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dc.contributor.authorHerrera-Gómez, Francisco
dc.contributor.authorChimeno, M. Montserrat
dc.contributor.authorMartín-García, Débora
dc.contributor.authorLizaraso-Soto, Frank
dc.contributor.authorMaurtua-Briseno-Meiggs, Álvaro
dc.contributor.authorGrande-Villoria, Jesús
dc.contributor.authorBustamante-Munguira, Juan
dc.contributor.authorAlamartine, Eric
dc.contributor.authorVilardell, Miquel
dc.contributor.authorOchoa-Sangrador, Carlos
dc.contributor.authorÁlvarez, F. Javier
dc.date.accessioned2020-05-21T20:44:39Z
dc.date.available2020-05-21T20:44:39Z
dc.date.issued2019
dc.identifier.citationHerrera F., Chimeno M., Martín D., Lizaraso F., Maurtua A., Grande J., et al. Cholesterol-lowering treatment in chronic kidney disease: multistage pairwise and network meta-analyses. Sci Rep. 2019; 9: 8951es_PE
dc.identifier.urihttps://hdl.handle.net/20.500.12727/6096
dc.description.abstractPairwise and network meta-analyses on the relationship between the efficacy of the use of statins with or without ezetimibe and reductions in low-density lipoprotein cholesterol (LDLc) and C-reactive protein (CRP) in patients with chronic kidney disease (CKD) are presented. In the pairwise meta-analysis, statins with or without ezetimibe were shown to be efficacious in reducing major adverse cardiovascular events (MACE) in patients with CKD and an estimated glomerular filtration rate (eGFR) of less than 60 ml/min/1.73 m2, in the context of both primary prevention [odds ratio (OR)/95% confidence interval (95% CI)/I2/number of studies (n): 0.50/0.40-0.64/0%/6] and primary/secondary prevention (0.66/0.57-0.76/57%/18). However, in the Bayesian network meta-analysis, compared to the placebo, only atorvastatin 80 mg daily and atorvastatin and rosuvastatin at doses equivalent to simvastatin 20 mg daily reduced the odds of MACEs in this patient population. The network meta-analysis for LDLc and CRP treatment objectives also showed that, regardless of eGFR and excluding dialysis patients, the number of MACEs decreased in patients with CKD, with reductions in both LDLc and CRP of less than 50% (surface under the cumulative ranking (SUCRA)/heterogeneity (vague)/n: 0.77/0.14/3). The evaluation of the benefits of drugs may lead to individualized therapy for CKD patients: Cholesterol-lowering treatment for CKD patients with high levels of both LDLc and CRP is suggested.es_PE
dc.description.sponsorshipConsejería de Educación, Junta de Castilla y León, Spaines_PE
dc.format.extentpp. 8951es_PE
dc.language.isoenges_PE
dc.publisherSpringer Naturees_PE
dc.relation.ispartofurn:issn:0143-4004
dc.relation.ispartofseriesScientific reports;vol. 9
dc.relation.urihttps://doi.org/10.1038/s41598-019-45431-5es_PE
dc.rightsinfo:eu-repo/semantics/openAccesses_PE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/es_PE
dc.sourceRepositorio Académico USMPes_PE
dc.sourceUniversidad San Martín de Porres - USMPes_PE
dc.subjectColesteroles_PE
dc.subjectInsuficiencia renal crónicaes_PE
dc.subjectRevisión de la investigación por pareses_PE
dc.subjectMetaanálisises_PE
dc.titleCholesterol-lowering treatment in chronic kidney disease: multistage pairwise and network meta-analyseses_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
thesis.degree.nameMedicina Humanaes_PE
thesis.degree.grantorUniversidad de San Martín de Porres. Facultad de Medicina Humanaes_PE
thesis.degree.disciplineMedicinaes_PE
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.00es_PE


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