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Updated: Aug 24, 2025

Quantitative Polymerase Chain Reaction-based Analyses of Murine Intestinal Microbiota After Oral Antibiotic Treatment
Published on: November 17, 2018
"Growth-Promoting Effect" of Antibiotic Use Could Explain the Global Obesity Pandemic: A European Survey
Gábor Ternák1, Márton Németh2, Martin Rozanovic2
1Institute of Migration Health, Medical School, University of Pécs, H-7624 Pécs, Hungary.
Insights
Early antibiotic use is linked to childhood obesity. Certain antibiotic classes may promote obesity by altering the gut microbiome, potentially explaining the global obesity pandemic.
Area of Science:
- Microbiology
- Public Health
- Epidemiology
Background:
- Clinical observations suggest a link between early-life antibiotic exposure and increased childhood obesity rates.
- Experimental studies implicate a modified gut microbiome in obesity development.
- Antibiotic-induced dysbiosis is a potential factor in the rising obesity epidemic.
Purpose of the Study:
- To identify specific antibiotic classes associated with promoting or inhibiting obesity-related gut dysbiosis.
- To analyze correlations between antibiotic consumption patterns and obesity prevalence across European countries.
Main Methods:
- Compiled a database of average yearly antibiotic consumption (2008-2018) from European Centre for Disease Prevention and Control (ECDC) reports for 30 European countries.
- Compared antibiotic consumption data with childhood and adult obesity prevalence from the Obesity Atlas.
- Utilized Pearson's chi-square test, one-way ANOVA, and logistic regression analysis to assess correlations and odds ratios.
Main Results:
- Found strong positive associations between childhood obesity and consumption of systemic antibiotics, broad-spectrum, beta-lactamase-resistant penicillin, cephalosporin, and quinolone.
- Identified a negative correlation between obesity and consumption of tetracycline, broad-spectrum, beta-lactamase-sensitive penicillin, and narrow-spectrum, beta-lactamase-sensitive penicillin.
- Specific antibiotic classes may have a 'growth-promoting effect' contributing to obesity.
Conclusions:
- Certain antibiotic classes are significantly associated with increased obesity rates.
- The "growth-promoting effect" of specific antibiotics on gut microbiota may be a key factor in the obesity pandemic.
- Further research into antibiotic stewardship is warranted to mitigate obesity risks.
Abstract:
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".
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