Why the study?
Is a novel VNTR polymorphism in the renin gene associated with essential hypertension?
Is a novel VNTR polymorphism in the renin gene associated with essential hypertension?
A newly discovered VNTR polymorphism in the renin gene is not associated with essential hypertension.
No association detected in this case-control study; leaves open need for larger cohorts to assess modest effects.
The aims of the present study were to find new genetic markers of essential hypertension (EH) and to investigate relationships between EH and polymorphisms of the renin gene. Using single strand conformation polymorphism, we discovered a new variable number of tandem repeat (VNTR) polymorphism in intron 7 that is 18 bp upstream from the boundary with exon 8. Nucleotide sequencing revealed that this VNTR polymorphism is a tandem repeat of the 4-nucleotide sequence TCTG. There were 6 alleles of this VNTR polymorphism, ranging from 7 repeats to 12 repeats. We analyzed the association between EH and this VNTR polymorphism. There was no significant difference in the overall distribution of this VNTR polymorphism between the EH and normotensive subjects. In summary, we discovered a novel VNTR polymorphism in the renin gene, and this polymorphism was not associated with EH.
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Hasimu et al. (2003) studied this question.
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