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Genetics and genomics of hypertension associated with microinflammation, oxidative stress, chronic renal disease and heart failure.

Genetics and genomics of hypertension associated with microinflammation, oxidative stress, chronic renal disease and heart failure. - InGenious HyperCare

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33614
Enrollment
200
Registered
2009-02-20
Start date
2009-09-07
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

essential hypertension high blood pressure

Interventions

None listed

Sponsors

Interne Geneeskunde
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Men or women between 18 and 60 years of age at time of enrolment - Essential hypertension diagnosed before the age of 50 years. - At least 3 first-degree relatives of whom at least 1 should have hypertension and at least one from a different generation, willing to participate in the study. - Written informed consent

Exclusion criteria

Exclusion criteria: - Any known form of secondary hypertension, - Any known previous clinical complications of hypertension (angina, myocardial infarction, stroke, TIA, peripheral artery disease) at any time - known renal disease, including GFR

Design outcomes

Primary

MeasureTime frame
To analyse genetic and genomic factors involved in the pathogenesis of hypertension. To analyse genetic, genomic and proteomic factors involved in changes in microalbuminuria. To analyse genetic, genomic and proteomic factors involved in changes in cardiac and large artery structure and function.

Secondary

MeasureTime frame
To analyse the proteomic factors involves in the pathogenesis of hypertension. To explore the role of oxidative stress and microinflammation in the pathogenesis of hypertension. To analyse genetic, genomic and proteomic factors associated with renal phenotypes in hypertensive subjects: elevated urinary albumin excretion (microalbuminuria, proteinuria) salt-sensitivity, reduced GFR, and end-stage renal disease. To analyse genetic, genomic and proteomic factors associated with presence or development of heart dysfunction and failure in hypertensive patients.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)