# Serum Vitamin D and Pyridinoline Cross-Linked Carboxyterminal Telopeptide of Type I Collagen in Patients with Ankylosing Spondylitis

**Authors:** Pingping Zhang, Qiuxia Li, Qiujing Wei, Zetao Liao, Zhiming Lin, Linkai Fang, Jieruo Gu

PMC · DOI: 10.1155/2015/543806 · BioMed Research International · 2015-07-26

## TL;DR

This study found that patients with ankylosing spondylitis have lower vitamin D and higher ICTP levels, which are linked to bone loss and disease activity.

## Contribution

The study identifies vitamin D and ICTP as potential biomarkers for bone loss in ankylosing spondylitis.

## Key findings

- AS patients had significantly lower vitamin D and higher ICTP levels compared to controls.
- Low vitamin D and high ICTP were associated with reduced hip bone mineral density in AS patients.
- ICTP levels were higher in male AS patients and those with juvenile-onset AS.

## Abstract

Objective. To assess the serum vitamin D and ICTP levels in patients with ankylosing spondylitis (AS) and investigate their relationship with disease activity and bone mineral density (BMD). Method. 150 patients and 168 controls were included. Serum 25(OH)D, ICTP, C-reaction protein (CRP), Bath AS Disease Activity Index (BASDAI), Bath AS Functional Index (BASFI), and Hip BMD were assessed in patients. 25(OH)D and ICTP were detected in controls. Results. The serum 25(OH)D in AS was 57.92 ± 24.42 nmol/L, significantly lower than controls (91.24 ± 42.02 nmol/L). Serum ICTP in AS was 5.72 ± 3.88 ug/L, significantly higher than controls (3.69 ± 1.26 ug/L). ICTP level was higher in men than in women patients (6.07 ± 4.05 versus 3.84 ± 1.96 ug/L, P ≤ 0.01); it was also higher in JAS than in AAS (9.52 ± 3.79 versus 5.27 ± 3.65 ug/L, P ≤ 0.01). Furthermore, 25(OH)D was negatively correlated with ICTP. Low 25(OH)D and high ICTP were one of the reasons of AS patients' low hip BMD. Besides, a significant relationship was found between serum ICTP and CRP. Conclusion. There was a high incidence of vitamin D inadequacy in AS. Serum ICTP level was elevated in AS, especially in JAS and male patients. 25(OH)D and ICTP seem to be valuable markers to detect bone loss in AS.

## Linked entities

- **Diseases:** Ankylosing Spondylitis (MONDO:0005306), juvenile ankylosing spondylitis (MONDO:0020655)

## Full-text entities

- **Genes:** BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632] {aka BGP, OC, OCN}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}, CYP24A1 (cytochrome P450 family 24 subfamily A member 1) [NCBI Gene 1591] {aka CP24, CYP24, HCAI, HCINF1, P450-CC24}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CYP27A1 (cytochrome P450 family 27 subfamily A member 1) [NCBI Gene 1593] {aka CP27, CTX, CYP27}, HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}
- **Diseases:** BMD (MESH:D001851), diabetes mellitus (MESH:D003920), chronic renal or hepatic disease (MESH:D006521), bone resorption (MESH:D001862), inflammatory disease (MESH:D007249), malnutrition (MESH:D044342), bone metastases (MESH:D009362), bone pain (MESH:D010146), autoimmune disorder (MESH:D001327), ligament calcifications (MESH:D017887), bone loss (MESH:D001847), spinal deformity (MESH:D013122), rheumatic disease (MESH:D012216), ankylosis of the spine and sacroiliac joints (MESH:C563037), parathyroid or thyroid disease (MESH:D010279), Vitamin D deficiency (MESH:D014808), AAS (MESH:D013167), inflammatory bowel disease (MESH:D015212), fractures (MESH:D050723), osteoporosis (MESH:D010024)
- **Chemicals:** pyridinoline (MESH:C015484), 25-Hydroxyvitamin D (MESH:C104450), sulfasalazine (MESH:D012460), bisphosphonates (MESH:D004164), 25(OH)D (-), Vitamin D (MESH:D014807), secosteroid (MESH:D012632), coumarin derivatives (MESH:D003374), phosphorus (MESH:D010758), calcium (MESH:D002118), calcitriol (MESH:D002117),  (MESH:D010455),  (MESH:D015415),  (MESH:C052929)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC4529939/full.md

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Source: https://tomesphere.com/paper/PMC4529939