Chaudhary Prateek, Chen Xing, Assassi Shervin, Gorlova Olga, Draeger Hilda, Harper Brock E, Gonzalez Emilio, McNearney Terry, Perry Marilyn, Arnett Frank C, Mayes Maureen D
University of Texas Health Science Center at Houston, Houston, TX, USA.
Arthritis Rheum. 2011 Oct;63(10):3098-102. doi: 10.1002/art.30492.
To investigate the association of cigarette smoking with susceptibility to systemic sclerosis (SSc) in a large, well-defined patient population.
We conducted a review of 1,379 patients with SSc enrolled in the Scleroderma Family Registry and DNA Repository and/or the Genetics versus Environment in Scleroderma Outcome Study cohort. Smoking history was obtained from chart review or via telephone interview. Patients with SSc were subsequently categorized as never smokers or ever smokers. Patients with SSc for whom smoking data were available were matched 2:1 by age, sex, ethnicity, and state of residence to control subjects, using the Behavioral Risk Factor Surveillance System.
The majority of patients were white (74.2%), with Hispanics and blacks representing 11.3% and 9.7%, respectively. Most patients had limited cutaneous involvement (54%). For our comparative analyses, 621 patients were matched with control subjects. There was no significant difference in age, sex, ethnicity, and SSc subtype between matched versus unmatched patients. The majority of patients had never smoked (57%), while 43% of patients were classified as ever smokers. The patients with SSc did not differ from control subjects in terms of their smoking behavior (odds ratio [OR] 1.020, 95% confidence interval [95% CI] 0.839-1.240, P=0.842). Anti-topoisomerase I antibody-positive patients were more likely to be never smokers (OR 0.648, 95% CI 0.421-0.998, P=0.049), whereas no such association was observed with anticentromere and anti-RNA polymerase III antibodies.
Unlike its role in rheumatoid arthritis, smoking does not confer a risk for development of SSc, although it may impact disease severity.
在一个大型、明确界定的患者群体中,研究吸烟与系统性硬化症(SSc)易感性之间的关联。
我们对1379例纳入硬皮病家族登记处和DNA储存库及/或硬皮病结局研究队列中的遗传因素与环境因素研究的SSc患者进行了回顾性分析。吸烟史通过病历审查或电话访谈获得。随后,将SSc患者分为从不吸烟者或曾经吸烟者。利用行为危险因素监测系统,将有吸烟数据的SSc患者按年龄、性别、种族和居住州以2:1的比例与对照受试者进行匹配。
大多数患者为白人(74.2%),西班牙裔和黑人分别占11.3%和9.7%。大多数患者有局限性皮肤受累(54%)。在我们的比较分析中,621例患者与对照受试者进行了匹配。匹配患者与未匹配患者在年龄、性别、种族和SSc亚型方面无显著差异。大多数患者从不吸烟(57%),而43%的患者被归类为曾经吸烟者。SSc患者与对照受试者在吸烟行为方面无差异(优势比[OR]为1.020,95%置信区间[95%CI]为0.839 - 1.240,P = 0.842)。抗拓扑异构酶I抗体阳性的患者更可能从不吸烟(OR为0.648,95%CI为0.421 - 0.998,P = 0.049),而在抗着丝点抗体和抗RNA聚合酶III抗体方面未观察到此类关联。
与吸烟在类风湿关节炎中的作用不同,吸烟虽然可能影响疾病严重程度,但不会增加患SSc的风险。