Monogenic hypertension

Acta Biomed. 2019 Sep 30;90(10-S):50-52. doi: 10.23750/abm.v90i10-S.8759.

Abstract

Hypertension is a significant public health problem. Thirty percent of cases are caused by a single genetic mutation. Hypertension is the predominant and usually the only manifestation in monogenic hypertension Monogenic hypertension may involve mineralcorticoid-dependent or -independent increase in Na+ transport. Diagnosis is based on routine physical examination, blood pressure measurement and laboratory analysis of renin, aldosterone, cortisol and potassium. Genetic testing is useful for confirming diagnosis and for differential diagnosis. Monogenic hypertension has autosomal dominant or autosomal recessive inheritance.

Publication types

  • Review

MeSH terms

  • Aldosterone / metabolism
  • Genetic Testing
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Hydrocortisone / metabolism
  • Hypertension / diagnosis*
  • Hypertension / genetics*
  • Hypertension / metabolism
  • Mutation / genetics
  • Potassium / metabolism
  • Renin / metabolism

Substances

  • Aldosterone
  • Renin
  • Potassium
  • Hydrocortisone