Literature DB >> 1626916

Variation of sweat sodium and chloride with age in cystic fibrosis and normal populations: further investigations in equivocal cases.

J M Kirk1, M Keston, I McIntosh, S al Essa.   

Abstract

Patients attending cystic fibrosis clinics had sweat sodium and chloride concentrations measured, were reassessed clinically and had DNA studies performed. Sweat test results were compared with a matched control population. In both populations sweat sodium increased with age up to 12 years, and did not change significantly thereafter. The age-related increase was significantly less in the cystic fibrosis group. Sweat chloride increased with age in normal, but not in cystic fibrosis children. After age 12 years there was no age-related change in the normal group, and a fall with age in the cystic fibrosis group. Sweat chloride provided the best discrimination between normal and cystic fibrosis populations and this was particularly important in older subjects. Combining sweat sodium and chloride results did not improve discrimination. Nine patients were identified with equivocal sweat chloride results. DNA studies showed six of these subjects were heterozygous for the delta F508 mutation in the cystic fibrosis gene. Clinical assessment did not always resolve cases with borderline sweat chloride results.

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Year:  1992        PMID: 1626916     DOI: 10.1177/000456329202900204

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  11 in total

1.  Australian guidelines for the performance of the sweat test for the diagnosis of cystic fibrosis: report from the AACB Sweat Testing Working Party.

Authors:  John Coakley; Sue Scott; James Doery; Ronda Greaves; Peter Talsma; Elaine Whitham; Janet Winship
Journal:  Clin Biochem Rev       Date:  2006-05

2.  The limitations of sweat electrolyte reference intervals for the diagnosis of cystic fibrosis: a systematic review.

Authors:  Avantika Mishra; Ronda Greaves; John Massie
Journal:  Clin Biochem Rev       Date:  2007-05

3.  P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population.

Authors:  A Gilfillan; J P Warner; J M Kirk; T Marshall; A Greening; L P Ho; T Hargreave; B Stack; D McIntyre; R Davidson; J C Dean; W Middleton; D J Brock
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

4.  The relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era.

Authors:  Avantika Mishra; Ronda Greaves; John Massie
Journal:  Clin Biochem Rev       Date:  2005-11

5.  Indirect measurements of sweat electrolyte concentration in the laboratory diagnosis of cystic fibrosis.

Authors:  M E Heeley; D A Woolf; A F Heeley
Journal:  Arch Dis Child       Date:  2000-05       Impact factor: 3.791

Review 6.  Working Up a Good Sweat - The Challenges of Standardising Sweat Collection for Metabolomics Analysis.

Authors:  Joy N Hussain; Nitin Mantri; Marc M Cohen
Journal:  Clin Biochem Rev       Date:  2017-02

7.  Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype.

Authors:  V Dumur; R Gervais; J M Rigot; E Delomel-Vinner; B Decaestecker; J J Lafitte; P Roussel
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

Review 8.  Detection of cystic fibrosis transmembrane conductance regulator activity in early-phase clinical trials.

Authors:  Steven M Rowe; Frank Accurso; John P Clancy
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

9.  Sources of Variation in Sweat Chloride Measurements in Cystic Fibrosis.

Authors:  Joseph M Collaco; Scott M Blackman; Karen S Raraigh; Harriet Corvol; Johanna M Rommens; Rhonda G Pace; Pierre-Yves Boelle; John McGready; Patrick R Sosnay; Lisa J Strug; Michael R Knowles; Garry R Cutting
Journal:  Am J Respir Crit Care Med       Date:  2016-12-01       Impact factor: 21.405

10.  Performance Evaluation of a New Coulometric Endpoint Method in Sweat Testing and Its Comparison With Classic Gibson&Cooke and Chloridometer Methods in Cystic Fibrosis.

Authors:  Yasemin Gokdemir; Pinar Vatansever; Bulent Karadag; Tuncay Seyrekel; Ozgur Baykan; Nilay Bas Ikızoglu; Refika Ersu; Fazilet Karakoc; Goncagul Haklar
Journal:  Front Pediatr       Date:  2018-05-22       Impact factor: 3.418

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