Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory Findings

Although the number of patients reaching end-stage kidney disease without a biopsy- proven diagnosis is increasing, kidney biopsies play a key role in diagnosing kidney disease. We analyzed prospective data from patients with kidney disease who underwent percutaneous native kidney biopsies from Janu...

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Main Authors: Ehab Mohammed, Issa Al Salmi, Ahmed Atris, Mohammed Al Ghonaim, Shilpa Ramaiah, Suad Hannawi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Saudi Journal of Kidney Diseases and Transplantation
Online Access:http://www.sjkdt.org/article.asp?issn=1319-2442;year=2022;volume=33;issue=3;spage=380;epage=392;aulast=Mohammed
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author Ehab Mohammed
Issa Al Salmi
Ahmed Atris
Mohammed Al Ghonaim
Shilpa Ramaiah
Suad Hannawi
author_facet Ehab Mohammed
Issa Al Salmi
Ahmed Atris
Mohammed Al Ghonaim
Shilpa Ramaiah
Suad Hannawi
author_sort Ehab Mohammed
collection DOAJ
description Although the number of patients reaching end-stage kidney disease without a biopsy- proven diagnosis is increasing, kidney biopsies play a key role in diagnosing kidney disease. We analyzed prospective data from patients with kidney disease who underwent percutaneous native kidney biopsies from January 2006 to December 2017. Demographic data, clinical presentations, and the laboratory and radiological findings at the time of biopsy were analyzed. Of 530 patients, 42.8% were male. The mean age was 33.9 (32.8–34.9.2) years; 66.3% were aged 25–64 years. Edema was the main clinical presentation (61.9%), with clinical urine changes seen in 66.7%. Most (89.6%) were nondiabetic; 46.8% had high blood pressure or were on antihypertensive therapy. Most patients (77.5%) were in Stages I, II, and III, and 12.3% underwent hemodialysis at the time of admission. Most (54.4%) were obese. Low hemoglobin (31.8%), high triglycerides (30%), high total cholesterol (58.2%), low serum albumin (73.9%), nephrotic proteinuria (61.8.6%), and microscopic hematuria (79.8%) were the main laboratory findings. The immunological investigations showed that antinuclear antibodies, positive anti-double-stranded DNA (anti–dsDNA), and extractable nuclear antigens were positive in 29.6%, 20.7%, and 19.7%, respectively. Perinuclear antineutrophil cytoplasmic antibodies (ANCA) were positive in 9.6% and cytoplasmic ANCA were positive in 5.4%, whereas immunoglobulin A was detected in 4.6%. More than one- third of the patients had reached advanced chronic kidney disease (CKD) Stages IIIB, IV, and V. This indicates the need to increase awareness about CKD, greater utilization of kidney biopsies, and earlier investigations to enable accurate diagnoses, and proper and timely management.
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spelling doaj.art-fe4d90bf01a04ede98988ee32b33059d2023-10-30T11:57:41ZengWolters Kluwer Medknow PublicationsSaudi Journal of Kidney Diseases and Transplantation1319-24422022-01-0133338039210.4103/1319-2442.385961Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory FindingsEhab MohammedIssa Al SalmiAhmed AtrisMohammed Al GhonaimShilpa RamaiahSuad HannawiAlthough the number of patients reaching end-stage kidney disease without a biopsy- proven diagnosis is increasing, kidney biopsies play a key role in diagnosing kidney disease. We analyzed prospective data from patients with kidney disease who underwent percutaneous native kidney biopsies from January 2006 to December 2017. Demographic data, clinical presentations, and the laboratory and radiological findings at the time of biopsy were analyzed. Of 530 patients, 42.8% were male. The mean age was 33.9 (32.8–34.9.2) years; 66.3% were aged 25–64 years. Edema was the main clinical presentation (61.9%), with clinical urine changes seen in 66.7%. Most (89.6%) were nondiabetic; 46.8% had high blood pressure or were on antihypertensive therapy. Most patients (77.5%) were in Stages I, II, and III, and 12.3% underwent hemodialysis at the time of admission. Most (54.4%) were obese. Low hemoglobin (31.8%), high triglycerides (30%), high total cholesterol (58.2%), low serum albumin (73.9%), nephrotic proteinuria (61.8.6%), and microscopic hematuria (79.8%) were the main laboratory findings. The immunological investigations showed that antinuclear antibodies, positive anti-double-stranded DNA (anti–dsDNA), and extractable nuclear antigens were positive in 29.6%, 20.7%, and 19.7%, respectively. Perinuclear antineutrophil cytoplasmic antibodies (ANCA) were positive in 9.6% and cytoplasmic ANCA were positive in 5.4%, whereas immunoglobulin A was detected in 4.6%. More than one- third of the patients had reached advanced chronic kidney disease (CKD) Stages IIIB, IV, and V. This indicates the need to increase awareness about CKD, greater utilization of kidney biopsies, and earlier investigations to enable accurate diagnoses, and proper and timely management.http://www.sjkdt.org/article.asp?issn=1319-2442;year=2022;volume=33;issue=3;spage=380;epage=392;aulast=Mohammed
spellingShingle Ehab Mohammed
Issa Al Salmi
Ahmed Atris
Mohammed Al Ghonaim
Shilpa Ramaiah
Suad Hannawi
Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory Findings
Saudi Journal of Kidney Diseases and Transplantation
title Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory Findings
title_full Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory Findings
title_fullStr Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory Findings
title_full_unstemmed Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory Findings
title_short Late Presentation for Kidney Biopsy: Clinical Presentations and Laboratory Findings
title_sort late presentation for kidney biopsy clinical presentations and laboratory findings
url http://www.sjkdt.org/article.asp?issn=1319-2442;year=2022;volume=33;issue=3;spage=380;epage=392;aulast=Mohammed
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AT ahmedatris latepresentationforkidneybiopsyclinicalpresentationsandlaboratoryfindings
AT mohammedalghonaim latepresentationforkidneybiopsyclinicalpresentationsandlaboratoryfindings
AT shilparamaiah latepresentationforkidneybiopsyclinicalpresentationsandlaboratoryfindings
AT suadhannawi latepresentationforkidneybiopsyclinicalpresentationsandlaboratoryfindings