dc.creatorPOP-BUSUI, Rodica
dc.creatorLU, Jiang
dc.creatorLOPES, Neuza
dc.creatorJONES, Teresa L. Z.
dc.creatorBARI 2D Investigators
dc.date.accessioned2012-10-19T17:00:24Z
dc.date.accessioned2018-07-04T15:03:44Z
dc.date.available2012-10-19T17:00:24Z
dc.date.available2018-07-04T15:03:44Z
dc.date.created2012-10-19T17:00:24Z
dc.date.issued2009
dc.identifierJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, v.14, n.1, p.1-13, 2009
dc.identifier1085-9489
dc.identifierhttp://producao.usp.br/handle/BDPI/21272
dc.identifier10.1111/j.1529-8027.2009.00200.x
dc.identifierhttp://dx.doi.org/10.1111/j.1529-8027.2009.00200.x
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1618047
dc.description.abstractWe evaluated the associations between glycemic therapies and prevalence of diabetic peripheral neuropathy (DPN) at baseline among participants in the Bypass Angioplasty Revascularization Investigation 2 Diabetes (BARI 2D) trial on medical and revascularization therapies for coronary artery disease (CAD) and on insulin-sensitizing vs. insulin-providing treatments for diabetes. A total of 2,368 patients with type 2 diabetes and CAD was evaluated. DPN was defined as clinical examination score > 2 using the Michigan Neuropathy Screening Instrument (MNSI). DPN odds ratios across different groups of glycemic therapy were evaluated by multiple logistic regression adjusted for multiple covariates including age, sex, hemoglobin A1c (HbA1c), and diabetes duration. Fifty-one percent of BARI 2D subjects with valid baseline characteristics and MNSI scores had DPN. After adjusting for all variables, use of insulin was significantly associated with DPN (OR = 1.57, 95% CI: 1.15-2.13). Patients on sulfonylurea (SU) or combination of SU/metformin (Met)/thiazolidinediones (TZD) had marginally higher rates of DPN than the Met/TZD group. This cross-sectional study in a cohort of patients with type 2 diabetes and CAD showed association of insulin use with higher DPN prevalence, independent of disease duration, glycemic control, and other characteristics. The causality between a glycemic control strategy and DPN cannot be evaluated in this cross-sectional study, but continued assessment of DPN and randomized therapies in BARI 2D trial may provide further explanations on the development of DPN.
dc.languageeng
dc.publisherWILEY-BLACKWELL PUBLISHING, INC
dc.relationJournal of the Peripheral Nervous System
dc.rightsCopyright WILEY-BLACKWELL PUBLISHING, INC
dc.rightsrestrictedAccess
dc.subjectcoronary artery disease
dc.subjectdiabetic peripheral neuropathy
dc.subjectglycemic control therapy
dc.subjectMichigan Neuropathy Screening Instrument
dc.subjecttype 2 diabetes
dc.titlePrevalence of diabetic peripheral neuropathy and relation to glycemic control therapies at baseline in the BARI 2D cohort
dc.typeArtículos de revistas


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