| Literature DB >> 33925441 |
Won Jung Choi1, Yu A Hong1, Ji Won Min2, Eun Sil Koh3, Hyung Duk Kim4, Tae Hyun Ban5, Young Soo Kim6, Yong Kyun Kim7, Seok Joon Shin8, Seok Young Kim1, Young Ok Kim6, Chul Woo Yang4, Yoon-Kyung Chang1.
Abstract
Hyperuricemia is a significant risk factor for cardiovascular morbidity and chronic kidney disease progression. IgA nephropathy (IgAN) is a well-known primary glomerular nephropathy. Hyperuricemia is associated with a poor prognosis in IgAN patients. We evaluated the association of hyperuricemia with the histopathological severity of IgAN in male and female patients; 658 patients diagnosed with IgAN via kidney biopsy were initially included. Baseline patient data were collected by eight university hospitals affiliated with the College of Medicine of the Catholic University of Korea. Pathological features were independently evaluated by eight expert pathologists working in the hospitals, and the consensus was reached. Of the initial 658 patients, 517 were finally included (253 males and 264 females). Hyperuricemia was defined as a serum uric acid (UA) level >7.0 mg/dL for males and >5.6 mg/dL for females; 108 (42.7%) males and 95 (35.9%) females exhibited hyperuricemia. Compared to the patients with normal UA levels, the global glomerulosclerosis, segmental sclerosis, mesangial matrix expansion (MME), endocapillary proliferation (ECP), interstitial fibrosis (IF), and tubular atrophy (TA) scores were higher in hyperuricemic males and females. In multivariable linear regression, the serum UA level correlated significantly with the MME, ECP, IF, and TA scores of female IgAN patients only.Entities:
Keywords: IgA nephropathy; glomerular sclerosis; kidney biopsy; mesangial matrix expansion; uric acid
Year: 2021 PMID: 33925441 DOI: 10.3390/jcm10091885
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241