Article Summary
王龙影,许文强,顾丽霞,赵雅璇,曹君阳.不同病程自身免疫性卵巢早衰患者血清BMP15、IL-1β、INHB、MIF的变化及与性激素和T淋巴细胞亚群的相关性研究[J].现代生物医学进展英文版,2022,(18):3568-3572.
不同病程自身免疫性卵巢早衰患者血清BMP15、IL-1β、INHB、MIF的变化及与性激素和T淋巴细胞亚群的相关性研究
Changes of Serum BMP15, IL-1β, INHB and MIF in Patients with Different Stages of Autoimmune Premature Ovarian Failure and Their Correlation Study with Sex Hormones and Peripheral Blood T Lymphocyte Subsets
Received:February 27, 2022  Revised:March 24, 2022
DOI:10.13241/j.cnki.pmb.2022.18.032
中文关键词: 自身免疫性卵巢早衰  BMP15  IL-1β  INHB  MIF  性激素  T淋巴细胞亚群  相关性
英文关键词: Autoimmune premature ovarian failure  BMP15  IL-1β  INHB  MIF  Sex hormones  T lymphocyte subsets  Correlation
基金项目:河北省医学科学研究重点课题计划项目(201800836)
Author NameAffiliationE-mail
王龙影 河北北方学院附属第一医院妇产科 河北 张家口 075000 wanglongyingzjks@163.com 
许文强 河北北方学院附属第一医院妇产科 河北 张家口 075000  
顾丽霞 河北北方学院附属第一医院妇产科 河北 张家口 075000  
赵雅璇 河北北方学院附属第一医院妇产科 河北 张家口 075000  
曹君阳 河北北方学院附属第一医院妇产科 河北 张家口 075000  
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中文摘要:
      摘要 目的:分析不同病程的自身免疫性卵巢早衰(APOF)患者血清骨形态发生蛋白15(BMP15)、白介素-1β(IL-1β)、血清抑制素B(INHB)、巨噬细胞移动抑制因子(MIF)变化及其与血清性激素、外周血T淋巴细胞亚群相关指标表达的关系。方法:选取2021年1月至12月期间在河北北方学院附属第一医院就诊且被确诊为APOF的52例患者纳入APOF组,另选取同期在河北北方学院附属第一医院体检且确定为卵巢功能正常的健康女性50例纳入健康组,比较APOF组与健康组、不同病程的APOF患者血清BMP15、IL-1β、INHB、MIF水平差异,比较APOF组与健康组血清性激素水平和外周血T淋巴细胞亚群水平差异,分析血清BMP15、IL-1β、INHB、MIF与血清性激素水平和外周血T淋巴细胞亚群水平的相关性。结果:APOF组血清BMP15、INHB水平较健康组明显降低,APOF组血清IL-1β、MIF水平较健康组均明显升高(均P<0.05);病程>3年的患者血清BMP15、INHB水平较病程≤3年的患者明显降低,血清IL-1β、MIF水平明显升高(均P<0.05);APOF组促卵泡激素(FSH)较健康组明显升高,血清雌二醇(E2)水平较健康组明显降低(均P<0.05);APOF组CD4+水平较健康组明显降低(P<0.05);血清BMP15、INHB与FSH及CD4+呈明显负相关,与E2呈明显正相关,血清IL-1β、MIF与FSH及CD4+呈明显正相关,与E2呈明显负相关(均P<0.05)。结论:APOF患者随着病程延长,其血清BMP15、INHB水平呈下降趋势,血清IL-1β、MIF水平呈上升趋势,且上述各指标与患者性激素水平及外周血T淋巴细胞亚群水平密切相关。
英文摘要:
      ABSTRACT Objective: To analyze the changes of serum bone morphogenetic protein-15 (BMP15), interleukin-1β (IL-1β), serum inhibin B (INHB) and macrophage migration inhibitory factor (MIF) in patients with autoimmune premature ovarian failure (APOF) and their relationship with the expression of serum sex hormones and peripheral blood T lymphocyte subsets. Methods: 52 patients diagnosed with APOF who visited The First Affiliated Hospital of Hebei North University from January to December 2021 were included in the APOF group, and 50 healthy women with normal ovarian function who underwent physical examination in The First Affiliated Hospital of Hebei North University during the same period were included in the health group. The levels differences of serum BMP15, IL-1β, INHB and MIF between APOF group and healthy group, patients with different stages of APOF were compared, and the levels differences of serum sex hormones and peripheral blood T lymphocyte subsets were compared between APOF group and healthy group. The correlation of serum BMP15, IL-1β, INHB, MIF with serum sex hormone levels and peripheral blood T lymphocyte subsets was analyzed. Results: The levels of serum BMP15 and INHB in APOF group were significantly lower than those in healthy group, while the levels of serum IL-1β and MIF in APOF group were significantly higher than those in healthy group (all P<0.05). The levels of serum BMP15 and INHB in patients with course of disease > 3 years were significantly lower than those in patients with course of disease ≤3 years, while the levels of serum IL-1β and MIF were significantly increased (all P<0.05). Follicle stimulating hormone (FSH) in APOF group was significantly higher than that in healthy group, the level of serum estradiol (E2) was significantly lower than that in healthy group (all P<0.05). The level of CD4+ in APOF group was significantly lower than that in healthy group (P<0.05). Serum BMP15 and INHB were negatively correlated with FSH and CD4+, and positively correlated with E2, serum IL-1β and MIF were positively correlated with FSH and CD4+, and negatively correlated with E2 (all P<0.05). Conclusion: With the prolongation of the course of APOF, the levels of serum BMP15 and INHB are decreased, while the levels of serum IL-1β and MIF are increased, and the above indicators are closely related to the levels of sex hormones and peripheral blood T lymphocyte subsets.
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