Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/52991
Campo DC Valoridioma
dc.contributor.authorPerez, JCR
dc.contributor.authorNovoa, JN
dc.contributor.authorCaballero, A
dc.contributor.authorAnabitarte, A
dc.contributor.authorPlaza, C
dc.contributor.authorPalop, L
dc.contributor.authorEsparragon, FR
dc.contributor.otherRodriguez-Esparragon, Francisco
dc.contributor.otherRodriguez-Perez, J.C.
dc.date.accessioned2019-02-04T14:38:13Z-
dc.date.available2019-02-04T14:38:13Z-
dc.date.issued2005
dc.identifier.issn0211-6995
dc.identifier.urihttp://hdl.handle.net/10553/52991-
dc.description.abstractArterial hypertension and diabetes mellitus give rise to a situation of high cardiovascular risk. The potential renoprotection from inhibition of the renin-angiotensin system is a valid option in this type of patient.Objective: Evaluate the effect of valsartan on blood pressure (BP) and renal function in albuminuric patients with type 2 diabetes and arterial hypertension. Patients and methods: This was a prospective, observational study. Seventy-four diabetic patients with a blood pressure of >= 140/90 mmHg, with micro or macroalbuminuria and a) blood creatinine levels lower 1.5 mg/dl (group 1) or b) blood creatinine levels between 1.5 and 2 mg/dl (group 2), were studied and followed up for a 12-week period. Treatment was started with valsartan 80 mg/d, increasing to 760 mg/d, adding torasemide at a dose of 5 mg/d if the target blood pressure of 730185 mmHg has not been achieved. The degree of BP reduction was analyzed comparatively using a mercury sphygmomanometer and a semi-automatic monitor, the Omron HEM 705 CP.Results: All patients showed a significant reduction of the systolic (SBP) and diastolic (DBP) blood pressures (p < 0.001) over the study period, decreasing from 150.7 +/- 72.8 to 130.8 +/- 9.6 and from 94.7 +/- 7.7 to 76.8 +/- 6.3 mmHg, respectively. A significant reduction was observed only for diastolic blood pressure (101.4 +/- 8.8 to 79.4 +/- 5.6; p < 0.001) in the group 2 of patients. Lowest BP values were always obtained with the semiautomatic device. At the end of the study, 9.5% maintained valsartan 80 mg/d and 36.5% required the addition of a second or third drug to valsartan 160 mg in order to achieve the therapeutic target BP A significant reduction was observed in the microalbuminuria (75.5 +/- 9.5 to 54.7 +/- 7.3 mu g/min; p < 0.007) and macroalbuminuria (n = 20; 0.93 +/- 0.4 to 0.68 +/- 0.4 g/day; p < 0.001).Conclusion: Valsartan significantly reduced SBP and DBP Valsartan at 760 mg/d had a significantly greater effect in reducing micro and macroalbuminuria. No changes were observed in renal function, HbA1c or serum potassium. The rate of adverse events was very low.
dc.publisher0211-6995
dc.relation.ispartofNefrologia
dc.sourceNefrologia[ISSN 0211-6995],v. 25 (5), p. 500-508
dc.subject.otherBlood-Pressure
dc.subject.otherAntihypertensive Treatment
dc.subject.otherProgression
dc.subject.otherOutcomes
dc.subject.otherRisk
dc.titleValsartan in patients with arterial hypertension and type 2 diabetes mellitus. The lapaval study
dc.typeinfo:eu-repo/semantics/Article
dc.typeArticle
dc.identifier.isi000234179900006
dcterms.isPartOfNefrologia
dcterms.sourceNefrologia[ISSN 0211-6995],v. 25 (5), p. 500-508
dc.description.lastpage508
dc.identifier.issue5
dc.description.firstpage500
dc.relation.volume25
dc.type2Artículo
dc.identifier.wosWOS:000234179900006
dc.contributor.daisngid245684
dc.contributor.daisngid10589224
dc.contributor.daisngid1300413
dc.contributor.daisngid615955
dc.contributor.daisngid3092642
dc.contributor.daisngid315895
dc.contributor.daisngid1265413
dc.contributor.daisngid751953
dc.contributor.daisngid1305938
dc.identifier.investigatorRIDD-2810-2013
dc.identifier.investigatorRIDC-1247-2010
dc.contributor.wosstandardWOS:Perez, JCR
dc.contributor.wosstandardWOS:Novoa, JN
dc.contributor.wosstandardWOS:Caballero, A
dc.contributor.wosstandardWOS:Anabitarte, A
dc.contributor.wosstandardWOS:Plaza, C
dc.contributor.wosstandardWOS:Palop, L
dc.contributor.wosstandardWOS:Esparragon, FR
dc.date.coverdate2005
dc.identifier.ulpgces
dc.description.jcr0,466
dc.description.jcrqQ4
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Patología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptGIR IUSA-ONEHEALTH 5: Reproducción Animal, Oncología y Anestesiología Comparadas-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.orcid0000-0003-0023-1063-
crisitem.author.orcid0000-0003-1663-3673-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.fullNameRodríguez Pérez,José Carlos-
crisitem.author.fullNameRodríguez Esparragón,Francisco Javier-
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