干扰素- α和利巴韦林诱导的甲状腺功能障碍与巴基斯坦亚裔慢性丙型肝炎患者疾病严重程度和治疗反应的关系

Hepatitis research and treatment Pub Date : 2012-01-01 Epub Date: 2012-09-02 DOI:10.1155/2012/864315
Amina Nadeem, Muhammad Aslam
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引用次数: 9

摘要

目标。目的:探讨慢性丙型肝炎患者甲状腺功能障碍与疾病严重程度及治疗反应的关系。队列研究。病人。167例非肝硬化慢性丙型肝炎患者分为治疗组(n = 107)和对照组(n = 60)。测量。化学发光法测定基线S. ALT、S. AST及S. TSH、S.游离T4、S. t3水平。采用肝活检Knodell组织病理学指数(HPI)测定疾病的严重程度。研究组患者接受了24周的干扰素和利巴韦林治疗,并在第0、12和24周检测甲状腺功能。通过聚合酶链反应-丙型肝炎病毒试验确定对治疗的反应。结果:20例(18.69%)患者出现甲状腺功能障碍,相对危险度(RR)为11.25,归因危险度(AR)为91%。女性患病风险更高。甲状腺功能减退较甲状腺功能亢进常见。甲状腺功能障碍与疾病严重程度(P = 0.81)和对治疗的反应(P = 0.79)之间无显著相关性。结论。干扰素- α和利巴韦林治疗可诱导慢性丙型肝炎患者甲状腺功能障碍。疾病的严重程度和对干扰素诱导的甲状腺功能障碍的治疗反应之间没有关联。
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Association of interferon-alpha and ribavirin-induced thyroid dysfunction with severity of disease and response to treatment in pakistani asian patients of chronic hepatitis C.

Objective. To determine the association of thyroid dysfunction with the severity of the disease and response to treatment in patients of chronic hepatitis C. Design. Cohort study. Patients. One hundred and sixty seven noncirrhotic chronic hepatitis C patients were grouped into treatment group (n = 107) and control group (n = 60). Measurements. Baseline S. ALT and S. AST by IFCC and S. TSH, S. free T4, and S.T3 level were measured by chemiluminescence method. The severity of the disease was measured by Knodell histopathological index (HPI) on liver biopsy. Study group patients underwent 24-weeks IFN and ribavirin therapy and thyroid functions were determined at weeks 0, 12, and 24. Response to therapy was determined by PCR-HCV test. Results. 20 treated patients (18.69%) developed thyroid dysfunction with relative risk (RR) of 11.25 and attributable risk (AR) of 91%. Females were at higher risk. Hypothyroidism was common than hyperthyroidism. There was no significant association between thyroid dysfunction and severity of the disease (P = 0.81) and response to therapy (P = 0.79). Conclusion. Interferon-alpha and ribavirin therapy induces thyroid dysfunction in chronic hepatitis C patients. There is no association between severity of disease and response to therapy with interferon-induced thyroid dysfunction.

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