Fouda Mona A, Khan Aliya A, Sultan Muhammad Saad, Rios Lorena P, McAssey Karen, Armstrong David
College of Medicine, King Saudi University, Riyadh, Saudi Arabia.
Can J Gastroenterol. 2012 Nov;26(11):819-29. doi: 10.1155/2012/823648.
To review the evaluation and management of skeletal health in patients with celiac disease (CD), and to make recommendations on screening, diagnosis, treatment and follow-up of low bone mineral density (BMD) in CD patients.
A multidisciplinary team developed clinically relevant questions for review. An electronic search of the literature was conducted using the MEDLINE and EMBASE databases from 1996 to 2010. All original studies, reviews and guidelines, both pediatric and adult, were included. A document summarizing the results of the review and proposed recommendations was prepared and underwent multiple revisions until consensus was reached.
At diagnosis, approximately one-third of adult CD patients have osteoporosis, one-third have osteopenia and one-third have normal BMD. Children with CD have low bone mass at diagnosis. Adult and pediatric CD patients are at increased risk of fractures.
For adults, serum calcium, albumin, 25(OH) vitamin D3, parathyroid hormone and 24 h urine calcium testing should be performed at diagnosis; patients with 'classic' CD and those at risk for osteoporosis should undergo a dual x-ray absorptiometry scan. An abnormal baseline dual x-ray absorptiometry scan should be repeated one to two years after initiation of a gluten-free diet (GFD). For children, BMD should be assessed one year after diagnosis if GFD adherence is not strict. A GFD is the most important treatment for bone loss. Supplemental antiresorptives may be justified in those who remain at high fracture risk (eg, postmenopausal women, older men) after implementation of a GFD.
Current evidence does not support the screening of all CD patients for low BMD at diagnosis. Follow-up BMD assessment should be performed one to two years after initiation of a GFD.
回顾乳糜泻(CD)患者骨骼健康的评估与管理,并就CD患者低骨密度(BMD)的筛查、诊断、治疗及随访提出建议。
一个多学科团队提出了具有临床相关性的问题以供回顾。使用MEDLINE和EMBASE数据库对1996年至2010年的文献进行了电子检索。纳入了所有儿科和成人的原始研究、综述及指南。编写了一份总结回顾结果并提出建议的文件,该文件经过多次修订直至达成共识。
在诊断时,约三分之一的成年CD患者患有骨质疏松症,三分之一患有骨质减少,三分之一的骨密度正常。CD患儿在诊断时骨量较低。成年和儿科CD患者骨折风险增加。
对于成年人,诊断时应进行血清钙、白蛋白、25(OH)维生素D3、甲状旁腺激素和24小时尿钙检测;患有“典型”CD的患者以及有骨质疏松症风险的患者应接受双能X线吸收测定扫描。异常基线双能X线吸收测定扫描应在开始无麸质饮食(GFD)后1至2年重复进行。对于儿童,如果GFD依从性不严格,应在诊断后1年评估骨密度。GFD是治疗骨质流失最重要的方法。对于在实施GFD后仍处于高骨折风险的患者(如绝经后女性、老年男性),补充抗吸收药物可能是合理的。
目前的证据不支持在诊断时对所有CD患者进行低骨密度筛查。应在开始GFD后1至2年进行随访骨密度评估。