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Low Bone Mass in Microscopic Colitis

Overview
Publisher Biomed Central
Specialty Gastroenterology
Date 2011 May 21
PMID 21595910
Citations 2
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Abstract

Background: Microscopic colitis presents with similar symptoms to classic inflammatory bowel diseases. Osteoporosis is a common complication of Crohn's disease but there are no data concerning bone metabolism in microscopic colitis.

Aims: The aim of the present study was to evaluate bone density and metabolism in patients with microscopic colitis.

Methods: Fourteen patients microscopic colitis were included in the study, and 28 healthy persons and 28 age and gender matched Crohn's disease patients were enrolled as controls. Bone mineral density was measured using dual x-ray absorptiometry at the lumbar spine, femoral neck and the radius. Serum bone formation and bone resorption markers (osteocalcin and beta-crosslaps, respectively) were measured using immunoassays.

Results: Low bone mass was measured in 57.14% patients with microscopic colitis. Bone mineral density at the femoral neck in patients suffering from microscopic colitis and Crohn's disease was lower than in healthy controls (0.852 ± 0.165 and 0.807 ± 0.136 vs. 1.056 ± 0.126 g/cm²; p < 0.01). Bone mineral density at the non-dominant radius was decreased in microscopic colitis patients (0.565 ± 0.093 vs. 0.667 ± 0.072 g/cm²; p < 0.05) but unaffected in Crohn's disease patients (0.672 ± 0.056 g/cm²). Mean beta-crosslaps concentration was higher in microscopic colitis and Crohn's disease patients than controls (417.714 ± 250.37 and 466.071 ± 249.96 vs. 264.75 ± 138.65 pg/ml; p < 0.05). A negative correlation between beta-crosslaps concentration and the femoral and radius t-scores was evident in microscopic colitis patients.

Conclusions: Low bone mass is frequent in microscopic colitis, and alterations to bone metabolism are similar to those present in Crohn's disease. Therefore, microscopic colitis-associated osteopenia could be a significant problem in such patients.

Citing Articles

Microscopic colitis in older adults: impact, diagnosis, and management.

Fedor I, Zold E, Barta Z Ther Adv Chronic Dis. 2022; 13:20406223221102821.

PMID: 35813189 PMC: 9260565. DOI: 10.1177/20406223221102821.


Muramyl dipeptide responsive pathways in Crohn's disease: from NOD2 and beyond.

Salem M, Seidelin J, Rogler G, Nielsen O Cell Mol Life Sci. 2013; 70(18):3391-404.

PMID: 23275943 PMC: 11113952. DOI: 10.1007/s00018-012-1246-4.

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