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Impaired fasting glucose and chronic kidney disease, albuminuria, or worsening kidney function: a secondary analysis of SPRINT
| dc.contributor.author | Vieira, Miguel Bigotte | |
| dc.contributor.author | Neves, João Sérgio | |
| dc.contributor.author | Leitão, Lia | |
| dc.contributor.author | Baeta Baptista, Rute | |
| dc.contributor.author | Magriço, Rita | |
| dc.contributor.author | Viegas Dias, Catarina | |
| dc.contributor.author | Oliveira, Ana | |
| dc.contributor.author | Carvalho, Davide | |
| dc.contributor.author | Mc Causland, Finnian R | |
| dc.date.accessioned | 2022-05-09T15:40:03Z | |
| dc.date.available | 2022-05-09T15:40:03Z | |
| dc.date.issued | 2019 | |
| dc.description | Copyright © 2019 Endocrine Society | pt_PT |
| dc.description.abstract | Purpose: Diabetes mellitus is a risk factor for the development and progression of chronic kidney disease (CKD). However, the association of prediabetes with adverse kidney outcomes is uncertain. Methods: We performed a secondary analysis of the Systolic Blood Pressure Intervention Trial (SPRINT), including 9,361 participants without diabetes at baseline. We categorized participants according to fasting glucose as having impaired fasting glucose (≥100 mg/dL [(≥5.6 mmol/L]) or normoglycemia (<100 mg/dL [(<5.6 mmol/L]). Unadjusted and adjusted proportional hazards models were fit to estimate the association of impaired fasting glucose (versus normoglycemia) with a composite outcome of worsening kidney function (≥30% decrease in eGFR to <60 ml/min/1.73 m2 in participants without baseline CKD; ≥50% decrease in eGFR or need of long-term dialysis/kidney transplantation in participants with CKD) or incident albuminuria (doubling of urinary albumin to creatinine ratio from <10 mg/g to >10 mg/g). These outcomes were also evaluated separately, and according to CKD status at baseline. Results: The mean age was 67.9 ± 9.4 years, 35.5% were female, and 31.4% were black. The median follow-up was 3.3 years and 41.8% had impaired fasting glucose. Impaired fasting glucose was not associated with higher rates of the composite outcome (HR 0.97; 95%CI 0.81-1.16), worsening kidney function (HR 1.02; 95%CI 0.75-1.37), or albuminuria (HR 0.98; 95%CI 0.78-1.23). Similarly, there was no association of impaired fasting glucose with outcomes according to baseline CKD status. Conclusions: Impaired fasting glucose at baseline was not associated with the development of worsening kidney function or albuminuria in participants of SPRINT. | pt_PT |
| dc.description.sponsorship | The SPRINT trial was sponsored by the National Heart, Lung, and Blood Institute (NHLBI), with cosponsorship by the National Institute of Diabetes and Digestive and Kidney Diseases, the National Institute of Neurological Disorders and Stroke, and the National Institute on Aging. F.R.M. is supported by the National Institute of Diabetes and Digestive and Kidney Diseases grant K23DK102511. | pt_PT |
| dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
| dc.identifier.citation | J Clin Endocrinol Metab. 2019 May 7;104(9):4024-4032 | pt_PT |
| dc.identifier.doi | 10.1210/jc.2019-00073 | pt_PT |
| dc.identifier.eissn | 1945-7197 | |
| dc.identifier.issn | 0021-972X | |
| dc.identifier.uri | http://hdl.handle.net/10451/52812 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.publisher | Oxford University Press | pt_PT |
| dc.relation.publisherversion | https://academic.oup.com/jcem | pt_PT |
| dc.title | Impaired fasting glucose and chronic kidney disease, albuminuria, or worsening kidney function: a secondary analysis of SPRINT | pt_PT |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 4032 | pt_PT |
| oaire.citation.issue | 9 | pt_PT |
| oaire.citation.startPage | 4024 | pt_PT |
| oaire.citation.title | The Journal of Clinical Endocrinology & Metabolism | pt_PT |
| oaire.citation.volume | 104 | pt_PT |
| person.familyName | Bigotte Vieira | |
| person.familyName | Baeta Baptista | |
| person.givenName | Miguel | |
| person.givenName | Rute | |
| person.identifier | 591378 | |
| person.identifier.ciencia-id | FF17-2C76-E2CC | |
| person.identifier.ciencia-id | 7614-FA6B-270F | |
| person.identifier.orcid | 0000-0003-0528-2716 | |
| person.identifier.orcid | 0000-0002-7572-2812 | |
| person.identifier.rid | V-4629-2018 | |
| person.identifier.scopus-author-id | 57192837006 | |
| rcaap.rights | restrictedAccess | pt_PT |
| rcaap.type | article | pt_PT |
| relation.isAuthorOfPublication | 8d118e09-0abf-4347-8e5c-cc53c7cbd4bd | |
| relation.isAuthorOfPublication | c13d7193-7985-4594-9954-4d138bd9317a | |
| relation.isAuthorOfPublication.latestForDiscovery | c13d7193-7985-4594-9954-4d138bd9317a |
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