Jois Asha, Perera Sajini, Simm Peter, Alex George
Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Victoria, Australia.
General Medicine, Royal Children's Hospital, Victoria, Australia.
Pediatr Gastroenterol Hepatol Nutr. 2022 Nov;25(6):473-480. doi: 10.5223/pghn.2022.25.6.473. Epub 2022 Nov 2.
Low bone mineral density (BMD) is a complication in children with inflammatory bowel disease (IBD). There are limited data evaluating dual-energy x-ray absorptiometry (DXA) as a screening tool for low BMD in children with IBD. We performed a single site retrospective analysis of DXA use.
Children aged 5-18 years with IBD diagnosed between 2013 to 2017 at the Royal Children's Hospital, Australia, were included. Patient demographics, measures of disease activity, DXA scores, and factors related to BMD were collected.
Over a median follow up of 5.1 (4-6.4) years, 72/239 (30.1%) children underwent DXA, and 28/239 (11.7%) children had a second DXA. Our DXA practice differed to consensus guidelines regarding initial screening based on height and/or body mass index (BMI) z-score (8/17 [47.1%]), and repeat surveillance (13/42 [31.0%]). Children had a median lumbar spine (LS) z-score -0.80 (-1.65-0.075). Children with LS z-score≤-2.0 (n=14) had lower weight (6.57 [1.78-23.7] vs. 51.1 [26.5-68.7], =0.0002) and height centiles (3.62 [1.17-17.1] vs. 42 [16.9-67.1], =0.0001), and higher faecal calprotectin (FCP) (3041 [1182-4192] vs. 585 [139-2419], =0.009) compared to children with LS z-score>-2.0. No fractures were reported. Of 28 children who underwent a second DXA 1.6 (1.1-2.2) years following initial DXA, no significant change in z-scores occurred.
Children with IBD had low BMD. In addition to height centile and weight centile, FCP was associated with lower BMD, and should be considered in DXA screening guidelines. Greater clinician awareness of DXA consensus guidelines is required. Future prospective studies are required.
低骨矿物质密度(BMD)是炎症性肠病(IBD)患儿的一种并发症。评估双能X线吸收法(DXA)作为IBD患儿低BMD筛查工具的数据有限。我们对DXA的使用进行了单中心回顾性分析。
纳入2013年至2017年在澳大利亚皇家儿童医院诊断为IBD的5至18岁儿童。收集患者人口统计学资料、疾病活动度指标、DXA评分以及与BMD相关的因素。
在中位随访5.1(4 - 6.4)年期间,72/239(30.1%)名儿童接受了DXA检查,28/239(11.7%)名儿童进行了第二次DXA检查。我们的DXA实践在基于身高和/或体重指数(BMI)z评分进行初始筛查(8/17 [47.1%])以及重复监测(13/42 [31.0%])方面与共识指南存在差异。儿童腰椎(LS)z评分的中位数为 -0.80(-1.65 - 0.075)。LS z评分≤ -2.0的儿童(n = 14)体重更低(6.57 [1.78 - 23.7] 对比 51.1 [26.5 - 68.7],P = 0.0002),身高百分位数更低(3.62 [1.17 - 17.1] 对比 42 [16.9 - 67.1],P = 0.0001),且粪便钙卫蛋白(FCP)更高(3041 [1182 - 4192] 对比 585 [139 - 2419],P = 0.009),这与LS z评分 > -2.0的儿童相比。未报告骨折情况。在初次DXA检查后1.6(1.1 - 2.2)年接受第二次DXA检查的28名儿童中,z评分无显著变化。
IBD患儿存在低BMD。除了身高百分位数和体重百分位数外,FCP与较低的BMD相关,应在DXA筛查指南中予以考虑。临床医生需要更好地了解DXA共识指南。未来需要进行前瞻性研究。