- 现金
- 62111 元
- 精华
- 26
- 帖子
- 30437
- 注册时间
- 2009-10-5
- 最后登录
- 2022-12-28
|
Assessment of Bone Mineral Density in Tenofovir-Treated Patients With Chronic Hepatitis B: Can the Fracture Risk Assessment Tool Identify Those at Greatest Risk?
Upkar S. Gill1,
Alexandra Zissimopoulos2,
Safa Al-Shamma2,
Katherine Burke2,
Mark J. W. McPhail3,
David A. Barr4,
Yiannis N. Kallis2,
Richard T. C. Marley2,
Paul Kooner2,
Graham R. Foster1 and
Patrick T. F. Kennedy1
+ Author Affiliations
1Hepatology Unit, Centre for Digestive Diseases, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London
2Department of Hepatology, Barts Health NHS Trust
3Department of Hepatology, Faculty of Medicine, Imperial College London, St Mary's Hospital, Paddington
4Department of Infectious Diseases, Brownlee Centre for Infectious and Communicable Diseases, NHS Greater Glasgow and Clyde, United Kingdom
Correspondence: Patrick T. F. Kennedy, MD, Blizard Institute, Barts and The London School of Medicine & Dentistry, Queen Mary University of London, 4 Newark St, London, UK, E1 2AT ([email protected]).
Presented in part: British Society of Gastroenterology (BSG), Birmingham, United Kingdom, March 2011. PTH-085; European Association for the Study of Liver (EASL), Berlin, Germany, April 2011. S32; British Association for the Study of Liver (BASL), London, United Kingdom, September 2011. 61; American Association for the Study of Liver Disease (AASLD), San Francisco, November 2011. 1012; American Association for the Study of Liver Disease (AASLD), Boston, November 2012. 201; British Society of Gastroenterology (BSG), Glasgow, United Kingdom, March 2013. PWE-144.
Abstract
Background. Tenofovir disoproxil fumarate (TDF) is an established nucleotide analogue in the treatment of chronic hepatitis B. Bone mineral density loss has been described in TDF-treated patients with human immunodeficiency virus infection, but limited data exist for patients with chronic hepatitis B. Dual X-ray absorptiometry (DEXA) was used to determine bone mineral density changes in TDF-exposed patients. We evaluated the accuracy of the Fracture Risk Assessment Tool (FRAX) as an alternative to DEXA in clinical practice.
Methods. A total of 170 patients were studied: 122 were exposed to TDF, and 48 were controls. All patients underwent DEXA, and demographic details were recorded. FRAX scores (before and after DEXA) were calculated.
Results. TDF was associated with a lower hip T score (P = .02). On univariate and multivariate analysis, advancing age, smoking, lower body mass index, and TDF exposure were independent predictors of low bone mineral density. In addition, the pre-DEXA FRAX score was an accurate predictor of the post-DEXA FRAX treatment recommendation (100% sensitivity and 83% specificity), area under the curve 0.93 (95% CI, .87–.97, P < .001).
Conclusions. TDF-treated patients with chronic hepatitis B have reduced bone mineral density, but the reduction is limited to 1 anatomical site. Age and advanced liver disease are additional contributing factors, underlining the importance of multifactorial fracture risk assessment. FRAX can accurately identify those at greatest risk of osteoporotic fracture.
|
|