Prevalence and predictors of female sexual dysfunction among sexually active women in the diabetes prevention program outcomes study

Author:

Gupta Priyanka1ORCID,Doherty Lindsay2,Temprosa Marinella2,Pop‐Busui Rodica3,Gadde Kishore M.4,Singh Prachi5,Owora Arthur H.6,Wessells Hunter7,Sarma Aruna V.1ORCID,

Affiliation:

1. Department of Urology University of Michigan Ann Arbor Michigan USA

2. Department of Biostatistics and Bioinformatics, Biostatistics Center, Milken Institute School of Public Health George Washington University Washington District of Columbia USA

3. Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine University of Michigan Ann Arbor Michigan USA

4. Department of Surgery University of California Irvine Orange California USA

5. Pennington Biomedical Research Center Louisiana State University System Baton Rouge Louisiana USA

6. Department of Epidemiology and Biostatistics Indiana University School of Public Health Bloomington Indiana USA

7. Department of Urology and Diabetes, Research Center University of Washington School of Medicine Seattle Washington USA

Abstract

AbstractObjectiveTo 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).MethodsThe 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.ResultsOne 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).ConclusionsFSD is prevalent in women with PreD and T2D. Our findings suggest that FSD is associated with neuropathic complications commonly observed in PreD and T2D.

Publisher

Wiley

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