Literature DB >> 18728376

[Standardized sweat chloride analysis for the diagnosis of cystic fibrosis in Korea].

Sue Jung Kim1, Mingoo Lee, Seung-Ick Cha, Hwa Young Park, Kang Mo Ahn, Chang-Seok Ki, Jeong-Ho Kim.   

Abstract

BACKGROUND: Cystic fibrosis is a chronic progressive autosomal recessive disorder caused by the CFTR gene mutations. It is quite common in Caucasians, but very rare in Asians. Sweat chloride test is known to be a screening test for the cystic fibrosis due to the fact that electrolyte levels in sweat are elevated in patients. In this study, sweat chloride levels in Korean population were measured and analyzed by using standardized pilocarpine iontophoresis sweat chloride test.
METHODS: The sweat chloride test was performed in 47 patients referred to Yondong Severance Hospital from August, 2001 to April, 2007 and 41 healthy volunteers. The sweat chloride tests were conducted according to the CLSI C34-A2 guideline using pilocarpine iontophoresis method, and the chloride concentrations in sweat were measured by mercurimetric titration.
RESULTS: Four patients showed sweat chloride concentrations higher than 60 mmol/L. Reference interval was calculated as 1.4-44.5 mmol/L by analysis of the results of healthy volunteers (n=41). Four patients who exhibited high sweat chloride levels, had characteristic clinical features of cystic fibrosis and their diagnoses were confirmed either by repeated sweat chloride test or genetic analysis.
CONCLUSIONS: Standardized sweat chloride test can be utilized as a useful diagnostic tool for cystic fibrosis in Koreans. In cases of sweat chloride levels higher than 40 mmol/L, the test should be repeated for the possible diagnosis of cystic fibrosis. All the confirmed Korean cases of cystic fibrosis showed sweat chloride level above 60 mmol/L.

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Year:  2008        PMID: 18728376     DOI: 10.3343/kjlm.2008.28.4.274

Source DB:  PubMed          Journal:  Korean J Lab Med        ISSN: 1598-6535


  3 in total

1.  Heterogeneous spectrum of CFTR gene mutations in Korean patients with cystic fibrosis.

Authors:  Haiyoung Jung; Chang-Seok Ki; Won-Jung Koh; Kang-Mo Ahn; Sang-Il Lee; Jeong-Ho Kim; Jae Sung Ko; Jeong Kee Seo; Seung-Ick Cha; Eun-Sil Lee; Jong-Won Kim
Journal:  Korean J Lab Med       Date:  2011-06-28

2.  Chest CT Features of Cystic Fibrosis in Korea: Comparison with Non-Cystic Fibrosis Diseases.

Authors:  So Yeon Yang; Kyung Soo Lee; Min Jae Cha; Tae Jung Kim; Tae Sung Kim; Hyun Jung Yoon
Journal:  Korean J Radiol       Date:  2017-01-05       Impact factor: 3.500

3.  Multicenter Surveillance of Cystic Fibrosis in Korean Children.

Authors:  Hyung Young Kim; Soo-Jong Hong; Kangmo Ahn; Dong In Suh; Shin Hye Noh; Soo Yeon Kim; Jinho Yu; Jung Min Ko; Min Goo Lee; Kyung Won Kim
Journal:  Allergy Asthma Immunol Res       Date:  2022-09       Impact factor: 5.096

  3 in total

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