Moisey Robert, Swinburne Julie, Orme Steve
Department of Endocrinology, Leeds General Infirmary, Great George Street, Leeds, UK.
Clin Endocrinol (Oxf). 2008 Oct;69(4):642-7. doi: 10.1111/j.1365-2265.2008.03251.x. Epub 2008 Apr 3.
To investigate the loading regimen for intramuscular (IM) testosterone undecanoate (Nebido) to determine whether testosterone and bioavailable testosterone levels achieved correlate with age or body size of subjects studied.
Retrospective observational study of testosterone naïve patients and patients previously treated with an alternative testosterone therapy.
51 hypogonadal men (35, 68.6% secondary hypogonadism). 8 (16%) had not previously received testosterone therapy.
Patients received an IM injection of Nebido (1000 mg) at baseline and a second injection after 6 weeks. Serum was assayed at baseline and 18 weeks after commencing Nebido for total testosterone (TT) and SHBG. Bioavailable testosterone was calculated (cBioT) using TT and SHBG. Measurements were taken for weight, body mass index (BMI) and body surface area (BSA).
Baseline TT (mean 11.5 nmol/l, range 0.3-54.8) increased by 50% after commencing Nebido (17.2 nmol/l (5.4-32.8), P = 0.0001). 75% of subjects had a TT within the reference range (8.0-25.0 nmol/l). Subjects with primary hypogonadism had a higher 18-week TT [20.9 nmol/l (9.8-32.8) vs. 15.5 (5.4-32.6), P = 0.02] and SHBG [39.2 nmol/l (11-82) vs. 25.7 (9.0-60.0), P = 0.003] although the cBioT was not significantly different [4.9 nmol/l (2.9-7.3) vs. 4.2 (2.0-7.9), P = 0.12]. The 18-week TT positively correlated with age (R = 0.36, P = 0.01) and negatively correlated with weight (R = -0.38, P = 0.006), BMI (R = -0.42, P = 0.002) and BSA (R =-0.38, P = 0.007). Similarly cBioT correlated with age (R = 0.28, P = 0.04), weight (R = -0.29, P = 0.03), BMI (R = -0.30, P = 0.03) and BSA (R = -0.27, P = 0.05). Age (t = 2.04, P = 0.05) and baseline testosterone (t = -9.26, P < 0.0001) were independent variables of the increase in TT at 18 weeks.
This starting regimen is simple and provides the majority of men with a TT within the reference range. Age and baseline TT are independent variables of the increase in TT with IM testosterone undecanoate. At week 18 age and body size correlated with the cBioT and TT and this may then be used to estimate dosing frequency for this therapy.
研究肌肉注射十一酸睾酮(耐必多)的给药方案,以确定所达到的睾酮和生物可利用睾酮水平是否与所研究受试者的年龄或体型相关。
对未接受过睾酮治疗的患者和先前接受过其他睾酮治疗的患者进行回顾性观察研究。
51名性腺功能减退男性(35名,继发性性腺功能减退占68.6%)。8名(16%)此前未接受过睾酮治疗。
患者在基线时接受一次耐必多肌肉注射(1000毫克),6周后再注射一次。在开始使用耐必多后的基线和18周时检测血清中的总睾酮(TT)和性激素结合球蛋白(SHBG)。使用TT和SHBG计算生物可利用睾酮(cBioT)。测量体重、体重指数(BMI)和体表面积(BSA)。
开始使用耐必多后,基线TT(平均11.5纳摩尔/升,范围0.3 - 54.8)增加了50%(17.2纳摩尔/升(5.4 - 32.8),P = 0.0001)。75%的受试者TT在参考范围内(8.0 - 25.0纳摩尔/升)。原发性性腺功能减退的受试者18周时的TT[20.9纳摩尔/升(9.8 - 32.8)对15.5(5.4 - 32.6)纳摩尔/升,P = 0.02]和SHBG[39.2纳摩尔/升(11 - 82)对25.7(9.0 - 60.0)纳摩尔/升,P = 0.003]更高,尽管cBioT无显著差异[4.9纳摩尔/升(2.9 - 7.3)对4.2(2.0 - 7.9)纳摩尔/升,P = 0.12]。18周时TT与年龄呈正相关(R = 0.36,P = 0.01),与体重呈负相关(R = -0.38,P = 0.006)、与BMI呈负相关(R = -0.42,P = 任002)、与BSA呈负相关(R = -0.38,P = 0.007)。同样,cBioT与年龄相关(R = 0.28,P = 0.04)、与体重相关(R = -0.任29,P = 0.03)、与BMI相关(R = -0.30,P = 0.03)、与BSA相关(R = -0.27,P = 0.05)。年龄(t = 2.04,P = 0.05)和基线睾酮(t = -9.26,P < 0.0001)是18周时TT增加的独立变量。
这种起始给药方案简单,能使大多数男性的TT处于参考范围内。年龄和基线TT是肌肉注射十一酸睾酮后TT增加的独立变量。在第18周时,年龄和体型与cBioT和TT相关,这可用于估计该疗法的给药频率。