Ternák Gábor, Németh Márton, Rozanovic Martin, Márovics Gergely, Bogár Lajos
Institute of Migration Health, Medical School, University of Pécs, H-7624 Pécs, Hungary.
Department of Anesthesiology and Intensive Care, Medical School, University of Pécs, H-7624 Pécs, Hungary.
Antibiotics (Basel). 2022 Sep 28;11(10):1321. doi: 10.3390/antibiotics11101321.
Clinical observations indicated a higher rate of obesity among children who received antibiotics at early ages. Experimental studies supported the role of the modified gut microbiome in the development of obesity as well. For identifying antibiotic classes that might promote or inhibit obesity-related dysbiosis, a database of the average yearly antibiotic consumption (2008-2018) has been developed using the European Center for Disease Prevention and Control (ECDC) yearly reports of antibiotic consumption in the community for the major antibiotic classes in 30 European countries, which were compared to the childhood and adult obesity prevalence featured in the Obesity Atlas. Pearson's chi-square test was applied to estimate positive/negative correlations between antibiotic consumption and obesity. One-way ANOVA has been applied to test the differences in antibiotic consumption between groups, and logistic regression analysis was performed to determine the odds ratios (OR) of antibiotic consumption for obesity. Strong, positive associations were estimated between childhood obesity and the total consumption of systemic antibiotics, broad-spectrum, beta-lactamase-resistant penicillin, cephalosporin, and quinolone, and a negative correlation was found with the consumption of tetracycline, broad-spectrum, beta-lactamase-sensitive penicillin, and narrow-spectrum, beta-lactamase-sensitive penicillin. Our observation indicated that the "growth-promoting effect" of the consumption of certain antibiotic classes might be identified as a possible etiology in the development of obesity and might be the explanation for the obesity "pandemic".
临床观察表明,早年接受抗生素治疗的儿童肥胖率较高。实验研究也支持了肠道微生物群改变在肥胖发展中的作用。为了确定可能促进或抑制肥胖相关生态失调的抗生素类别,利用欧洲疾病预防控制中心(ECDC)关于30个欧洲国家主要抗生素类别的社区抗生素年度消费报告,建立了一个2008 - 2018年平均年度抗生素消费数据库,并将其与《肥胖地图集》中的儿童和成人肥胖患病率进行比较。采用Pearson卡方检验来估计抗生素消费与肥胖之间的正/负相关性。应用单因素方差分析来检验各组之间抗生素消费的差异,并进行逻辑回归分析以确定抗生素消费导致肥胖的优势比(OR)。估计儿童肥胖与全身用抗生素、广谱、β-内酰胺酶耐药青霉素、头孢菌素和喹诺酮的总消费量之间存在强正相关,而与四环素、广谱、β-内酰胺酶敏感青霉素和窄谱、β-内酰胺酶敏感青霉素的消费量呈负相关。我们的观察表明,某些抗生素类别的消费所产生的“促生长效应”可能被确定为肥胖发展的一种可能病因,并且可能是肥胖“大流行”的解释。