Preston and Wang 2006 — Sex Mortality Differences in the United States The Role of Cohort Smoking Patterns

mortalitysex-differencessmokingcohort-effectsdemographyage-period-cohortforecastingperiod-mortalitycohort-mortality

Summary

Preston and Wang (2006) demonstrate that U.S. sex differences in all-cause mortality from 1948 to 2003 follow a cohort diagonal rather than a period pattern: the gap between male and female death rates is best explained by which birth cohort is being observed, not which calendar year. Using an age-period-cohort (APC) negative binomial regression with mean years of pre-age-40 smoking as the cohort covariate, they attribute most of the widening and subsequent narrowing of the sex mortality gap to differential cohort smoking histories. Controlling for smoking, the underlying mortality decline over 1948–2003 was 56%—substantially larger than the naive 48% estimate—because men's higher smoking prevalence had masked genuine improvement.

Key Claims

Concepts Introduced or Extended

Entities Mentioned

Quotes

"Mortality differences between the sexes in the United States have followed a course that is largely explicable by reference to the different smoking behaviors of male and female birth cohorts."

"Controlling for smoking, mortality fell by 56% during 1948–2003 rather than the 48% estimated without this control."

"The peak in sex differences in mortality occurs for cohorts born approximately 1903–1908, not for any particular calendar period."

My Take

This paper is methodologically exemplary: the cohort diagonal finding is not merely descriptive but generates a falsifiable prediction (future narrowing of the sex gap as later cohorts age) that has largely been borne out. The APC framework here is cleaner than in most applications because the cohort covariate (smoking history) is observable and theoretically motivated, not just a birth-year fixed effect. The period-distortion finding — that naive analysis underestimates mortality improvement by 8 percentage points — has direct implications for any forecasting model that uses all-cause period death rates without a smoking adjustment: such models import a downward bias into estimated baseline improvement rates. The key limitation is that "mean years smoked before age 40" is a retrospective cohort summary derived from survey data with potential recall bias, and the authors assume a fixed functional form for the smoking-mortality dose-response that may not hold across cohorts with different cigarette types and smoking intensities.