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Published on: June 10, 2015
Hereditary intermediate phenotypes in African American hypertension
M T Kailasam1, D T O'Connor, R J Parmer
1Department of Medicine, University of California, San Diego 92161, USA.
Insights
Researchers identified key physiological and biochemical markers linked to hypertension in African Americans. These intermediate phenotypes may help pinpoint genes contributing to high blood pressure in this population.
Area of Science:
- Cardiovascular research
- Genetics of hypertension
- African American health
Background:
- Essential hypertension disproportionately affects African Americans.
- The genetic basis of hypertension remains largely unknown.
- Intermediate phenotypes offer a strategy to identify hypertension-related genes.
Purpose of the Study:
- To identify and characterize intermediate phenotypes relevant to hypertension in African Americans.
- To explore potential pathophysiological factors preceding high blood pressure.
- To suggest candidate genes for hypertension heritability.
Main Methods:
- Studied physiological and biochemical candidate intermediate phenotypes.
- Included untreated black and white patients with essential hypertension.
- Utilized normotensive individuals stratified by genetic risk.
Main Results:
- Identified promising intermediate phenotypes for African American hypertension studies.
- These include baroreceptor sensitivity, cold pressor test responses, and specific biochemical markers.
- Biochemical markers include plasma chromogranin A, dopamine-beta-hydroxylase, and urinary kallikrein.
Conclusions:
- The intermediate phenotype approach can aid gene identification in complex traits like hypertension.
- This strategy, combined with quantitative genetics and linkage mapping, shows promise.
- Further research is necessary to identify specific genes involved in African American hypertension.
Objective:
Essential hypertension is a heterogeneous and multifactorial disorder and is at least twice as frequent among African Americans as in the general population. Inheritance of high blood pressure is complex, with the gene(s) responsible for hypertension still remaining elusive. A useful strategy for investigating the heritability of hypertension is to evaluate 'intermediate phenotypes'--simple Mendelian or monogenic traits that are associated with hypertension. These intermediate steps may identify potential pathophysiological factors that antedate the development of high blood pressure and suggest candidate genes. We are attempting to identify and characterize several such intermediate phenotypes, in particular as these might apply to hypertension in African Americans.
Methods:
We studied several physiological and biochemical candidate intermediate phenotypes in untreated black and white patients with essential hypertension and in their normotensive counterparts stratified by genetic risk of hypertension.
Results And Conclusions:
Promising intermediate phenotypes, which may be useful for studies in African American families, include baroreceptor sensitivity to low and high pressure stimuli, cold pressor test responses, and biochemical markers such as plasma chromogranin A, dopamine-beta-hydroxylase and urinary kallikrein excretion. Identification of genes involved in complex traits such as hypertension may be facilitated by the intermediate phenotype approach, combined with recent advances in quantitative genetics and linkage mapping. Further studies are needed to pinpoint the nature of genes in African American hypertension.
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