Summary
Definition
History and exam
Key diagnostic factors
- hematúria
Other diagnostic factors
- proteinúria
- hipertensão
- edema
Risk factors
- história familiar de nefropatia por imunoglobulina A
- sexo masculino
- idade entre 20 e 30 anos
- ancestralidade asiática/branca/de nativos norte-americanos
- Vasculite por IgA
- doença hepática crônica
- Infecção pelo vírus da imunodeficiência humana (HIV)
Diagnostic tests
1st tests to order
- urinálise
- microscopia e cultura de urina
- bioquímica básica, incluindo taxa de filtração glomerular (TFG) estimada
- níveis dos complementos C3 e C4
- ultrassonografia renal
- tomografia computadorizada (RUB)
- biópsia renal
Tests to consider
- cistoscopia flexível
- biópsia de pele
Treatment algorithm
baixo risco de progressão
risco moderado de progressão
risco elevado de progressão
lesão renal aguda
Contributors
Authors
Jonathan Barratt, PhD, FRCP
The Mayer Professor of Renal Medicine
Department of Cardiovascular Sciences
University of Leicester
Honorary Consultant Nephrologist
John Walls Renal Unit
Leicester General Hospital
UK
Disclosures
JB has consultancies with Alnylam, argenx, Astellas, Calliditas, Chinook, Dimerix, Novartis, Omeros, Travere Therapeutics, Vera Therapeutics and Visterra. He is also an author of a number of references cited in this topic.
See Cheng Yeo, MBBS, M.Med (Int Med), FRCP (London), MD
Adjunct Assistant Professor
Head & Senior Consultant
Department of Renal Medicine
Tan Tock Seng Hospital
Singapore
Disclosures
SCY is an author of a reference cited in this topic.
Acknowledgements
Professor Jonathan Barratt and Dr See Cheng Yeo would like to gratefully acknowledge Dr Hani Bleibel and Dr Chike Nzerue, previous contributors to this topic.
Disclosures
HB and CN declare that they have no competing interests.
Peer reviewers
Richard Lafayette, MD
Associate Professor of Medicine
Nephrology Division
Stanford University Medical Center
Stanford
CA
Disclosures
RL declares that he has no competing interests.
Alan Salama, MA, MBBS, PhD, FRCP
Professor of Nephrology
UCL Centre for Nephrology
Royal Free Hospital
London
UK
Disclosures
AS declares that he has no competing interests.
Peer reviewer acknowledgements
BMJ Best Practice topics are updated on a rolling basis in line with developments in evidence and guidance. The peer reviewers listed here have reviewed the content at least once during the history of the topic.
Disclosures
Peer reviewer affiliations and disclosures pertain to the time of the review.
References
Key articles
Wyatt RJ, Julian BA. IgA nephropathy. N Engl J Med. 2013 Jun 20;368(25):2402-14. Abstract
Trimarchi H, Barratt J, Cattran DC, et al; IgAN Classification Working Group of the International IgA Nephropathy Network and the Renal Pathology Society; Conference Participants. Oxford Classification of IgA nephropathy 2016: an update from the IgA Nephropathy Classification Working Group. Kidney Int. 2017 May;91(5):1014-21. Abstract
Barratt J, Feehally J. Primary IgA nephropathy: new insights into pathogenesis. Semin Nephrol. 2011 Jul;31(4):349-60. Abstract
Kidney Disease: Improving Global Outcomes (KDIGO) Glomerular Diseases Work Group. KDIGO 2021 clinical practice guideline for the management of glomerular diseases. Kidney Int. 2021 Oct;100(4s):S1-S276.Full text Abstract
Lv J, Zhang H, Wong MG, et al; TESTING Study Group. Effect of oral methylprednisolone on clinical outcomes in patients with IgA nephropathy: the TESTING randomized clinical trial. JAMA. 2017 Aug 1;318(5):432-42. Abstract
Rauen T, Eitner F, Fitzner C, et al. Intensive supportive care plus immunosuppression in IgA nephropathy. N Engl J Med. 2015 Dec 3;373(23):2225-36.Full text Abstract
Tumlin JA, Hennigar RA. Clinical presentation, natural history, and treatment of crescentic proliferative IgA nephropathy. Semin Nephrol. 2004 May;24(3):256-68. Abstract
Reference articles
A full list of sources referenced in this topic is available to users with access to all of BMJ Best Practice.
Differentials
- Vasculite por IgA (conhecida como púrpura de Henoch-Schönlein [PHS])
- Doença da membrana basal glomerular fina
- Síndrome de Alport
More DifferentialsGuidelines
- KDIGO 2021 clinical practice guidelines for the management of glomerular diseases
More GuidelinesLog in or subscribe to access all of BMJ Best Practice
Use of this content is subject to our disclaimer