Menopause is associated with postprandial metabolism, metabolic health and lifestyle: The ZOE PREDICT study.

Bermingham, Kate M; Linenberg, Inbar; Hall, Wendy L; Kadé, Kirstin; Franks, Paul W; Davies, Richard; Wolf, Jonathan; Hadjigeorgiou, George et al. · EBioMedicine · 2022

prospective_cohort · Level II

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Abstract

The menopause transition is associated with unfavourable alterations in health. However, postprandial metabolic changes and their mediating factors are poorly understood. The PREDICT 1 UK cohort (n=1002; pre- n=366, peri- n=55, and post-menopausal females n=206) assessed phenotypic characteristics, anthropometric, diet and gut microbiome data, and fasting and postprandial (0-6 h) cardiometabolic blood measurements, including continuous glucose monitoring (CGM) data. Differences between menopausal groups were assessed in the cohort and in an age-matched subgroup, adjusting for age, BMI, menopausal hormone therapy (MHT) use, and smoking status. Post-menopausal females had higher fasting blood measures (glucose, HbA1c and inflammation (GlycA), 6%, 5% and 4% respectively), sugar intakes (12%) and poorer sleep (12%) compared with pre-menopausal females (p<0.05 for all). Postprandial metabolic responses for glucose<sub>2hiauc</sub> and insulin<sub>2hiauc</sub> were higher (42% and 4% respectively) and CGM measures (glycaemic variability and time in range) were unfavourable post- versus pre-menopause (p<0.05 for all). In age-matched subgroups (n=150), postprandial glucose responses remained higher post-menopause (peak<sub>0-2h</sub> 4%). MHT was associated with favourable visceral fat, fasting (glucose and insulin) and postprandial (triglyceride<sub>6hiauc</sub>) measures. Mediation analysis showed that associations between menopause and metabolic health indicators (visceral fat, GlycA<sub>360mins</sub> and glycaemia (peak<sub>0-2h</sub>)) were in part mediated by diet and gut bacterial species. Findings from this large scale, in-depth nutrition metabolic study of menopause, support the importance of monitoring risk factors for type-2 diabetes and cardiovascular disease in mid-life to older women to reduce morbidity and mortality associated with oestrogen decline. Zoe Ltd.

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