Literature DB >> 2915747

Cause of persistent hypouricemia in outpatients.

I Hisatome1, K Ogino, H Kotake, R Ishiko, M Saito, J Hasegawa, H Mashiba, S Nakamoto.   

Abstract

We measured serum urate in 3,258 Japanese outpatients. Five of them had persistent hypouricemia. Three also had microhematuria. Four of the five patients were proven to have renal uricosuria with hypouricemia, but otherwise normal tubular function. When tested with both pyrazinamide and benzbromarone, 1 patient had a presecretory reabsorption defect, 2 had postabsorption defects, and 1 an enhanced renal tubular secretion of urate. These results suggest that persistent hypouricemia in outpatients is of very low incidence, is usually caused by an isolated metabolic error of urate transport, and is not related to drug ingestion or systemic disease.

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Year:  1989        PMID: 2915747     DOI: 10.1159/000185233

Source DB:  PubMed          Journal:  Nephron        ISSN: 1660-8151            Impact factor:   2.847


  23 in total

Review 1.  Roles of organic anion transporters (OATs) and a urate transporter (URAT1) in the pathophysiology of human disease.

Authors:  Atsushi Enomoto; Hitoshi Endou
Journal:  Clin Exp Nephrol       Date:  2005-09       Impact factor: 2.801

2.  Homozygous frameshift mutation in the SLC22A12 gene in a patient with primary gout and high levels of serum uric acid.

Authors:  J Vázquez-Mellado; V Alvarado-Romano; R Burgos-Vargas; A L Jiménez-Vaca; G Pozo-Molina; S A Cuevas-Covarrubias
Journal:  J Clin Pathol       Date:  2007-08       Impact factor: 3.411

3.  Acute kidney injury after acute gastroenteritis in an infant with hereditary hypouricemia.

Authors:  Koichi Kamei; Masao Ogura; Shingo Ishimori; Hiroshi Kaito; Kazumoto Iijima; Shuichi Ito
Journal:  Eur J Pediatr       Date:  2013-05-08       Impact factor: 3.183

4.  Recurrent URAT1 gene mutations and prevalence of renal hypouricemia in Japanese.

Authors:  Tsutomu Takahashi; Satoko Tsuchida; Tasuku Oyamada; Tadashi Ohno; Masahiro Miyashita; Seiji Saito; Kazuo Komatsu; Kouei Takashina; Goro Takada
Journal:  Pediatr Nephrol       Date:  2005-03-17       Impact factor: 3.714

5.  A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1.

Authors:  Ayami Ochi; Takashi Takei; Akiko Ichikawa; Chiari Kojima; Takahito Moriyama; Mitsuyo Itabashi; Toshio Mochizuki; Atsuo Taniguchi; Kosaku Nitta
Journal:  Clin Exp Nephrol       Date:  2011-11-03       Impact factor: 2.801

6.  Uric acid levels in southern Germany in 1989. A comparison with studies from 1962, 1971, and 1984.

Authors:  U Gresser; B Gathof; N Zöllner
Journal:  Klin Wochenschr       Date:  1990-12-17

7.  Familial hypouricaemia due to an isolated tubular defect of urate reabsorption.

Authors:  D Barajas de Frutos; B Bravo Mancheño; N Palomino Urda; J Pedrero Vera
Journal:  Pediatr Nephrol       Date:  1993-02       Impact factor: 3.714

8.  The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia.

Authors:  Fusako Komoda; Takashi Sekine; Jun Inatomi; Atsushi Enomoto; Hitoshi Endou; Toshiyuki Ota; Takeshi Matsuyama; Tsutomu Ogata; Masahiro Ikeda; Midori Awazu; Koji Muroya; Isamu Kamimaki; Takashi Igarashi
Journal:  Pediatr Nephrol       Date:  2004-03-31       Impact factor: 3.714

Review 9.  Gout, uric acid and purine metabolism in paediatric nephrology.

Authors:  J S Cameron; F Moro; H A Simmonds
Journal:  Pediatr Nephrol       Date:  1993-02       Impact factor: 3.714

10.  Oxidative imbalance in idiopathic renal hypouricemia.

Authors:  Kazunari Kaneko; Naho Taniguchi; Yuko Tanabe; Takahide Nakano; Masafumi Hasui; Kandai Nozu
Journal:  Pediatr Nephrol       Date:  2008-10-21       Impact factor: 3.714

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