Markers for Risk of Type 1 Diabetes in Relatives of Alsacian Patients with Type 1 Diabetes
2002

Genetic Markers for Type 1 Diabetes Risk in Relatives

Sample size: 218 publication Evidence: high

Author Information

Author(s): JEAN CLAUDE ONGAGNA, REMI SAPIN, MICHEL PINGET, ALAIN BELCOURT

Primary Institution: Centre Europeen d'Etude du Diabete-Hopitaux Universitaires de Strasbourg

Hypothesis

The CTLA-4 49 (Thr/Ala) polymorphism is associated with an increased risk of type 1 diabetes in first-degree relatives of diabetic patients.

Conclusion

The CTLA-4 49 Ala allele increases the risk of type 1 diabetes, regardless of age and HLA-DQ genetic markers.

Supporting Evidence

  • The CTLA-4 49 Ala allele was found in 75.8% of type 1 diabetic patients.
  • First-degree relatives had a 68.1% frequency of the CTLA-4 49 Ala allele.
  • The relative risk of type 1 diabetes conferred by the Ala/Ala genotype was 18.8.
  • Significant differences in allele frequencies were observed between diabetic patients and controls.

Takeaway

Some people have genes that make them more likely to get type 1 diabetes, especially if they have family members with the disease.

Methodology

The study analyzed genetic markers in 62 type 1 diabetic patients, 72 first-degree relatives, and 84 control subjects using PCR-RFLP.

Limitations

The study's sample size may limit the generalizability of the findings.

Participant Demographics

Participants included 62 type 1 diabetic patients and 72 first-degree relatives, with a mix of genders and ages.

Statistical Information

P-Value

p<0.001

Statistical Significance

p<0.001

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication