Wawro Nina, Amann Ute, Butt Julia, Meisinger Christa, Akmatov Manas K, Pessler Frank, Peters Annette, Rathmann Wolfgang, Kääb Stefan, Waterboer Tim, Linseisen Jakob
German Research Center for Environmental Health (GmbH), Institute of Epidemiology II, Munich, Germany.
German Center for Diabetes Research (DZD e.V.), Munich, Germany.
Front Public Health. 2019 Apr 24;7:96. doi: 10.3389/fpubh.2019.00096. eCollection 2019.
() is a common infection and known risk factor for gastric cancer. We assessed cross-sectional and longitudinal associations to study the impact of seropositivity on metabolic diseases. seropositivity in serum samples of the KORA study was analyzed by multiplex serology. We calculated sex-specific prevalence of seropositivity for the year 2007 based on the first follow-up survey (termed F4) of the KORA study S4. We identified factors associated with seropositivity in the F4 survey. Further, we assessed relative risks of incident metabolic diseases/risk factors at the time of the second follow-up survey of S4 (termed FF4) and seropositivity at the F4 survey as a determinant. Models were adjusted for age, sex, overweight status, physical activity, smoking status, education level, alcohol intake, and other metabolic diseases. Based on 3,037 persons aged 32 to 82 years, the prevalence for 2007 was 30.2% in men ( = 1,465) and 28.1% in women ( = 1,572). Increasing age, current smoking, low education and no alcohol intake were significantly associated with seropositivity in the F4 survey. However, no association between seropositivity and BMI, metabolic diseases (type 2 diabetes, hypertension and dyslipidemia, gout or increased uric acid) and gastrointestinal diseases (gastritis, inflammatory bowel disease, and gastric or duodenal ulcer) was observed. No significant associations between seropositivity and one of the five investigated incident metabolic diseases/risk factors were detected in the longitudinal analysis. We identified associations between age, smoking, education and alcohol intake and seropositivity but no impact of seropositivity on incident metabolic diseases/risk factors.
()是一种常见感染,也是已知的胃癌危险因素。我们评估了横断面和纵向关联,以研究血清阳性对代谢性疾病的影响。通过多重血清学分析了德国社区健康研究(KORA)血清样本中的血清阳性情况。我们根据KORA研究S4的首次随访调查(称为F4)计算了2007年血清阳性的性别特异性患病率。我们在F4调查中确定了与血清阳性相关的因素。此外,我们将S4的第二次随访调查(称为FF4)时发生的代谢性疾病/危险因素的相对风险以及F4调查时的血清阳性作为决定因素进行了评估。模型针对年龄、性别、超重状况、身体活动、吸烟状况、教育水平、酒精摄入量和其他代谢性疾病进行了调整。基于3037名年龄在32至82岁之间的人,2007年男性患病率为30.2%(n = 1465),女性为28.1%(n = 1572)。在F4调查中,年龄增加、当前吸烟、低教育水平和不饮酒与血清阳性显著相关。然而,未观察到血清阳性与体重指数、代谢性疾病(2型糖尿病、高血压、血脂异常、痛风或尿酸升高)和胃肠道疾病(胃炎、炎症性肠病以及胃或十二指肠溃疡)之间存在关联。在纵向分析中,未检测到血清阳性与所调查的五种新发代谢性疾病/危险因素之一之间存在显著关联。我们确定了年龄、吸烟、教育和酒精摄入与血清阳性之间的关联,但血清阳性对新发代谢性疾病/危险因素没有影响。