Efficacy and Effect on Plasma B-type Natriuretic Peptide Concentration of Losartan-hydrochlorothiazide for Hypertension Uncontrolled by Losartan-based Therapy: Subanalysis of a Multicentre Prospective Observational Study

التفاصيل البيبلوغرافية
العنوان: Efficacy and Effect on Plasma B-type Natriuretic Peptide Concentration of Losartan-hydrochlorothiazide for Hypertension Uncontrolled by Losartan-based Therapy: Subanalysis of a Multicentre Prospective Observational Study
المؤلفون: K. Kobayashi, Y. Nakamura, Yoshihiro Tsuchiya, M. Tanaka, H. Meno, T. Inou, I. Kubara, T. Ota, Yuhei Shiga
المصدر: Arzneimittelforschung. 62:414-419
بيانات النشر: Georg Thieme Verlag KG, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Combination therapy, medicine.drug_class, medicine.medical_treatment, Losartan/hydrochlorothiazide, Urology, Blood Pressure, Angiotensin II receptor antagonist, Pharmacology, Losartan, Hydrochlorothiazide, Natriuretic Peptide, Brain, Drug Discovery, Natriuretic peptide, Humans, Medicine, Prospective Studies, Diuretics, Antihypertensive Agents, Aged, business.industry, Middle Aged, Uric Acid, Blood pressure, Hypertension, Drug Therapy, Combination, Female, Diuretic, business, Angiotensin II Type 1 Receptor Blockers, Follow-Up Studies, medicine.drug
الوصف: Many patients with hypertension have difficulty achieving their target blood pressure (BP). Therefore combination therapy, for example with an angiotensin II receptor blocker (ARB) and a diuretic, may be recommended. We previously evaluated the efficacy and safety of losartan (LOS) 50 mg - hydrochlorothiazide (HCTZ) 12.5 mg, as well as its effect on the plasma concentration of B-type natriuretic peptide (BNP, a prognostic marker for cardiovascular events), in patients with hypertension uncontrolled by ≥3 months of ARB-based therapy. The present subanalysis used data from patients who received LOS-based therapy before switching to LOS-HCTZ. Efficacy, safety, and changes in blood biochemical variables including BNP were evaluated. After excluding 4 patients with protocol violations, data from 35 patients (aged 36-79 years, mean 63 years; 66% male) were used in the safety analysis. The efficacy analysis used data from the 30 patients who were followed up for 12 months. Systolic/diastolic BP decreased from 156±12/87±11 mmHg at baseline to 125±11/73±10 mmHg at 12 months (p0.001). After 12 months, half of the patients achieved their target BP as defined by the Japanese Society of Hypertension Guidelines for the Management of Hypertension 2004. In 12 patients with baseline plasma BNP concentration ≥20 pg/mL, BNP decreased from 78.3±18.8 pg/mL to 57.3±17.7 pg/mL (p0.01). 3 patients experienced adverse events, one of which was cardiovascular. LOS-HCTZ is efficacious, has a good safety profile, and decreases plasma BNP concentration.
تدمد: 1616-7066
0004-4172
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91a29c556eb2a7b1a6083a9dbe9fffdbTest
https://doi.org/10.1055/s-0032-1316376Test
رقم الانضمام: edsair.doi.dedup.....91a29c556eb2a7b1a6083a9dbe9fffdb
قاعدة البيانات: OpenAIRE