A Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension (GENRES)
Primary Purpose
Hypertension, Pharmacogenetics
Status
Completed
Phase
Phase 4
Locations
Finland
Study Type
Interventional
Intervention
Amlodipine
Bisoprolol
Hydrochlorothiazide
Losartan
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Hypertension
Eligibility Criteria
Inclusion Criteria:
- essential hypertension diagnosed on an earlier occasion or during the present study (three diastolic blood pressure readings >=95 mmHg on separate occasions are required).
Exclusion Criteria (before and during the study):
- usage of three or more antihypertensive drugs
- secondary hypertension
- left ventricular hypertrophy
- drug-treated diabetes mellitus
- coronary heart disease
- stroke and other disorders of cerebral circulation
- renal disease
- obstructive pulmonary disease
- a disease treated with corticosteroids
- a disease with drug treatment potentially influencing blood pressure levels
- significant obesity (BMI >=32 kg/m2)
- allergic reaction towards any of the study drugs
- The patient is excluded from the study if his blood pressure level rises to 200/120 mmHg or above during the study.
Sites / Locations
- Helsinki University Central Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Active Comparator
Active Comparator
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
Amlodipine
Bisoprolol
Hydrochlorothiazide
Losartan
Placebo
Arm Description
One of the four monotherapy treatment periods.
One of the four monotherapy treatment periods.
One of the four monotherapy treatment periods.
One of the four monotherapy treatment periods.
Placebo treatment period.
Outcomes
Primary Outcome Measures
Blood pressure
Change in blood pressure
Secondary Outcome Measures
Full Information
NCT ID
NCT03276598
First Posted
September 6, 2017
Last Updated
September 8, 2017
Sponsor
Helsinki University Central Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03276598
Brief Title
A Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension
Acronym
GENRES
Official Title
A Randomised Double-blind Cross-over Single-centre Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
November 25, 1999 (Actual)
Primary Completion Date
April 1, 2004 (Actual)
Study Completion Date
April 1, 2004 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Helsinki University Central Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Blood pressure variation and the risk of essential hypertension have an important genetic component. In most cases susceptibility to essential hypertension is likely determined by the action of more than one gene.
The identification of genes causing susceptibility to hypertension is important, since it would give new tools for the diagnosis and enable better etiological classification and specific treatment of the disease.
The innovation of this study is to use the response to antihypertensive therapy as an intermediate phenotype.
In the study, each subject uses one of four antihypertensive drugs, each as a monotherapy in a rotational fashion, for 28 days in a randomized order. The antihypertensive drugs to be tested include a thiazide diuretic, a beta-adrenergic antagonist, an angiotensin-II receptor antagonist and a calcium channel blocker. The drugs that are selected for the study are "typical" representatives of their groups and long-acting, and the dosages are sufficient but well tolerable.
Detailed Description
Blood pressure variation and the risk of essential hypertension have an important genetic component. In most cases susceptibility to essential hypertension is likely determined by the action of more than one gene.
The identification of genes causing susceptibility to hypertension is important, since it would give new tools for the diagnosis and enable better etiological classification and specific treatment of the disease. Finland is an ideal place for a study like this because of the genetic homogeneity of the population, the relatively high prevalence of the disease and the established protocols for the treatment and follow-up of hypertension in public health care.
The molecular genetic studies on hypertension performed so far (by 1999) have primarily been association studies, which are based on case-control classification and may produce erroneous results. Particularly, a reliable phenotyping of cases and controls has been difficult. Consequently, more attention should be paid to the phenotyping of patients, and novel intermediate phenotypes characteristic of certain subtypes of hypertension should be used to facilitate the search for hypertension genes. The innovation of this study is to use the response to antihypertensive therapy as an intermediate phenotype.
In the study, each subject uses one of four antihypertensive drugs, each as a monotherapy in a rotational fashion, for 28 days in a randomized order. The antihypertensive drugs to be tested include a thiazide diuretic, a beta-adrenergic antagonist, an angiotensin-II receptor antagonist and a calcium channel blocker. The drugs that are selected for the study are "typical" representatives of their groups and long-acting, and the dosages are sufficient but well tolerable. The study design does not necessitate the use of equipotent doses of the various agents, since the study is not designed to compare the antihypertensive effectiveness of the study drugs or, due to the short treatment periods, their effects on clinical endpoints.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Pharmacogenetics
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
The design of the study is a randomized placebo-controlled cross-over study. The study starts with a run-in placebo period lasting for four weeks. The four monotherapy treatment periods last for four weeks and they are separated by placebo periods lasting also for four weeks. Randomization occurs after the first placebo period in blocks of 24 (all possible drug sequences).
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The placebo tablets and drugs are packed in similar gelatin capsules.
Allocation
Randomized
Enrollment
233 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Amlodipine
Arm Type
Active Comparator
Arm Description
One of the four monotherapy treatment periods.
Arm Title
Bisoprolol
Arm Type
Active Comparator
Arm Description
One of the four monotherapy treatment periods.
Arm Title
Hydrochlorothiazide
Arm Type
Active Comparator
Arm Description
One of the four monotherapy treatment periods.
Arm Title
Losartan
Arm Type
Active Comparator
Arm Description
One of the four monotherapy treatment periods.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo treatment period.
Intervention Type
Drug
Intervention Name(s)
Amlodipine
Intervention Description
Treatment for four weeks. Dose: 5 mg o.d.
Intervention Type
Drug
Intervention Name(s)
Bisoprolol
Intervention Description
Treatment for four weeks. Dose: 5 mg o.d.
Intervention Type
Drug
Intervention Name(s)
Hydrochlorothiazide
Intervention Description
Treatment for four weeks. Dose: 25 mg o.d.
Intervention Type
Drug
Intervention Name(s)
Losartan
Intervention Description
Treatment for four weeks. Dose: 50 mg o.d.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Treatment for four weeks. Dose: 1 tablet per day.
Primary Outcome Measure Information:
Title
Blood pressure
Description
Change in blood pressure
Time Frame
4 weeks
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Based on self-representation of gender identity
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
essential hypertension diagnosed on an earlier occasion or during the present study (three diastolic blood pressure readings >=95 mmHg on separate occasions are required).
Exclusion Criteria (before and during the study):
usage of three or more antihypertensive drugs
secondary hypertension
left ventricular hypertrophy
drug-treated diabetes mellitus
coronary heart disease
stroke and other disorders of cerebral circulation
renal disease
obstructive pulmonary disease
a disease treated with corticosteroids
a disease with drug treatment potentially influencing blood pressure levels
significant obesity (BMI >=32 kg/m2)
allergic reaction towards any of the study drugs
The patient is excluded from the study if his blood pressure level rises to 200/120 mmHg or above during the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kimmo K Kontula, Professor
Organizational Affiliation
Helsinki University Central Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Helsinki University Central Hospital
City
Helsinki
Country
Finland
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
17324745
Citation
Hiltunen TP, Suonsyrja T, Hannila-Handelberg T, Paavonen KJ, Miettinen HE, Strandberg T, Tikkanen I, Tilvis R, Pentikainen PJ, Virolainen J, Kontula K. Predictors of antihypertensive drug responses: initial data from a placebo-controlled, randomized, cross-over study with four antihypertensive drugs (The GENRES Study). Am J Hypertens. 2007 Mar;20(3):311-8. doi: 10.1016/j.amjhyper.2006.09.006. Erratum In: Am J Hypertens. 2018 Nov 13;31(12):1333.
Results Reference
result
PubMed Identifier
18475165
Citation
Suonsyrja T, Hannila-Handelberg T, Paavonen KJ, Miettinen HE, Donner K, Strandberg T, Tikkanen I, Tilvis R, Pentikainen PJ, Kontula K, Hiltunen TP. Laboratory tests as predictors of the antihypertensive effects of amlodipine, bisoprolol, hydrochlorothiazide and losartan in men: results from the randomized, double-blind, crossover GENRES Study. J Hypertens. 2008 Jun;26(6):1250-6. doi: 10.1097/HJH.0b013e3282fcc37f.
Results Reference
result
PubMed Identifier
25622599
Citation
Hiltunen TP, Donner KM, Sarin AP, Saarela J, Ripatti S, Chapman AB, Gums JG, Gong Y, Cooper-DeHoff RM, Frau F, Glorioso V, Zaninello R, Salvi E, Glorioso N, Boerwinkle E, Turner ST, Johnson JA, Kontula KK. Pharmacogenomics of hypertension: a genome-wide, placebo-controlled cross-over study, using four classes of antihypertensive drugs. J Am Heart Assoc. 2015 Jan 26;4(1):e001521. doi: 10.1161/JAHA.115.001778.
Results Reference
result
PubMed Identifier
35213289
Citation
Nuotio ML, Sanez Tahtisalo H, Lahtinen A, Donner K, Fyhrquist F, Perola M, Kontula KK, Hiltunen TP. Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design. Epigenetics. 2022 Nov;17(11):1432-1445. doi: 10.1080/15592294.2022.2038418. Epub 2022 Feb 25.
Results Reference
derived
PubMed Identifier
29580174
Citation
Ala-Mutka EM, Rimpela JM, Fyhrquist F, Kontula KK, Hiltunen TP. Effect of hydrochlorothiazide on serum uric acid concentration: a genome-wide association study. Pharmacogenomics. 2018 Apr;19(6):517-527. doi: 10.2217/pgs-2017-0184. Epub 2018 Mar 27.
Results Reference
derived
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A Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension
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