The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism.
Charley XiaSarah J PickettDavid C M LiewaldAlexander WeissGavin HudsonW David HillPublished in: Nature communications (2023)
Neuroticism is a heritable trait composed of separate facets, each conferring different levels of protection or risk, to health. By examining mitochondrial DNA in 269,506 individuals, we show mitochondrial haplogroups explain 0.07-0.01% of variance in neuroticism and identify five haplogroup and 15 mitochondria-marker associations across a general factor of neuroticism, and two special factors of anxiety/tension, and worry/vulnerability with effect sizes of the same magnitude as autosomal variants. Within-haplogroup genome-wide association studies identified H-haplogroup-specific autosomal effects explaining 1.4% variance of worry/vulnerability. These H-haplogroup-specific autosomal effects show a pleiotropic relationship with cognitive, physical and mental health that differs from that found when assessing autosomal effects across haplogroups. We identify interactions between chromosome 9 regions and mitochondrial haplogroups at P < 5 × 10 -8 , revealing associations between general neuroticism and anxiety/tension with brain-specific gene co-expression networks. These results indicate that the mitochondrial genome contributes toward neuroticism and the autosomal links between neuroticism and health.
Keyphrases
- mitochondrial dna
- copy number
- mental health
- oxidative stress
- genome wide
- public health
- healthcare
- dna methylation
- climate change
- gene expression
- physical activity
- poor prognosis
- cell death
- social media
- health information
- genome wide association
- reactive oxygen species
- blood brain barrier
- multiple sclerosis
- endoplasmic reticulum
- resting state