Polycystic ovary syndrome (PCOS) is considered the most common reproductive disorder, affecting 8-18% of women of reproductive age (March et al.). Insulin resistance and PCOS are tightly linked (Dunaif). Here’s some news in the field, on research published in the last month.
Insulin resistance is a symptom of polycystic ovary syndrome (PCOS), independent of obesity. A polymorphism in human Tribbles 3 (TRB3) gene is associated with insulin resistance. However, the TRB3 polymorphism genotype is no more prevalent in women with PCOS versus control (n= 336 women with PCOS and n=116 women undergoing infertility treatments who do not have PCOS) when body mass index is controlled for (Zhang et al.). TRB3 gene does not appear to be a candidate for further investigation into PCOS causes.
A polymorphism of melatonin receptor 1A (SNP rs2119882) was found to be more prevalent in women with insulin resistant PCOS versus healthy and non-IR PCOS controls in Li et al‘s study published last week.
Polymorphisms in the human lipin 1 gene (SNPs rs11693809 and rs2716610) are no more prevalent in women with PCOS versus controls. However, women with PCOS that have the rs11693809 polymorphism are less likely to experience alterations in glucose and lipid metabolism (Mlinar et al.), and presumably the after effects of altered metabolism.
Neurotransmission of endogenous opiods in the limbic system (nucleus accumbens, ventral pallidum and amygdala) is disrupted in some women with PCOS, particularly when they are also insulin resistant (Farrell and Antoni). Using PET scans and anatomical MRIs Berent-Spillson et al.‘s new study showed that insulin-resistant PCOS women had significantly fewer opiod-bound receptors in their limbic systems versus women with PCOS who were not insulin resistant. This was successfully treated with a 4 month metaformin protocol. The study size was small (n=12), but opens a potentially important avenue for understanding and treating alterations in apetite and mood in women with PCOS.