Comparative effects of nebivolol and atenolol on blood pressure and insulin sensitivity in hypertensive subjects with type II diabetes

The aim of this double-blind, parallel group study was to compare the effects of nebivolol and atenolol on blood pressure (BP) and insulin sensitivity in hypertensive patients with type II, non-insulin dependent diabetes mellitus (NIDDM). After a 4-week run-in period on placebo, 30 patients (14 male...

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Veröffentlicht in:Journal of human hypertension 1997-11, Vol.11 (11), p.753-757
Hauptverfasser: FOGARI, R, ZOPPI, A, LAZZARI, P, MUGELLINI, A, LUSARDI, P, PRETI, P, VAN NUETEN, L, VERTOMMEN, C
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container_issue 11
container_start_page 753
container_title Journal of human hypertension
container_volume 11
creator FOGARI, R
ZOPPI, A
LAZZARI, P
MUGELLINI, A
LUSARDI, P
PRETI, P
VAN NUETEN, L
VERTOMMEN, C
description The aim of this double-blind, parallel group study was to compare the effects of nebivolol and atenolol on blood pressure (BP) and insulin sensitivity in hypertensive patients with type II, non-insulin dependent diabetes mellitus (NIDDM). After a 4-week run-in period on placebo, 30 patients (14 males and 16 females) aged 43 to 69 years, with stable NIDDM and mild to moderate hypertension (DBP > or =95 and
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After a 4-week run-in period on placebo, 30 patients (14 males and 16 females) aged 43 to 69 years, with stable NIDDM and mild to moderate hypertension (DBP &gt; or =95 and &lt;116 mm Hg) were randomised to receive either nebivolol 5 mg or atenolol 50 mg, both administered once daily for 6 months. At the end of the placebo and the active treatment periods, supine and standing BP was measured, 24-h urinary C-peptide, HbA1c, plasma glucose and lipid levels were evaluated and an euglycaemic hyperinsulinaemic clamp was performed to evaluate insulin sensitivity: glucose infusion rate during the last 60 min of clamp and total glucose requirements were evaluated. Nebivolol 5 mg once daily was of an equivalent efficacy as atenolol 50 mg once daily at reducing supine and standing systolic and diastolic BP values. Neither beta-blocker adversely affected carbohydrate metabolism in terms of insulin sensitivity, whole body glucose utilization, HbA1c and 24-h urinary C-peptide excretion. No significant changes in cholesterol (total, high density and low density lipoprotein) and triglycerides plasma levels were observed with both beta-blockers. These findings indicate that, in hypertensive patients with NIDDM, ie, in subjects who have established insulin resistance, treatment with nebivolol and atenolol neither further deteriorated insulin sensitivity nor adversely affected the lipid profile.</description><identifier>ISSN: 0950-9240</identifier><identifier>EISSN: 1476-5527</identifier><identifier>DOI: 10.1038/sj.jhh.1000533</identifier><identifier>PMID: 9416986</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing</publisher><subject>Adrenergic beta-Antagonists - adverse effects ; Adrenergic beta-Antagonists - therapeutic use ; Adult ; Aged ; Antihypertensive agents ; Antihypertensive Agents - adverse effects ; Antihypertensive Agents - therapeutic use ; Atenolol ; Atenolol - adverse effects ; Atenolol - therapeutic use ; Benzopyrans - adverse effects ; Benzopyrans - therapeutic use ; Biological and medical sciences ; Blood pressure ; Blood Pressure - drug effects ; Carbohydrate metabolism ; Cardiovascular system ; Cholesterol ; Diabetes ; Diabetes mellitus (insulin dependent) ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 ; Diabetic Angiopathies - drug therapy ; Diabetic Angiopathies - physiopathology ; Double-Blind Method ; Ethanolamines - adverse effects ; Ethanolamines - therapeutic use ; Female ; Glucose ; Glucose metabolism ; Humans ; Hypertension ; Hypertension - drug therapy ; Insulin ; Insulin Resistance ; Low density lipoprotein ; Male ; Medical sciences ; Middle Aged ; Nebivolol ; Patients ; Peptides ; Pharmacology. 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After a 4-week run-in period on placebo, 30 patients (14 males and 16 females) aged 43 to 69 years, with stable NIDDM and mild to moderate hypertension (DBP &gt; or =95 and &lt;116 mm Hg) were randomised to receive either nebivolol 5 mg or atenolol 50 mg, both administered once daily for 6 months. At the end of the placebo and the active treatment periods, supine and standing BP was measured, 24-h urinary C-peptide, HbA1c, plasma glucose and lipid levels were evaluated and an euglycaemic hyperinsulinaemic clamp was performed to evaluate insulin sensitivity: glucose infusion rate during the last 60 min of clamp and total glucose requirements were evaluated. Nebivolol 5 mg once daily was of an equivalent efficacy as atenolol 50 mg once daily at reducing supine and standing systolic and diastolic BP values. Neither beta-blocker adversely affected carbohydrate metabolism in terms of insulin sensitivity, whole body glucose utilization, HbA1c and 24-h urinary C-peptide excretion. No significant changes in cholesterol (total, high density and low density lipoprotein) and triglycerides plasma levels were observed with both beta-blockers. These findings indicate that, in hypertensive patients with NIDDM, ie, in subjects who have established insulin resistance, treatment with nebivolol and atenolol neither further deteriorated insulin sensitivity nor adversely affected the lipid profile.</description><subject>Adrenergic beta-Antagonists - adverse effects</subject><subject>Adrenergic beta-Antagonists - therapeutic use</subject><subject>Adult</subject><subject>Aged</subject><subject>Antihypertensive agents</subject><subject>Antihypertensive Agents - adverse effects</subject><subject>Antihypertensive Agents - therapeutic use</subject><subject>Atenolol</subject><subject>Atenolol - adverse effects</subject><subject>Atenolol - therapeutic use</subject><subject>Benzopyrans - adverse effects</subject><subject>Benzopyrans - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Blood pressure</subject><subject>Blood Pressure - drug effects</subject><subject>Carbohydrate metabolism</subject><subject>Cardiovascular system</subject><subject>Cholesterol</subject><subject>Diabetes</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2</subject><subject>Diabetic Angiopathies - drug therapy</subject><subject>Diabetic Angiopathies - physiopathology</subject><subject>Double-Blind Method</subject><subject>Ethanolamines - adverse effects</subject><subject>Ethanolamines - therapeutic use</subject><subject>Female</subject><subject>Glucose</subject><subject>Glucose metabolism</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension - drug therapy</subject><subject>Insulin</subject><subject>Insulin Resistance</subject><subject>Low density lipoprotein</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nebivolol</subject><subject>Patients</subject><subject>Peptides</subject><subject>Pharmacology. Drug treatments</subject><subject>Placebos</subject><subject>Plasma levels</subject><subject>Sensitivity analysis</subject><subject>Single-Blind Method</subject><subject>Triglycerides</subject><issn>0950-9240</issn><issn>1476-5527</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1LxDAQhoMoun5cvQkBvXZN06Zpj7L4sSB40XNJ2imb0k1qJlX2D_i7za7FQ5hk3neeMC8h1ylbpiwr77Ff9ptNvDMmsuyILNJcFokQXB6TBasESyqeszNyjtgzthfLU3Ja5WlRlcWC_KzcdlReBfMFFLoOmoDUddSCNl9ucANVtqUqgD08nKV6cK6lowfEycNBNhanwViKYNFEkgm72KOb3Qg-7HuRjZPuD_BvEzY0RImu17Q1SkMAvCQnnRoQruZ6QT6eHt9XL8nr2_N69fCaNFkpQ9KykkOrmliL_SpFxjmvhGy1AKULXVYyZ1IKpllelrwquEjTJledFPGoNrsgt3_c0bvPCTDUvZu8jV_WvMiZkJms0uha_rka7xA9dPXozVb5XZ2yep96jX0dU6_n1OPAzYyd9Bbaf_scc9TvZl1ho4bOK9sY_LfxuBaTPPsFoxeNBg</recordid><startdate>19971101</startdate><enddate>19971101</enddate><creator>FOGARI, R</creator><creator>ZOPPI, A</creator><creator>LAZZARI, P</creator><creator>MUGELLINI, A</creator><creator>LUSARDI, P</creator><creator>PRETI, P</creator><creator>VAN NUETEN, L</creator><creator>VERTOMMEN, C</creator><general>Nature Publishing</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope></search><sort><creationdate>19971101</creationdate><title>Comparative effects of nebivolol and atenolol on blood pressure and insulin sensitivity in hypertensive subjects with type II diabetes</title><author>FOGARI, R ; ZOPPI, A ; LAZZARI, P ; MUGELLINI, A ; LUSARDI, P ; PRETI, P ; VAN NUETEN, L ; VERTOMMEN, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-d082edacd086147663222957db5eab6b897407750b04882962511c4af75af7ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adrenergic beta-Antagonists - adverse effects</topic><topic>Adrenergic beta-Antagonists - therapeutic use</topic><topic>Adult</topic><topic>Aged</topic><topic>Antihypertensive agents</topic><topic>Antihypertensive Agents - adverse effects</topic><topic>Antihypertensive Agents - therapeutic use</topic><topic>Atenolol</topic><topic>Atenolol - adverse effects</topic><topic>Atenolol - therapeutic use</topic><topic>Benzopyrans - adverse effects</topic><topic>Benzopyrans - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Blood pressure</topic><topic>Blood Pressure - drug effects</topic><topic>Carbohydrate metabolism</topic><topic>Cardiovascular system</topic><topic>Cholesterol</topic><topic>Diabetes</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2</topic><topic>Diabetic Angiopathies - drug therapy</topic><topic>Diabetic Angiopathies - physiopathology</topic><topic>Double-Blind Method</topic><topic>Ethanolamines - adverse effects</topic><topic>Ethanolamines - therapeutic use</topic><topic>Female</topic><topic>Glucose</topic><topic>Glucose metabolism</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Hypertension - drug therapy</topic><topic>Insulin</topic><topic>Insulin Resistance</topic><topic>Low density lipoprotein</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nebivolol</topic><topic>Patients</topic><topic>Peptides</topic><topic>Pharmacology. 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After a 4-week run-in period on placebo, 30 patients (14 males and 16 females) aged 43 to 69 years, with stable NIDDM and mild to moderate hypertension (DBP &gt; or =95 and &lt;116 mm Hg) were randomised to receive either nebivolol 5 mg or atenolol 50 mg, both administered once daily for 6 months. At the end of the placebo and the active treatment periods, supine and standing BP was measured, 24-h urinary C-peptide, HbA1c, plasma glucose and lipid levels were evaluated and an euglycaemic hyperinsulinaemic clamp was performed to evaluate insulin sensitivity: glucose infusion rate during the last 60 min of clamp and total glucose requirements were evaluated. Nebivolol 5 mg once daily was of an equivalent efficacy as atenolol 50 mg once daily at reducing supine and standing systolic and diastolic BP values. Neither beta-blocker adversely affected carbohydrate metabolism in terms of insulin sensitivity, whole body glucose utilization, HbA1c and 24-h urinary C-peptide excretion. No significant changes in cholesterol (total, high density and low density lipoprotein) and triglycerides plasma levels were observed with both beta-blockers. These findings indicate that, in hypertensive patients with NIDDM, ie, in subjects who have established insulin resistance, treatment with nebivolol and atenolol neither further deteriorated insulin sensitivity nor adversely affected the lipid profile.</abstract><cop>Basingstoke</cop><pub>Nature Publishing</pub><pmid>9416986</pmid><doi>10.1038/sj.jhh.1000533</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Adrenergic beta-Antagonists - adverse effects
Adrenergic beta-Antagonists - therapeutic use
Adult
Aged
Antihypertensive agents
Antihypertensive Agents - adverse effects
Antihypertensive Agents - therapeutic use
Atenolol
Atenolol - adverse effects
Atenolol - therapeutic use
Benzopyrans - adverse effects
Benzopyrans - therapeutic use
Biological and medical sciences
Blood pressure
Blood Pressure - drug effects
Carbohydrate metabolism
Cardiovascular system
Cholesterol
Diabetes
Diabetes mellitus (insulin dependent)
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2
Diabetic Angiopathies - drug therapy
Diabetic Angiopathies - physiopathology
Double-Blind Method
Ethanolamines - adverse effects
Ethanolamines - therapeutic use
Female
Glucose
Glucose metabolism
Humans
Hypertension
Hypertension - drug therapy
Insulin
Insulin Resistance
Low density lipoprotein
Male
Medical sciences
Middle Aged
Nebivolol
Patients
Peptides
Pharmacology. Drug treatments
Placebos
Plasma levels
Sensitivity analysis
Single-Blind Method
Triglycerides
title Comparative effects of nebivolol and atenolol on blood pressure and insulin sensitivity in hypertensive subjects with type II diabetes
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