Oxidative stress as a hidden cost of attractiveness in postmenopausal women

. 2020 Dec 15 ; 10 (1) : 21970. [epub] 20201215

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid33319813

Grantová podpora
T32 AG000243 NIA NIH HHS - United States

Odkazy

PubMed 33319813
PubMed Central PMC7738509
DOI 10.1038/s41598-020-76627-9
PII: 10.1038/s41598-020-76627-9
Knihovny.cz E-zdroje

Perceived facial attractiveness, a putative marker of high biological fitness, is costly to maintain throughout a lifetime and may cause higher oxidative stress (OS). We investigated the association between the facial features of 97 postmenopausal women and their levels of OS biomarkers 8-hydroxy-2'-deoxyguanosine (8-OHdG), superoxide dismutase (Cu-Zn SOD), and thiobarbituric acid reactive substances (TBARS). In study 1, 966 judges rated the composites (facial averages) of women with higher OS as more attractive, healthier, younger, and less symmetric. In study 2, Geometric Morphometric analysis did not reveal significant differences in facial morphology depending on OS levels. In study 3, measured facial averageness and symmetry were weakly negatively related to 8-OHdG levels. Maintaining higher perceived facial attractiveness may be costly due to increased oxidative damage in the postmenopausal period. These costs may remain hidden during the reproductive period of life due to the protective mechanisms of oxidative shielding and revealed only after menopause when shielding has ceased.

Zobrazit více v PubMed

Marcinkowska UM, Holzleitner IJ. Stability of women’s facial shape throughout the menstrual cycle. Proc. R. Soc. B. 2020;287:20192910. doi: 10.1098/rspb.2019.2910. PubMed DOI PMC

Thornhill R, Gangestad SW. Facial attractiveness. Trends Cogn. Sci. 1999;3:452–460. doi: 10.1016/S1364-6613(99)01403-5. PubMed DOI

Rhodes G. The evolutionary psychology of facial beauty. Annu. Rev. Psychol. 2006;57:199–226. doi: 10.1146/annurev.psych.57.102904.190208. PubMed DOI

Peters M, Rhodes G, Simmons LW. Contributions of the face and body to overall attractiveness. Anim. Behav. 2007;73:937–942. doi: 10.1016/j.anbehav.2006.07.012. DOI

Langlois JH, et al. Maxims or myths of beauty? A meta-analytic and theoretical review. Psychol. Bull. 2000;126:390. doi: 10.1037/0033-2909.126.3.390. PubMed DOI

Samuels CA, Ewy R. Aesthetic perception of faces during infancy. Br. J. Dev. Psychol. 1985;3:221–228. doi: 10.1111/j.2044-835X.1985.tb00975.x. DOI

Boothroyd LG, Scott I, Gray AW, Coombes CI, Pound N. Male facial masculinity as a cue to health outcomes. Evol. Psychol. 2013;11:147470491301100500. doi: 10.1177/147470491301100508. PubMed DOI

Kamachi MG, Chiba T, Kurosumi M, Mizukoshi K. Perception of human age from faces: Symmetric versus asymmetric movement. Symmetry (Basel) 2019;11:650. doi: 10.3390/sym11050650. DOI

Rhodes G, Simmons LW, Peters M. Attractiveness and sexual behavior: Does attractiveness enhance mating success? Evol. Hum. Behav. 2005;26:186–201. doi: 10.1016/j.evolhumbehav.2004.08.014. DOI

Boothroyd LG, Cross CP, Gray AW, Coombes C, Gregson-Curtis K. Perceiving the facial correlates of sociosexuality: Further evidence. Pers. Individ. Dif. 2011;50:422–425. doi: 10.1016/j.paid.2010.10.017. DOI

Gangestad SW, Thornhill R, Yeo RA. Facial attractiveness, developmental stability, and fluctuating asymmetry. Ethol. Sociobiol. 1994;15:73–85. doi: 10.1016/0162-3095(94)90018-3. DOI

Valentine T, Darling S, Donnelly M. Why are average faces attractive? The effect of view and averageness on the attractiveness of female faces. Psychon. Bull. Rev. 2004;11:482–487. doi: 10.3758/BF03196599. PubMed DOI

Burriss RP, Marcinkowska UM, Lyons MT. Gaze properties of women judging the attractiveness of masculine and feminine male faces. Evol. Psychol. 2014;12:147470491401200100. doi: 10.1177/147470491401200102. PubMed DOI

Andre CM, Larondelle Y, Evers D. Dietary antioxidants and oxidative stress from a human and plant perspective: A review. Curr. Nutr. Food Sci. 2010;6:2–12. doi: 10.2174/157340110790909563. DOI

Svensson PA, Wong BBM. Carotenoid-based signals in behavioural ecology: A review. Behaviour. 2011;148:131–189. doi: 10.1163/000579510X548673. DOI

Foo YZ, Simmons LW, Rhodes G. The relationship between health and mating success in humans. R. Soc. Open Sci. 2017;4:160603. doi: 10.1098/rsos.160603. PubMed DOI PMC

Ip FWL, Lewis GJ, Lefevre CE. Carotenoid skin colouration enhances face and body attractiveness: A cross-cultural study. Q. J. Exp. Psychol. 2019;72:2565–2573. doi: 10.1177/1747021819850970. PubMed DOI

Harman D. Free radical theory of aging. Mutat. Res. 1992;275:257–266. doi: 10.1016/0921-8734(92)90030-S. PubMed DOI

Cesari M, et al. Oxidative damage, platelet activation, and inflammation to predict mobility disability and mortality in older persons: Results from the health aging and body composition study. J. Gerontol. Ser. A Biomed. Sci. Med. Sci. 2012;67:671–676. doi: 10.1093/gerona/glr246. PubMed DOI PMC

Mutlu B, Bas AY, Aksoy N, Taskin A. The effect of maternal number of births on oxidative and antioxidative systems in cord blood. J. Matern. Neonatal Med. 2012;25:802–805. doi: 10.3109/14767058.2011.594920. PubMed DOI

Shoji H, Koletzko B. Oxidative stress and antioxidant protection in the perinatal period. Curr. Opin. Clin. Nutr. Metab. Care. 2007;10:324–328. doi: 10.1097/MCO.0b013e3280a94f6d. PubMed DOI

Ziomkiewicz A, et al. Evidence for the cost of reproduction in humans: High lifetime reproductive effort is associated with greater oxidative stress in post-menopausal women. PLoS ONE. 2016;11:e0145753. doi: 10.1371/journal.pone.0145753. PubMed DOI PMC

Ziomkiewicz A, Frumkin A, Zhang Y, Sancilio A, Bribiescas RG. The cost of reproduction in women: Reproductive effort and oxidative stress in premenopausal and postmenopausal American women. Am. J. Hum. Biol. 2018;30:e23069. doi: 10.1002/ajhb.23069. PubMed DOI

Cai Z, et al. No evidence that facial attractiveness, femininity, averageness, or coloration are cues to susceptibility to infectious illnesses in a university sample of young adult women. Evol. Hum. Behav. 2019;40:156–159. doi: 10.1016/j.evolhumbehav.2018.10.002. DOI

Little AC, Jones BC, DeBruine LM. Facial attractiveness: Evolutionary based research. Philos. Trans. R. Soc. B Biol. Sci. 2011;366:1638–1659. doi: 10.1098/rstb.2010.0404. PubMed DOI PMC

von Schantz T, Bensch S, Grahn M, Hasselquist D, Wittzell H. Good genes, oxidative stress and condition–dependent sexual signals. Proc. R. Soc. Lond. Ser. B Biol. Sci. 1999;266:1–12. doi: 10.1098/rspb.1999.0597. PubMed DOI PMC

Zahavi A. Mate selection—A selection for a handicap. J. Theor. Biol. 1975;53:205–214. doi: 10.1016/0022-5193(75)90111-3. PubMed DOI

Gangestad SW, Merriman LA, Thompson ME. Men’s oxidative stress, fluctuating asymmetry and physical attractiveness. Anim. Behav. 2010;80:1005–1013. doi: 10.1016/j.anbehav.2010.09.003. DOI

Foo YZ, Simmons LW, Rhodes G. Predictors of facial attractiveness and health in humans. Sci. Rep. 2017;7:39731. doi: 10.1038/srep39731. PubMed DOI PMC

Dowling DK, Simmons LW. Reactive oxygen species as universal constraints in life-history evolution. Proc. R. Soc. B Biol. Sci. 2009;276:1737–1745. doi: 10.1098/rspb.2008.1791. PubMed DOI PMC

Livshits G, Kobyliansky E. Fluctuating asymmetry as a possible measure of developmental homeostasis in humans: A review. Hum. Biol. 1991;63:441–466. PubMed

Colleran H, Jasienska G, Nenko I, Galbarczyk A, Mace R. Fertility decline and the changing dynamics of wealth, status and inequality. Proc. Biol. Sci. 2015;282:20150287. PubMed PMC

Colleran H, Jasienska G, Nenko I, Galbarczyk A, Mace R. Community-level education accelerates the cultural evolution of fertility decline. Proc. Biol. Sci. 2014;281:20132732. PubMed PMC

Lee KMN, Rogers MP, Galbarczyk A, Jasienska G, Clancy KBH. Physical activity in women of reproductive age in a transitioning rural Polish population. Am. J. Hum. Biol. 2019 doi: 10.1002/ajhb.23231. PubMed DOI

Colleran H. Farming in transition: Land and property inheritance in a rural Polish population. Soc. Biol. Hum. Aff. 2014;78:7.

Jasienska G. The Fragile Wisdom: An Evolutionary View on Women’s Biology and Health. Cambridge: Harvard University Press; 2013.

Marcinkowska UM, et al. Costs of reproduction are reflected in women’s faces: Post-menopausal women with fewer children are perceived as more attractive, healthier and younger than women with more children. Am. J. Phys. Anthropol. 2017 doi: 10.1002/ajpa.23362. PubMed DOI

Tiddeman B, Burt M, Perrett D. Prototyping and transforming facial textures for perception research. IEEE Comput. Graph. Appl. 2001;21:42–50. doi: 10.1109/38.946630. DOI

Rohlf FJ. The tps series of software. Hystrix. 2015;26:9.

Kleisner K, Pokorný Š, Saribay SA. Towards a new approach to cross-cultural distinctiveness and typicality of human faces: The cross-group typicality/distinctiveness metric. Front. Psychol. 2019;10:124. doi: 10.3389/fpsyg.2019.00124. PubMed DOI PMC

Saribay SA, et al. The Bogazici face database: Standardized photographs of Turkish faces with supporting materials. PLoS ONE. 2018;13:e0192018. doi: 10.1371/journal.pone.0192018. PubMed DOI PMC

Adams DC, Otárola-Castillo E. geomorph: An R package for the collection and analysis of geometric morphometric shape data. Methods Ecol. Evol. 2013;4:393–399. doi: 10.1111/2041-210X.12035. DOI

Dryden IL, Mardia KV. Statistical Analysis of Shape. Hoboken: Wiley; 1998.

Jones AL, Jaeger B. Biological bases of beauty revisited: The effect of symmetry, averageness, and sexual dimorphism on female facial attractiveness. Symmetry (Basel) 2019;11:279. doi: 10.3390/sym11020279. DOI

Blount JD, Vitikainen EIK, Stott I, Cant MA. Oxidative shielding and the cost of reproduction. Biol. Rev. 2016;91:483–497. doi: 10.1111/brv.12179. PubMed DOI

Vaanholt LM, et al. Oxidative costs of reproduction: Oxidative stress in mice fed standard and low antioxidant diets. Physiol. Behav. 2016;154:1–7. doi: 10.1016/j.physbeh.2015.11.009. PubMed DOI PMC

Viblanc VA, et al. Maternal oxidative stress and reproduction: Testing the constraint, cost and shielding hypotheses in a wild mammal. Funct. Ecol. 2018;32:722–735. doi: 10.1111/1365-2435.13032. DOI

Vitikainen EIK, et al. Evidence of oxidative shielding of offspring in a wild mammal. Front. Ecol. Evol. 2016;4:58. doi: 10.3389/fevo.2016.00058. DOI

Simons MJP, Cohen AA, Verhulst S. What does carotenoid-dependent coloration tell? Plasma carotenoid level signals immunocompetence and oxidative stress state in birds–a meta-analysis. PLoS ONE. 2012;7:e43088. doi: 10.1371/journal.pone.0043088. PubMed DOI PMC

Van Dongen S, Gangestad SW. Human fluctuating asymmetry in relation to health and quality: A meta-analysis. Evol. Hum. Behav. 2011;32:380–398. doi: 10.1016/j.evolhumbehav.2011.03.002. DOI

Scutiero G, et al. Oxidative stress and endometriosis: A systematic review of the literature. Oxid. Med. Cell. Longev. 2017 doi: 10.1155/2017/7265238. PubMed DOI PMC

Vercellini P, et al. Attractiveness of women with rectovaginal endometriosis: A case-control study. Fertil. Steril. 2013;99:212–218. doi: 10.1016/j.fertnstert.2012.08.039. PubMed DOI

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

FACEDIG automated tool for placing landmarks on facial portraits for geometric morphometrics users

. 2025 Jul 07 ; 15 (1) : 24330. [epub] 20250707

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...