Your browser doesn't support javascript.
loading
Clinical manifestations and associated factors in acquired hypoaldosteronism in endocrinological practice.
Ruiz-Sánchez, Jorge Gabriel; Calle-Pascual, Alfonso Luis; Rubio-Herrera, Miguel Ángel; De Miguel Novoa, María Paz; Gómez-Hoyos, Emilia; Runkle, Isabelle.
Afiliación
  • Ruiz-Sánchez JG; Servicio de Endocrinología y Nutrición, Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD, UAM), Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
  • Calle-Pascual AL; Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain.
  • Rubio-Herrera MÁ; Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain.
  • De Miguel Novoa MP; Servicio de Endocrinología y Nutrición, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Hospital Clínico San Carlos, Madrid, Spain.
  • Gómez-Hoyos E; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Madrid, Spain.
  • Runkle I; Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain.
Front Endocrinol (Lausanne) ; 13: 990148, 2022.
Article en En | MEDLINE | ID: mdl-36303866
Introduction: Hypoaldosteronism can be congenital or acquired, isolated or part of primary adrenal insufficiency, and caused by an aldosterone deficit, resistance, or a combination of both. Reduced mineralocorticoid action can induce a decrease in urine K+ and H+ excretion and an increase in urine Na+ excretion, leading to hyperkalemia, and/or hyponatremia, often combined with metabolic acidosis. We aimed to characterize the clinical manifestations of hypoaldosteronism, and their associated factors. Methods: Retrospective analysis of 112 episodes of hypoaldosteronism diagnosed in 86 adult patients from 2012-2019 by the Endocrinology and Nutrition Department of a tertiary hospital. The frequency of hyperkalemia, hypovolemic hyponatremia (HH) and metabolic acidosis (MA), and their associated factors were evaluated. Results: Patients had a median age of 77 [65 - 84], 55.4% were male. 94.6% cases showed hyperkalemia, 54.5% HH, and 60.3% MA. The mean serum K+ of all cases was 5.4 ± 0.5 mmol/L, Na+: 132.1 ± 6.3 mmol/L, HCO3: 22.6 ± 3.3 mmol/L. Hypoaldosteronism was isolated in the majority of cases: only 6/112 (5%) had primary adrenal insufficiency. Hypovolemia was associated with hyponatremia and a more florid clinical presentation. HH was associated with a combined presence of aldosterone-lowering and mineralocorticoid resistance factors. MA was associated with the presence of mineralocorticoid resistance factors. Conclusions: Hypoaldosteronism in adult endocrinological clinical practice is primarily isolated, and acquired. It predisposes not only to the development of hyperkalemia and MA, but also to that of HH. Hypoaldosteronism must be considered in the differential diagnosis of HH with urinary sodium wasting.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Acidosis / Hipoaldosteronismo / Enfermedad de Addison / Hiperpotasemia / Hiponatremia Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2022 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Acidosis / Hipoaldosteronismo / Enfermedad de Addison / Hiperpotasemia / Hiponatremia Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2022 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza