Mortality and causes of death in different celiac disease phenotypes during long-term follow-up

Inka Koskinen1, Kaisa Hervonen2, Heini Huhtala3

  • 1Celiac Disease Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland; Department of Internal Medicine, Central Finland Central Hospital, Jyväskylä, Finland.

Insights

Long-term studies show overall mortality is not increased in celiac disease patients. However, risks for lymphoproliferative and central nervous system diseases are higher, while alcohol-related disease risk is lower.

Area of Science:

  • Gastroenterology
  • Epidemiology
  • Clinical Medicine

Background:

  • Celiac disease (CD) diagnosis has been linked to increased mortality, but comprehensive long-term data are limited.
  • Understanding long-term survival trends is crucial for managing celiac disease patients effectively.

Purpose of the Study:

  • To investigate the long-term overall and cause-specific mortality in a large cohort of celiac disease patients.
  • To compare mortality risks in celiac disease patients against a matched general population.

Main Methods:

  • A cohort of 1,392 celiac disease patients diagnosed between 1960-2000 was established.
  • Patients were categorized by demographics and disease characteristics.
  • Mortality data were collected over a median follow-up of 26.5 years and compared to 4,177 matched controls.

Main Results:

  • Over 41 years, all-cause mortality was not significantly increased in celiac disease patients (HR 0.96).
  • Increased mortality was observed for lymphoproliferative diseases (HR 2.42) and central nervous system diseases (HR 2.14).
  • A decreased risk was noted for alcohol-related diseases (HR 0.31).

Conclusions:

  • Overall mortality in celiac disease patients is not elevated, even with extended follow-up.
  • Specific causes of death, including certain cancers and neurological conditions, warrant continued monitoring in celiac disease management.
  • No significant mortality differences were found across various celiac disease phenotypes.
Abstract

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