Official Title
Genetics Study of Salt-Sensitive Hypertension in a Chinese Population
Brief Title
Salt-sensitive Hypertension Study in Lantian County
Protocol ID
NCT02915315
Lead Sponsor
First Affiliated Hospital Xi'an Jiaotong University
Brief Summary
Essential hypertension is a complex trait which results from interaction between
environmental factors and genetic factors. Our study aimed to detect the differential
expression of LncRNAs and epigenetic changes such as DNA methylation associated with salt
sensitive hypertension in human based on a chronic salt loading study conducted in
Lantian county, China. Firstly, a chronic salt loading study will be conducted in a
Chinese population to differentiate salt-sensitive and salt-resistant individuals.
Second, LncRNAs and DNA methylation Chip analysis will be performed using samples
collected from salt-sensitive and salt resistant individual, and the results will be
analyzed by modern bioinformatics methods to seek for differential genetic markers. In
addition, the investigators also try to examine the effects of chronic salt loading on
BP, ambulatory BP, microalbuminuria and baPWV and other biochemical indexes. This project
had great significance to reveal molecular genetics mechanism in the development of salt,
salt-sensitive and hypertension.
Detailed Description
The main contents include: (1) Questionnaire design: questionnaire is designed according
to the research contents and purposes. The standard questionnaires will be used to
collect the general information, dietary habits, lifestyle, medical history and family
history etc.(2)Anthropometric measurements: blood pressure, height, body weight, waist
and hip, pulse will be acquired by medical practitioners who received professional
trainings based on World Health Organization (WHO) standards, and passed relevant
examinations.(3) Dietary intervention: The dietary intervention comprise a 3-day baseline
observation period, a low-salt diet for 7 days (3g of salt or 51.3mmol of sodium per day)
and a high-salt diet for 7 days (18g of salt or 307.8mmol of sodium per day). During the
baseline period, each subject is given detailed dietary instructions to avoid table salt,
cooking salt, and high-salt foods for the 21-day study duration. To ensure compliance of
study participants with the intervention program, they are required to have their
breakfast, lunch, and dinner at the study kitchen under supervision of the study staff
during the entire study period. All foods are cooked without salt. Onsite study staff
members add prepackaged salt to the meals of individual subjects as indicated by the
study protocol. (4) Blood and urine samples collection: morning fasting blood, nocturnal
enuresis, and 24-hour urine specimen will be collected by medical staffs, and blind tubes
will be set up according to 5% of the total samples. Blood biochemistries including serum
total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides, fasting glucose,
creatinine and hsCRP can be measured using automatic biochemical analyzer. The sodium and
potassium concentrations in the urine will be measured by flame photometry. The total
sodium and potassium excretions in urine in 24h were calculated by multiplying the
concentration and 24-h volume of urine. (5) DNA methylation and LncRNA detection: Using a
method of modifying a hydrogen sulfite salt and gene chip technology to detect DNA
methylation and LncRNA. (6) LncRNA: LncRNA will be measured with gene chip technology
after the high salt intervention period. (7) Auxiliary examinations: Auxiliary
examinations including carotid intima-media thickness, endothelium-dependent vasodilation
(FMD), measurements of brachial-ankle pulse wave velocity (baPWV) and
electrocardiographic parameters. The measurement will be done in hospitals by medical
practitioners who received professional trainings and passed relevant examinations. (8)
Data processing and statistics: the investigators should input the data to the database,
and utilize software such as SPSS, STATA, Haploview and FBAT to analyze. (9)Quality
control: ① Questionnaire is strictly designed and amended by epidemiologist and clinical
experts. ② A standardized "Investigator Handbook" will be stipulated according to the
guidelines. ③ Staff members are required to do a rigorous training and pass the exam. ④
The investigation process will be strictly supervised by the principal investigator. ⑤
Data entry use the parallel double entry method. ⑥ During laboratory testing, blank
control and blind detection are applied to ensure the quality. ⑦Data analysis is
performed by 2-3 postgraduates, inconsistent data need to be double checked.
Study Period
Enrollment Count
70 participants
Eligibility Criteria
Inclusion Criteria:
- Han individuals in rural northern China
- adults aged 18-65 years
- individuals who had a mean systolic BP (SBP) between 130-160 mmHg and/or a diastolic
BP (DBP) between 85-100 mmHg and no use of antihypertensive medications were
identified as the proband
- the probands'parents,siblings, spouses, and offspring were recruited for the study.
Exclusion Criteria:
- Secondary hypertension
- a history of severe cardiovascular disease
- chronic kidney disease or liver disease
- unable to complete the examination
- unable/refuse to sign the informed consent form
Filters
Hypertension
UNKNOWN
ADULT
OLDER_ADULT