Literature DB >> 19445912

Does the Macroduct collection system reliably define sweat chloride concentration in subjects with intermediate results?

J B Rose1, L Ellis, B John, S Martin, T Gonska, M Solomon, E Tullis, M Corey, K Adeli, P R Durie.   

Abstract

OBJECTIVES: The sweat test remains the current diagnostic gold standard for CF disease. Many CF testing centres have switched from the Gibson and Cooke to the Macroduct. Since the validity and sensitivity of Macroduct has not been tested in patients with intermediate sweat chloride concentrations, we compared both methods simultaneously including subjects expected to have intermediate results. DESIGN AND METHODS: We prospectively evaluated controls, obligate heterozygotes, patients with CF and with an uncertain diagnosis of CF (congenital absence of the vas deferens, pancreatitis and sinopulmonary disease).
RESULTS: We assessed 82 subjects (3.7-60.1 years); 14 healthy controls, 7 obligate heterozygotes, 20 CF (15 pancreatic insufficient, 5 pancreatic sufficient), and 41 with unproven diagnosis. Mean test difference was close to 0 (95% CI+/-20 mmol/L) and test values were highly correlated (r=0.93, p < or =0.0001). Discrepancies between the two testing methods occurred in 22% of subjects.
CONCLUSION: Sweat chloride measured by Macroduct highly correlates with Gibson and Cooke for concentrations in all ranges, including the intermediate range. This study reveals the limitations of sweat testing for excluding a diagnosis of CF since 38% of subjects had intermediate range results.

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Year:  2009        PMID: 19445912     DOI: 10.1016/j.clinbiochem.2009.05.001

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  3 in total

1.  Ivacaftor in subjects with cystic fibrosis who are homozygous for the F508del-CFTR mutation.

Authors:  Patrick A Flume; Theodore G Liou; Drucy S Borowitz; Haihong Li; Karl Yen; Claudia L Ordoñez; David E Geller
Journal:  Chest       Date:  2012-09       Impact factor: 9.410

2.  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

3.  Soft, skin-interfaced sweat stickers for cystic fibrosis diagnosis and management.

Authors:  Tyler R Ray; Maja Ivanovic; Paul M Curtis; Daniel Franklin; Kerem Guventurk; William J Jeang; Joseph Chafetz; Hannah Gaertner; Grace Young; Steve Rebollo; Jeffrey B Model; Stephen P Lee; John Ciraldo; Jonathan T Reeder; Aurélie Hourlier-Fargette; Amay J Bandodkar; Jungil Choi; Alexander J Aranyosi; Roozbeh Ghaffari; Susanna A McColley; Shannon Haymond; John A Rogers
Journal:  Sci Transl Med       Date:  2021-03-31       Impact factor: 17.956

  3 in total

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