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Osteoporosis in scleroderma.

机译:硬皮病中的骨质疏松症。

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摘要

Objective To review the literature describing the association of osteoporosis (OP) with scleroderma (SSc). Methods A Medline (PubMed) search identified all studies from 1966 to 2004 that investigated the association between OP and SSc. Search terms included "scleroderma," systemic sclerosis, densitometry," and "prevalence." Results Eight case control studies and 1 retrospective study (comparing OP status to a reference standard) were identified. There is no clear association between bone mineral density (BMD) scores and scleroderma. Two of 4 studies have reported lower BMD scores in SSc, but appear not to have considered possible confounding risk factors. Earlier age of menopause has been reported in 2 of 3 studies, and thus, may be a confounder in some samples of women with SSc. Studies of bone metabolism markers have not provided any consistent explanatory mechanism for increased OP in SSc, and such markers may be unreliable in SSc as these are affected by the altered collagen turnover and fibrosis characteristic of SSc. Conclusions It is unknown whether OP is truly increased in SSc or whether this association has been observed in some studies as a result of other confounding risk factors for OP. Clinical heterogeneity of SSc study samples and small sample sizes have contributed to the difficulty in obtaining valid estimates of the risk for the development of OP. There is no strong evidence in the literature for consistently lower BMD scores in SSc, or for altered biomarkers of bone resorption. Earlier menopause, corticosteroid use in some patients, and other factors secondary to SSc (such as malabsorption and inflammation), may be causal factors or may be confounders in studies of OP in SSc.
机译:目的回顾描述骨质疏松症(OP)与硬皮病(SSc)的相关文献。方法Medline(PubMed)搜索确定了1966年至2004年的所有研究,这些研究调查了OP和SSc之间的关系。搜索词包括“硬皮病”,“系统性硬化症”,“密度测定法”和“患病率”。结果确定了8例病例对照研究和1项回顾性研究(将OP状态与参考标准进行比较)。分数和硬皮病4项研究中有2项报告SSc的BMD分数较低,但似乎没有考虑可能的混杂危险因素。3项研究中有2项报告了更年期的提前,因此在某些研究中可能是混杂因素SSc妇女的样本。骨代谢标志物的研究尚未提供任何一致的解释来解释SSc OP的增加机制,并且这些标志物在SSc中可能不可靠,因为这些标志物受SSc胶原转换和纤维化特性改变的影响。尚不知道SS中OP是否确实增加,或者是否由于其他混杂的OP危险因素而在某些研究中观察到这种关联。 SSc研究样本的有效性和样本量小,导致难以获得有效的OP风险估计值。文献中没有强有力的证据表明SSc中的BMD分数始终较低,或者骨吸收的生物标志物发生了改变。更年期更早,某些患者使用皮质类固醇激素以及SSc继发的其他因素(例如吸收不良和炎症)可能是因果关系,也可能是SSc OP研究中的混杂因素。

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