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The association of RBC sodium-lithium countertransport (Vmax) with left ventricular mass in African American women
Insights
Increased sodium-lithium countertransporter activity (SLC) in young African American women is linked to higher blood pressure and left ventricular mass, indicating potential early cardiovascular risk. This finding suggests SLC activity may help identify those at risk before hypertension develops.
Area of Science:
- Cardiovascular Physiology
- Renal Physiology
- Metabolic Syndrome
Background:
- Increased red blood cell sodium-lithium countertransporter activity (SLC) is a marker for vascular disease complications in Caucasian hypertensives and diabetics.
- A subset of African Americans with high Vmax for SLC exhibit correlations with dyslipidemia, insulin resistance, microalbuminuria, and elevated blood pressure.
Purpose of the Study:
- To investigate the correlation between sodium-lithium countertransporter activity (Vmax) and left ventricular mass (LVM) in premenopausal African American women prior to diagnosed hypertension.
Main Methods:
- Evaluated 35 non-diabetic African American women (mean age 31) for cardiovascular risk factors, including blood pressure, oral glucose tolerance tests, and insulin sensitivity via euglycemic hyperinsulinemic clamp.
- Assayed fasting blood for SLC activity (Vmax) and lipids.
- Determined cardiac structure using 2-D echocardiography, calculating LVM index adjusted for height.
Main Results:
- Vmax significantly correlated with systolic, diastolic, and mean blood pressure.
- Vmax showed significant correlations with fasting insulin, total insulin response, and insulin sensitivity.
- A notable association was found between Vmax and LVM index.
- No significant relationship was observed between Vmax and body mass or lipid profiles.
Conclusions:
- Sodium-lithium countertransporter activity (Vmax) correlates with cardiac structure (LVM index) in premenopausal African American women.
- Vmax is associated with insulin sensitivity and insulin resistance in this non-diabetic cohort.
- SLC activity may serve as a biomarker for identifying young African American women with early left ventricular hypertrophy and insulin resistance, preceding clinical hypertension or diabetes.
Abstract:
In Caucasian hypertensives and diabetics, increased RBC sodium-lithium countertransporter activity (SLC) is a marker for end-organ complications of vascular disease. A subgroup of African Americans with high Vmax for SLC show strong correlations with dyslipidaemia, insulin resistance, microalbuminuria and higher blood pressure. The purpose of our study was to determine if Vmax in premenopausal African American women correlates with left ventricular mass (LVM) before the onset of clinically diagnosed hypertension. Non-diabetic African American women (n = 35, mean age 31 years) were evaluated for cardiovascular disease risk factors, including anthropometric and blood pressure measurements, oral glucose tolerance test (OGTT), and euglycaemic hyperinsulinaemic clamp for insulin sensitivity. Fasting blood specimens were assayed for SLC activity (Vmax) and lipids. Cardiac structure was determined by 2-D echocardiography. LVM was calculated by the cube root formula and adjusted for height (LVM index). Vmax correlated significantly with average systolic blood pressure (r = 0.45, P = 0.007), diastolic blood pressure (r = 0.48, P = 0.004), mean blood pressure (r = 0.48, P = 0.003) and LVM index (r = 0.40, P = 0.02). Vmax was also associated with fasting insulin (r = 0.39, P = 0.01), the sum of insulin (r = 0.52, P = 0.002), and insulin sensitivity adjusted for fat-free mass (r = -0.55, P = 0.001). There was no statistically significant relationship between Vmax and body mass or lipids. Vmax for SLC correlates with cardiac structure in premenopausal African American women. Vmax is also associated with insulin sensitivity and insulin resistance in this non-diabetic sample. SLC activity may be useful in identifying a subgroup of young African American women with left ventricular hypertrophy and insulin resistance before the onset of clinically diagnosed hypertension and diabetes. Journal of Human Hypertension (2000) 14, 213-219.
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