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肝硬化患者骨质疏松症的患病率:一项系统评价和荟萃分析。

Prevalence of Osteoporosis in Cirrhosis: A Systematic Review and Meta-Analysis.

作者信息

Kang Jennifer, Gopakumar Harishankar, Puli Srinivas R

机构信息

Gastroenterology and Hepatology, University of Illinois, Peoria, USA.

出版信息

Cureus. 2023 Jan 12;15(1):e33721. doi: 10.7759/cureus.33721. eCollection 2023 Jan.

Abstract

The prevalence of osteoporosis in individuals with cirrhosis varies based on the diagnostic approach and etiology of the underlying liver disease. This systematic review aims to evaluate the prevalence of osteoporosis in individuals with cirrhosis. Electronic databases were searched for studies reporting the prevalence of osteoporosis among patients with cirrhosis. The primary outcome was the presence of osteoporosis, as determined by a dual-energy x-ray absorptiometry (DEXA) scan. Secondary outcomes were levels of biochemical markers of bone metabolism, including calcium, vitamin D, phosphorus, and parathormone (PTH) levels. A cohort of 836 patients from 10 studies was included in the final analysis. The pooled rate of osteoporosis was 14.80% (95% CI: 14.19-15.49). Pooled levels of biochemical markers of bone metabolism were as follows: calcium 9.09 mg/dL (95% CI: 8.73-9.45), 25-hydroxyvitamin D (25-OH vitamin D) 15.41 ng/mL (95% CI: 14.79-16.03), phosphorus 15.41 mg/dL (95% CI: 2.99-3.51), and PTH 26.58 pg/mL (95% CI: 25.45-27.71). Pooled levels of liver biochemistries were: bilirubin 3.04 mg/dL (95% CI: 2.84-3.25), aspartate aminotransferase (AST) 65.35 U/L (95% CI: 61.39-69.31), alanine aminotransferase (ALT) 50.17 U/L (95% CI: 46.18-54.10), alkaline phosphatase 133.31 U/L (95% CI: 124.89-141.73), and albumin 3.25 g/dL (95% CI: 3.05-3.45). Cirrhosis appears to be associated with an increased risk for osteoporosis, with a pooled prevalence of 15%. This can include men and individuals younger than 50 years of age, a cohort not typically considered to be at an increased risk of osteoporosis. Levels of 25-hydroxyvitamin D and insulin-like growth factor-1 (IGF-1) were also significantly low. Further studies are required to evaluate the risk of osteoporosis based on the etiology and stage of cirrhosis, especially in younger males, to incorporate this into future prediction models for fragility fractures.

摘要

肝硬化患者骨质疏松症的患病率因潜在肝病的诊断方法和病因不同而有所差异。本系统评价旨在评估肝硬化患者骨质疏松症的患病率。通过电子数据库检索报告肝硬化患者骨质疏松症患病率的研究。主要结局是通过双能X线吸收测定法(DEXA)扫描确定的骨质疏松症的存在情况。次要结局是骨代谢生化标志物的水平,包括钙、维生素D、磷和甲状旁腺激素(PTH)水平。最终分析纳入了来自10项研究的836例患者队列。骨质疏松症的合并患病率为14.80%(95%CI:14.19 - 15.49)。骨代谢生化标志物的合并水平如下:钙9.09mg/dL(95%CI:8.73 - 9.45),25 - 羟基维生素D(25 - OH维生素D)15.41ng/mL(95%CI:14.79 - 16.03),磷15.41mg/dL(95%CI:2.99 - 3.51),PTH 26.58pg/mL(95%CI:25.45 - 27.71)。肝脏生化指标的合并水平为:胆红素3.04mg/dL(95%CI:2.84 - 3.25),天冬氨酸转氨酶(AST)65.35U/L(95%CI:61.39 - 69.31),丙氨酸转氨酶(ALT)50.17U/L(95%CI:46.18 - 54.10),碱性磷酸酶133.31U/L(95%CI:124.89 - 141.73),白蛋白3.25g/dL(95%CI:3.05 - 3.45)。肝硬化似乎与骨质疏松症风险增加有关,合并患病率为15%。这包括男性和年龄小于50岁的个体,这一群体通常不被认为骨质疏松症风险增加。25 - 羟基维生素D和胰岛素样生长因子 - 1(IGF - 1)水平也显著降低。需要进一步研究根据肝硬化的病因和阶段评估骨质疏松症风险,尤其是在年轻男性中,以便将其纳入未来脆性骨折预测模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1cf/9922208/1f5e030dd11b/cureus-0015-00000033721-i01.jpg

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