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Does hemochromatosis predispose to celiac disease? A study of 29,096 celiac disease patients
Jonas F Ludvigsson1, Joseph A Murray, Paul C Adams
1Department of Paediatrics, Örebro University Hospital, Sweden. jonasludvigsson@yahoo.com
Insights
Hereditary hemochromatosis (HH) appears to increase the risk of celiac disease (CD). This population-based study found a significant association between these two conditions, highlighting a potential link for further research.
Area of Science:
- Gastroenterology
- Genetics
- Epidemiology
Background:
- Case reports suggest a link between hereditary hemochromatosis (HH) and celiac disease (CD).
- Quantitative estimates of this association are currently lacking in population-based studies.
Purpose of the Study:
- To estimate the association between HH and CD using a population-based study design.
- To investigate the risk of CD in individuals diagnosed with HH.
Main Methods:
- A case-control study was conducted using biopsy reports from all Swedish pathology departments.
- 29,096 individuals with biopsy-verified CD (Marsh stage III) were identified.
- The risk of HH diagnosis in CD patients was compared to 144,522 matched controls using conditional logistic regression.
Main Results:
- Hereditary hemochromatosis was observed in 30 patients with CD and 60 matched controls.
- HH was associated with an increased risk of CD, with an odds ratio (OR) of 2.30 (95% CI = 1.53-3.45).
- Restricting HH to individuals with at least two records, the OR for CD was 2.54 (95% CI = 1.57-4.11), and when HH preceded CD diagnosis, the OR was 2.64 (95% CI = 1.24-5.60).
Conclusions:
- Hereditary hemochromatosis is associated with an increased risk of developing celiac disease.
- The findings suggest a significant link between these two conditions that warrants further investigation.
Background And Aim:
Case reports suggest an association between hereditary hemochromatosis (HH) and celiac disease (CD), but estimates of association are lacking. We estimated the association between HH and CD in a population-based study.
Material And Methods:
Case-control study. We identified 29,096 individuals with biopsy-verified CD (equal to villous atrophy, Marsh stage III) through biopsy reports from all 28 pathology departments in Sweden. We then investigated the risk of a clinical diagnosis of HH in CD and in 144,522 controls matched for age, sex, county and calendar year. Conditional logistic regression was used to calculate odds ratios (ORs) for CD in patients with HH.
Results:
HH was seen in 30 patients with CD and in 60 matched controls. HH was hence associated with an increased risk of CD (OR = 2.30; 95% CI = 1.53-3.45). Restricting HH to individuals with at least two records of HH, the OR for CD was 2.54 (95% CI = 1.57-4.11), with a similar risk estimate when we only looked at HH diagnosed before CD (and matched date in controls) (OR = 2.64; 95% CI = 1.24-5.60).
Conclusion:
HH seems to be associated with an increased risk of CD.
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