Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Diabetes Care. 2013 Mar;36(3):701-7. doi: 10.2337/dc12-1089. Epub 2012 Nov 16.
Ad36, a human adenovirus, increases adiposity but improves glycemic control in animal models. Similarly, natural Ad36 infection is cross-sectionally associated with greater adiposity and better glycemic control in humans. This study compared longitudinal observations in indices of adiposity (BMI and body fat percentage) and glycemic control (fasting glucose and insulin) in Ad36-infected versus uninfected adults.
Baseline sera from Hispanic men and women (n = 1,400) were screened post hoc for the presence of Ad36-specific antibodies. Indices of adiposity and glycemic control at baseline and at ~10 years past the baseline were compared between seropositive and seronegative subjects, with adjustment for age and sex. In addition to age and sex, indices of glycemic control were adjusted for baseline BMI and were analyzed only for nondiabetic subjects.
Seropositive subjects (14.5%) had greater adiposity at baseline, compared with seronegative subjects. Longitudinally, seropositive subjects showed greater adiposity indices but lower fasting insulin levels. Subgroup analyses revealed that Ad36-seropositivity was associated with better baseline glycemic control and lower fasting insulin levels over time in the normal-weight group (BMI ≤25 kg/m(2)) and longitudinally, with greater adiposity in the overweight (BMI 25-30 kg/m(2)) and obese (BMI >30 kg/m(2)) men. Statistically, the differences between seropositive and seronegative individuals were modest in light of the multiple tests performed.
This study strengthens the plausibility that in humans, Ad36 increases adiposity and attenuates deterioration of glycemic control. Panoptically, the study raises the possibility that certain infections may modulate obesity or diabetes risk. A comprehensive understanding of these under-recognized factors is needed to effectively combat such metabolic disorders.
人腺病毒 36(Ad36)在动物模型中可增加肥胖度,但改善血糖控制。同样,Ad36 的自然感染与人类的更大肥胖度和更好的血糖控制呈横断面相关。本研究比较了 Ad36 感染与未感染成年人的肥胖指标(BMI 和体脂百分比)和血糖控制(空腹血糖和胰岛素)的纵向观察结果。
对西班牙裔男性和女性(n = 1400)的基础血清进行了 Ad36 特异性抗体的事后筛查。比较了血清阳性和血清阴性受试者的基线和基线后约 10 年的肥胖和血糖控制指标,调整了年龄和性别。除了年龄和性别外,血糖控制指标还根据基线 BMI 进行了调整,仅对非糖尿病患者进行了分析。
与血清阴性者相比,血清阳性者(14.5%)基线时肥胖度更大。纵向研究显示,血清阳性者的肥胖指数较高,但空腹胰岛素水平较低。亚组分析显示,在正常体重组(BMI ≤25 kg/m²)中,Ad36 血清阳性与更好的基线血糖控制和随时间推移的空腹胰岛素水平降低相关,而在超重(BMI 25-30 kg/m²)和肥胖(BMI >30 kg/m²)男性中,Ad36 血清阳性与随时间推移的肥胖程度增加相关。从统计学角度来看,考虑到进行了多次测试,血清阳性者与血清阴性者之间的差异不大。
本研究进一步证实了 Ad36 在人类中可增加肥胖度并减轻血糖控制恶化的可能性。总体而言,该研究提出了一种可能性,即某些感染可能会调节肥胖或糖尿病风险。为了有效治疗这些被低估的代谢疾病,需要全面了解这些未被充分认识的因素。