» Articles » PMID: 12483296

Mitochondrial DNA Polymorphisms Associated with Longevity in a Finnish Population

Overview
Journal Hum Genet
Specialty Genetics
Date 2002 Dec 17
PMID 12483296
Citations 95
Authors
Affiliations
Soon will be listed here.
Abstract

Sequence variation in mitochondrial DNA (mtDNA) may cause slight differences both in the functioning of the respiratory chain and in free radical production, and an association between certain mtDNA haplogroups and longevity has been suggested. In order to determine further the role of mtDNA in longevity, we studied the frequencies of mtDNA haplogroups and haplogroup clusters among elderly subjects and controls in a Finnish population. Samples were obtained from 225 persons aged 90-91 years (Vitality 90+) and from 400 middle-aged controls and 257 infants. MtDNA haplogroups were determined by restriction fragment length polymorphism. The haplogroup frequencies of the Vitality 90+ group differed from both those of the middle-aged controls ( P=0.01) and the infants ( P=0.00005), haplogroup H being less frequent than among the middle-aged subjects ( P=0.001) and infants ( P=0.00001), whereas haplogroups U and J were more frequent. Haplogroup clusters also differed between Vitality 90+ and both the middle-aged subjects ( P=0.002) and infants ( P=0.00001), the frequency of haplogroup cluster HV being lower in the former and that of UK and WIX being higher. These data suggest an association between certain mtDNA haplogroups or haplogroup clusters and longevity. Furthermore, our data appear to favour the presence of advantageous polymorphisms and support a role for mitochondria and mtDNA in the degenerative processes involved in ageing.

Citing Articles

Sexual dimorphism in immunity and longevity among the oldest old.

Arakelyan N, Kupriyanova D, Vasilevska J, Rogaev E Front Immunol. 2025; 16:1525948.

PMID: 40034689 PMC: 11872714. DOI: 10.3389/fimmu.2025.1525948.


Mitochondrial DNA variants and their impact on epigenetic and biological aging in young adulthood.

Mareckova K, Mendes-Silva A, Jani M, Pacinkova A, Piler P, Goncalves V Transl Psychiatry. 2025; 15(1):16.

PMID: 39837837 PMC: 11751369. DOI: 10.1038/s41398-025-03235-4.


Neurological manifestations in adult patients with the m.3243A>G variant in mitochondrial DNA.

Majamaa K, Karppa M, Moilanen J BMJ Neurol Open. 2024; 6(2):e000825.

PMID: 39324021 PMC: 11423728. DOI: 10.1136/bmjno-2024-000825.


The shared ancestry between the C9orf72 hexanucleotide repeat expansion and intermediate-length alleles using haplotype sharing trees and HAPTK.

Rautila O, Kaivola K, Rautila H, Hokkanen L, Launes J, Strandberg T Am J Hum Genet. 2024; 111(2):383-392.

PMID: 38242117 PMC: 10870140. DOI: 10.1016/j.ajhg.2023.12.019.


Mitochondrial DNA in Human Diversity and Health: From the Golden Age to the Omics Era.

Hernandez C Genes (Basel). 2023; 14(8).

PMID: 37628587 PMC: 10453943. DOI: 10.3390/genes14081534.