgur Muhammet Koc, Volkan Demirhan Yumuk, Zeynep Banu Gungor, Ger H. Koek

PMC · DOI: 10.3390/nu18040599 · 2026-02-11

## TL;DR

Higher vitamin D levels are linked to lower odds of MASLD in adults at risk, suggesting it may help prevent or manage the condition.

## Contribution

This study reveals a dose-dependent protective effect of vitamin D on MASLD, beyond current sufficiency thresholds.

## Key findings

- Vitamin D sufficiency was associated with lower odds of MASLD and significant fibrosis.
- Participants in the highest vitamin D quartile had 61% lower odds of MASLD compared to the lowest quartile.
- The protective effect of vitamin D on MASLD was dose-dependent, but not on fibrosis.

## Abstract

Background and Aims: Vitamin D plays a pivotal role in liver health, influencing multiple steps in the development of steatosis, fibrosis, and extrahepatic complications in metabolic dysfunction-associated steatotic liver disease (MASLD). However, serum vitamin D concentrations that confer optimal hepatic protection in MASLD remain unclear. We therefore aimed to investigate the association between vitamin D status and MASLD and to explore whether higher vitamin D concentrations confer incremental protection beyond current sufficiency cut-offs. Method: We conducted a multicenter cross-sectional study of 1039 adults with at least one cardiometabolic risk factor for MASLD diagnosis, recruited between 2022 and 2024. Participants that reported excessive alcohol intake (>30 g/day for men, >20 g/day for women) and other etiologies of liver disease were excluded. Serum vitamin D levels were measured, with ≥20 ng/mL defined as sufficiency. MASLD (controlled attenuation parameter [CAP] ≥ 248 dB/m) and significant fibrosis (liver stiffness measurement [LSM] ≥ 8 kPa) were assessed using vibration-controlled transient elastography. Missing vitamin D values were imputed with multiple imputation. Associations between vitamin D status, MASLD and fibrosis were examined using multivariable logistic regression models adjusted for potential confounders. Results: Participants had a mean age of 52.2 ± 13.0 years; 51.6% were male and mean BMI was 30.1 ± 5.8 kg/m2. Vitamin D sufficiency and obesity were present in 81.2% (95% CI: 78.4–84.9) and 54.7% (95% CI: 51.3–58.0), respectively. Vitamin D sufficiency was associated with lower odds of MASLD (crude OR = 0.47, 95% CI: 0.33–0.67) and significant fibrosis (crude OR = 0.46, 95% CI: 0.28–0.76). After adjusting for potential confounders, the association between Vitamin D sufficiency and MASLD remained clinically relevant but did not reach statistical significance (adjusted OR = 0.60, 95% CI: 0.36–1.03, p = 0.06). In contrast, the association between Vitamin D sufficiency and significant fibrosis was both clinically relevant and statistically significant (adjusted OR = 0.48, 95% CI: 0.246–0.916, p = 0.03). When Vitamin D was categorized into quartiles, participants in the highest quartile (≥44 ng/dL) had 61% lower odds of MASLD in the adjusted model (adjusted OR = 0.39, 95% CI: 0.21–0.71) compared with participants in the lowest quartile (≤22 ng/mL). No significant dose-dependent associations were observed for fibrosis. Conclusions: Vitamin D levels showed a dose-dependent decrease in the odds of MASLD among at-risk adults. While the protective effect on fibrosis was not dose-dependent, these findings collectively suggest vitamin D as a potentially modifiable factor in MASLD prevention and management.

## Linked entities

- **Diseases:** metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), MASLD (MONDO:0013209)

## Full-text entities

- **Genes:** GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}
- **Diseases:** CAP (MESH:C538265), hepatocellular carcinoma (MESH:D006528), metabolic diseases (MESH:D008659), LSM (MESH:D017093), Vitamin D insufficiency (MESH:D014808), Obesity (MESH:D009765), VCTE (MESH:D053421), hepatic fat accumulation (MESH:D005218), Steatosis (MESH:D005234), type 2 diabetes (MESH:D003924), Insulin resistance (MESH:D007333), DM (MESH:D009223), liver fibrosis (MESH:D008103), Diabetes (MESH:D003920), cardiovascular disease (MESH:D002318), smoker (MESH:C000719328), impaired glucose regulation (MESH:C565631), Dyslipidemia (MESH:D050171), hypertension (MESH:D006973), IR (MESH:C537629), Metabolic syndrome (MESH:D024821), Fibrosis (MESH:D005355), MASLD (MESH:D008107), inflammation (MESH:D007249), injury to (MESH:D014947)
- **Chemicals:** cholesterol (MESH:D002784), glucose (MESH:D005947), alcohol (MESH:D000438), lipid (MESH:D008055), triglycerides (MESH:D014280), TC (MESH:D013667), mercury (MESH:D008628), Vitamin D (MESH:D014807), TAG (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943758/full.md

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Source: https://tomesphere.com/paper/PMC12943758