IgA Nephropathy: Presentation, Clinical Course, and Prognosis in Children and Adults

Robert J. Wyatt, Bruce A. Julian, Dinyar B. Bhathena, Bonnie L. Mitchell, Nancy H. Holland, Hartmut H. Malluche

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Abstract

Eighty-two patients, 56 male and 26 female, biopsied since 1972 had IgA nephropathy. At the time of kidney biopsy, 24 patients were children and 58 were adults. In both groups the clinical course was documented in sufficient detail to allow prediction of disease outcome. Twenty-six (45%) of the adult patients had chronic renal insufficiency either at first evaluation or subsequently. Fourteen eventually required chronic hemodialysis. Hypertension as the initial sign of disease was seen more frequently in patients with chronic renal insufficiency. Adult males were more likely to have chronic renal insufficiency. The life table method was used to predict age at initiation of dialysis and kidney survival from date of onset of clinically apparent disease. Thirty-five percent of the male patients were predicted to require dialysis by age 40. Kidney death was predicted at 10 years from onset for 33% of male and 22% of all patients biopsied as adults. While all patients with progressive disease had over 2.0 g/24 h urinary protein excretion at least once, many individuals with serum creatinine concentration below 1.5 mg/dL showed marked fluctuation in degree of proteinuria, often exceeding 2.0 g/24 h. Thus, in some cases, degree of proteinuria was not a reliable predictor of outcome.

Original languageEnglish
Pages (from-to)192-200
Number of pages9
JournalAmerican Journal of Kidney Diseases
Volume4
Issue number2
DOIs
StatePublished - 1984

Bibliographical note

Funding Information:
From the Department of Pediatrics, Department of Pathology, Division of Nephrology. Bone and Mineral Metabolism, and the Department of Medicine, University of Kentucky, College of Medicine, Lexington; the Department of M edicine, Central Baptist Hospital, Lexington, Kentucky; and the Department of Pathology, Wayne State University, School of Medicine, Detroit. Financial support: Clinical Investigator Award AM0777 (Dr Wyatt) from the National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases a nd A ward No. 114 from Dialysis Clinics, Inc (Dr Julian). Presented in part at the annual meeting of the American Society of Nephrology, December 3, 1982. Address reprint requests to Robert J. Wyatt, MD, University of Tennessee Center for H ealth Sciences, 956 Court, Room 3 B~, Memphis, TN 38163. © 1984 by The National Kidney Foundation, Inc. 0272-6386/84/020192-15$03.00/0

Keywords

  • IgA nephropathy
  • chronic renal insufficiency
  • glomerulonephritis

ASJC Scopus subject areas

  • Nephrology

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