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Clinical and histopathological spectrum of IgA nephropathy in Kuwait
BACKGROUND: Little is known about the nature and the course of IgA nephropathy (IgAN) in Arab countries. The aim of this work was to study the spectrum of clinical presentation and histopathological findings at our institution. DESIGN AND SETTING: Retrospective review, all renal biopsies at the Muba...
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102474/ https://www.ncbi.nlm.nih.gov/pubmed/21403411 http://dx.doi.org/10.4103/0256-4947.77491 |
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author | Ghani, Amal Abdel Al Waheeb, Salah Al Homoud, Ekhlas Al Helal, Bassam Hussain, Naser |
author_facet | Ghani, Amal Abdel Al Waheeb, Salah Al Homoud, Ekhlas Al Helal, Bassam Hussain, Naser |
author_sort | Ghani, Amal Abdel |
collection | PubMed |
description | BACKGROUND: Little is known about the nature and the course of IgA nephropathy (IgAN) in Arab countries. The aim of this work was to study the spectrum of clinical presentation and histopathological findings at our institution. DESIGN AND SETTING: Retrospective review, all renal biopsies at the Mubarak Al Kabeer Hospital between January 2000 and December 2004. METHODS: Cases of IgA nephropathy were selected, and their medical records and biopsy findings were reviewed. RESULTS: Eighty patients (9.2% of all native kidney biopsies) were diagnosed to have IgAN nephropathy. Sixty-nine biopsies were included in the study;11 were excluded. Forty-three (62.3%) patients were male and 26 (37.7) patients were female. Fifty (72.5%) patients were below the age of 40 years. Mean (SD) duration of follow-up was 3.6 (1.3) years. The first presentation included nephritic-range proteinuria (49.3%) and renal impairment (50.7%). During the follow-up period, 56 (81.2%) patients were stable or improved. Hass classification of biopsies showed 36.2% had class I, 27.5% had class II, 13.0% had class III, 5.8% had class IV, and 17.4% had class V IgAN. Females had milder forms of the disease than males. Macroscopic hematuria and renal impairment at presentation were seen more in patients with class IV and V IgAN. The presenting serum creatinine and uric acid values were higher in those with Hass classes III to V. Deterioration of renal function during the follow-up period was more significant in the presence of hypertension, renal impairment, or macroscopic hematuria at the time of biopsy . CONCLUSION: The prevalence of IgAN in Kuwait is about 9.2%. Renal impairment or macroscopic hematuria at presentation was seen in patients with more aggressive renal lesions and contributed to poor outcome. |
format | Text |
id | pubmed-3102474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31024742011-06-14 Clinical and histopathological spectrum of IgA nephropathy in Kuwait Ghani, Amal Abdel Al Waheeb, Salah Al Homoud, Ekhlas Al Helal, Bassam Hussain, Naser Ann Saudi Med Original Article BACKGROUND: Little is known about the nature and the course of IgA nephropathy (IgAN) in Arab countries. The aim of this work was to study the spectrum of clinical presentation and histopathological findings at our institution. DESIGN AND SETTING: Retrospective review, all renal biopsies at the Mubarak Al Kabeer Hospital between January 2000 and December 2004. METHODS: Cases of IgA nephropathy were selected, and their medical records and biopsy findings were reviewed. RESULTS: Eighty patients (9.2% of all native kidney biopsies) were diagnosed to have IgAN nephropathy. Sixty-nine biopsies were included in the study;11 were excluded. Forty-three (62.3%) patients were male and 26 (37.7) patients were female. Fifty (72.5%) patients were below the age of 40 years. Mean (SD) duration of follow-up was 3.6 (1.3) years. The first presentation included nephritic-range proteinuria (49.3%) and renal impairment (50.7%). During the follow-up period, 56 (81.2%) patients were stable or improved. Hass classification of biopsies showed 36.2% had class I, 27.5% had class II, 13.0% had class III, 5.8% had class IV, and 17.4% had class V IgAN. Females had milder forms of the disease than males. Macroscopic hematuria and renal impairment at presentation were seen more in patients with class IV and V IgAN. The presenting serum creatinine and uric acid values were higher in those with Hass classes III to V. Deterioration of renal function during the follow-up period was more significant in the presence of hypertension, renal impairment, or macroscopic hematuria at the time of biopsy . CONCLUSION: The prevalence of IgAN in Kuwait is about 9.2%. Renal impairment or macroscopic hematuria at presentation was seen in patients with more aggressive renal lesions and contributed to poor outcome. Medknow Publications 2011 /pmc/articles/PMC3102474/ /pubmed/21403411 http://dx.doi.org/10.4103/0256-4947.77491 Text en Copyright: © Annals of Saudi Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ghani, Amal Abdel Al Waheeb, Salah Al Homoud, Ekhlas Al Helal, Bassam Hussain, Naser Clinical and histopathological spectrum of IgA nephropathy in Kuwait |
title | Clinical and histopathological spectrum of IgA nephropathy in Kuwait |
title_full | Clinical and histopathological spectrum of IgA nephropathy in Kuwait |
title_fullStr | Clinical and histopathological spectrum of IgA nephropathy in Kuwait |
title_full_unstemmed | Clinical and histopathological spectrum of IgA nephropathy in Kuwait |
title_short | Clinical and histopathological spectrum of IgA nephropathy in Kuwait |
title_sort | clinical and histopathological spectrum of iga nephropathy in kuwait |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102474/ https://www.ncbi.nlm.nih.gov/pubmed/21403411 http://dx.doi.org/10.4103/0256-4947.77491 |
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