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Aldosterone synthase (CYP11B2) -344 C/T polymorphism is related to antihypertensive response : result from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA) trial

Kurland, Lisa (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Akut- och internmedicin,Department of Internal Medicine, Uppsala University Hospital, Uppsala, Sweden, Department of Internal Medicine, Uppsala University Hospital, SE-751 85 Uppsala, Sweden
Melhus, Håkan (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Melhus, H.åkan, Department of Internal Medicine, Uppsala University Hospital, Uppsala, Sweden
Karlsson, Julia (author)
Department of Internal Medicine, Uppsala University Hospital, Uppsala, Sweden
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Kahan, Thomas (author)
Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Danderyd, Sweden
Malmqvist, Karin (author)
Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Danderyd, Sweden
Öhman, Peter (author)
Linköpings universitet,Klinisk farmakologi,Hälsouniversitetet
Nyström, Fredrik (author)
Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Internmedicin,Endokrin- och magtarmmedicinska kliniken US
Hägg, Anders (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Akut- och internmedicin,Hägg, A., Department of Internal Medicine, Uppsala University Hospital, Uppsala, Sweden
Lind, Lars (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Akut- och internmedicin,Department of Internal Medicine, Uppsala University Hospital, Uppsala, Sweden
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 (creator_code:org_t)
Elsevier, 2002
2002
English.
In: American Journal of Hypertension. - : Elsevier. - 0895-7061 .- 1941-7225. ; 15:5, s. 389-93
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Our aim was to determine whether the aldosterone synthase (CYP11B2) -344 C/T polymorphism was associated with the blood pressure (BP)-lowering response to antihypertensive treatment. METHODS: Patients with mild-to-moderate primary hypertension and left ventricular hypertrophy were randomized in a double-blind study to receive treatment with either the angiotensin II type 1 (AT1) receptor antagonist irbesartan (n = 43), or the beta1-adrenergic receptor blocker atenolol (n = 43). The aldosterone synthase (CYP11B2) -344 C/T polymorphism was analyzed using solid-phase minisequencing and related to BP reduction after 3 months treatment. Serum aldosterone levels were measured. RESULTS: After 3 months treatment the mean reductions in BP were similar for both treatment groups. When assessing the systolic BP reduction in the irbesartan group, patients with the TT variant had a more pronounced reduction (-21 +/- 19 SD mm Hg, n = 17) than both the TC (-14 +/- 18 mm Hg, n= 18) and CC (0 +/- 17 mm Hg, n = 8) genotypes (P = .04). There was no association between this polymorphism and the diastolic BP response. The -344 C/T polymorphism was not associated with the BP response to atenolol. Nor was it related to the baseline serum aldosterone level. CONCLUSIONS: The aldosterone synthase -344 C/T polymorphism was related to the BP-lowering response in hypertensive patients treated with the AT1-receptor antagonist irbesartan.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Keyword

Adrenergic beta-Antagonists/*therapeutic use
Aldosterone/blood
Aldosterone Synthase/*genetics
Antihypertensive Agents/*therapeutic use
Atenolol/*therapeutic use
Base Sequence/genetics
Biphenyl Compounds/*therapeutic use
Blood Pressure
Comparative Study
Cytosine
Double-Blind Method
Female
Humans
Hypertension/blood/*drug therapy/*genetics/physiopathology
Hypertrophy; Left Ventricular/drug therapy
Male
Middle Aged
Polymorphism; Genetic
Receptor; Angiotensin; Type 1
Receptors; Angiotensin/antagonists & inhibitors
Research Support; Non-U.S. Gov't
Tetrazoles/*therapeutic use
Thymine
Treatment Outcome
MEDICINE
MEDICIN

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