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首页> 外文期刊>Journal of viral hepatitis. >Prospective study of bone mineral density and metabolism in patients with chronic hepatitis C during pegylated interferon alpha and ribavirin therapy.
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Prospective study of bone mineral density and metabolism in patients with chronic hepatitis C during pegylated interferon alpha and ribavirin therapy.

机译:聚乙二醇干扰素α和利巴韦林治疗期间慢性丙型肝炎患者骨矿物质密度和代谢的前瞻性研究。

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The importance of osteoporosis as a complication of end-stage liver disease is well known. However, significant osteopenia may occur in earlier stages of chronic hepatitis C (CHC). Furthermore, antiviral therapy may influence bone metabolism. Thirty patients with CHC genotype 1 infection and without established cirrhosis were treated with peginterferon-alfa and ribavirin. Dual-energy x-ray absorptiometry was performed at baseline, after 48 weeks of therapy, and by the end of a 24-week follow-up period. Bone mineral density (BMD), T-scores, and Z-scores were assessed. Serum C-terminal propeptide of type I collagen (CICP) and osteocalcin levels were measured. Thirteen patients had osteopenia (43%) and osteoporosis was present in four patients (13%). Antiviral therapy led to significant on-treatment increases of lumbar spine and hip BMD (P < or = 0.05) as well as T-scores (P < or = 0.05) and Z-scores (P < or = 0.01) irrespective of subsequent treatment response. Further analyses showed that in patients with sustained virological response (n = 19) most parameters remained highly above baseline values by the end of the 24-week follow-up period, while patients with virological relapse (n = 11) had decreases of BMD, T-scores and Z-scores thereafter that did not differ from baseline. Serum CICP and osteocalcin levels decreased during therapy. Osteocalcin levels remained below baseline in sustained responder, but showed an increase in relapsers by the end of the 24-week follow-up (P < or = 0.05). Osteopenia is detectable in a substantial proportion of CHC patients without established cirrhosis. Antiviral therapy leads to an on-treatment increase of BMD, which may last in those patients who achieve a sustained virological response.
机译:骨质疏松作为终末期肝病并发症的重要性众所周知。但是,在慢性丙型肝炎(CHC)的早期阶段可能会发生大量骨质减少。此外,抗病毒治疗可能会影响骨代谢。接受聚乙二醇干扰素-α和利巴韦林治疗的30例CHC基因1型感染且无肝硬化的患者。在治疗后48周,以及在24周的随访期结束时,在基线进行了双能X线骨密度仪。评估骨矿物质密度(BMD),T分数和Z分数。测量血清I型胶原C末端前肽(CICP)和骨钙素水平。 13名患者患有骨质减少(43%),四名患者中存在骨质疏松症(13%)。抗病毒治疗导致腰椎和髋部BMD(P <或= 0.05)以及T分数(P <或= 0.05)和Z分数(P <或= 0.01)的治疗中显着增加,而与后续治疗无关响应。进一步的分析表明,在持续病毒学应答(n = 19)的患者中,到24周随访期结束时,大多数参数仍远远高于基线值,而病毒学复发的患者(n = 11)的BMD降低了,其后的T分数和Z分数与基线无差异。治疗期间血清CICP和骨钙蛋白水平降低。持续响应者的骨钙素水平仍低于基线,但在24周随访结束时复发率增加(P <或= 0.05)。在绝大部分未确诊肝硬化的CHC患者中可检测到骨质减少。抗病毒治疗会导致治疗中BMD的升高,这可能在获得持续病毒学应答的患者中持续存在。

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