EVALUATION OF ETIOLOGIC CAUSES OF RECURRENT PREGNANCY LOSS

M. Obut, M. Evsen, H. E. Soydinç, M. Sak, Ali Özler, M. Fidanboy, M. Balkan, A. Türkyılmaz, T. Gül
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引用次数: 1

Abstract

SUMMARY Objective: The aim of the present study is to evaluate etiologic factors in patients with recurrent pregnancy loss (RPL). Material and methods: The records of patients admitted to Obstetrics& Gynecology Clinic of Dicle University Medical Faculty Hospital, from 2008 to 2011 were evaluated. Of the 114 patients who all tests were applied for diagnosis in our hospital were enrolled to study. For etiologic evaluation; Parental chromosome analysis, maternal antiphospholipid antibodies, hysterosalpingography for mullerian anomalies, thrombophilic disorders (factor V leiden mutation, prothrombin gene mutation) and endocrine (diabetes mellitus, thyroid hormone disorder) tests applied to patients. Results: The mean age and mean number of abortus were 29.7±6.6, 3.2±1.3 respectively. Fifty (43.9%) patients had at least one etiologic factor where as 64 (56.1%) were idiopathic. Major chromosomal aberrations were detected in four (%3.5) couples as inversion of the ninth chromosome. The frequency for other pathologies; mullerian anomaly:14 (%12.3), factor V leiden mutation:7 (%6.1), prothrombin gene mutation:6 (%5.3) and antiphospholipid antibodies in 10 (%8.8) patients. Conclusion: The prevalance for major chromosomal aberrations, mullerian anomalies, thrombopylic disorders and other pathologic conditions which evaluated in the study were found similar to reported previously. Polymorphism of 9qh+ (heterochromatic centromeric regions) was seen in 39 (%34.2) parents. Further studies are needed to understand that, if this result related to the genetic polymorpisym of the study population? or the pathology associated with RPL?.
复发性流产的病因分析
摘要目的:本研究的目的是评估复发性妊娠丢失(RPL)患者的病因。材料与方法:对2008 - 2011年在迪勒大学医学院附属医院妇产科门诊就诊的患者进行回顾性分析。选取我院应用各项指标诊断的114例患者作为研究对象。病原学评价;亲本染色体分析,母体抗磷脂抗体,子宫输卵管造影检查苗勒管异常,血栓性疾病(因子V leiden突变,凝血酶原基因突变)和内分泌(糖尿病,甲状腺激素紊乱)检测应用于患者。结果:平均流产年龄29.7±6.6岁,平均流产次数3.2±1.3次。50例(43.9%)患者至少有一种病因,64例(56.1%)为特发性病因。在4对(%3.5)夫妇中发现主要染色体畸变为第9染色体倒置。其他病理的发生频率;缪勒管异常14例(%12.3),V因子leiden突变7例(%6.1),凝血酶原基因突变6例(%5.3),抗磷脂抗体10例(%8.8)。结论:本研究评估的主要染色体畸变、苗勒管异常、血栓形成障碍及其他病理情况的患病率与文献报道相似。在39(%34.2)对亲本中发现9qh+(异色着丝粒区)多态性。需要进一步的研究来了解,这个结果是否与研究人群的遗传多态性有关?还是与RPL相关的病理?
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