Evolutionary Medicine Perspectives: Helicobacter pylori, Lactose Intolerance, and 3 Hypotheses for Functional and Inflammatory Gastrointestinal and Hepatobiliary Disorders

乳糖不耐受 幽门螺杆菌 医学 胃肠病学 内科学 有机化学 化学 乳糖
作者
Grigorios I. Leontiadis,George F. Longstreth
出处
期刊:The American Journal of Gastroenterology [American College of Gastroenterology]
被引量:3
标识
DOI:10.14309/ajg.0000000000001681
摘要

Many clinicians have suboptimal knowledge of evolutionary medicine. This discipline integrates social and basic sciences, epidemiology and clinical medicine, providing explanations, especially ultimate causes, for many conditions. Principles include genetic variation from population bottleneck and founder effects, evolutionary trade-offs and coevolution. For example, host-microbe coevolution contributes to the inflammatory and carcinogenic variability of Helicobacter pylori . Antibiotic-resistant strains are evolving, but future therapy could target pro-mutagenic proteins. Ancient humans practicing dairying achieved survival and reproduction advantages of post-weaning lactase persistence and passed this trait to modern descendants, delegitimizing lactose intolerance as “disease” in the majority of people with lactase non-persistence. Three evolutionary hypotheses are each relevant to multiple diseases: 1) The polyvagal hypothesis posits that prehistoric adaptation of autonomic nervous system reactions to stress is beneficial acutely but, when continued chronically, predisposes individuals to painful functional gastrointestinal disorders, in whom it may be a biomarker. 2) The thrifty gene hypothesis proposes genetic adaptation to feast-famine cycles among Pleistocene migrants to America that is mismatched with Indigenous Americans’ current diet and physical activity, predisposing them to obesity, nonalcoholic fatty liver disease, gallstones and their complications. 3) The hygiene hypothesis proposes alteration of the gut microbiome, with which humans have coevolved, in allergic and autoimmune disease pathogenesis; for example, association of microbiome-altering proton pump inhibitor use with pediatric eosinophilic esophagitis, early life gastrointestinal infection with celiac disease, and infant antibiotic use and an economically advanced environment with inflammatory bowel disease. Evolutionary perspectives broaden physicians’ understanding of disease processes, improve care, and stimulate research.
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