scholarly journals WNT7A (rs104893832) polymorphism increases the risk of recurrent spontaneous abortion in Iranian women

2018 ◽  
Vol 37 (3) ◽  
pp. 167
Author(s):  
Manouchehr Mazdapour ◽  
Mahmood Dehghani Ashkezari ◽  
Seyed Morteza Seifati
Keyword(s):  
Spontaneous Abortion ◽  
Recurrent Spontaneous Abortion ◽  
Control Group ◽  
Chi Square ◽  
Pcr Rflp ◽  
History Of ◽  
Spss Software ◽  
And Control ◽  
Regression Tests ◽  
Control Study

BACKGROUND<br />Recurrent spontaneous abortion is defined as the occurrence of three or more clinical miscarriages in one woman. Several factors, including genetics and environmental factors, are involved in this kind of infertility, in which WNT7A (rs104893832) polymorphism plays a major role. The aim of the present study was to determine the association between a common polymorphism of WNT7A (rs104893832) with recurrent spontaneous abortion in females. <br /><br />METHODS<br />In the present case-control study, the WNT7A (rs104893832) polymorphism was investigated in 70 women with recurrent spontaneous abortion as cases and 100 women with at least one child and no history of infertility or abortion as controls. Polymerase chain reaction- restriction fragment length polymorphism (PCR-RFLP) was used to investigate the WNT7A (rs104893832) polymorphism in both case and control groups. The data were subsequently analyzed using the chi-square and logistic regression tests by SPSS software (version 18.0). <br /><br />RESULTS<br />A significant association was found between the WNT7A (rs104893832) polymorphism and recurrent spontaneous abortion (OR=25.00, 95% CI=5.52-157.09; p&lt;0.0001). Our finding showed that G allele frequency in women with recurrent spontaneous abortion was significantly different compared to the control group. (OR=6.42, 95% CI=2.82-15.16; p&lt;0.0001).Therefore, genetic variation in WNT7A (rs104893832) polymorphism may play a role in recurrent spontaneous abortion. <br /><br />Conclusion<br />This study revealed that WNT7A (rs104893832) polymorphism increased the risk of recurrent spontaneous abortion. Knowledge of these mutations and polymorphisms can provide an insight into the prognosis for individual patients. Therefore, further studies are necessary to establish the association of WNT7A (rs104893832) polymorphism with recurrent spontaneous abortion in a larger population.

scholarly journals Association between HOXA10 (rs267601473) polymorphism and recurrent spontaneous abortion

2019 ◽  
Author(s):  
Manouchehr Mazdapour ◽  
Mahmood DehghaniAshkezari ◽  
SeyedMorteza Seifati
Keyword(s):  
Spontaneous Abortion ◽  
Recurrent Spontaneous Abortion ◽  
Infertile Woman ◽  
Control Group ◽  
P Value ◽  
Chi Square ◽  
Significant Difference ◽  
Pcr Rflp ◽  
Chi Square Test ◽  
Spss Software

Introduction: Recurrent spontaneous abortion is defined as the occurrence of more than two clinical miscarriages in one woman. Several factors, including endocrine irregularities, genetics and environmental factors, are involved in this kind of infertility.The aim of this study was to survey the association of HOXA10 (rs267601473) polymorphism with the risk of recurrent spontaneous abortion in our population. Methods: In the present case-control study, the HOXA10 (rs267601473) polymorphism was investigated in 70 infertile woman and 100 healthy participants using PCR-RFLP methods. Then, the data were analyzed by SPSS software version 18 and also were compared using Chi-square test and Logistic regression model. The p-value was found to be statistically significant (p<0.05). Results: Our results showed significant association between the HOXA10 (rs267601473) polymorphism and recurrent spontaneous abortion (OR=0.143, 95% CI=0.056-0.368; p<0.0001). Our findings showed that T allele frequency in women with recurrent spontaneous abortion had significant difference compared to the control group (OR=0.2, 95% CI=0.11-0.4; p<0.0001). Conclusion: The results of this study reveal that the HOXA10 (rs267601473) polymorphism is significantly associated with recurrent spontaneous abortion in our population.

scholarly journals iTRAQ and PRM-based quantitative proteomics in early recurrent spontaneous abortion: biomarkers discovery

2019 ◽  
Vol 16 (1) ◽  
Author(s):  
Ying Cui ◽  
Ling He ◽  
Chun-Yan Yang ◽  
Qian Ye
Keyword(s):  
Spontaneous Abortion ◽  
Early Stage ◽  
Pregnancy Termination ◽  
Diagnostic Value ◽  
Differentially Expressed ◽  
Recurrent Spontaneous Abortion ◽  
Control Group ◽  
Case Group ◽  
Differentially Expressed Proteins ◽  
History Of

Abstract Background Early recurrent spontaneous abortion (ERSA) is a common condition in pregnant women. To prevent ERSA is necessary to look for abortion indicators, such as hormones and proteins, in an early stage. Methods Thirty patients with ERSA were enrolled in the case group. In the control group, we recruited 30 healthy women without a history of miscarriage undergoing voluntary pregnancy termination. The differentially expressed proteins in the serum were identified between the two groups using PRM and iTRAQ. Results Seventy-eight differentially expressed proteins were identified. Using GO functional annotation and KEGG pathway analysis, we detected that the most significant changes occurred in the pathway of Fc gamma R-mediated phagocytosis. Meanwhile, using PRM, we identified three proteins that were closely related to abortion, B4DTF1 (highly similar to PSG1), P11464 (PSG1), and B4DF70 (highly similar to Prdx-2). The levels of B4DTF1 and P11464 were down-regulated, while the level of B4DF70 was up-regulated. Conclusions CD45, PSG1, and Prdx-2, were significantly dysregulated in the samples of ERSA and could become important biomarkers for the prediction and diagnosis of ERSA. Larger‑scale studies are required to confirm the diagnostic value of these biomarkers.

scholarly journals Does the Polymorphism in the Length of the Polyalanine Tract ofFOXE1Gene Influence the Risk of Thyroid Dysgenesis Occurrence?

2017 ◽  
Vol 2017 ◽  
pp. 1-6
Author(s):  
Clebson Pantoja Pimentel ◽  
Erik Artur Cortinhas-Alves ◽  
Edivaldo Herculano Correa de Oliveira ◽  
Luiz Carlos Santana-da-Silva
Keyword(s):  
Genomic Dna ◽  
Case Control Study ◽  
Case Control ◽  
Control Group ◽  
Thyroid Dysgenesis ◽  
Susceptibility Factor ◽  
History Of ◽  
And Control ◽  
Polyalanine Tract ◽  
Control Study

Background.Recent data have suggested that polymorphisms in the length of the polyalanine tract (polyA) ofFOXE1gene may act as a susceptibility factor for thyroid dysgenesis. The main purpose of this study was to investigate the influence of polyA ofFOXE1gene on the risk of thyroid dysgenesis.Method.A case-control study was conducted in a sample of 90 Brazilian patients with thyroid dysgenesis and 131 controls without family history of thyroid disease. Genomic DNA was isolated from peripheral blood samples and the genotype of each individual was determined by automated sequencing.Results.More than 90% of genotypes found in the group of patients with thyroid dysgenesis and in controls subjects were represented by sizes 14 and 16 polymorphisms in the following combinations: 14/14, 14/16, and 16/16. Genotypes 14/16 and 16/16 were more frequent in the control group, while genotype 14/14 was more frequent in the group of patients with thyroid dysgenesis. There was no difference between agenesis group and control group. Genotype 14/14 when compared to genotypes 14/16 and 16/16A showed an association with thyroid dysgenesis.Conclusion.PolyA ofFOXE1gene alters the risk of thyroid dysgenesis, which may explain in part the etiology of this disease.

scholarly journals PCR detection of Toxoplasma gondii B1 gene in women suffering from abortion

2019 ◽  
Vol 13 (1) ◽  
pp. 12-15
Author(s):  
Aseel S. Mahmood ◽  
Sabeeha A. Al-Sarray ◽  
Abdulkareem Al-Kazaz
Keyword(s):  
Toxoplasma Gondii ◽  
Complex Disease ◽  
Control Group ◽  
Chi Square ◽  
Nested Polymerase Chain Reaction ◽  
B1 Gene ◽  
History Of ◽  
Polymerase Chain ◽  
And Control ◽  
Apparently Healthy

Background: Primary infection of maternal with toxoplasmosis during gestation and this infection transmission to the fetus continue to be the cause complex disease in offspring. Objective: This study was conducted to test the utility of nested Polymerase Chain Reaction (nPCR) assay to detect recent infections with Toxoplasma in abortive women. Material and methods: Toxoplasma gondii DNA was detected by using B1 gene as a target for amplification which was highly specific for T. gondii and is well conserved among all of the tested strains. Blood from 60 abortive women and 25 apparently healthy pregnant women with no history of abortion (as control group) were taken in this current study. Results: The results revealed that nPCR was positive in 48(80%) subjects and negative in 12(20%), Chi-square- χ2 for patients and control was ( 13.82 , 15.75 ) respectively. Conclusion: It can be concluded that nPCR assay in blood has advantage in detection of recent and active toxoplasmosis.

scholarly journals Study of the association between DRD2 Gene Ser311Cys and GSTM1 Gene Polymorphism in Schizophrenia

2019 ◽  
Author(s):  
Sanaz poorshekar ◽  
Afsaneh Firoozfar ◽  
Mohammadreza Dehghani ◽  
Seyed Mojtaba Yassini Ardekani ◽  
Seyed Mehdi Kalantar
Keyword(s):  
Frequency Distribution ◽  
Case Control Study ◽  
Control Group ◽  
Chi Square ◽  
Gstm1 Gene ◽  
Study Population ◽  
Regression Tests ◽  
Healthy Participants ◽  
Gstm1 Polymorphism ◽  
Control Study

Introduction: Schizophrenia is a mental disorder affecting 1% of the world's population. Two of genes have been recognized to be involved in development of this disease: DRD2 and GSTM1. Methods: This case-control study included 100 patients suffering from schizophrenia who referred to Yazd Neuropsychiatry Hospital. Also, 100 healthy patients without schizophrenia were selected as the control group. After DNA extraction, it was genotyped 100 schizophrenic and 100 healthy controls by use of restricted fragment of length polymorphism (RFLP) for Ser311Cys polymorphism and multiplex PCR for GSTM1. After performing relevant experiments and gaining some results, statistical analysis was performed using SPSS software16. In this study, Chi-square and logistic regression tests were used to investigate the relation between genotype of polymorphism and schizophrenia. Results: Data analysis showed that frequency distribution of Ser311Cys polymorphism genotypes between the patients and healthy participants was not significant (P: 0.121). Also, for GSTM1, there was no association between the polymorphism and schizophrenia. In general, the frequency distribution of the deleting gene between the patients and the control group was not significant (P= 0.089). And this polymorphism was significantly associated with symptoms (P = 0.012). Conclusion: The results of this study show that Ser311Cys polymorphism and GSTM1 polymorphism is not common among the studied patients, therefore it indicates its non-effectiveness in the study population. However, because the study population is not representative of the entire Iranian population, further studies with larger population are needed.  

Hypothyroidism In Women With Recurrent Spontaneous Abortion

2020 ◽  
Vol 7 (10) ◽  
pp. 71-77
Author(s):  
MOHAMED S. A. EMARAH ◽  
MOHAMED A. EL-NAGGAR ◽  
ABEER EL SHABACY ◽  
SAHAR H. QUSHWA
Keyword(s):  
Pregnant Women ◽  
Spontaneous Abortion ◽  
First Trimester ◽  
Reproductive Age ◽  
Recurrent Spontaneous Abortion ◽  
Control Group ◽  
Study Group ◽  
Uterine Anomalies ◽  
History Of ◽  
Living Children

Recurrent miscarriage, defined as loss of two or more consecutive pregnancies, occurs in 1–2% of couples attempting to bear children. The major causes of recurrent pregnancy loss (RPL) based on the literature include parental structural chromosome rearrangement, immunologic factors (i.e. antiphospholipid syndrome), thrombophilic factors (both inherited and acquired), anatomic factors of uterine anomalies, and endocrinologic disorders. Luteal phase defect, polycystic ovarian syndrome (PCOS), diabetes mellitus, thyroid disease and hyperprolactinemia are among the endocrinologic disorders implicated in approximately 17% to 20% of RPL. The prevalence of hypothyroidism in the general population of reproductive age is about 2-3%. The aim of this study is to observe the benefit of screening for hypothyroidism amongst women with recurrent spontaneous abortion early in the first trimester. The study included one hundred and sixty (160) women, in the reproductive age of life, where there ages ranged from 20 – 33 years, and divided into two groups. Study group which included eighty (80), non pregnant women with a history of two or more consecutive spontaneous abortions early in the first trimester, with no living children and control group which included eighty (80), non pregnant women having one or more living children without any history of abortion. Hypothyroidism was noted in ten (10) cases (12.5%) in the study group and noted in two (2) cases (2.5%) in the control group with a statistically significant difference (P < 0.01). The mean levels of TSH in the study group was 22.71  13.13 Iu/ml. Conclusion: Screening for hypothyroidism has clinical significance and would help to reduce miscarriage rate in women with recurrent spontaneous abortion.

scholarly journals CHARACTERS, DETERMINANTS, AND ASSOCIATION BETWEEN CHRONIC ANEMIA AND ATRIAL FIBRILLATION: CASE–CONTROL STUDY

2019 ◽  
pp. 192-196
Author(s):  
HAIDER SHAHEED MOHAMMED
Keyword(s):  
Atrial Fibrillation ◽  
Case Control Study ◽  
Case Control ◽  
Control Group ◽  
Chi Square ◽  
Chronic Anemia ◽  
Exact Test ◽  
Significant Difference ◽  
And Control ◽  
Control Study

Objective: The objective of this study was carried out to study the characters, determinants of anemia among atrial fibrillation (AF) patients and to estimate the link between chronic anemia and AF. Methods: This is a case–control study, administrated in Al-Hussein Teaching Hospital among admitted patients in the cardiac care unit from 1st week of January 2018 to the last week of April 2019. A random sample of 100 patients was included in the study based cut of time, where a special form of inquiry sheet was constructed to gather data and it was reviewed and revised by matter experts for testing the validity and enrichment of it. Both cases of AF and control with sinus rhythm were divided into anemic and non-anemic, anemia is defined as hemoglobin <13 and <12 in male and female, respectively. A Statistical Package for the Social Sciences (SPSS) version (25) was used for data analysis. Descriptive statistics Chi-square Fischer exact test, and ANOVA tests of significance, correlation and logistic regression analysis had been estimated where p<0.05 was set as statistically significant. Results: A total of 100 individuals had been included in the study, 50 cases with AF and 50 control with mean of age was 62.74003±13.424 years 58 females with 42 males, total non-anemic was 57 while total anemic was 43, 74.4% of AF cases was anemic while 25.6% of control group was anemic, there was statistically significant difference between cases and control according to the presence and absence of anemia where p<0.05. Conclusion: The first study done in the region to prove the direct relation of anemia on incident AF, thus in conclusion, chronic anemia had a relation with AF.

scholarly journals Do diabetes and family history influence the rheumatoid arthritis? - results from a case-control study

1970 ◽  
Vol 10 (4) ◽  
pp. 230-234
Author(s):  
MM Efterkharian ◽  
Z Basiri ◽  
KM Kashani
Keyword(s):  
Rheumatoid Arthritis ◽  
Family History ◽  
Case Control Study ◽  
Case Control ◽  
Chi Square ◽  
Chi Square Test ◽  
History Of ◽  
Diabetes Family History ◽  
And Control ◽  
Control Study

Introduction: Up to now, several studies have been performed about the role of different factors on incidence and severity of Rheumatoid arthritis (RA) in the world. This 2009 study was carried out to investigate the association between History of diabetes and Family history of RA with RA incidence in Hamedan, a western city of Iran. Methods: As a case-control study, information from 128 cases and 130 controls, matched for age and Sex, were collected by questionnaire and analyzed using SPSS (chi-square test). Results: In case and control groups, females were 116 and 118 persons respectively and the rest were males. Statistical analysis showed that there is significant and no significant association between Family history of RA and history of diabetes with RA respectively. Conclusion: Considering previous global investigations on these topics and the results of our study, it seems that more studies will be needed to describe the association between history of diabetes and RA, but about another checked risk factor, there is a definite significant association between family history of RA and RA. Keywords: Rheumatoid arthritis; diabetes; family history; risk factors. DOI: http://dx.doi.org/10.3329/bjms.v10i4.9492 BJMS 2011; 10 (4): 230-234

scholarly journals Decreased Toll-like Receptor (TLR) 2 and 4 Expression in Spermatozoa in Couples with Unexplained Recurrent Spontaneous Abortion (URSA)

2020 ◽  
Author(s):  
Nasrin Sereshki ◽  
Alireza Andalib ◽  
Ataollah Ghahiri ◽  
Ferdos Mehrabian ◽  
Roya Sherkat ◽  
...  
Keyword(s):  
Spontaneous Abortion ◽  
Recurrent Spontaneous Abortion ◽  
Control Group ◽  
Toll Like Receptor ◽  
Tlr4 Expression ◽  
Tlr2 Expression ◽  
Unexplained Recurrent Spontaneous Abortion ◽  
Toll Like Receptor 2 ◽  
And Control ◽  
Reproductive Processes

Studies have shown that toll-like receptors (TLRs) play some important roles in reproductive processes such as ovulation, spermatogenesis, sperm capacitation, fertilization, and pregnancy to the best of our knowledge, no study has evaluated the expression and role of these molecules and their impairment in spermatozoa; accompanied by pregnancy complications such as recurrent spontaneous abortion (RSA). Therefore, this study investigates the alteration of toll-like receptor 2 (TLR2) and toll-like receptor 4 (TLR4) expression in spermatozoa in men whose spouse have unexplained RSA. Fifteen fertile couples and fifteen couples with unexplained recurrent spontaneous abortion (URSA) were included in this study. The level of TLR2 and TLR4 expression in untreated and lipopolysaccharide (LPS) or PAM3CYS in treated spermatozoa were examined by flow cytometry. The results showed reduced expression of TLR4 in untreated spermatozoa and decreased LPS or PAM3CYS levels in treated spermatozoa in the URSA group compared to the control group. No significant differences were found in TLR2 expression of untreated spermatozoa in RSA and control groups. After the treatment of spermatozoa with LPS, the TLR2 expression was decreased in both groups. After the treatment of spermatozoa with PAM3CYS, the level of TLR2 expression was significantly increased in the URSA group; while no significant differences were shown in the control group in comparison to untreated spermatozoa. We have concluded that decreased TLR4 expression and a differently increased TLR2 expression in response to ligand treatment in spermatozoa is associated with URSA.

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