| Texto completo | |
| Autor(es): Mostrar menos - |
Freitas, Thais C.
;
Maciel, Ana Alice W.
;
Fagundes, Gustavo F. C.
;
Petenuci, Janaina
;
Santana, Lucas S.
;
Guimaraes, Augusto G.
;
Freitas-Castro, Felipe
;
Srougi, Victor
;
Tanno, Fabio Y.
;
Chambo, Jose L.
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Pereira, Maria Adelaide A.
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Brito, Luciana P.
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Pio-Abreu, Andrea
;
Bortolotto, Luiz A.
;
Latronico, Ana Claudia
;
Fragoso, Maria Candida B., V
;
Drager, Luciano F.
;
Mendonca, Berenice B.
;
Almeida, Madson Q.
Número total de Autores: 19
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| Tipo de documento: | Artigo Científico |
| Fonte: | JOURNAL OF THE ENDOCRINE SOCIETY; v. 8, n. 1, p. 10-pg., 2023-12-01. |
| Resumo | |
Context: Confirmatory tests represent a fundamental step in primary aldosteronism (PA) diagnosis, but they are laborious and often require a hospital environment due to the risks involved.Objective: To evaluate the efficacy of oral furosemide as a new confirmatory test for PA diagnosis.Methods: We prospectively evaluated the diagnostic performance of 80 mg of oral furosemide in 64 patients with PA and 22 with primary hypertension (controls). Direct renin concentration (DRC) was measured before, and 2 hours and 3 hours after the oral furosemide. In addition, the oral furosemide test was compared with 2 other confirmatory tests: the furosemide upright test (FUT) and saline infusion test (SIT) or captopril challenge test (CCT) in all patients with PA.Results: The cut-off of 7.6 mu U/mL for DRC at 2 hours after oral furosemide had a sensitivity of 92%, specificity of 82%, and accuracy of 90% for PA diagnosis. In 5 out of 6 controls with low-renin hypertension, which might represent a PA spectrum, renin remained suppressed. Excluding these 6 controls with low-renin hypertension, the DRC cut-off of 10 mu U/mL at 2 hours after oral furosemide had a sensitivity of 95.3%, specificity of 93.7% and accuracy of 95% for PA diagnosis. DRC after 3 hours of oral furosemide did not improve diagnostic performance. Using the cut-off of 10 mu U/mL, the oral furosemide test and the FUT were concordant in 62 out of 64 (97%) patients with PA. Only 4 out of 64 cases with PA (6.4%) ended the oral furosemide test with potassium <3.5 mEq/L. Hypotension was not evidenced in any patient with PA during the test.Conclusion: The oral furosemide test was safe, well-tolerated and represents an effective strategy for PA investigation. (AU) | |
| Processo FAPESP: | 21/10101-5 - Investigação de novas alterações genética associadas à patogênese dos Aldosteronomas por sequenciamento exômico |
| Beneficiário: | Augusto Garcia Guimarães |
| Modalidade de apoio: | Bolsas no Brasil - Doutorado Direto |
| Processo FAPESP: | 21/11240-9 - Sequenciamento completo do exoma para investigação de novas causas genéticas dos Feocromocitomas e Paragangliomas metastáticos |
| Beneficiário: | Felipe Freitas de Castro |
| Modalidade de apoio: | Bolsas no Brasil - Pós-Doutorado |
| Processo FAPESP: | 21/10363-0 - Sequenciamento completo do exoma para investigação de novas causas genéticas do Hiperaldosteronismo primário causado por hiperplasia adrenal bilateral |
| Beneficiário: | Lucas Santos de Santana |
| Modalidade de apoio: | Bolsas no Brasil - Pós-Doutorado |
| Processo FAPESP: | 19/15873-6 - Investigação de novos aspectos genéticos, clínicos e anatomopatológicos da hipertensão arterial de origem endócrina |
| Beneficiário: | Madson Queiroz Almeida |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |
| Processo FAPESP: | 21/09879-1 - Investigação clínica e genética da associação entre Hiperaldosteronismo Primário e Câncer Papilífero de Tireoide |
| Beneficiário: | Ana Alice Wolf Maciel |
| Modalidade de apoio: | Bolsas no Brasil - Doutorado Direto |