Home Different vitamin D status in common multiorgan autoimmune disease patients
Article
Licensed
Unlicensed Requires Authentication

Different vitamin D status in common multiorgan autoimmune disease patients

  • Erfu Xie ORCID logo , Zhongjian Zhao , Chengjing Yan , Yiting Zhang , Qiaodi Zhang and Shiyang Pan EMAIL logo
Published/Copyright: September 6, 2019
Become an author with De Gruyter Brill

Abstract

Background

Vitamin D plays a key role in calcium homeostasis and contributes to the regulation of the immune system. Furthermore, vitamin D deficiency has been reported to be associated with autoimmune diseases (AIDs), especially with multiorgan AIDs. Various multiorgan AIDs may be different based on the vitamin D status. This study aims to investigate the serum 25-hydroxyvitamin D (25(OH)D) levels in patients with different common multiorgan AIDs.

Methods

A total of 295 patients with multiorgan AIDs treated in our hospital from January 2012 to September 2018 were recruited, including 137 cases of rheumatoid arthritis (RA), 85 cases of systemic lupus erythematosus (SLE), 32 cases of Sjögren’s syndrome (SS) and 41 cases of mixed connective tissue disease (MCTD); 47 apparently healthy individuals were also recruited as controls. The serum 25(OH)D levels in patients with different multiorgan AIDs were measured with Roche electrochemiluminescence immunoassay and statistically analyzed the proportion of patients with normal, insufficiency and deficiency in 25(OH)D levels in different multiorgan diseases. The 25(OH)D levels of different multiorgan AID groups and healthy controls were also compared.

Results

Incidences of 25(OH)D deficiency in the RA, SLE, SS and MCTD groups were 21.2%, 35.3%, 25.0% and 22.0%, respectively, with significant inter-group differences (p < 0.05). The incidence in the SLE group was higher than in the RA, SS and MCTD groups, indicating severe 25(OH)D deficiency in patients with SLE. Significant inter-group differences (p < 0.05) were detected in the serum 25(OH)D levels in different multiorgan AID groups and in the healthy control group. Further pairwise comparison found a significantly higher level of 25(OH)D in the healthy control group than in the SLE, SS, RA and MCTD groups (p < 0.05). Moreover, the 25(OH)D status in the SLE group was significantly lower than that in the SLE, SS, RA and MCTD groups (p < 0.05).

Conclusions

Serum 25(OH)D deficiency and a low 25(OH)D status are commonly seen in patients with different multiorgan AIDs compared to healthy controls, warranting vitamin D supplementation. Severe 25(OH)D deficiency and a lower 25(OH)D status were found in patients with SLE.

Reviewed Publication:

Conrad K. Sack U. Edited by:


Award Identifier / Grant number: ZDXKB2016005

Award Identifier / Grant number: 81672100

Funding statement: This study was supported by grants from the Key Laboratory for Laboratory Medicine of Jiangsu Province of China (No. ZDXKB2016005), A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions, the National Natural Science Foundation of China (81672100, funder id: http://dx.doi.org/10.13039/501100001809).

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Employment or leadership: None declared.

  3. Honorarium: None declared.

  4. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Wang L, Wang FS, Gershwin ME. Human autoimmune diseases: a comprehensive update. J Intern Med 2015;278:369–95.10.1111/joim.12395Search in Google Scholar

2. Baeke F, Korf H, Overbergh L, Verstuyf A, Thorrez L, Van Lommel L, et al. The vitamin D analog, TX527, promotes a human CD4+CD25highCD127low regulatory T cell profile and induces a migratory signature specific for homing to sites of inflammation. J Immunol 2011;186:132–42.10.4049/jimmunol.1000695Search in Google Scholar

3. Mathieu C, Adorini L. The coming of age of 1,25-dihydroxyvitamin D(3) analogs as immunomodulatory agents. Trends Mol Med 2002;8:174–9.10.1016/S1471-4914(02)02294-3Search in Google Scholar

4. Reichel H, Koeffler HP, Norman AW. The role of the vitamin D endocrine system in health and disease. N Engl J Med 1989;320:980–91.10.1056/NEJM198904133201506Search in Google Scholar PubMed

5. Adorini L, Penna G. Dendritic cell tolerogenicity: a key mechanism in immunomodulation by vitamin D receptor agonists. Hum Immunol 2009;70:345–52.10.1016/j.humimm.2009.01.016Search in Google Scholar PubMed

6. Achinger SG, Ayus JC. The role of vitamin D in left ventricular hypertrophy and cardiac function. Kidney Int Suppl 2005;95: S37–42.10.1111/j.1523-1755.2005.09506.xSearch in Google Scholar PubMed

7. Ponsonby AL, Lucas RM, van der Mei IA. UVR, vitamin D and three autoimmune diseases–multiple sclerosis, type 1 diabetes, rheumatoid arthritis. Photochem Photobiol 2005;81:1267–75.10.1562/2005-02-15-IR-441Search in Google Scholar PubMed

8. Chiu KC, Chu A, Go VL, Saad MF. Hypovitaminosis D is associated with insulin resistance and beta cell dysfunction. Am J Clin Nutr 2004;79:820–5.10.1093/ajcn/79.5.820Search in Google Scholar PubMed

9. Holick MF. The use and interpretation of assays for vitamin D and its metabolites. J Nutr 1990;120 Suppl 11:1464–9.10.1093/jn/120.suppl_11.1464Search in Google Scholar PubMed

10. Dall’Ara F, Cutolo M, Andreoli L, Tincani A, Paolino S. Vitamin D and systemic lupus erythematous: a review of immunological and clinical aspects. Clin Exp Rheumatol 2018;36:153–62.Search in Google Scholar

11. Lee YH, Bae SC. Vitamin D level in rheumatoid arthritis and its correlation with the disease activity: a meta-analysis. Clin Exp Rheumatol 2016;34:827–33.Search in Google Scholar

12. Sandhya P, Mahasampath G, Mashru P, Bondu JD, Job V, Danda D. Vitamin D levels and associations in Indian patients with primary Sjogren’s syndrome. J Clin Diagn Res 2017;11: OC33–6.10.7860/JCDR/2017/28493.10697Search in Google Scholar PubMed PubMed Central

13. Bischoff-Ferrari HA, Giovannucci E, Willett WC, Dietrich T, Dawson-Hughes B. Estimation of optimal serum concentrations of 25-hydroxyvitamin D for multiple health outcomes. Am J Clin Nutr 2006;84:18–28.10.1093/ajcn/84.1.18Search in Google Scholar PubMed

14. Ascherio A, Munger KL, White R, Kochert K, Simon KC, Polman CH, et al. Vitamin D as an early predictor of multiple sclerosis activity and progression. JAMA Neurol 2014;71:306–14.10.1001/jamaneurol.2013.5993Search in Google Scholar PubMed PubMed Central

15. Emerah AA, El-Shal AS. Role of vitamin D receptor gene polymorphisms and serum 25-hydroxyvitamin D level in Egyptian female patients with systemic lupus erythematosus. Mol Biol Rep 2013;40:6151–62.10.1007/s11033-013-2726-9Search in Google Scholar PubMed

16. Shirinskiy VS. Autoimmune diseases: problems of pathogenesis, diagnostics and treatment. Russ J Immunol 1999;4:261–3.Search in Google Scholar

17. Martins-Costa P, Martins H, Bravo F, Cruz M, Reis J, Oliveira JC. Comparison of automated methods for measurement of 25-hydroxyvitamin D. Clin Lab 2013;59:885–91.10.7754/Clin.Lab.2012.120924Search in Google Scholar

18. Attar SM, Siddiqui AM. Vitamin D deficiency in patients with systemic lupus erythematosus. Oman Med J 2013;28:42–7.10.5001/omj.2013.10Search in Google Scholar PubMed PubMed Central

19. Ruiz-Irastorza G, Egurbide MV, Olivares N, Martinez-Berriotxoa A, Aguirre C. Vitamin D deficiency in systemic lupus erythematosus: prevalence, predictors and clinical consequences. Rheumatology (Oxford) 2008;47:920–3.10.1093/rheumatology/ken121Search in Google Scholar PubMed

20. Prietl B, Treiber G, Pieber TR, Amrein K. Vitamin D and immune function. Nutrients 2013;5:2502–21.10.3390/nu5072502Search in Google Scholar PubMed PubMed Central

Received: 2019-06-28
Accepted: 2019-08-13
Published Online: 2019-09-06
Published in Print: 2019-10-25

© 2019 Walter de Gruyter GmbH, Berlin/Boston

Downloaded on 24.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/labmed-2019-0104/html
Scroll to top button