Rabin Medical Center, Institute of Endocrinology, Beilinson Hospital, 4941492, Petah-Tikva, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Pituitary. 2022 Dec;25(6):882-890. doi: 10.1007/s11102-022-01259-3. Epub 2022 Aug 29.
To study the baseline characteristics predicting hypogonadotropic hypogonadism (HH) persistence in men with macroprolactinoma that achieved prolactin normalization.
Retrospective cohort study.
Male patients diagnosed with macroprolactinoma and HH that received cabergoline treatment with subsequent prolactin normalization were included: men that achieved eugonadism, and men that remained hypogonadal. Patient's demographic, clinical and biochemical parameters, sellar imaging, and visual fields tests were obtained. Univariate and multivariate models were used to identify predictors of HH persistence.
Fifty-eight male patients (age 49.2 ± 12.6 years) with a median baseline prolactin of 1154 ng/mL (IQR 478-2763 ng/mL) and adenoma (maximal) diameter of 25.9 ± 14.8 mm were followed for a median of 5.6 years (IQR 3.0-10.7). Twelve men (21%) suffered from HH persistence at the end of follow-up and 46 men achieved eugonadism. Forty-two out of 46 men (91%) accomplished eugonadism within the first year following prolactin normalization. In a multivariate logistic regression model, hypopituitarism (OR 10.1; 95% CI 1.10-101.94), visual field defect (OR 9.9; 95% CI 1.07-92.33), and low baseline testosterone levels (OR 0.5; 95% CI 0.29-0.93) were independent predictors of HH persistence.
In our cohort of men with macroprolactinoma that reached prolactin normalization with cabergoline treatment, 21% had HH persistence. Pituitary hormone deficiency, visual field defects, and low baseline testosterone levels were independently associated with HH persistence. 91% of men achieved eugonadism within the first year following prolactin normalization. These findings may support informed clinical decision-making regarding the initiation of testosterone replacement in men with macroprolactinomas.
研究催乳素正常化的男性大泌乳素瘤患者中预测促性腺激素低下性性腺功能减退症(HH)持续存在的基线特征。
回顾性队列研究。
纳入接受卡麦角林治疗且催乳素正常化后诊断为大泌乳素瘤和 HH 的男性患者:达到正常生育力的男性和仍然存在性腺功能减退的男性。获得患者的人口统计学、临床和生化参数、鞍区成像和视野测试。使用单变量和多变量模型来确定 HH 持续存在的预测因素。
58 名男性患者(年龄 49.2±12.6 岁)的基线催乳素中位数为 1154ng/mL(IQR 478-2763ng/mL),腺瘤(最大)直径为 25.9±14.8mm,中位随访时间为 5.6 年(IQR 3.0-10.7)。12 名男性(21%)在随访结束时出现 HH 持续存在,46 名男性达到正常生育力。46 名男性中有 42 名(91%)在催乳素正常化后第一年达到正常生育力。在多变量逻辑回归模型中,垂体功能减退(OR 10.1;95%CI 1.10-101.94)、视野缺损(OR 9.9;95%CI 1.07-92.33)和低基线睾酮水平(OR 0.5;95%CI 0.29-0.93)是 HH 持续存在的独立预测因素。
在我们的队列中,接受卡麦角林治疗的催乳素正常化的男性大泌乳素瘤患者中,有 21%存在 HH 持续存在。垂体激素缺乏、视野缺损和低基线睾酮水平与 HH 持续存在独立相关。91%的男性在催乳素正常化后第一年达到正常生育力。这些发现可能为男性大泌乳素瘤患者启动睾酮替代治疗提供临床决策依据。