Exploring the causal effect of hearing loss on Alzheimers disease: a Mendelian randomisation study
Jacobs, B. M.; Noyce, A. J.; Hardy, C. J.; Warren, J. D.; Marshall, C. R.
Show abstract
BackgroundHearing loss has been identified as one of the most important risk factors for Alzheimers disease (AD). However, the causality of this association has not been established. MethodsWe used publicly available GWAS summary statistics to construct instrumental variables for age-related hearing difficulty. We tested these genetic instruments for association with the outcome of AD using AD GWAS summary statistics in a two-sample Mendelian randomisation analysis. We used inverse-variance weighted meta-analysis to estimate the causal effect of hearing-related traits on AD, followed by secondary sensitivity analyses including a mixture of experts approach. ResultsThere was no strong evidence for a causal relationship between genetically-determined hearing difficulty (ORFE-IVW 1.27, 95% CI 0.89 to 1.82, p=0.189) and AD risk. There was no evidence to suggest that unbalanced horizontal pleiotropy was biasing the result. Power calculations indicated our instruments were sufficiently powered to detect the magnitude of effect described in case-control and cohort settings. ConclusionsOur results suggest that the size of the observed relationship between hearing loss and AD cannot be completely accounted for by a direct causal influence. Hearing loss may have more utility as a risk marker for AD than as a modifiable risk factor.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Frequency of Variants in Mendelian Alzheimer’s Disease Genes within the Alzheimer’s Disease Sequencing Project (ADSP) 93%
- Brain and Blood Transcriptome-Wide Association Studies Identify Five Novel Genes Associated with Alzheimer’s Disease 93%
- Sex Differences in Cognitive Performance in Alzheimer's Disease: Insights from the ADAS-Cog-13 93%
Similar papers in this journal
- Failure to detect synergy between variants in transferrin and hemochromatosis and Alzheimer’s disease in large cohort 95%
- Pupillary dilation responses as a midlife indicator of risk for Alzheimer’s Disease: Association with Alzheimer’s disease polygenic risk 94%
- Mitonuclear interactions influence Alzheimer’s disease risk 94%
Similar papers in this journal
Similar papers in this journal
- Unbiased data-driven analysis of five amyloid-beta peptides for biomarker investigations in familial Alzheimer's disease 93%
- Scalable biological-cognitive profiling for Alzheimer's disease in the population 93%
- The contribution of Apoliproprotein E genetic variation to dementia risk in British South Asians 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.