Analysis of Clinical Risk Factors for Idiopathic Hypogonadotropic Hypogonadism
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摘要:
目的 分析特发性低促性腺激素性性腺功能减退症(IHH)患者的临床指标危险因素。 方法 选取云南省第一人民医院内分泌科2008年1月至2021年12月确诊为IHH的患者120例(男性82例,女性38例,其中卡尔曼综合征15例)为病例组,年龄(22.43±6.08)岁,选取性腺功能正常的健康人群95例(男性75例,女性20例)为对照组,年龄(21.47±2.67)岁;收集病例组与对照组的一般临床资料,剔除部分数据缺失的患者,分析病例组与对照组指标是否具有统计学差异,对有统计学意义的进行多因素分析;病例组中,收集IHH患者的骨密度共48例(骨密度降低组31例(男性22例,女性9例),骨密度正常组17例(男性6例,女性11例);分析导致IHH患者骨密度异常的危险因素。 结果 病例组与对照组年龄、体重、E2、Testo、LH、FSH、CHOL、血糖差异有统计学意义(P < 0.05),性别、身高、TSH、T3、T4、FT3、FT4、TG、HDL-C、LDL-C无统计学差异(P > 0.05);无序二元 Logistic 回归分析显示E2、Testo是患者发生IHH的保护因素(P < 0.05)。IHH患者中骨密度减低组与骨密度正常组比较:2组中性别、年龄有统计学差异(P < 0.05),E2、Prog、Testo、PRL、LH、FSH无统计学差异,无序二元 Logistic 回归分析显示年龄是IHH患者发生骨密度减低的危险因素,性别是IHH患者发生骨密度减低的保护因素(P < 0.05)。 结论 IHH会导致患者血糖、血脂及骨密度减低,E2、Testo是患者发生IHH的保护因素,年龄是IHH患者发生骨密度减低的危险因素,性别是保护因素。 -
关键词:
- 特发性低促性腺激素性性腺功能减退症 /
- 骨密度 /
- 危险因素
Abstract:Objective To analyze the clinical risk factors in idiopathic hypogonadotropic hypogonadism patients (IHH). Methods We selected 120 patients with hypogonadism from the Endocrinology Department of the First People's Hospital of Yunnan Province from January 2008 to December 2021 (82 males, 38 females, including 25 Kalman syndrome patients; 22.43 ± 6.08 years) as the case group. We also selected 95 healthy patients with normal gonadal function (75 males and 20 females21.47±2.67 years) as the control group. General clinical data of patients in the case group and control group were collected, excluding the patients with some missing data. We analyzed whether the indicators were statistically different between the case and control groups by multivariate analysis. The data on the bone mineral density of 48 IHH patients, including 31 patients with reduced bone mineral density (22 males, 9 Females) and 17 patients with normal bone mineral density (6 males, 11 females), were collected in the case group. The risk factors leading to abnormal BMD were analyzed in IHH patients. Results There were significant differences in age, weight, E2, Testo, LH, FSH, CHOL and blood glucose (P < 0.05), and no significant differences in gender, height, TSH, T3, T4, FT3, FT4, TG, HDL-C, LDL-C (P > 0.05). Unordered binary Logistic regression analysis showed that E2 and Testo were the protective factors for IHH patients (P < 0.05). Comparison between the IHH patients for the reduced BMD group and the IHH patients for the normal BMD group: there were significant differences in sex and age (P < 0.05), while E2, Prog, Testo, PRL, LH, L H, FSH was not significant. Disordered binary Logistic regression analysis showed that age was the risk factor for BMD in IHH patients, and sex was the protective factor for BMD in IHH patients (P < 0.05). Conclusions IHH can lead to decrease of blood glucose, lipid and bone density. E2 and T are the protective factors for IHH, age is the risk factor for decreased bone density in IHH patients, and gender is the protective factor. -
表 1 病例组与对照组单因素分析[n(%)/M(P25,P75)]
Table 1. Univariate analysis of the related indexes between case group and control group [n(%)/M(P25,P75)]
变量 病例组(n = 120) 对照组(n = 95) χ2/Z P 性别 男 82(68.3) 75(79.0) 3.032 0.082 女 38(31.7) 20(21.0) 年龄(岁) 21(18,26.75) 25(21,28) −3.118 0.002* 体重(kg) 57(49,68.75) 66(60,69) −3.369 0.001* 身高(cm) 168(160,175) 169(165,172) −0.847 0.397 TSH(mIU/mL) 2.25(1.38,3.25) 1.86(1.4,2.56) −1.224 0.221 T4(nmol/L) 99.79(85.79,113.15) 101.42(88.41,113.51)
−0.976
0.329T3(nmol/L) 1.80(1.58,2.13) 1.74(1.59,1.93) −1.055 0.291 FT3(pmol/L) 5.25(4.7,5.83) 5.16(4.81,5.58) −0.355 0.722 FT4(pmol/L) 16.72(14.77,18.76) 16.88(15.45,18.55) −0.587 0.557 E2(pmol/L) 34.70(18.35,56.8) 161(131,184.9) −12.592 0.000* Prog(nmol/L) 0.57(0.32,0.97) 0.48(0.40,0.7) −0.337 0.736 PRL(ng/mL) 10.73(7.64,16.76) 12.34(8.96,16.22) −1.346 0.178 Testo(nmol/L) 0.52(0.31,1.09) 13.6(9.94,18.7) −11.136 < 0.001* FSH(mIU/mL) 0.72(0.43,1.26) 4.42(3.1,8.18) −11.864 < 0.001* LH(mIU/mL) 0.19(0.1,0.51) 5.02(3.51,7.5) −12.6544 < 0.001* TG(mmol/L) 1.09(0.77,1.62) 1.11(0.72,1.52) −0.752 0.452 HDL-C(mmol/L) 1.24(1.05,1.39) 1.22(1.02,1.41) −0.365 0.715 LDL-C(mmol/L) 2.35(1.9,3.02) 2.61(2.22,3.07) −1.444 0.149 血糖(mmol/L) 4.5(4.3,4.8) 4.6(4.5,4.9) −1.99 0.047* *P < 0.05。 表 2 IHH患者骨密度减低组与骨密度正常组资料比较 [n(%)/M(P25,P75)]
Table 2. Data comparison between the IHH patients in reduced BMD group and the IHH patients in normal BMD group [n(%)/M(P25,P75)]
变量 骨密度减低组(n = 31) 骨密度正常组(n = 17) χ2/U P 性别 男 22(71.0) 6(35.3) 5.749 0.017* 女 9(29.0) 11(64.7) 年龄 17~25岁 9(29.0) 10(58.9) 4.075 0.044* 26~40岁 22(71.0) 7(41.1) E2(pmol/L) 41.46(18.35,74.42) 60.86(32.24,68.60) 209.0 0.234 Prog(nmol/L) 0.70(0.32,1.15) 0.82(0.41,1.09) 247.5 0.730 PRL(ng/mL) 9.10(7.33,14.28) 11.25(5.3.18.51) 231.0 0.484 Testo(nmol/L) 0.52(0.23,0.9) 0.53(0.42,0.89) 223.0 0.383 FSH(mIU/mL) 0.59(0.42,1.16) 0.76(0.28,2.46) 225.5 0.413 LH(mIU/mL) 0.10(0.1,0.59) 0.18(0.10,1.15) 206.0 0.189 *P < 0.05。 表 3 IHH患者的变量与赋值
Table 3. Variables and assignments in patients with IHH
因素 变量名 赋值说明 研究对象编号 ID 性别 X1 男 = 1;女 = 0 年龄 X2 1 = 21~40岁;0 = 17~20岁 Testo X3 E2 X4 体重 X5 IHH Y 1 = 是,0 = 否 表 4 IHH患者骨密度危险因素分析研究的变量与赋值
Table 4. Variables and assignments of BMD analysis of risk factors in IHH patients
因素 变量名 赋值说明 研究对象编号 ID 性别 X1 男 = 1;女 = 0 年龄 X2 1 = 26~40岁;0 = 17~25岁 Testo X3 E2 X4 骨密度 Y 1 = 减低;0 = 正常 表 5 IHH患者危险因素 Logistic 回归
Table 5. Logistic regression of IHH patients risk factors
因素 Wald OR 95%CI P E2(pmol/L) 9.526 0.846 0.761-0.941 0.002* Testo(nmol/L) 4.259 0.780 0.616-0.988 0.039* *P < 0.05。 表 6 IHH患者骨密度危险因素 Logistic 回归
Table 6. Logistic regression of BMD risk factors in IHH patients
因素 Wald OR 95%CI P 性别(男/女) 6.731 0.129 0.027-0.606 0.009* 年龄(17~25岁/26~40岁) 5.583 1.182 1.029-1.358 0.018* *P < 0.05。 -
[1] 中华医学会内分泌学分会性腺学组. 特发性低促性腺激素性性腺功能减退症诊治专家共识[J]. 中华内科杂志,2015,54(8):739-744. doi: 10.3760/cma.j.issn.0578-1426.2015.08.021 [2] 李晨曦,张小倩,章秋,等. 男性特发性低促性腺激素性性腺功能减退症患者心理健康状况研究[J]. 中国全科医学,2015,18(23):2787-2791. [3] Nakauchi M,Suda K,Kadoya S,et al. Technical aspects and short and longterm outcomes of totally laparoscopic total gastrectomy for advanced gastric cancer: a single-institution retrospective study[J]. Surg Endosc,2016,30(10):4632-4639. doi: 10.1007/s00464-015-4726-4 [4] 罗有文,张忆聪. 不同临床特征IHH女性患者相关激素含量特征的风险[J]. 实用妇科内分泌电子杂志,2022,9(1):23-26. [5] 郭建华,高彬,王琼,等. 垂体功能减退症患者和低促性腺激素性性腺功能减退症患者糖脂代谢的研究[J]. 现代生物医学进展,2017,17(20):3876-3879,3924. [6] Zheng R,Cao L,Cao W,et al. Risk factors for hypogonadism in male patients with type 2 diabetes[J]. J Diabetes Res,2016,2016:5162167. [7] Hu Y,Huang C,Sun Y,et al. Morbidity and mortality of laparoscopic versus open d2 distal gastrectomy for advanced gastric cancer:A randomized controlled trial[J]. J Clin Oncol,2016,34(12):1350-1357. doi: 10.1200/JCO.2015.63.7215 [8] Caruso S,Patriti A,Roviello F,et al. Laparoscopic and robotassisted gastrectomy for gastric cancer: Current considerations[J]. World J Gastroenterol,2016,22(25):5694-5717. doi: 10.3748/wjg.v22.i25.5694 [9] Jiang A,Chen L J,Wang Y X,et al. The effects of different methods of anaesthesia for laparoscopic radical gastrectomy with monitoring of entropy[J]. Anticancer Res,2016,36(3):1305-1308. [10] 陈青,孙斯曼,孙卫霞,等. 特发性低促性腺激素性性腺功能减退症合并1型糖尿病一例[J]. 中华糖尿病杂志,2021,13(3):262-264. [11] Zhang R,Mao J,Wang X,et al. Increased bone mineral density in male patients with idiopathic hyp-ogonadotropic hypogonadism who undergo sex hormone therapy: findings from cros-s-sectional and longitudinal studies[J]. Endocr Pract,2021,27(9):934-940. doi: 10.1016/j.eprac.2021.05.004 [12] Margaret F,Lippincott,Wanxue,Xu,et al. The p190 RhoGAPs,ARHGAP35,and ARHGAP5 are implicated in GnRH neuronal development:Evidence from patients with idiopathic hypogonadotropic hypogonadism,zebrafish,and in vitro GAP activity assay[J]. Genetics in Medicine:Official Journal of the American College of Medical Genetics,2022,24(12):2501-2515. [13] Wu J Y,Fang Z H,Wang X Y,et al. SLIT2 rare sequencing variants identified in idiopathic hypogonadotropic hypogonadism[J]. Hormone research in paediatrics,2022,95(4):384-392. [14] 解一丹,郑瑞芝,韩宾宾,等. 22例低促性腺激素性性腺功能减退症患者CHD7基因变异分析[J]. 中华医学遗传学杂志,2022,39(6):571-575. [15] Sun T T,Xu W C,Xu H,et al. Hormonal therapy is effective and safe for cryptorchidism caused by idiopathic hypogonadotropic hypogonadism in adult males[J]. Frontiersin Endocrinology,2022,13:1095950.