Cardiomyopathy (CM) is a progressive disease of the myocardium or heart muscle, resulting in heart failure [1].
Heart muscle disorders occur due to a heterogeneous group of CM. In the absence of abnormal loading conditions or ischemic heart disease, abnormal myocardial structure and function is present in CM [2]. In the autosomal dominant forms of CM incomplete expression is common. On the basis of morphology and function, CM is classified into four groups: dilated CM (DCM), hypertrophic CM (HCM), restrictive CM (RCM) and arrhythmogenic right ventricular (RV) CM/dysplasia (ARVC/D) [2]. Worldwide, the most widespread CM is DCM. Dilated CM is a disorder in heart muscles, in which left or both ventricles become dilated and perform poor function [3]. More than 1400 mutations are associated with CM. Most of these mutations are located on genes encoding the proteins of thick and thin sarcomere filaments. Small numbers of mutations have been observed in genes which encode Z-disc components and handle calcium proteins [4]. The most common causes of CM are viral infection, alcohol, family history, age, sex, hyperglycemia, diabetes mellitus, abnormal thyroid function and heart attack. Symptoms of heart failure (HF) may include shortness of breath, fatigue, cough, orthopnea, paroxysmal nocturnal dyspnea, and edema [5,6]. Some physical activities (vigorous, moderate and sedentary life style) and etiological attributes may contribute in this disease [7].
Cardiotrophin-1 (CT-1) is an interleukin-6 (IL-6) family cytokine and is an active inducer capable of cardiac hypertrophy and vascular stiffness in hypertensive heart disease [8]. It is capable of recapitulating the physiological growth of the heart including transient and reversible hypertrophy of the myocardium [9]. In the human aortic vascular smooth muscle cells, CT-1 stimulate the proliferation, migration and collagen-1 (COL1) expression. In vascular endothelial cells and monocyte migration, proatherogenic expression is stimulated by CT-1. Atherosclerotic lesions formed by formation of foam cells and COL1 production [10]. The purpose of present study was to examine the expression of
The cross-sectional study was conducted at the Fatima Memorial Hospital (FMH) of Lahore, Pakistan. Permission for sampling was obtained from the Ethics Committee of the institution. Samples were collected from the Cardiology Department of FMH between January and June 2016. The sample size was calculated using sample calculator on Raosoft Inc. (
The study population was divided into two groups: the control group consisted of 20 healthy individuals and the CM group included 20 subjects. Inclusion and exclusion criteria were made for appropriate selection of patients which were as follows: patients with suspected HF, patients with left ventricular (LV) dilatation and dysfunction were included in the study. Other acquired or congenital cardiac diseases such as myocardial infarction, other coronary vascular disease, myocarditis, pericardial diseases (not mild pericardial effusion that may be secondary to HF) and patients of any cardiac/genetic disease were excluded from the study. Written informed consent was obtained from the subjects before their participation in the study. A structured questionnaire used for data collection regarding age, gender, habits, duration of disease and family history of disease. A blood sample (3 mL) was drawn from the enrolled subjects and transferred immediately to EDTA-containing vacutainers and mixed gently for 1 min. to prevent blood clotting and inhibiting activity of nucleases. The sequence of human gene
RNA was isolated by the trizole method [10]. RNA quantity and quality was determined using the Nano Drop™ 2000/2000c spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA). Then, cDNA synthesis was done by the reverse transcriptase method. Furthermore, cellular gene expression was determined by reverse-transcriptase-polymerase chain reaction (RT-PCR). Statistical analysis was done using the Statistical Package for the Social Sciences (SPSS), version 23 (IBM Corporation, Armonk, NY, USA). The statistical difference between the groups was analyzed by the Student’s
The demographic characteristics are presented in Table 1. In the control group, 80.0% were males and 20.0% were females. In the CM group, 45.0% were males and 55.0% were females. Systolic blood pressure (SBP) and diastolic BP (DBP) of the CM group was 124.0±0.7 and 83.0±0.8 mmHg, respectively, as compared to the control group in which SBP was 103.0±0.9 and DBP was 79.0±1.5 mmHg, respectively. Etiological attributes of the disease were idiopathic 65.0%, nutritional 15.0% and multifactorial 15.0%. In the CM group, 15.0% were former smokers but in control group no one was a smoker. Symptomatology of the disease includes 85.0% breathlessness, palpitation 75.0% and chest pain was observed in 40.0% of the subjects. On the basis of physical activity, three categories were formed: vigorous activity, moderate activity and sedentary life style. In control group, 20.0% showed vigorous activity, 10.0% sedentary lifestyle and 70.0% were moderately active. In DCM group, 5.0% showed vigorous activity, 20.0% showed moderate activity and 75.0% had sedentary lifestyle (Table 2).
Demographic parameters of the cardiomyopathy and control groups.
Parameters | CM Group ( |
Control Group ( |
---|---|---|
Age (years) | 40.10±6.03 | 35.00±3.71 |
BMI (kg/m2) | 25.11±0.39 | 24.22±0.66 |
SBP (mmHg) | 124.0±0.7 | 103.0±0.9 |
DBP (mmHg) | 83.0±0.8 | 79.0±1.5 |
5.29±0.34 | 1.00 |
CM: pressure; cardiomyopathy; DBP: diastolic BMI: blood body pressure; mass index;
Prevalence of physical activity, etiological attributes and symptomatology in the cardiomyopathy group.
Variables | CM Group ( |
---|---|
Physical activity (%) | |
vigorous | 5.0 |
moderate | 20.0 |
sedentary | 75.0 |
Etiological attributes (%) | |
idiopathic | 65.0 |
nutritional | 15.0 |
multifactorial | 15.0 |
Symptomatology (%) | |
breathless | 85.0 |
palpitations | 75.0 |
chest pain | 45.0 |
The expression of
Pearson correlation coefficient between CT-1 and other parameters revealed a highly significant relationship with age and BMI (Figure 2), while non significant correlation with SBP and DBP (Table 3). In the control group, the value of expression is one so correlation cannot be calculated.
Correlation between the
Parameters | ||
---|---|---|
Age (years) | 0.54a | <0.05 |
BMI (kg/m2) | 0.46b | <0.01 |
SBP (mmHg) | –0.079 | >0.05 |
DBP (mmHg) | 0.069 | >0.05 |
BMI: body mass index; SBP: systolic blood pressure; DBP: diastolic blood pressure.
a Significant difference.
b Highly significant difference.
Among cardiovascular problems, CM is one of the leading causes of heart transplantation. Dilated CM occu- pies a significant position among all types of CM. In CM, more than 1400 mutations are linked [4]. Approximately 80.0% of identified mutations relating to cardiac β-myosin heavy chain and cardiac myosin binding protein C are present in eight sarcomere genes in CM [11]. Left ventricular dilation and dysfunction characterized by primary myocardial disease is known as DCM. Ventricular hypertrophy is increased mainly due to volume overload [12]. Prevalence of CM in the USA is as low as 0.02 to 0.2% in the population. It is found to be only 0.5% within unselected patients referred for echocardiography examination. Occurrence of one form of CM in Japan is the same as in the western population, namely 17.3/100,000 [13]. In Pakistan, data regarding the occurrence of CM has hardly been reported.
In comparison to the control group, the alteration in “
The studies revealed that direct relationship exist between increased expression of
It was concluded that expression of the