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Prevalence and predictors of female sexual dysfunction among sexually active women in the diabetes prevention program outcomes study.
Gupta, Priyanka; Doherty, Lindsay; Temprosa, Marinella; Pop-Busui, Rodica; Gadde, Kishore M; Singh, Prachi; Owora, Arthur H; Wessells, Hunter; Sarma, Aruna V.
Affiliation
  • Gupta P; Department of Urology, University of Michigan, Ann Arbor, Michigan, USA.
  • Doherty L; Department of Biostatistics and Bioinformatics, Biostatistics Center, Milken Institute School of Public Health, George Washington University, Washington, District of Columbia, USA.
  • Temprosa M; Department of Biostatistics and Bioinformatics, Biostatistics Center, Milken Institute School of Public Health, George Washington University, Washington, District of Columbia, USA.
  • Pop-Busui R; Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Gadde KM; Department of Surgery, University of California Irvine, Orange, California, USA.
  • Singh P; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, Louisiana, USA.
  • Owora AH; Department of Epidemiology and Biostatistics, Indiana University School of Public Health, Bloomington, Indiana, USA.
  • Wessells H; Department of Urology and Diabetes, Research Center, University of Washington School of Medicine, Seattle, Washington, USA.
  • Sarma AV; Department of Urology, University of Michigan, Ann Arbor, Michigan, USA.
Neurourol Urodyn ; 43(4): 977-990, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38501372
ABSTRACT

OBJECTIVE:

To determine the burden and identify correlates of female sexual dysfunction (FSD) among women with prediabetes (PreD) and type 2 diabetes (T2D) enrolled in the Diabetes Prevention Program (DPP) Outcomes Study (DPPOS).

METHODS:

The DPPOS visit included the Female Sexual Function Index (FSFI) to determine sexual function. Of 1464 participants, 1320 (90%) completed the (FSFI) and 426 were sexually active. A backward selection multivariable logistic regression model estimated the odds of FSD for sociodemographic, clinical, and diabetes-related covariates.

RESULTS:

One hundred and eighty-five (43%) had a score of ≤26.55 and met the criteria for FSD. After adjustment for DPP treatment and age, urinary incontinence (UI) (odds ratio [OR] = 1.91, 95% confidence interval [CI] = 1.15-3.17) and hysterectomy (OR = 1.89, 95% CI = 1.01-3.53) were associated with increased odds of FSD. Increased body mass index was protective for FSD (OR = 0.93 per kg/m2, 95% CI = 0.89-0.96). Michigan Neuropathy Screening Instrument-based peripheral neuropathy (mean±SD scores 1.1±1.3 vs. 0.9±1.1, p < 0.0001) and Electrocardiogram (ECG)-based autonomic dysfunction measures (mean ± SD heart rate levels 64.3 ± 6.8 vs. 65.6 ± 10.2, p = 0.008) were associated with FSD. There were no differences in diabetes rates between women who did (66.5%) and did not (66%) have (p = 0.7).

CONCLUSIONS:

FSD is prevalent in women with PreD and T2D. Our findings suggest that FSD is associated with neuropathic complications commonly observed in PreD and T2D.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sexual Dysfunction, Physiological / Sexual Dysfunctions, Psychological / Diabetes Mellitus, Type 2 Limits: Female / Humans Language: En Journal: Neurourol Urodyn Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sexual Dysfunction, Physiological / Sexual Dysfunctions, Psychological / Diabetes Mellitus, Type 2 Limits: Female / Humans Language: En Journal: Neurourol Urodyn Year: 2024 Type: Article Affiliation country: United States