The complex interplay where the effect of an environmental exposure on a physiological trait or disease risk is conditional on an individual’s specific genetic makeup. This concept acknowledges that an individual’s response to factors like diet, stress, or exogenous hormones is not solely determined by genes or environment alone. Understanding this interaction is crucial for personalized medicine, allowing clinicians to tailor interventions based on an individual’s genetic susceptibility.
Origin
This term emerged from the fields of quantitative genetics and epidemiology, gaining prominence as genetic sequencing became more accessible in the late 20th and early 21st centuries. It moved beyond simple Mendelian inheritance to explain the multifactorial nature of common chronic diseases. In endocrinology, it explains why hormonal interventions yield varied responses among different patients.
Mechanism
The mechanism often involves environmental factors influencing gene expression through epigenetic modifications, which are then contingent upon specific genetic polymorphisms. For example, a genetic variation in a hormone-metabolizing enzyme might only manifest as a clinical problem when a certain dietary component is consumed. The environment acts as a switch, activating or modulating the expression of a pre-existing genetic predisposition, thus altering the individual’s metabolic or hormonal phenotype.
We use cookies to personalize content and marketing, and to analyze our traffic. This helps us maintain the quality of our free resources. manage your preferences below.
Detailed Cookie Preferences
This helps support our free resources through personalized marketing efforts and promotions.
Analytics cookies help us understand how visitors interact with our website, improving user experience and website performance.
Personalization cookies enable us to customize the content and features of our site based on your interactions, offering a more tailored experience.