» Articles » PMID: 30874797

Advanced Parental Age at Conception and Sex Affects Mitochondrial DNA Copy Number in Human and Fruit Flies

Overview
Specialty Geriatrics
Date 2019 Mar 16
PMID 30874797
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Aging is a multifactorial trait caused by early as well as late-life circumstances. A society trend that parents deliberately delay having children is of concern to health professionals, for example as advanced parental age at conception increases disease risk profiles in offspring. We here aim to study if advanced parental age at conception affects mitochondrial DNA content, a cross-species biomarker of general health, in adult human twin offspring and in a model organism. We find no deteriorated mitochondrial DNA content at advanced parental age at conception, but human mitochondrial DNA content was higher in females than males, and the difference was twofold higher at advanced maternal age at conception. Similar parental age effects and sex-specific differences in mitochondrial DNA content were found in Drosophila melanogaster. In addition, parental longevity in humans associates with both mitochondrial DNA content and parental age at conception; thus, we carefully propose that a poorer disease risk profile from advanced parental age at conception might be surpassed by superior effects of parental successful late-life reproduction that associate with parental longevity.

Citing Articles

Associations of Prenatal Mercury Exposure and PUFA with Telomere Length and mtDNA Copy Number in 7-Year-Old Children in the Seychelles Child Development Nutrition Cohort 2.

Stajnko A, Pineda D, Klus J, Love T, Thurston S, Mulhern M Environ Health Perspect. 2025; 133(2):27002.

PMID: 39903555 PMC: 11793161. DOI: 10.1289/EHP14776.


Advanced maternal age has negative multigenerational impacts during embryogenesis.

Ostberg H, Boehm Vock L, Bloch-Qazi M Curr Res Insect Sci. 2024; 4:100068.

PMID: 38161993 PMC: 10757284. DOI: 10.1016/j.cris.2023.100068.


Systemic Evidence for Mitochondrial Dysfunction in Age-Related Macular Degeneration as Revealed by mtDNA Copy Number Measurements in Peripheral Blood.

Koller A, Lamina C, Brandl C, Zimmermann M, Stark K, Weissensteiner H Int J Mol Sci. 2023; 24(22).

PMID: 38003595 PMC: 10671207. DOI: 10.3390/ijms242216406.


Parental age at conception on mouse lemur's offspring longevity: Sex-specific maternal effects.

Martine P, Aude A PLoS One. 2022; 17(12):e0265783.

PMID: 36580457 PMC: 9799291. DOI: 10.1371/journal.pone.0265783.


Interrelationships and determinants of aging biomarkers in cord blood.

Reimann B, Martens D, Wang C, Ghantous A, Herceg Z, Plusquin M J Transl Med. 2022; 20(1):353.

PMID: 35945616 PMC: 9361565. DOI: 10.1186/s12967-022-03541-1.


References
1.
Mengel-From J, Thinggaard M, Dalgard C, Kyvik K, Christensen K, Christiansen L . Mitochondrial DNA copy number in peripheral blood cells declines with age and is associated with general health among elderly. Hum Genet. 2014; 133(9):1149-59. PMC: 4127366. DOI: 10.1007/s00439-014-1458-9. View

2.
Zhu J, Vestergaard M, Madsen K, Olsen J . Paternal age and mortality in children. Eur J Epidemiol. 2008; 23(7):443-7. DOI: 10.1007/s10654-008-9253-3. View

3.
Brieger K, Schiavone S, Miller Jr F, Krause K . Reactive oxygen species: from health to disease. Swiss Med Wkly. 2012; 142:w13659. DOI: 10.4414/smw.2012.13659. View

4.
Knez J, Winckelmans E, Plusquin M, Thijs L, Cauwenberghs N, Gu Y . Correlates of Peripheral Blood Mitochondrial DNA Content in a General Population. Am J Epidemiol. 2015; 183(2):138-46. PMC: 4706678. DOI: 10.1093/aje/kwv175. View

5.
Fragouli E, Spath K, Alfarawati S, Kaper F, Craig A, Michel C . Altered levels of mitochondrial DNA are associated with female age, aneuploidy, and provide an independent measure of embryonic implantation potential. PLoS Genet. 2015; 11(6):e1005241. PMC: 4454688. DOI: 10.1371/journal.pgen.1005241. View