国际医药卫生导报 ›› 2025, Vol. 31 ›› Issue (6): 996-1000.DOI: 10.3760/cma.j.cn441417-20241011-06023

• 临床研究 • 上一篇    下一篇

血清AMH、INHB、TGF-β1水平联合检测对卵巢早衰的诊断价值分析

田波  史冬冬  申延兴   

  1. 濮阳油田总医院医学检验科,濮阳 457001

  • 收稿日期:2024-10-11 出版日期:2025-03-15 发布日期:2025-03-17
  • 通讯作者: 田波,Email:tian1015TT@163.com
  • 基金资助:

    河南省医学科技攻关联合共建项目(LHGJ20221084)

Value of combined detection of serum AMH, INHB, and TGF-β1 levels in diagnosis of premature ovarian failure

Tian Bo, Shi Dongdong, Shen Yanxing   

  1. Department of Medical Laboratory, Puyang Oilfield General Hospital, Puyang 457001, China

  • Received:2024-10-11 Online:2025-03-15 Published:2025-03-17
  • Contact: Tian Bo, Email: tian1015TT@163.com
  • Supported by:

    Problem-tackling Co-construction Project of Medical Science and Technology in Henan (LHGJ20221084)

摘要:

目的 探究血清抗苗勒管激素(AMH)、抑制素B(INHB)、转化生长因子β受体1(TGF-β1)水平联合检测对卵巢早衰的诊断价值。方法 采用回顾性研究,选取濮阳油田总医院2023年3月至2024年3月收治的105例卵巢早衰患者为观察组,另选取同期月经周期正常的健康体检女性105名为对照组。观察组:年龄25~39(32.15±2.78)岁,体重指数19.9~26.8(23.24±1.62)kg/m2;对照组:年龄24~38(31.51±3.04)岁,体重指数19.7~26.9(22.96±1.58)kg/m2。对比两组血清AMH、INHB、TGF-β1水平,分析血清AMH、INHB、TGF-β1水平与卵巢早衰发生的相关性与危险度,以及对卵巢早衰的诊断价值。统计学方法采用t检验。结果 观察组血清AMH、INHB、TGF-β1水平均低于对照组[(2.51±0.62)μg/L比(13.74±3.45)μg/L、(41.12±10.58)ng/L比(106.24±30.62)ng/L、(151.54±15.27)ng/L比(285.44±34.38)ng/L],差异均有统计学意义(t=-32.829、-20.597、-36.473,均P<0.05)。血清AMH、INHB、TGF-β1水平均与卵巢早衰发生呈负相关(r=-0.648、-0.623、-0.659,均P<0.05)。血清AMH(OR=7.306,95%CI 5.983~8.921)、INHB(OR=7.680,95%CI 6.387~9.234)、TGF-β1(OR=8.762,95%CI 7.245~10.597)水平均是患者发生卵巢早衰的独立影响因素(均P<0.05)。血清AMH、INHB、TGF-β1水平及联合检测诊断卵巢早衰发生的曲线下面积(AUC)分别为0.631、0.619、0.702、0.849(均P<0.05);血清AMH、INHB、TGF-β1高水平者发生卵巢早衰分别是低水平的0.470倍、0.530倍、0.391倍(均P<0.05)。结论 血清AMH、INHB、TGF-β1水平与卵巢早衰发生关系密切,各指标联合检测可为临床诊断卵巢早衰提供参考。

关键词:

卵巢早衰, 抗苗勒管激素, 抑制素B, 转化生长因子β受体1

Abstract:

Objective To explore the value of combined detection of serum anti-Müllerian hormone (AMH), inhibin B (INHB), and transforming growth factor beta receptor 1 (TGF-β1) levels in the diagnosis of premature ovarian failure. Methods A total of 105 patients with premature ovarian failure treated at Puyang Oilfield General Hospital from March 2023 to March 2024 were selected as an observation group; 105 healthy female examinees with normal menstrual cycles in the same period were selected as a control group. The observation group were 25-39 (32.15±2.78) years old; their body mass index was 19.9-26.8 (23.24±1.62) kg/m2. The control group were 24-38 (31.51±3.04) years old; their body mass index was 19.7-26.9 (22.96±1.58) kg/m2. The serum levels of AMH, INHB and TGF-β1 were compared between the two groups. The correlation of the serum levels of AMH, INHB and TGF-β1 with the occurrence of premature ovarian failure was analyzed. The risk of premature ovarian failure was analyzed. The diagnostic value of serum levels of AMH, INHB and TGF-β1 for premature ovarian failure was analyzed. t test was used for the statistical analysis. Results The levels of serum AMH, INHB, and TGF-β1 in the observation group were lower than those in the control group [(2.51±0.62) μg/L vs. (13.74±3.45) μg/L, (41.12±10.58) ng/L vs. (106.24±30.62) ng/L, and (151.54±15.27) ng/L vs. (285.44±34.38) ng/L; t=-32.829, -20.597, and -36.473; all P<0.05]; the levels of serum AMH, INHB, and TGF-β1 were negatively correlated with the occurrence of premature ovarian failure (r=-0.648, -0.623, and -0.659; all P<0.05); the levels of serum AMH (OR=7.306,95%CI 5.983-8.921), INHB(OR=7.680,95%CI 6.387-9.234), and TGF-β1 (OR=8.762,95%CI 7.245-10.597) were independent influencing factors for the occurrence of premature ovarian failure in the patients ( all P<0.05). The areas under the curves (AUC) of AMH, INHB, TGF-β1, and their combination in the diagnosis of premature ovarian failure were 0.631, 0.619, 0.702, and 0.849, respectively (P<0.05). The individuals with high serum levels of AMH, INHB, and TGF-β1 were 0.470, 0.530, and 0.391 times more likely to experience premature ovarian failure compared to those with low levels (all P<0.05). Conclusion The serum levels of AMH, INHB, and TGF-β1 are closely related to the occurrence of premature ovarian failure, and the combined detection of these indicators can provide references for the clinical diagnosis of premature ovarian failure.

Key words:

Premature ovarian failure, Anti-Müllerian hormone, Inhibin B, Transforming growth factor beta receptor 1