Abstract

Polycystic ovary syndrome (PCOS) is the most common female endocrine disorder and has important evolutionary implications for female reproduction and health. PCOS presents an interesting paradox, as it results in significant anovulation and potential sub-fecundity in industrialized populations, yet it has a surprisingly high prevalence and has a high heritability. In this review, we discuss an overview of PCOS, current diagnostic criteria, associated hormonal pathways and a review of proposed evolutionary hypotheses for the disorder. With a multifactorial etiology that includes ovarian function, metabolism, insulin signaling and multiple genetic risk alleles, PCOS is a complex disorder. We propose that PCOS is a mismatch between previously neutral genetic variants that evolved in physically active subsistence settings that have the potential to become harmful in sedentary industrialized environments. Sedentary obesogenic environments did not exist in ancestral times and exacerbate many of these pathways, resulting in the high prevalence and severity of PCOS today. Overall, the negative impacts of PCOS on reproductive success would likely have been minimal during most of human evolution and unlikely to generate strong selection. Future research and preventative measures should focus on these gene-environment interactions as a form of evolutionary mismatch, particularly in populations that are disproportionately affected by obesity and metabolic disorders.Lay SummaryThe most severe form of polycystic ovary syndrome (PCOS) is likely a result of interactions between genetic predispositions for PCOS and modern obesogenic environments. PCOS would likely have been less severe ancestrally and the fitness reducing effects of PCOS seen today are likely a novel product of sedentary, urban environments.

Highlights

  • Polycystic ovary syndromeBroadly, polycystic ovary syndrome (PCOS) symptoms include hyperandrogenism, anovulation and polycystic ovaries [1]; these symptoms are subject to wide clinical heterogeneity across patients and populations [2, 3]

  • Previous statements by PCOS taskforces have stated that insulin resistance and metabolic dysfunction are not aspects of health that need to be considered in the diagnosis or treatment of PCOS [51]

  • It is clear that insulin plays a crucial role in the pathophysiology of PCOS and can intersect with other root causes to generate different phenotypes of varying severity

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Summary

Polycystic ovary syndrome

Polycystic ovary syndrome (PCOS) symptoms include hyperandrogenism, anovulation and polycystic ovaries [1]; these symptoms are subject to wide clinical heterogeneity across patients and populations [2, 3]. Global estimates of the prevalence of PCOS range from 6 to 15%, but reach as high as 21% in the Northern Territory Aborigines of Australia [1, 7, 8] Despite such a large frequency of the disorder, it remained undiagnosed in up to 70% of a birth cohort of females from Australia with the condition [9]. We propose that PCOS is a mismatch between previously neutral genetic variants that evolved in physically active subsistence settings that have the potential to become harmful in sedentary industrialized environments. This summary of PCOS is an important case study of the connections between energy regulation and the female reproductive system and critically considers the clinical implications of the Western obesogenic environment on that relationship

Why take an evolutionary perspective on PCOS?
Clinical diagnostic criteria
Type II classic X
Comorbidity and burden of disease
Treatments vary in efficacy for different PCOS phenotypes
Pathways to dysregulation
Genetic polymorphisms attributed to PCOS pathogenesis
GENERATING ULTIMATE EVOLUTIONARY HYPOTHESES FOR THE ORIGINS OF PCOS
Would the PCOS phenotype be different in ancestral environments?
What are possible adaptive explanations for PCOS in ancestral environments?
Findings
CONCLUSIONS

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