Center for Evidence-based Healthcare, Medizinische Fakultät Carl Gustav Carus, TU Dresden, Dresden, Germany; University Allergy Center, TU Dresden, Dresden, Germany.
Center for Evidence-based Healthcare, Medizinische Fakultät Carl Gustav Carus, TU Dresden, Dresden, Germany.
J Allergy Clin Immunol. 2016 Jan;137(1):130-136. doi: 10.1016/j.jaci.2015.06.029. Epub 2015 Aug 4.
Atopic dermatitis (AD) is characterized by epidermal barrier failure and immune-mediated inflammation. Evidence on AD as a potential risk factor for inflammatory comorbidities is scarce.
We sought to test the hypothesis that prevalent AD is a risk factor for incident rheumatoid arthritis (RA) and inflammatory bowel disease (IBD; Crohn disease [CD], ulcerative colitis [UC]) and is inversely related to type 1 diabetes (T1D) and to investigate established RA, IBD, and T1D susceptibility loci in AD.
This cohort study used data from German National Health Insurance beneficiaries aged 40 years or younger (n = 655,815) from 2005 through 2011. Prevalent AD in the period 2005 to 2006 was defined as primary exposure, and incident RA, IBD, and T1D in the period 2007 to 2011 were defined as primary outcomes. Risk ratios were calculated with generalized linear models. Established RA, IBD, and T1D loci were explored in high-density genotyping data from 2,425 cases with AD and 5,449 controls.
Patients with AD (n = 49,847) were at increased risk for incident RA (risk ratio [RR], 1.72; 95% CI, 1.25-2.37) and/or IBD (CD: RR, 1.34; 95% CI, 1.11-1.61; UC: RR, 1.25; 95% CI, 1.03-1.53). After adjusting for health care utilization, there was a nominally significant inverse effect on T1D risk (RR, 0.72; 95% CI, 0.53-0.998). There was no disproportionate occurrence of known RA, CD, UC, or T1D risk alleles in AD.
AD is a risk factor for the development of RA and IBD. This excess comorbidity cannot be attributed to major known IBD and RA genetic risk factors.
特应性皮炎(AD)的特征是表皮屏障功能障碍和免疫介导的炎症。AD 是炎症性合并症潜在危险因素的证据很少。
我们试图验证以下假设,即现患 AD 是发生类风湿关节炎(RA)和炎症性肠病(IBD;克罗恩病[CD]、溃疡性结肠炎[UC])的危险因素,并且与 1 型糖尿病(T1D)呈负相关,并研究 AD 中的已确定的 RA、IBD 和 T1D 易感性基因座。
本队列研究使用了 2005 年至 2011 年期间德国国家健康保险受益人的数据,年龄在 40 岁或以下(n=655815)。2005 年至 2006 年期间患有的 AD 定义为主要暴露,2007 年至 2011 年期间发生的 RA、IBD 和 T1D 定义为主要结局。使用广义线性模型计算风险比。在 2425 例 AD 患者和 5449 例对照的高密度基因分型数据中探索了已确定的 RA、IBD 和 T1D 基因座。
AD 患者(n=49847)发生 RA(风险比[RR],1.72;95%CI,1.25-2.37)和/或 IBD(CD:RR,1.34;95%CI,1.11-1.61;UC:RR,1.25;95%CI,1.03-1.53)的风险增加。在调整医疗保健利用率后,T1D 风险呈名义上的显著降低趋势(RR,0.72;95%CI,0.53-0.998)。AD 中未出现不成比例的已知 RA、CD、UC 或 T1D 风险等位基因。
AD 是 RA 和 IBD 发展的危险因素。这种合并症的增加不能归因于主要的已知的 IBD 和 RA 遗传危险因素。