Nephrotic proteinuria in hypertensive nephrosclerosis: Clinical and evolution characteristics

Nàdia Martín Alemany, Jaume Almirall Daly, Ruth Orellana Fernández, Xavier Andreu

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Abstract

Background and objective Nephrotic range proteinuria can occur in patients with biopsy proven hypertensive nephrosclerosis (HN). We analysed the differential clinical and evolution characteristics of these patients compared with other glomerular diseases.Material and method This is a case-control descriptive analysis obtained from the renal pathology registry of our hospital. Clinical features, treatment and evolution of these patients (cases) were compared with nephrotic patients with other glomerular diseases (controls).Results Five point one percent of biopsies with HN diagnosis. Case/control characteristics were: proteinuria 4.7 [3-11.4] versus 5.5 [3-28.1] g/24 h/1.73 m2 (P = NS). Normal albumin compared with controls (39.5 [6.4] versus 29.4 [10] g/dL; P =.001), significant oedemas only in 10 versus 63% of controls. HN were older (58.8 [12.6] versus 45.5 [19.6] years), had longer hypertension duration before renal biopsy and more previous cardiovascular events (39 versus 16%). Mean blood pressure was higher (166/90 versus 133/75 mmHg; P =.01) and had worse renal outcome.Conclusions HN must be included in the differential diagnosis of nephrotic range proteinuria in hypertensive patients. The absence of oedema and normal serum albumin are distinctive clinical characteristics that can help in decision-making before performing a renal biopsy. © 2013 Elsevier España, S.L.U.
Original languageEnglish
Pages (from-to)392-394
JournalMedicina Clinica
Volume143
Issue number9
DOIs
Publication statusPublished - 1 Jan 2014

Keywords

  • Hipertensión
  • Nefroangioesclerosis
  • Palabras clave
  • Síndrome nefrótico

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    Martín Alemany, N., Almirall Daly, J., Orellana Fernández, R., & Andreu, X. (2014). Nephrotic proteinuria in hypertensive nephrosclerosis: Clinical and evolution characteristics. Medicina Clinica, 143(9), 392-394. https://doi.org/10.1016/j.medcli.2013.09.015