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本文引用的文献

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Inflammation in Preeclampsia: Genetic Biomarkers, Mechanisms, and Therapeutic Strategies.子痫前期中的炎症:遗传生物标志物、机制和治疗策略。
Front Immunol. 2022 Jul 8;13:883404. doi: 10.3389/fimmu.2022.883404. eCollection 2022.
2
Second-trimester serum high mobility group box-1 and uterine artery Doppler to predict preeclampsia.中孕期血清高迁移率族蛋白 B1 联合子宫动脉多普勒预测子痫前期。
Sci Rep. 2022 Apr 27;12(1):6886. doi: 10.1038/s41598-022-10861-1.
3
The mechanism of HMGB1 secretion and release.HMGB1分泌与释放的机制。
Exp Mol Med. 2022 Feb;54(2):91-102. doi: 10.1038/s12276-022-00736-w. Epub 2022 Feb 25.
4
The etiology of preeclampsia.子痫前期的病因。
Am J Obstet Gynecol. 2022 Feb;226(2S):S844-S866. doi: 10.1016/j.ajog.2021.11.1356.
5
Etiological Value of Sterile Inflammation in Preeclampsia: Is It a Non-Infectious Pregnancy Complication?子痫前期无菌性炎症的病因学价值:它是一种非感染性妊娠并发症吗?
Front Cell Infect Microbiol. 2021 Aug 16;11:694298. doi: 10.3389/fcimb.2021.694298. eCollection 2021.
6
The PRISMA 2020 statement: an updated guideline for reporting systematic reviews.《PRISMA 2020声明:系统评价报告的更新指南》
Rev Esp Cardiol (Engl Ed). 2021 Sep;74(9):790-799. doi: 10.1016/j.rec.2021.07.010.
7
The Role of Oxidative Stress in Hypertensive Disorders of Pregnancy (Preeclampsia, Gestational Hypertension) and Metabolic Disorder of Pregnancy (Gestational Diabetes Mellitus).氧化应激在妊娠高血压疾病(先兆子痫、妊娠高血压)及妊娠代谢紊乱(妊娠期糖尿病)中的作用
Oxid Med Cell Longev. 2021 May 31;2021:5581570. doi: 10.1155/2021/5581570. eCollection 2021.
8
Targeting HMGB1 for the treatment of sepsis and sepsis-induced organ injury.针对高迁移率族蛋白 B1 治疗脓毒症及脓毒症诱导的器官损伤。
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9
Upregulated HMGB1 levels in maternal-fetal interface of patients with unexplained recurrent spontaneous abortion from different sources.不同来源不明原因复发性自然流产患者母胎界面中高迁移率族蛋白 B1 水平上调。
J Matern Fetal Neonatal Med. 2022 Dec;35(25):6542-6549. doi: 10.1080/14767058.2021.1918084. Epub 2021 May 4.
10
Exploring the therapeutic promise of targeting HMGB1 in rheumatoid arthritis.探讨靶向 HMGB1 在类风湿关节炎中的治疗潜力。
Life Sci. 2020 Oct 1;258:118164. doi: 10.1016/j.lfs.2020.118164. Epub 2020 Jul 31.

高迁移率族蛋白 B1 水平与子痫前期的关联:系统评价和荟萃分析。

Association between high-mobility group box 1 levels and preeclampsia: a systematic review and meta-analysis.

机构信息

School of Pharmacy, Fujian Medical University, Fuzhou, Fujian, China.

Department of Pharmacy, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, 18 Daoshan Road, Fuzhou, Fujian, 350001, China.

出版信息

J Assist Reprod Genet. 2024 Mar;41(3):551-561. doi: 10.1007/s10815-024-03021-z. Epub 2024 Jan 11.

DOI:10.1007/s10815-024-03021-z
PMID:38200286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10957809/
Abstract

PURPOSE

Previous studies had demonstrated that high-mobility group box 1 (HMGB1) levels were elevated in preeclampsia (PE). However, the conclusion remains controversial. This study aimed to investigate the association between blood and placenta HMGB1 levels and PE in pregnant women.

METHODS

After a systematic literature search, eligible literature was screened according to inclusion and exclusion criteria. Data extraction and quality assessment were performed independently by two reviewers. The extracted data were analyzed using Review Manager 5.4 and STATA 12.0 software. Subgroup analysis and meta-regression analysis were conducted to find potential sources of heterogeneity.

RESULTS

Twelve studies were included, with a total of 1145 participants. Compared with normal pregnancies, pregnant women with PE had significantly higher blood HMGB1 levels (SMD = 1.34, 95% CI: 0.72-1.95, p < 0.0001). Similarly, the expression of placental HMGB1 in PE was higher than that in normal controls by using Western blot (MD = 0.37, 95% CI: 0.27-0.47, p < 0.00001) or immunohistochemistry (OR = 6.36, 95% CI: 1.48-27.25, p = 0.01). In addition, the blood HMGB1 levels were positively correlated with the severity of PE, with higher blood HMGB1 levels in severe PE than those in mild PE (SMD = 3.35, 95% CI: 0.63-6.06, p = 0.02). The subgroup analysis indicated a close association of blood HMGB1 with PE in the Asian group, but not in the European group.

CONCLUSION

Both blood and placental HMGB1 levels in patients with PE were significantly elevated, and higher blood HMGB1 levels indicated a more serious disease condition, suggesting that higher levels of HMGB1 were associated with the risk of PE.

摘要

目的

先前的研究表明,高迁移率族蛋白 B1(HMGB1)水平在子痫前期(PE)中升高。然而,结论仍存在争议。本研究旨在探讨孕妇血液和胎盘 HMGB1 水平与 PE 之间的关系。

方法

经过系统的文献检索,根据纳入和排除标准筛选合格文献。两名评审员独立进行数据提取和质量评估。使用 Review Manager 5.4 和 STATA 12.0 软件分析提取的数据。进行亚组分析和荟萃回归分析以寻找潜在的异质性来源。

结果

纳入了 12 项研究,共 1145 名参与者。与正常妊娠相比,PE 孕妇的血液 HMGB1 水平显著升高(SMD=1.34,95%CI:0.72-1.95,p<0.0001)。同样,使用 Western blot(MD=0.37,95%CI:0.27-0.47,p<0.00001)或免疫组织化学(OR=6.36,95%CI:1.48-27.25,p=0.01)检测,PE 患者的胎盘 HMGB1 表达也高于正常对照组。此外,血液 HMGB1 水平与 PE 的严重程度呈正相关,重度 PE 患者的血液 HMGB1 水平高于轻度 PE 患者(SMD=3.35,95%CI:0.63-6.06,p=0.02)。亚组分析表明,血液 HMGB1 与亚洲组的 PE 密切相关,但与欧洲组无关。

结论

PE 患者的血液和胎盘 HMGB1 水平均显著升高,且血液 HMGB1 水平升高提示疾病状况更严重,表明 HMGB1 水平升高与 PE 的发病风险相关。