Increased Expression of Cardiotrophin-1 in Cardiomyopathy Patients.

IF 0.5 4区 医学 Q4 GENETICS & HEREDITY
Balkan Journal of Medical Genetics Pub Date : 2021-07-27 eCollection Date: 2021-06-01 DOI:10.2478/bjmg-2021-0008
S Sharif, A Saleem, S Naz, F Rashid, M Iqtedar, A Kaleem, A Latif
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引用次数: 1

Abstract

Cardiomyopathy (CM) is a condition of cardiac dysfunction. It is one of the leading causes of mortality in which both genetic and environmental factors are involved. Cardiotrophin-1 (CT-1) level in plasma is associated with CM. It affects the cardiomyocyte differentiation. To evaluate the expression of CT-1 in cardiomyopathy, this study was done on CM subjects attending the Fatima Memorial Hospital, Lahore, Pakistan, between January and June, 2016. A total of 40 subjects were enrolled who were divided into two groups; CM group (n = 20) and a control group (n = 20). A self-designed questionnaire was filled in by each subject to collect data regarding age, body mass index (BMI) and CM history. RNA was isolated from blood after its quantification, cDNA was prepared and reverse-transcriptase-polymerase chain reaction (RT-PCR) was performed for expression of CT-1. The mean age in CM subjects was 40.1±6.03 years, while it was 35.0±3.7 years in the control group. The mean expression of CT-1 in the CM subjects was 5.2±0.66, while it was 1.00±0.001 in the control group. A highly significant difference was observed in CT-1 expression in the CM group, and expression was significantly correlated with age and BMI in CM subjects.

Abstract Image

Abstract Image

心肌病患者心肌营养因子-1表达升高。
心肌病(CM)是一种心功能障碍。它是造成死亡的主要原因之一,涉及遗传和环境因素。血浆中心肌营养因子-1 (CT-1)水平与CM相关。影响心肌细胞分化。为了评估CT-1在心肌病中的表达,本研究于2016年1月至6月在巴基斯坦拉合尔法蒂玛纪念医院的CM受试者中进行。共招募了40名受试者,他们被分为两组;CM组(n = 20)和对照组(n = 20)。每位受试者填写自行设计的问卷,收集年龄、体重指数(BMI)和CM病史等数据。定量后从血液中分离RNA,制备cDNA,用RT-PCR法表达CT-1。CM组平均年龄为40.1±6.03岁,对照组平均年龄为35.0±3.7岁。CM组CT-1平均表达量为5.2±0.66,对照组为1.00±0.001。CM组CT-1表达差异极显著,且表达与CM组年龄、BMI显著相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Balkan Journal of Medical Genetics is a journal in the English language for publication of articles involving all branches of medical genetics: human cytogenetics, molecular genetics, clinical genetics, immunogenetics, oncogenetics, pharmacogenetics, population genetics, genetic screening and diagnosis of monogenic and polygenic diseases, prenatal and preimplantation genetic diagnosis, genetic counselling, advances in treatment and prevention.
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