Abnormal electrochemical skin conductance in cystic fibrosis

Journal of Cystic Fibrosis

Volumn 10, Issue 1, 2011, Pages 15-20

  Hubert, Dominique ^a   Brunswick, Philippe ^b   Calvet, Jean Henri ^b   Dusser, Daniel ^a,c   Fajac, Isabelle ^a,c  

^a université Paris Cité   (France)

^b Impeto Medical   (France)

^c UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Cystic fibrosis; Electrochemical conductance; Sweat test

Indexed keywords

NICKEL;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; CYSTIC FIBROSIS; DIAGNOSTIC ACCURACY; ELECTRIC POTENTIAL; ELECTRODE; ELECTRODERMAL RESPONSE; FEMALE; HUMAN; HUMAN EXPERIMENT; MALE; SENSITIVITY AND SPECIFICITY; SKIN CONDUCTANCE;

ADULT; CHLORIDE CHANNELS; CHLORIDES; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DIAGNOSTIC TECHNIQUES AND PROCEDURES; ELECTRODES; FEMALE; GALVANIC SKIN RESPONSE; GENOTYPE; HUMANS; MALE; SENSITIVITY AND SPECIFICITY; SWEAT; SWEAT GLANDS; SWEATING;

EID: 78651431031     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcf.2010.09.002     Document Type: Article

References (19)

1. Rowe S.M., Miller S., Sorscher E.J. Cystic fibrosis. N Engl J Med 2005, 352:1992-2001.
2. Cheng S.H., Gregory R.J., Marshall J., Paul S., Souza D.W., White G.A., et al. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis. Cell 1990, 63:827-834.
3. Quinton P.M. Cystic fibrosis: a disease in electrolyte transport. FASEB J 1990, 4:2709-2717.
4. Riordan J.R., Rommens J.M., Kerem B.-S., Alon N., Rozmahel R., Grzelczak Z., et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 1989, 245:1066-1073.
5. Stutts M.J., Canessa C.M., Olsen J.C., Hamrick M., Cohn J.A., Rossier B.C., et al. CFTR as a cAMP-dependent regulator of sodium channels. Science 1995, 269:847-850.
6. Gibson L.E., Cooke R.E. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis. Pediatrics 1959, 23:545-549.
7. Di Sant'Agnese P.A., Darling R.C., Perera G.A., Shea E. Abnormal electrolyte composition of sweat in cystic fibrosis of the pancreas; clinical significance and relationship to the disease. Pediatrics 1953, 12:549-563.
8. Baumer J.H. Evidence based guidelines for the performance of the sweat test for the investigation of cystic fibrosis in the UK. Arch Dis Child 2003, 88:1126-1127.
9. LeGrys V.A. Sweat testing for the diagnosis of cystic fibrosis: practical considerations. J Pediatr 1996, 129:892-897.
10. LeGrys V.A., Yankaskas J.R., Quittell L.M., Marshall B.C., Mogayzel P.J. Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelines. J Pediatr 2007, 151:85-89.
11. De Boeck K., Wilschanski M., Castellani C., Taylor C., Cuppens H., Dodge J., et al. Cystic fibrosis: terminology and diagnostic algorithms. Thorax 2006, 61:627-635.
12. Mayer-Hamblett N., Ramsey B.W., Kronmal R.A. Advancing outcome measures for the new era of drug development in cystic fibrosis. Proc Am Thorac Soc 2007, 4:370-377.
13. Quinton P.M. Chloride impermeability in cystic fibrosis. Nature 1983, 301:421-422.
14. Gonska T., Ip W., Turner D., Han W.S., Rose J., Durie P., et al. Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis. Thorax 2009, 64:932-938.
15. Brunswick P., Mayaudon H., Albin V., Lair V., Ringuede A., Cassir M. Use of Ni electrodes chronoamperometry for improved diagnostics of diabetes and cardiac diseases. Conf Proc IEEE Eng Med Biol Soc 2007, 2007:4544-4547.
16. Hubert D., Dusser D., Bry A., Fajac I. Evaluation of a new tool for measurement of sweat chloride concentration. J Cyst Fibrosis 2009, 8:S5.
17. Bland J.M., Altman D.G. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986, 1:307-310.
18. Chizmadzhev Y.A., Indenbom A.V., Kuzmin P.I., Galichenko S.V., Weaver J.C., Potts R.O. Electrical properties of skin at moderate voltages: contribution of appendageal macropores. Biophys J 1998, 74:843-856.
19. Quinton P.M. Cystic fibrosis: lessons from the sweat gland. Physiology (Bethesda) 2007, 22:212-225.