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- W2892894469 abstract "Research has repeatedly pointed towards a multifactorial aetiology underlying female sexual dysfunction (FSD), in which genetic and environmental factors also play a role. As sexual functioning is a highly variable trait, epigenetics could provide a promising approach to tackle the origins of FSD and consequently offer a step-change in our understanding of these problems. The objective of this study was to identify differentially methylated CpG positions for sexual functioning in a sample of monozygotic (MZ) twin pairs discordant for sexual functioning. The sample consisted of 33 trait-discordant monozygotic twin pairs (age M 54.1 years, SD 9.05) from the TwinsUK registry. Phenotypic data on sexual desire, arousal, lubrication, orgasm, satisfaction, and pain were collected using the Female Sexual Function Index-Lifelong (FSFI-LL). The Illumina Infinium Human Methylation 450 DNA BeadChip was used for epigenome-wide analyses of DNA methylation in whole blood samples. DNA methylation patterns associated with the FSFI-LL total score and its six subdomains were compared." @default.
- W2892894469 created "2018-10-05" @default.
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- W2892894469 date "2018-07-01" @default.
- W2892894469 modified "2023-10-01" @default.
- W2892894469 title "151 Differential DNA Methylation in Monozygotic Twins Discordant for Female Sexual Functioning" @default.
- W2892894469 doi "https://doi.org/10.1016/j.jsxm.2018.04.152" @default.
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