SERUM TOTAL SIALIC ACID LEVELS AND SIALIC ACID ACETYL ESTERASE GENE VARIATION IN PATIENTS WITH PREECLAMPSIA

O. Gul, Ebru Öztürk, M. Uğur, F. B. Cebesoy, N. Kurtul, S. Pençe, S. Pehlivan, Ö. Balat
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引用次数: 3

Abstract

Objective: To evaluate the role of serum total sialic acid (SA) levels and sialic acid acetyl esterase (SIAE) gene variation in etiopathogenesis of preeclampsia (PE). Design: Prospective study Setting: Gaziantep Üniversity, Medical School, Department of Obstetrics and Gynecology Patients: This study was performed with 57 preeclamptic pregnant women and 50 pregnant women having no medical problems who has admitted to the Department of Obstetrics and Gynecology of Gaziantep University Medical Faculty between January 2008 and June 2008 Main outcome measures: Serum total SA levels were measured by Denny's colorimetric method and analysis of SIAE gene variation was performed by polymerase chain reaction -single stranded conformational polymorphism (PCR-SSCP). Statistical analyses were achieved using the SPSS 13.0 software. P<0.05 was considered to be statistically significant. Results: In this study, we observed higher serum total SA levels in PE (p<0.00001) and increased PE risk 10.4 times by SIAE gene variation. There was a weak-intermediate correlation between serum SA levels and diastolic blood pressure, uric acid levels (p=0.0001, r=0.34; p=0.0001, r=0.37 respectively). There was a strong correlation between serum SA levels and proteinuria (p=0.001, r=0.5). There was a significant association between SIAE gene variation and proteinuria (393±238 vs 107±185 mg\L, p= 0.021) , diastolic blood pressure (102.7±21.9 vs 85.7±20.6 mmHg, p=0.01). Conclusions: Further studies to reveal the importance of measurement of serum total SA levels in early pregnancy or preconceptional analysis of SIAE gene variation for prediction of PE are needed
子痫前期患者血清总唾液酸水平及唾液酸乙酰酯酶基因变异
目的:探讨血清总唾液酸(SA)水平和唾液酸乙酰酯酶(SIAE)基因变异在子痫前期(PE)发病中的作用。设计:前瞻性研究设置:加济安泰普Üniversity,医学院,妇产科患者:本研究在2008年1月至2008年6月期间在加济安泰普大学医学院妇产科住院的57名先兆子痫孕妇和50名无医疗问题的孕妇中进行。主要结果测量:采用Denny比色法检测血清总SA水平,采用聚合酶链反应-单链构象多态性(PCR-SSCP)分析SIAE基因变异。采用SPSS 13.0软件进行统计分析。P<0.05为差异有统计学意义。结果:本研究中,SIAE基因变异导致PE患者血清总SA水平升高(p<0.00001), PE发病风险增加10.4倍。血清SA水平与舒张压、尿酸水平呈弱中间相关性(p=0.0001, r=0.34;P =0.0001, r=0.37)。血清SA水平与蛋白尿有很强的相关性(p=0.001, r=0.5)。SIAE基因变异与蛋白尿(393±238 vs 107±185 mg\L, p= 0.021)、舒张压(102.7±21.9 vs 85.7±20.6 mmHg, p=0.01)有显著相关性。结论:需要进一步的研究来揭示妊娠早期血清总SA水平的测定或孕前分析SIAE基因变异对PE预测的重要性
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