SP152SHORT TERM EFFECTS OF PREDNISONE TREATMENT ON PROTEINURIA AND RENAL FUNCTION IN IGA NEPHROPATHY: RELATION WITH OXFORD CLASSIFICATION

2016 ◽  
Vol 31 (suppl_1) ◽  
pp. i136-i136
Author(s):  
Enoc Merino-Garcia ◽  
F.J. Borrego-Utiel ◽  
M.P. Perez-Del-Barrio ◽  
Manuel Polaina-Rusillo ◽  
M.C. Sanchez-Perales
2011 ◽  
Vol 34 (5) ◽  
pp. 435-444 ◽  
Author(s):  
Timothy Yau ◽  
Stephen M. Korbet ◽  
Melvin M. Schwartz ◽  
David J. Cimbaluk

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yoei Miyabe ◽  
Kazunori Karasawa ◽  
Kenichi Akiyama ◽  
Shota Ogura ◽  
Tomo Takabe ◽  
...  

AbstractThe Oxford classification of IgA nephropathy (IgAN) can evaluate each MEST-C score individually. We analysed a new grading system that utilised the total MEST-C score in predicting renal prognosis. Altogether, 871 IgAN patients were classified into three groups using the new Oxford classification system (O-grade) that utilised the total MEST-C score (O-grade I: 0–1, II: 2–4, and III: 5–7 points), and the 10-year renal prognosis was analysed. The clinical findings became significantly severer with increasing O-grades, and the renal survival rate by the Kaplan–Meier method was 94.1%, 86.9%, and 74.1% for O-grades I, II, and III, respectively. The hazard ratios (HRs) for O-grades II and III with reference to O-grade I were 2.8 (95% confidence interval [CI] 1.3–6.0) and 6.3 (95% CI 2.7–14.5), respectively. In the multivariate analysis, mean arterial pressure and eGFR, proteinuria at the time of biopsy, treatment of corticosteroids/immunosuppressors, and O-grade (HR 1.63; 95% CI 1.11–2.38) were the independent factors predicting renal prognosis. Among the nine groups classified using the O-grade and Japanese clinical-grade, the renal prognosis had an HR of 15.2 (95% CI 3.5–67) in the severest group. The O-grade classified by the total score of the Oxford classification was associated with renal prognosis.


2011 ◽  
Vol 12 (1) ◽  
Author(s):  
Kisara Onda ◽  
Isao Ohsawa ◽  
Hiroyuki Ohi ◽  
Mariko Tamano ◽  
Satoshi Mano ◽  
...  

2009 ◽  
Vol 76 (11) ◽  
pp. 1207 ◽  
Author(s):  
Gary S. Hill ◽  
Dominique Nochy ◽  
Khalil El Karoui

Author(s):  
K. Fukushi ◽  
H. Yamabe ◽  
K. Ozawa ◽  
H. Ohsawa ◽  
N. Chiba ◽  
...  

2021 ◽  
Author(s):  
Yong-Zhe Zhang ◽  
Geng Jian ◽  
Ping He ◽  
Rui Yu ◽  
Mi Tian ◽  
...  

Abstract Background: Wilson disease (WD) is a rare genetic disorder of copper metabolism. The difference in copper tissue accumulation lead to various clinical manifestations, including some atypical presentations. The complex clinical picture makes it easy to miss and misdiagnose, even delay the best chance for treatment. Case presentation: A 26-year-old male patient who had nephritis-range proteinuria and elevated serum creatinine. The renal pathology indicated Immunoglobulin A (IgA) nephropathy and tubular injury which was inconsistent with glomerular lesions. Cirrhosis was also detected by imaging examination. Considering both kidney injury and liver damage, WD was suspected. According to further detected results of abnormal copper metabolism, corneal Kayser-Fleischer rings(K-F rings), and genetic disorder of ATP7B gene, he was finally diagnosed as a case of WD.The patient was given oral penicillamine and zinc sulfate daily and he was also prescribed losartan to control proteinuria on the premise of monitoring renal function and blood pressure. During the 2 years follow-up, the patient’s 24h uric cooper dropped to normal. The sign of tremor hands disappeared. The Urine protein and renal function keep stable. The patient had normal liver function and maintained good quality of daily life. Conclusions: In some cases, IgA nephropathy patients with suspicious and unexplained neurological and liver symptoms cannot be ignored. They may eventually be diagnosed with WD.


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