血清YKL-40水平升高作为胎盘增生谱的诊断和预后标志物。

IF 1.3 Q4 OBSTETRICS & GYNECOLOGY Turkish Journal of Obstetrics and Gynecology Pub Date : 2022-06-27 DOI:10.4274/tjod.galenos.2022.94884
Neslihan Bayramoğlu Tepe, Denizhan Bayramoglu, İbrahim Taşkum
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引用次数: 1

摘要

目的:胎盘增生谱(PAS)是近年来剖宫产率上升的一个重要问题。目前仍没有诊断的血清标志物。我们确定血清YKL-40水平是否可用于PAS的诊断和预后。材料与方法:本研究纳入50例PAS患者,27例未PAS患者和33例正常孕妇。记录手术(CS +胎盘床缝合、CS +下段切除、CS-子宫切除术),并记录下段切除/CS-子宫切除术患者的组织病理学诊断(增生、增量、无增生)。分析血清YKL-40水平。结果:PAS患者血清YKL-40等级显著高于对照组(p=0.001)。手术干预包括4例CS +下节段切除,9例CS +胎盘床缝合,37例CS-子宫切除术。分别行下节段切除、cs子宫切除术并诊断为增生、增量和percreta的患者分别为6例、9例和26例的组织病理学结果。accreta组、increta组和percreta组血清YKL-40分级差异有统计学意义(p=0.001)。进行受试者工作特征分析,鉴别血清YKL-40截止水平为32.81 ng/mL,敏感性66%,特异性70.37%。YKL-40在PAS指标中的阳性预测值为80.5%,阴性预测值为52.8%。结论:血清YKL-40等级升高与PAS的诊断和严重程度相关。如果我们的发现得到更大患者系列的证实和阐述,YKL-40水平应与超声检查一起使用,以构建与非整倍体筛查相同的模型。
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Elevated serum YKL-40 levels as a diagnostic and prognostic marker in the placenta accreta spectrum.

Objective: Placenta accreta spectrum (PAS) is an important problem with increasing cesarean section (CS) rates recently. There is still no serum marker for the diagnosis. We determined whether serum YKL-40 levels can be used in the diagnosis and prognosis of PAS.

Materials and methods: The study was conducted with 50 patients with a PAS diagnosis, 27 individuals without PAS, and 33 normal pregnant women. The operations (CS + placental bed suture, CS + excision of the lower segment, CS-hysterectomy) and for individuals who had the excision of the lower segment /CS-hysterectomy, the histopathological diagnoses (accreta, increta, percreta) were recorded. Serum YKL-40 levels were analyzed.

Results: The individuals with PAS possessed significantly greater serum YKL-40 grades (p=0.001). The surgical interventions included 4 CS + excision of the lower segment, 9 CS + placental bed sutures, and 37 CS-hysterectomy. The histopathological outcomes of the individuals who had the excision of the lower segment, CS-hysterectomy and diagnosed 6, 9, and 26 patients with accreta, increta, and percreta, respectively. The accreta, increta, and percreta groups showed statistically significant different serum YKL-40 grades (p=0.001). The receiver operating characteristic analysis was performed to discriminate the cut-off serum YKL-40 level as 32.81 ng/mL with a sensitivity of 66% and specificity of 70.37%. The positive and negative predictive values of YKL-40 in the indicator of PAS were 80.5% and 52.8%, respectively.

Conclusion: Elevated serum YKL-40 grades were correlated with the diagnosis and severity of PAS. If our findings are corroborated and elaborated by larger patient series, the YKL-40 levels should be used along with ultrasonography to construct a model identical to that used in aneuploidy screening.

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