The Effect of Vitamin D on Intestinal Inflammation and Faecal Microbiota in Patients with Ulcerative Colitis

被引:102
作者
Garg, Mayur [1 ,2 ,3 ]
Hendy, Philip [3 ]
Ding, John Nik [3 ,4 ]
Shaw, Sophie [5 ]
Hold, Georgina [5 ,6 ]
Hart, Ailsa [3 ,7 ]
机构
[1] Eastern Hlth, Dept Gastroenterol, Level 3W,Bldg B,8 Arnold St, Box Hill, Vic 3128, Australia
[2] Monash Univ, Eastern Hlth Clin Sch, Clayton, Vic, Australia
[3] St Marks Hosp, Harrow, Middx, England
[4] St Vincents Hosp, Melbourne, Vic, Australia
[5] Univ Aberdeen, Aberdeen, Scotland
[6] Univ New South Wales, Fac Med, Sydney, NSW, Australia
[7] Imperial Coll, London, England
关键词
Basic science; experimental models and pathophysiology; clinical trials; C-REACTIVE PROTEIN; CROHNS-DISEASE; BOWEL-DISEASE; D-RECEPTOR; 1,25-DIHYDROXYVITAMIN D-3; ENDOSCOPIC ACTIVITY; DENDRITIC CELLS; D DEFICIENCY; TRANSPLANTATION; REMISSION;
D O I
10.1093/ecco-jcc/jjy052
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Vitamin D may be immunomodulatory and alter faecal microbiota, but results from clinical studies in humans to date have been inconclusive. This study aimed to assess the effect of vitamin D replacement in vitamin D-deficient patients with and without ulcerative colitis [UC] on inflammation and faecal microbiota. Methods: Vitamin D was replaced over 8 weeks in patients with active UC [defined by faecal calprotectin >=>= 100 mu g/g], inactive UC [faecal calprotectin < 100 mu g/g] and non-inflammatory bowel disease [IBD] controls with baseline serum 25[OH] vitamin D < 50 nmol/l, and markers of inflammation and faecal microbiota were analysed. Results: Eight patients with active UC, nine with inactive UC and eight non-IBD controls received 40 000 units cholecalciferol weekly for 8 weeks. Mean baseline 25[OH] vitamin D increased from 34 [range 12-49] to 111 [71-158] nmol/l [p < 0.001], with no difference across the groups [p = 0.32]. In patients with active UC, faecal calprotectin levels decreased from a median 275 to 111 mu g/g [p = 0.02], platelet count decreased [mean 375 to 313 x 109/l, p = 0.03] and albumin increased [mean 43 to 45 g/l, p = 0.04]. These parameters did not change in patients with inactive UC or non-IBD controls. No changes in overall faecal bacterial diversity were noted although a significant increase in Enterobacteriaceae abundance was observed in patients with UC [p = 0.03]. Conclusions: Vitamin D supplementation was associated with reduced intestinal inflammation in patients with active UC, with a concomitant increase in Enterobacteriaceae but no change in overall faecal microbial diversity.
引用
收藏
页码:963 / 972
页数:10
相关论文
共 61 条
[11]   Review article: vitamin D and inflammatory bowel disease - established concepts and future directions [J].
Garg, M. ;
Lubel, J. S. ;
Sparrow, M. P. ;
Holt, S. G. ;
Gibson, P. R. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2012, 36 (04) :324-344
[12]   Evaluation of a 12-week targeted vitamin D supplementation regimen in patients with active inflammatory bowel disease [J].
Garg, Mayur ;
Rosella, Ourania ;
Rosella, Gennaro ;
Wu, Yunqiu ;
Lubel, John S. ;
Gibson, Peter R. .
CLINICAL NUTRITION, 2018, 37 (04) :1375-1382
[13]   Association of Circulating Vitamin D Concentrations with Intestinal but Not Systemic Inflammation in Inflammatory Bowel Disease [J].
Garg, Mayur ;
Rosella, Ourania ;
Lubel, John S. ;
Gibson, Peter R. .
INFLAMMATORY BOWEL DISEASES, 2013, 19 (12) :2634-2643
[14]   Low Serum Vitamin D During Remission Increases Risk of Clinical Relapse in Patients With Ulcerative Colitis [J].
Gubatan, John ;
Mitsuhashi, Shuji ;
Zenlea, Talia ;
Rosenberg, Laura ;
Robson, Simon ;
Moss, Alan C. .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2017, 15 (02) :240-+
[15]   Standard Colonic Lavage Alters the Natural State of Mucosal-Associated Microbiota in the Human Colon [J].
Harrell, Laura ;
Wang, Yunwei ;
Antonopoulos, Dionysios ;
Young, Vincent ;
Lichtenstein, Lev ;
Huang, Yong ;
Hanauer, Stephen ;
Chang, Eugene .
PLOS ONE, 2012, 7 (02)
[16]   1,25-Dihydroxyvitamin D3 and IL-2 Combine to Inhibit T Cell Production of Inflammatory Cytokines and Promote Development of Regulatory T Cells Expressing CTLA-4 and FoxP3 [J].
Jeffery, Louisa E. ;
Burke, Fiona ;
Mura, Manuela ;
Zheng, Yong ;
Qureshi, Omar S. ;
Hewison, Martin ;
Walker, Lucy S. K. ;
Lammas, David A. ;
Raza, Karim ;
Sansom, David M. .
JOURNAL OF IMMUNOLOGY, 2009, 183 (09) :5458-5467
[17]   Immunological aspects of intestinal mucus and mucins [J].
Johansson, Malin E. V. ;
Hansson, Gunnar C. .
NATURE REVIEWS IMMUNOLOGY, 2016, 16 (10) :639-649
[18]   Ablation of Tumor Necrosis Factor Is Associated with Decreased Inflammation and Alterations of the Microbiota in a Mouse Model of Inflammatory Bowel Disease [J].
Jones-Hall, Yava L. ;
Kozik, Ariangela ;
Nakatsu, Cindy .
PLOS ONE, 2015, 10 (03)
[19]   Clinical trial: vitamin D3 treatment in Crohn's disease - a randomized double-blind placebo-controlled study [J].
Jorgensen, S. P. ;
Agnholt, J. ;
Glerup, H. ;
Lyhne, S. ;
Villadsen, G. E. ;
Hvas, C. L. ;
Bartels, L. E. ;
Kelsen, J. ;
Christensen, L. A. ;
Dahlerup, J. F. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2010, 32 (03) :377-383
[20]   Association of Vitamin D Level With Clinical Status in Inflammatory Bowel Disease: A 5-Year Longitudinal Study [J].
Kabbani, Toufi C. A. ;
Koutroubakis, Ioannis E. ;
Schoen, Robert E. ;
Ramos-Rivers, Claudia ;
Shah, Nilesh ;
Swoger, Jason ;
Regueiro, Miguel ;
Barrie, Arthur ;
Schwartz, Marc ;
Hashash, Jana G. ;
Baidoo, Leonard ;
Dunn, Michael A. ;
Binion, David G. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2016, 111 (05) :712-719