Efficacy of Oral Furosemide Test for Primary Aldosteronism Diagnosis

Author:

Freitas Thais C1,Maciel Ana Alice W1,Fagundes Gustavo F C1,Petenuci Janaina1,Santana Lucas S1,Guimaraes Augusto G1,Freitas-Castro Felipe1,Srougi Victor2ORCID,Tanno Fabio Y2,Chambo Jose L2,Pereira Maria Adelaide A1,Brito Luciana P1,Pio-Abreu Andrea3,Bortolotto Luiz A4,Latronico Ana Claudia1,Fragoso Maria Candida B V56ORCID,Drager Luciano F34,Mendonca Berenice B5,Almeida Madson Q16ORCID

Affiliation:

1. Divisão de Endocrinologia e Metabologia, Hospital das Clínicas, Unidade de Adrenal, Laboratório de Endocrinologia Molecular e Celular LIM/25, Faculdade de Medicina da Universidade de São Paulo , São Paulo, 05403-000 , Brazil

2. Divisão de Urologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo , São Paulo, 05403-000 , Brazil

3. Unidade de Hipertensão, Disciplina de Nefrologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo , São Paulo, 05403-000 , Brazil

4. Unidade de Hipertensão, Instituto do Coração (InCor), Faculdade de Medicna da Universidade de São Paulo , São Paulo, 05403-900 , Brazil

5. Divisão de Endocrinologia e Metabologia, Laboratório de Hormônios e Genética Molecular LIM/42, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo , São Paulo, 05403-000 , Brazil

6. Divisão de Oncologia Endócrina, Instituto do Câncer do Estado de São Paulo (ICESP), Faculdade de Medicina da Universidade de São Paulo , São Paulo, 01246-000 , Brazil

Abstract

Abstract 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 µU/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 µU/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 µU/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.

Funder

Sao Paulo Research Foundation

National Council for Scientific and Technological Development

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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