Use of polymorphic site in growth and differentiation factor 15 in predicting hypertensive secondary left ventricular hypertrophy
A technology of growth differentiation factors and polymorphic sites, applied in the field of medical molecular biology, can solve problems such as blood stasis, increased risk of stroke, and promotion of thrombosis, achieving high representation, improving feasibility and reliability , good sensitivity and specificity
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Embodiment 1
[0026] This study is a sub-project of investigation and research on the prevalence of left ventricular hypertrophy and related risk factors in hypertensive population in rural China. We used random cluster sampling to detect 5,421 patients with essential hypertension aged 40 to 75 from 7 natural villages in Xinyang, Henan, and performed echocardiography on 4,869 of them. From a total of 7 natural villages, we randomly selected 3, and all hypertensive patients who had undergone echocardiographic detection were included in this study, excluding all other cardiovascular diseases affecting left ventricular hypertrophy (hypertrophic cardiomyopathy, valvular heart disease, pulmonary hypertension, and coronary artery disease), resulting in a study population of 1,527 (506 men, 1021 women) patients with essential hypertension.
[0027] 1. Determination of clinical indicators:
[0028] 1. Blood pressure: measure the blood pressure of the right upper limb while sitting with a mercury s...
Embodiment 2
[0115] Example 2: A kit for predicting left ventricular hypertrophy secondary to hypertension
[0116] 1. Composition: The composition and content are as follows (50 servings), stored at -20°C:
[0117] 50 μL 10×PCR buffer (TaKaRa),
[0118] 50μL 10mmol / L dNTP mixture (TaKaRa),
[0119] 12 μL (5U / uL) Taq DNA polymerase (TaKaRa),
[0120] Each 20μL (10umol / L) of SEQ ID NO.1 and SEQ ID NO.2 primers (Beijing Aoke Biological Company)
[0121] 5ml deionized double distilled water (ddH2O),
[0122] 100 μL 10×BsrI restriction endonuclease reaction buffer (New England Biolabs, USA)
[0123] 35 μL (10U / μL) restriction endonuclease BsrI (New England Biolabs, USA)
[0124] 2. How to use
[0125] 1. Extract the subject's genomic DNA by conventional methods;
[0126] 2. PCR reaction:
[0127] Table 6
[0128] Reactive components
stock solution concentration
Volume (uL)
Final concentration
Upstream primer (SEQ ID NO.1)
Downstream pri...
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