The effect of inflammation on sexual desire and sexual function in pre- and post-menopausal women is moderated by sexual violence history.

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Inflammation may contribute to lower desire and arousal functioning in women; however, little research has examined effects across the reproductive lifespan. To examine associations between inflammation and sexual functioning in pre- and post-menopausal women. 103 healthy, sexually active cisgender women (48 pre-menopausal; 55 post-menopausal) completed a standardized sexual arousal induction paradigm. C-reactive protein (CRP), a marker of inflammation, was assessed from blood samples. Participants also completed validated clinical surveys and diagnostic interviews of sexual desire, arousal, and overall sexual functioning. Self-reported sexual arousal to a sexual film; survey indices of sexual desire and sexual functioning; and female sexual dysfunction diagnosis. While there was lower sexual functioning and higher CRP in the post-menopausal group, there was no significant association nor interaction between CRP and menopausal status in predicting sexual function, self-reported arousal, nor diagnosis. Exploratory analyses revealed a significant negative association between CRP and sexual desire among women with higher lifetime exposure to sexual violence, but positive association at lower levels of lifetime sexual violence exposure. Caution is warranted for interpreting CRP as a clinical marker of sexual dysfunction in either pre- or post-menopausal women. Strengths include well-validated clinical assessments of sexual function, direct measures of inflammation, and inclusion of women across the lifespan. Limitations include a cross-sectional design, limited racial/ethnic diversity, and reliance on one inflammation biomarker. CRP was not associated with subjective sexual arousal or sexual functioning in a sample of healthy women; further work may identify if more sensitive inflammation biomarkers are needed, or if inflammation has greater effects on sexual function in specific conditions such metabolic syndrome. Of note, CRP did predict lower sexual desire in women with sexual violence histories, suggesting that survivors of sexual violence may be particularly sensitive to inflammation-mediation suppression of sexual motivation and/or reward.

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(166) EXPLORING THE RELATIONSHIP BETWEEN PRE-AROUSAL CRP AND SEXUAL FUNCTION AND SUBJECTIVE SEXUAL AROUSAL IN PRE- AND POSTMENOPAUSAL WOMEN
  • Apr 25, 2025
  • The Journal of Sexual Medicine
  • M S Grosse-Rueschkamp + 1 more

Introduction At least 10% of women in the United States are affected by problems with sexual desire which can impact sexual satisfaction, relationship satisfaction and overall quality of life. Postmenopausal women are disproportionally at risk. The mechanisms and causes are still not well understood, contributing to a lack of treatment options. Inflammation might be an important component that has so far been overlooked. Given prior research showing links between elevated inflammation and reduced sensitivity to reward, a link between heightened inflammation and decreased sexual desire seems likely. A lack of anti-inflammatory effects of estrogen in postmenopausal women might exacerbate the effects. Objective The aim of this study was to explore the connection of inflammation and sexual desire, global function and self-reported sexual arousal in healthy pre- and postmenopausal women. Methods 48 premenopausal (M = 25.9, SD =9) and 7 postmenopausal participants completed in-person procedures while 55 postmenopausal participants completed remote procedures (M = 55.2, SD = 8) due to the COVID-19 restrictions. Participants were prescreened online and gave informed consent. All participants provided a sample of whole blood via dried blood spot, from which we derived a marker of inflammation, C-reactive protein (CRP). Self-reported subjective sexual arousal and emotional states were measured before and after exposure to an erotic film. Sexual function, desire and self-reported mental health symptoms were measured using validated questionnaires and a structured clinical interview. Data was transformed prior to data analysis and analyzed using general linear models. Results Postmenopausal women reported a significant lower global sexual function, measured by the Female Sexual Function Index (FSFI) (t (54.18) = - 2.64, p = 0.01) and lower desire, arousal and lubrication subscale scores. No significant group differences were observed in the Sexual Desire Inventory (SDI) or mental health outcomes. Premenopausal women had a significantly lower CRP than postmenopausal women (t (73.13) = −7.32, p < 0.001); however, CRP did not predict sexual function as measured by the FSFI. When controlling for BMI, diabetes, sexual trauma history, psychiatric disorders, and frequency of partnered sexual activity, CRP significantly predicted sexual desire as measured by the SDI (β = -19.57, SE = 8.28, t = -2.36, p = 0.037). There was no statistically significant relationship to self-reported subjective arousal. Menopausal status did not significantly moderate any of the main effects. Conclusions We did not find strong evidence for a link between baseline CRP and sexual desire, global sexual function or self-reported subjective arousal in pre- and postmenopausal women. However, there was some evidence that CRP may be a significant predictor of some elements of sexual desire when considering known predictors of inflammatory parameters such as metabolic conditions, sexual trauma history and partnered sex frequency. Possibly, CRP is not sensitive to subtle effects; future research may benefit from examining markers of inflammation that may be more sensitive to subjective sexual response, such as inflammatory cytokines. Disclosure No.

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Polycystic Ovary Syndrome (PCOS) is the most common endocrine disorder in women of fertile age. It is associated with somatic and psychological comorbidities and lower sexual function. To study which psychosocial factors predict sexual dysfunction, and dyadic and solitary sexual desire in women with PCOS. This is an observational case control study amongst healthy heterosexual women with (n= 68) and without PCOS (n= 67), aged 18-40years, in a steady relationship. All participants filled out questionnaires on sexuality (sexual function, sexual distress, sexual desire), psychosocial factors (general self-esteem, relationship satisfaction, body image, body self-consciousness, sexual esteem, sexual abuse), and mental health (anxiety and depression). Standard multiple regression analyses were performed to assess which factors predict sexual dysfunction and dyadic and solitary sexual desire. sexual dysfunction, dyadic sexual desire, solitary sexual desire. Women with PCOS reported significantly more often sexual dysfunction (41.2% vs. 11.9%, P< .001, φ: 0.331) and lower dyadic sexual desire (P: .005, η: 0.057), but no difference in solitary sexual desire (P: .160, η: 0.015) compared to women without PCOS. Also, women with PCOS reported significantly less positive body image (P: .012, η: 0.047), higher body self-consciousness (P: .011, η: 0.048), higher anxiety (P: .002, η: 0.072), higher depression scores (P: .006, η: 0.055), more sexual abuse experiences (P: .009, φ: 0.225), and less relationship satisfaction (P: .017, η: 0.042). No differences in general self-esteem (P: .169, η: 0.014) were found in contrast to sexual esteem (P: .021, η: 0.039). Body self-consciousness (P: .05, r= 0.242), depression (P: <.001, r= .357), relationship satisfaction (P: .05, r= -0.286), and sexual esteem (P: <.001, r= 0.644) showed significant correlations with sexual dysfunction; and sexual esteem (P: <.001, r= -0.475) and use of the combined oral contraceptive pill (P: .05, r= -0.270) with dyadic sexual desire. Regression showed the strongest associations (all P: <.001) between sexual esteem and sexual dysfunction and dyadic sexual desire, and between depression and sexual dysfunction with moderate explained variance. Sexual function should be discussed with women with PCOS and psycho-education on the association with sexual esteem and depression given. Other common psychosocial comorbidities in PCOS should be screened. Refer for psychotherapy or a tailormade psychosexual treatment including interventions targeted on sexual esteem and depression. Strengths are the broad assessment of psychosocial factors and sexual distress. A weakness is the relatively healthy population possibly underestimating the effect of psychosocial factors. Sexual dysfunction and dyadic sexual desire in women with PCOS are predicted by depression and sexual esteem suggesting psychosexual counseling might be helpful.

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