Division of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.
Department of Medicine, Michael E. DeBakey Veterans Affairs (VA) Medical Center, Houston, TX, United States.
Front Endocrinol (Lausanne). 2022 Jul 11;13:915309. doi: 10.3389/fendo.2022.915309. eCollection 2022.
Male hypogonadism adversely affects body composition, bone mineral density (BMD), and metabolic health. A previous report showed that pre-treatment testosterone (T) levels of <200 ng/dl is associated with greater improvement in spine BMD with T therapy. However, to date, there is no study that investigates whether baseline T levels also influence body composition and metabolic response to T therapy.
The aim of this study is to determine if there are differences in the changes in body composition, metabolic profile, and bone turnover markers, in addition to BMD, in response to T therapy in men with a baseline T level of <264 ng/dl compared to those with levels ≥264 ng/dl.
This is a secondary analysis of a single-arm, open-label clinical trial (NCT01378299) on pharmacogenetics of response to T therapy conducted between 2011 and 2016 involving 105 men (40-74 years old), with average morning T < 300 ng/dl, given intramuscular T cypionate 200 mg every 2 weeks for 18 months. Subjects were divided into those with baseline T levels of <264 ng/dl ( = 43) and those with ≥264 ng/dl ( = 57). T and estradiol (E2) were measured by liquid chromatography/mass spectrometry; serum bone turnover markers (C-telopeptide [CTX], osteocalcin, and sclerostin), adiponectin, and leptin were measured by enzyme-linked immunosorbent assay; glycated hemoglobin (HbA1c) was measured by high-performance liquid chromatography; and areal BMD and body composition was measured by dual-energy x-ray absorptiometry (DXA).
Men with T < 264 ng/dl showed greater increases in total fat-free mass (FFM) at 18 months compared to those with T ≥ 264 ng/dl (4.2 ± 4.1 vs. 2.7 ± 3.8%; = 0.047) and unadjusted appendicular FFM at 6 and 18 months (8.7 ± 11.5 vs. 4.4 ± 4.3%, 7.3 ± 11.6 vs. 2.4 ± 6.8%; = 0.033 and = 0.043, respectively). Men with T ≥ 264 ng/dl showed significant decreases in HbA1c at 12 months (-3.1 ± 9.2 vs. 3.2 ± 13.9%; = 0.005), fasting glucose at 18 months (-4.2 ± 31.9 vs. 13.0 ± 57.3%; = 0.040), LDL at 6 months (-6.4 ± 27.5 vs. 12.8 ± 44.1%; = 0.034), and leptin at 18 months (-40.2 ± 35.1 vs. -27.6 ± 31.0%; = 0.034) compared to those with T < 264 ng/dl. No significant differences in BMD and bone turnover markers were observed.
T therapy results in improvement in body composition irrespective of baseline T levels but T < 264 ng/dl is associated with greater improvement in FFM, whereas a T level of ≥264 ng/dl favors improvement in metabolic profile.
男性性腺功能减退症会对身体成分、骨密度(BMD)和代谢健康产生不利影响。之前有报道称,治疗前睾酮(T)水平<200ng/dl 与 T 治疗后脊柱 BMD 的改善程度更大有关。然而,迄今为止,尚无研究表明基线 T 水平是否也会影响 T 治疗对身体成分和代谢反应的影响。
本研究旨在确定基线 T 水平<264ng/dl 的男性与 T 水平≥264ng/dl 的男性相比,在接受 T 治疗后,除 BMD 外,身体成分、代谢谱和骨转换标志物的变化是否存在差异。
这是一项于 2011 年至 2016 年期间进行的关于 T 治疗反应的药物遗传学的单臂、开放性临床试验(NCT01378299)的二次分析,涉及 105 名(40-74 岁)男性,平均清晨 T<300ng/dl,给予肌内注射 T 环戊丙酸酯 200mg,每 2 周一次,共 18 个月。受试者分为基线 T 水平<264ng/dl(=43)和 T 水平≥264ng/dl(=57)两组。T 和雌二醇(E2)采用液相色谱/质谱法测定;血清骨转换标志物(CTX、骨钙素和硬骨素)、脂联素和瘦素采用酶联免疫吸附法测定;糖化血红蛋白(HbA1c)采用高效液相色谱法测定;双能 X 射线吸收法(DXA)测定面积 BMD 和身体成分。
T<264ng/dl 的男性在 18 个月时总去脂体重(FFM)的增加幅度明显大于 T≥264ng/dl 的男性(4.2±4.1%比 2.7±3.8%;=0.047),6 个月和 18 个月时的四肢去脂体重(FFM)也明显增加(8.7±11.5%比 4.4±4.3%,7.3±11.6%比 2.4±6.8%;=0.033 和=0.043)。T≥264ng/dl 的男性在 12 个月时 HbA1c 显著下降(-3.1±9.2%比 3.2±13.9%;=0.005),18 个月时空腹血糖(-4.2±31.9%比 13.0±57.3%;=0.040)、6 个月时 LDL(-6.4±27.5%比 12.8±44.1%;=0.034)和 18 个月时瘦素(-40.2±35.1%比-27.6±31.0%;=0.034)也显著下降。BMD 和骨转换标志物无显著差异。
T 治疗可改善身体成分,无论基线 T 水平如何,但 T<264ng/dl 与 FFM 的改善程度更大有关,而 T≥264ng/dl 有利于改善代谢谱。