Rachapalli Satish M, Kiely Patrick D, Bourke Brian E
St George's Hospital, Blackshaw Road, Tooting, London, UK.
Clin Rheumatol. 2009 May;28(5):587-90. doi: 10.1007/s10067-009-1099-x. Epub 2009 Feb 10.
Chronic inflammatory autoimmune conditions like rheumatoid arthritis and systemic lupus erythematosus are associated with an increased risk of accelerated atherosclerosis (ATS). Very limited data are available about the incidence of ATS in patients with primary Sjogren's syndrome (PSS). Ankle brachial index (ABI) is a recognized method of detecting subclinical atherosclerosis. The objective of this study was to compare the prevalence of abnormal ABI in patients with PSS and in controls without PSS. Twenty-five PSS patients were compared with an age-, ethnicity-, and sex-matched control group. Traditional risk factors such as smoking, high blood pressure, blood sugar, lipids, and family history of atherosclerosis were assessed in both groups. Baseline clinical and laboratory features of PSS patients were recorded. ABI was measured in both groups. ABI less than 1.0 is considered abnormal. Fifty individuals (25 in each group) were studied. PSS patients and controls did not differ significantly in age, sex, and ethnicity. The prevalence of traditional cardiovascular risk factors was the same in both groups. Five out of 25 PSS patients (20%) had an ABI < 1.0 compared to one of 25 (4%) in the control group [P = 0.189 (odds ratio (OR) = 6.000 and 95% confidence interval (CI) 0.6464 to 55.692)]. Eight out of 25 PSS patients (32%) had disease duration of more than 10 years. This group of patients had a higher prevalence of low ABI compared to the individuals with lesser disease duration [P = 0.02 (OR = 16, 95% CI 1.38 to 185)]. PSS patients had a higher prevalence of low ABI, although this did not reach statistical significance. The subgroup of PSS patients with a longer duration of disease had a significantly lower ABI. This study was underpowered and a larger study is required to confirm the findings of this pilot study.
类风湿关节炎和系统性红斑狼疮等慢性炎症性自身免疫性疾病与动脉粥样硬化加速(ATS)风险增加相关。关于原发性干燥综合征(PSS)患者中ATS的发病率,现有数据非常有限。踝臂指数(ABI)是一种公认的检测亚临床动脉粥样硬化的方法。本研究的目的是比较PSS患者和无PSS的对照组中ABI异常的患病率。将25例PSS患者与年龄、种族和性别匹配的对照组进行比较。两组均评估了吸烟、高血压、血糖、血脂和动脉粥样硬化家族史等传统危险因素。记录PSS患者的基线临床和实验室特征。两组均测量了ABI。ABI小于1.0被认为异常。共研究了50人(每组25人)。PSS患者和对照组在年龄、性别和种族方面无显著差异。两组传统心血管危险因素的患病率相同。25例PSS患者中有5例(20%)ABI<1.0,而对照组25例中有1例(4%)[P = 0.189(比值比(OR)= 6.000,95%置信区间(CI)0.6464至55.692)]。25例PSS患者中有8例(32%)病程超过10年。与病程较短的个体相比,这组患者低ABI的患病率更高[P = 0.02(OR = 16,95% CI 1.38至185)]。PSS患者低ABI的患病率较高,尽管未达到统计学意义。病程较长的PSS患者亚组的ABI显著较低。本研究样本量不足,需要更大规模的研究来证实这项初步研究的结果。