Type 2 & other diabetes

Thyroid Function, Diabetes, and Common Age-Related Eye Diseases: A Mendelian Randomization Study

ThyroidPublished Mendelian randomization study

Authors' conclusion

Genetic predisposition to AITD is associated with risk of diabetic retinopathy and cataract, mostly mediated through increased T1D risk. Reciprocal associations between AITD, diabetic retinopathy, and T1D imply a shared autoimmune origin.

Study context

Population
Publicly available genome-wide association study (GWAS) summary statistics from international consortia (ThyroidOmics, International AMD Genetics Consortium, deCODE, UK Biobank, FinnGen, DIAGRAM)
Comparison
Genetic predisposition to autoimmune thyroid disease (AITD), and genetically predicted free thyroxine (FT4) and thyroid stimulating hormone (TSH) within the reference range, vs common age-related eye diseases
Outcome
Common age-related eye diseases: diabetic retinopathy, cataract, early and late AMD, primary open-angle glaucoma
Methodological detailsbidirectional two-sample Mendelian randomization (MR), multivariable MR, mediation analysis
  • Bidirectional two-sample MR
  • Multivariable MR
  • Mediation analysis

Main finding

As reported in the abstract

Associations of genetic predisposition to AITD
AITD and increased risk of diabetic retinopathy
p = 3 × 10-4
AITD and increased risk of cataract
p = 3 × 10-3
AITD and increased risk of T1D
p = 1 × 10-3
AITD and less likely T2D
p = 0.01

Further findings

Genetic predisposition to T1D and T2D

Both T1D and T2D increased risk of diabetic retinopathy and cataract
P < 4 × 10-4

Genetically predicted higher FT4 within reference range and AMD

Increased risk of late AMD
P = 0.01
Late AMD, particularly in women
P = 7 × 10-3
No association between FT4 and early AMD, nor between TSH and early and late AMD
No other associations observed

Original publication

Thyroid Function, Diabetes, and Common Age-Related Eye Diseases: A Mendelian Randomization Study. Thyroid. Published 27 September 2024. doi:10.1089/thy.2024.0257

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.