Many studies have documented an obesity paradox—a survival advantage of being obese—in populations diagnosed with a medical condition. Whether obesity is causally associated with improved mortality in these conditions is unresolved.
We develop the logic of collider bias as it pertains to the association between smoking and obesity in a diseased population. Data from the National Health and Nutrition Examination Survey (NHANES) are used to investigate this bias empirically among persons with diabetes and prediabetes (dysglycemia). We also use NHANES to investigate whether reverse causal pathways are more prominent among people with dysglycemia than in the source population. Cox regression analysis is used to examine the extent of the obesity paradox among those with dysglycemia. In the regression analysis, we explore interactions between obesity and smoking, and we implement a variety of data restrictions designed to reduce the extent of reverse causality.
We find an obesity paradox among persons with dysglycemia. In this population, the inverse association between obesity and smoking is much stronger than in the source population, and the extent of illness and weight loss is greater. The obesity paradox is absent among never-smokers. Among smokers, the paradox is eliminated through successive efforts to reduce the extent of reverse causality.
Higher mortality among normal-weight people with dysglycemia is not causal but is rather a product of the closer inverse association between obesity and smoking in this subpopulation.
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From the Population Studies Center, University of Pennsylvania, Philadelphia, PA.
Supported by grant number R01AG040212 from the National Institute on Aging.
The authors report no conflicts of interest.
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Correspondence: Samuel H. Preston, Population Studies Center, University of Pennsylvania, 3718 Locust Walk, McNeil Building, Room 239, Philadelphia, PA 19104. E-mail: email@example.com.
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