医学
家族性地中海热
秋水仙碱
疾病
人口
内科学
炎症
门诊部
关节炎
免疫学
环境卫生
作者
Pnina Langevitz,Avi Livneh,Lily Neumann,Dan Buskila,Joshua Shemer,D Amolsky,M Pras
出处
期刊:PubMed
日期:2001-01-01
卷期号:3 (1): 9-12
被引量:97
摘要
Familial Mediterranean fever is a genetic disorder manifested by recurrent attacks of peritonitis, pleuritis and arthritis, and characterized by clinical, histological and laboratory evidence for localized and systemic inflammation. Colchicine treatment usually prevents the attacks and the associated inflammation. Inflammation may play an important role in the initiation and progression of atherosclerosis and ischemic heart disease.To study the effect of inflammation and its prevention on the occurrence of IHD, using FMF as a model.We studied the presence of IHD and its risk factors in 290 FMF patients aged 40 years or more, and in two control groups--233 spouses of the FMF patients, and 126 patients with inflammatory diseases obtained from other outpatient clinics, FMF patients were also compared with age and gender-matched individuals from the population reference data of the Israel Ministry of Health.The prevalence of IHD in FMF patients was significantly lower than in the group of controls from other outpatient clinics (15.5% vs. 30.2%, P < 0.05) and comparable with their spouses (11.2%) and with the matched general population in Israel (16%).These findings suggest that despite the evidence of recurrent inflammation, colchicine-treated FMF patients are not more predisposed to IHD than the normal population.
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