La Vignera Sandro, Cannarella Rossella, Garofalo Vincenzo, Crafa Andrea, Barbagallo Federica, Condorelli Rosita A, Calogero Aldo E
Department of Clinical and Experimental Medicine, University of Catania, Via S. Sofia 78, Catania, 95123, Italy.
Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
Reprod Biol Endocrinol. 2025 Jul 2;23(1):92. doi: 10.1186/s12958-025-01425-9.
Tirzepatide (TZP), a dual agonist of glucose-dependent insulinotropic peptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors, has recently been introduced in Italy for the treatment of obesity. Obesity is frequently associated with metabolic hypogonadism, which is characterized by low testosterone levels and normal low levels of gonadotropin. This condition exacerbates metabolic dysfunction and increases the risk of type 2 diabetes mellitus (DM). This study aims to evaluate the effects of TZP on metabolic hypogonadism in patients with obesity.
Male patients with obesity and metabolic hypogonadism were enrolled. Exclusion criteria included recent use of medications for hypertension, dyslipidemia, DM, anti-androgens, or hyperprolactinemia. All participants followed a hypocaloric diet and engaged in 20 min of daily brisk walking. Patients were allocated to one of the following treatment groups: Group A received 2.5 mg of TZP weekly for the first month, with the dose increased to 5 mg from the second month; Group B received no pharmacological treatment: Group C received transdermal testosterone. Clinical evaluations were conducted at 2 months including assessment of body composition, the Binge Eating Scale (BES), 5-item International Index of Erectile Function (IIEF-5) questionnaire to evaluate erectile dysfunction (ED), and serum levels of luteinizing hormone (LH), follicle-stimulating hormone (FSH), sex hormone-binding globulin (SHBG), total testosterone (TT), and 17β-estradiol (E). Free (fT) and bioavailable testosterone (bioT) were calculated using the Vermeulen formula.
A total of 83 patients with obesity (mean age 55.3 ± 5.5 years) were included in the study, divided into three groups: Group A (28 patients, mean age 56.3 ± 4.7 years), Group B (30 patients, mean age 55.1 ± 5.2 years), and Group C (25 patients, mean age 54.0 ± 6.5 years). At baseline, significant differences were observed in waist circumference (WC), which was higher in Group B, as well as in the BES score, lean mass (LM), and serum LH levels, all of which were higher in Group A. After 2 months, Group A showed significantly greater reductions in body weight, WC, BES score, and fat mass, along with a notable increase in LM and IIEF-5 score compared to Groups B and C. Additionally, Group A exhibited significantly higher serum levels of LH, FSH, SHBG, TT, fT, and bioT, while E levels were significantly lower than both Groups B and C.
The results of this study suggest that TZP is effective in improving both metabolic parameters, ED, and gonadal hormone levels in patients with obesity and metabolic hypogonadism. These findings position TZP as a promising treatment for obese patients with functional hypogonadism arising from metabolic-related alterations.
替尔泊肽(TZP)是一种葡萄糖依赖性促胰岛素多肽(GIP)和胰高血糖素样肽-1(GLP-1)受体的双重激动剂,最近已在意大利被用于治疗肥胖症。肥胖症常与代谢性性腺功能减退相关,其特征为睾酮水平低和促性腺激素水平正常偏低。这种情况会加剧代谢功能障碍,并增加2型糖尿病(DM)的风险。本研究旨在评估TZP对肥胖症患者代谢性性腺功能减退的影响。
纳入肥胖且患有代谢性性腺功能减退的男性患者。排除标准包括近期使用过治疗高血压、血脂异常、DM、抗雄激素或高催乳素血症的药物。所有参与者均遵循低热量饮食,并每天进行20分钟的轻快步行。患者被分配到以下治疗组之一:A组在第一个月每周接受2.5mg的TZP,从第二个月起剂量增加至5mg;B组不接受药物治疗;C组接受经皮睾酮治疗。在2个月时进行临床评估,包括身体成分评估、暴饮暴食量表(BES)、用于评估勃起功能障碍(ED)的5项国际勃起功能指数(IIEF-5)问卷,以及血清促黄体生成素(LH)、促卵泡生成素(FSH)、性激素结合球蛋白(SHBG)、总睾酮(TT)和17β-雌二醇(E)水平。游离(fT)和生物可利用睾酮(bioT)使用Vermeulen公式计算。
共有83例肥胖患者(平均年龄55.3±5.5岁)纳入研究,分为三组:A组(28例患者,平均年龄56.3±4.7岁)、B组(30例患者,平均年龄55.1±5.2岁)和C组(25例患者,平均年龄54.0±6.5岁)。在基线时,观察到腰围(WC)存在显著差异,B组的WC更高,同时在BES评分、瘦体重(LM)和血清LH水平方面也存在差异,A组的这些指标均更高。2个月后,与B组和C组相比,A组在体重、WC、BES评分和脂肪量方面的降低更为显著,同时LM和IIEF-5评分显著增加。此外,A组的血清LH、FSH、SHBG、TT、fT和bioT水平显著更高,而E水平显著低于B组和C组。
本研究结果表明,TZP在改善肥胖且患有代谢性性腺功能减退患者的代谢参数、ED和性腺激素水平方面是有效的。这些发现使TZP成为治疗因代谢相关改变引起的功能性性腺功能减退肥胖患者的一种有前景的治疗方法。