Vitamin D and its receptor in skeletal muscle are associated with muscle disease manifestation, lipid metabolism and physical fitness of patients with myositis
Language English Country England, Great Britain Media electronic
Document type Journal Article
Grant support
NU21-05-00322
Ministry of Health of the Czech Republic
023728
Ministry of Health of the Czech Republic
LM2023033
Large research infrastructure project BBMRI.cz
APVV 20/0466
The Ministry of Education, Research, Development and Youth of the Slovak Republic
SVV 260638
Ministry of Education Youth and Sports of the Czech Republic
PubMed
40038731
PubMed Central
PMC11877867
DOI
10.1186/s13075-025-03516-9
PII: 10.1186/s13075-025-03516-9
Knihovny.cz E-resources
- Keywords
- Lipid metabolism, Mitochondria, Muscle, Myositis, Physical activity, Vitamin D,
- MeSH
- 25-Hydroxyvitamin D3 1-alpha-Hydroxylase MeSH
- Exercise physiology MeSH
- Adult MeSH
- Muscle, Skeletal * metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- Lipid Metabolism * physiology MeSH
- Myositis * metabolism MeSH
- Receptors, Calcitriol * metabolism genetics MeSH
- Aged MeSH
- Physical Fitness * physiology MeSH
- Vitamin D * metabolism blood analogs & derivatives MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- 25-Hydroxyvitamin D3 1-alpha-Hydroxylase MeSH
- CYP27B1 protein, human MeSH Browser
- Receptors, Calcitriol * MeSH
- VDR protein, human MeSH Browser
- Vitamin D * MeSH
BACKGROUND: Low levels of vitamin D have been associated with several autoimmune diseases. A growing body of evidence supports the association of vitamin D with skeletal muscle damage, regeneration, and energy and lipid metabolism. The aim was to analyse vitamin D and its receptor (VDR) in the muscle tissue of patients with idiopathic inflammatory myopathies (IIM) and to relate them to clinical parameters and muscle lipid and energy metabolism. METHODS: Forty-six patients with IIM and 67 healthy controls (HC) were included in the study. 27 IIM patients participated in a 24-week exercise intervention. Muscle biopsies were obtained from 7 IIM patients before/after training, 13 non-exercising IIM controls, and 21 HC. Circulating concentrations of 25(OH)D and 1,25(OH)D were measured. Gene expression of VDR and CYP27B1, the enzyme converting 25(OH)D to hormonally active 1,25(OH)D, was determined by qPCR in muscle tissue and primary muscle cells. Lipid oxidative metabolism was assessed in muscle tissue (mRNA, qPCR) and primary muscle cells (radioactive assays). RESULTS: Lower levels of active 1,25(OH)D were observed in IIM patients compared with HC (mean ± SD: 125.0 ± 45.4 vs. 164.7 ± 49.2 pmol/L; p < 0.0001). 25(OH)D was associated with CRP (r = -0.316, p = 0.037), MITAX (r = -0.311, p = 0.040) and HAQ (r = -0.390, p = 0.009) in IIM. After 24 weeks of training, active 1,25(OH)D was associated with MMT8 (r = 0.866, p < 0.0001), FI-2 (r = 0.608, p = 0.013) and HAQ (r = -0.537, p = 0.032). Gene expression of both VDR and CYP27B1 in primary muscle cells decreased after training (p = 0.031 and p = 0.078, respectively). Associations of VDR mRNA in muscle tissue with MMT-8 (IIM: r = -0.559, p = 0.013), serum CK (HC: r = 0.484, p = 0.031), myoglobin (IIM: r = 0.510, p = 0.026) and myostatin (IIM: r = -0.519, p = 0.023) were observed. The expression of VDR in differentiated muscle cells correlated negatively with the complete oxidation of palmitic acid (r = -0.532, p = 0.028). Muscle mRNA of carnitine palmitoyl transferase 1 (CPT1) (downregulated in IIM, p = 0.001) correlated positively with serum 1,25(OH) vitamin D (r = 0.410, p = 0.042). CONCLUSION: Reduced biologically active vitamin D in circulation suggests its impaired metabolism in IIM. Serum vitamin D levels and gene expression of its receptor and activating enzyme in muscle tissue were modified by regular exercise and associated with disease manifestations, physical fitness, and muscle lipid metabolism of IIM patients.
Department of Rheumatology 1st Faculty of Medicine Charles University Prague Czech Republic
Faculty of Science Charles University Prague Czech Republic
Institute of Pathophysiology Faculty of Medicine Comenius University Bratislava Slovakia
Institute of Rheumatology Na Slupi 4 Prague 12850 Czech Republic
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