02211nas a2200229 4500000000100000008004100001260001200042653002200054653001900076653001700095653002400112653001400136653002200150100001200172700001200184700002400196700001800220700001900238245012200257520158800379022001401967 2026 d c07/202610aTrypanosoma cruzi10aChagas disease10aCohort study10aeffect modification10aMortality10aSurvival Analysis1 aDíaz M1 aRojas L1 aGonzález-Rugeles C1 aEcheverría L1 aGómez-Ochoa S00aChagas disease and mortality in a community-based cohort in Colombia: evidence for age-dependent effect modification.3 a

BACKGROUND:

Chagas disease (CD), caused by Trypanosoma cruzi, is a leading cause of cardiomyopathy in Latin America. Community-based prospective data on the CD-mortality association remain scarce.

METHODS:

We analysed the ANTORCHA prospective cohort, enrolling individuals from T. cruzi-endemic communities in Santander, Colombia (2015-2025). The primary exposure was serologically confirmed CD; the primary outcome was all-cause mortality. Cox proportional hazards models with hierarchical adjustment and restricted mean survival time (RMST) were used.

RESULTS:

Among 1509 participants (314 Chagas positive), 81 deaths occurred over a median follow-up of 5.6 y. After full multivariate adjustment, CD was not associated with overall mortality (hazard ratio [HR] 1.02 [95% confidence interval {CI} 0.61 to 1.72]). A significant age-dependent interaction was identified (p=0.007): CD was independently associated with increased mortality among participants <60 y of age (HR 4.96 [95% CI 1.80 to 13.71]) but not among those ≥60 y of age (HR 0.73 [95% CI 0.43 to 1.22]). RMST analysis confirmed an absolute survival loss of 121 d at approximately 10 y of follow-up in the younger subgroup (p=0.02).

CONCLUSIONS:

In this community-based cohort, CD was independently associated with markedly elevated mortality among adults <60 y of age. Younger T. cruzi-positive individuals warrant intensified cardiovascular surveillance.

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