Sexual Medicine and Andrology Unit, Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy.
Endocrinology Unit, Medical Department, Azienda USL, Maggiore-Bellaria Hospital, Bologna, Italy; Pituitary Unit, IRCCS Institute of Neurological Science of Bologna, Bologna, Italy.
J Sex Med. 2019 Jun;16(6):821-832. doi: 10.1016/j.jsxm.2019.03.006. Epub 2019 Apr 5.
Although the pathogenic role of metabolically complicated obesity (MCO) in erectile dysfunction (ED), major adverse cardiovascular events (MACE), and male infertility has been widely studied, that of metabolically healthy obesity (MHO) has been poorly investigated.
To assess the role of MHO in the pathogenesis of ED, prediction of MACE, and male reproductive health.
A consecutive series of 4,945 men (mean age, 50.5 ± 13.5 years) with sexual dysfunction (SD) (cohort 1) and 231 male partners of infertile couples (mean age, 37.9 ± 9.1 years; cohort 2) were studied. A subset of men with SD (n = 1,687) was longitudinally investigated to evaluate MACE. All patients underwent clinical, biochemical, erectile function, and flaccid penile color Doppler ultrasound (PCDU) assessment. Infertile men also underwent scrotal and transrectal ultrasound; semen analysis, including interleukin (IL-) 8; and prostatitis-like symptom assessment. MHO was defined as body mass index >30 kg/m with high-density lipoprotein cholesterol level >40 mg/dL and absence of diabetes or hypertension. The rest of the obesity sample was defined as MCO. MHO or MCO were compared with the rest of the sample, defined as normal weight (NW) individuals.
Clinical, biochemical, erectile, and PCDU assessment in MHO, MCO and NW men in both cohorts; longitudinal MACE incidence assessment in cohort 1.
In cohort 1, 816 men (16.5%) were obese, 181 (3.7%) were MHO, and 635 (12.8%) were MCO. In cohort 2, 68 men (28.4%) were obese, 19 (8.2%) were MHO, and 49 (21.2%) were MCO. After adjusting for confounders, in both samples, the men with MHO and MCO had lower total testosterone levels and worse PCDU parameters compared with the NW men. However, only MCO men had worse erectile function compared with NW men. In the longitudinal study, both MHO and MCO men independently had a higher incidence of MACE compared with NW men (P < .05 for both). In cohort 2, MHO and MCO men had a larger prostate volume, and MCO men also had higher ultrasound and biochemical (IL-8) features of prostatic inflammation compared with NW men, but no differences in prostatitis-like symptoms or seminal parameters.
MHO men should be considered at high cardiovascular risk like MCO men and followed-up for erectile dysfunction and prostate abnormalities overtime.
STRENGTHS & LIMITATIONS: The study simultaneously examined several endpoints with validated instruments within 2 different male populations, 1 with SD and 1 with infertility. As for limitations, there is no consensus in the scientific community regarding the definition of MHO, and the results are derived from patients with SD or infertility, which could have different characteristics than the general male population.
MHO is associated with subclinical ED, increased cardiovascular risk, and prostate enlargement. Lotti F, Rastrelli G, Maseroli E, et al. Impact of Metabolically Healthy Obesity in Patients with Andrological Problems. J Sex Med 2019:16;821-832.
尽管代谢异常肥胖(MCO)在勃起功能障碍(ED)、主要不良心血管事件(MACE)和男性不育中的致病作用已被广泛研究,但代谢健康肥胖(MHO)的作用却研究甚少。
评估 MHO 在 ED 发病机制、MACE 预测和男性生殖健康中的作用。
对有性功能障碍(SD)的 4945 名男性(平均年龄 50.5±13.5 岁;队列 1)和 231 名不育夫妇的男性伴侣(平均年龄 37.9±9.1 岁;队列 2)进行了连续系列研究。对一部分有 SD 的男性(n=1687)进行了纵向 MACE 评估。所有患者均接受了临床、生化、勃起功能和松弛阴茎彩色多普勒超声(PCDU)评估。不育男性还接受了阴囊和经直肠超声检查;精液分析,包括白细胞介素(IL)-8;前列腺炎样症状评估。MHO 定义为体重指数(BMI)>30kg/m2,高密度脂蛋白胆固醇(HDL-C)水平>40mg/dL,且无糖尿病或高血压。其余肥胖样本定义为 MCO。MHO 或 MCO 与其余定义为正常体重(NW)个体的样本进行比较。
在两个队列中,对 MHO、MCO 和 NW 男性进行了临床、生化、勃起和 PCDU 评估;在队列 1 中进行了纵向 MACE 发生率评估。
MHO 与亚临床 ED、心血管风险增加和前列腺增大有关。Lotti F, Rastrelli G, Maseroli E, et al. 代谢健康肥胖对有男科问题患者的影响。性医学杂志 2019;16:821-832。