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Published on: January 29, 2018
Bone Mineral Density in Patients with Pediatric Inflammatory Bowel Disease Using Dual Energy X-Ray Absorptiometry
Hasan M Isa1, Amira A Ezzaldin1, Mohamed M Alabbasi2
1Department of Pediatrics, Salmaniya Medical Complex, Arabian Gulf University, Manama, Bahrain.
Insights
Pediatric inflammatory bowel disease (IBD) is linked to a high prevalence of low bone mineral density (BMD). Factors like low BMI, specific disease locations, and certain medications are associated with osteoporosis in these children.
Area of Science:
- Pediatric Endocrinology
- Gastroenterology
- Rheumatology
Background:
- Inflammatory bowel disease (IBD) is a chronic immune-mediated condition affecting the gastrointestinal system.
- IBD can significantly impact bone growth and bone mineral density (BMD) in pediatric patients.
Purpose of the Study:
- To determine the prevalence of low BMD in children with IBD.
- To identify predictors associated with low BMD in this population.
Main Methods:
- Retrospective cross-sectional study of pediatric IBD patients.
- BMD assessed using dual-energy X-ray absorptiometry (total body and lumbar spine).
- Comparison of clinical and laboratory findings between patients with and without osteoporosis.
Main Results:
- High prevalence of low BMD observed: 27.1% osteoporosis and 33.3% osteopenia (total body); 39.5% osteoporosis and 32.6% osteopenia (spine).
- Significant predictors for total body osteoporosis included low BMI Z-score, ileocolonic disease, and low calcium levels.
- Significant predictors for spinal osteoporosis included low BMI Z-score, low hemoglobin, low calcium, and infliximab use.
Conclusions:
- Pediatric IBD patients exhibit a high prevalence of reduced bone mineral density.
- Low BMI, ileocolonic disease, low hemoglobin/calcium levels, and infliximab use are associated with osteoporosis in pediatric IBD.
Background:
Inflammatory bowel disease (IBD) is a chronic inflammatory immune-mediated condition that affects the gastrointestinal system and alters bone growth and bone mineral density (BMD). Here we aimed to study the prevalence and predictors of a low BMD in pediatric patients with IBD.
Methods:
This retrospective cross-sectional analytical study included pediatric patients with IBD in whom BMD was evaluated using dual energy X-ray absorptiometry of the total body and lumbar spine. Osteoporosis was defined as a BMD Z-score ≤-2, osteopenia as -2 to -1, and normal as >-1. Clinical and laboratory findings were compared between patients with and without osteoporosis.
Results:
Of the 48 patients, 30 (62.5%) were males, 35 (72.9%) had Crohn's disease, and 13 (27.1%) had ulcerative colitis. The mean age at diagnosis was 9.9±2.8 years. The median age at the time of the BMD scans was 11.9 (interquartile range, 9.9-14.3) years. Total body BMD scans identified 13 (27.1%) and 16 (33.3%) patients with osteoporosis and osteopenia, respectively. Spinal BMD scans revealed that 17 (39.5%) and 14 (32.6%) patients had osteoporosis and osteopenia, respectively. A low body mass index (BMI) Z-score (p=0.038), ileocolonic disease location (p=0.008), and a low calcium level (p=0.008) were significant predictors of osteoporosis on the total body BMD scans. A low BMI Z-score (p=0.039), decreased hemoglobin level (p=0.018), low calcium level (p=0.033), and infliximab use (p=0.019) were significant predictors of osteoporosis on the spinal BMD scans.
Conclusions:
This study showed a high prevalence of low BMD among pediatric patients with IBD. A low BMI, ileocolonic disease location, low hemoglobin and calcium levels, and infliximab use were significantly associated with osteoporosis.
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