Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis

Abstract Objective: Cystic fibrosis diagnosis is dependent on the chloride ion concentration in the sweat test (≥ 60 mEq/mL - recognized as the gold standard indicator for cystic fibrosis diagnosis). Moreover, the salivary glands express the CFTR protein in the same manner as sweat glands. Given this context, the objective was to verify the correlation of saliva chloride concentration and sweat chloride concentration, and between saliva sodium concentration and sweat sodium concentration, in patients with cystic fibrosis and healthy control subjects, as a tool for cystic fibrosis diagnosis. Methods: There were 160 subjects enrolled: 57/160 (35.70%) patients with cystic fibrosis and two known CFTR mutations and 103/160 (64.40%) healthy controls subjects. Saliva ion concentration was analyzed by ABL 835 Radiometer® equipment and, sweat chloride concentration and sweat sodium concentration, respectively, by manual titration using the mercurimetric procedure of Schales & Schales and flame photometry. Statistical analysis was performed by the chi-squared test, the Mann -Whitney test, and Spearman's correlation. Alpha = 0.05. Results: Patients with cystic fibrosis showed higher values of sweat chloride concentration, sweat sodium concentration, saliva chloride concentration, and saliva sodium concentration than healthy controls subjects (p-value < 0.001). The correlation between saliva chloride concentration and sweat chloride concentration showed a positive Spearman's Rho (correlation coefficient) = 0.475 (95% CI = 0.346 to 0.587). Also, the correlation between saliva sodium concentration and sweat sodium concentration showed a positive Spearman's Rho = 0.306 (95% CI = 0.158 to 0.440). Conclusions: Saliva chloride concentration and saliva sodium concentration are candidates to be used in cystic fibrosis diagnosis, mainly in cases where it is difficult to achieve the correct sweat amount, and/or CFTR mutation screening is difficult, and/or reference methods for sweat test are unavailable to implement or are not easily accessible by the general population.

Saved in:
Bibliographic Details
Main Authors: Gonçalves,Aline Cristina, Marson,Fernando Augusto Lima, Mendonça,Regina Maria Holanda, Bertuzzo,Carmen Sílvia, Paschoal,Ilma Aparecida, Ribeiro,José Dirceu, Ribeiro,Antônio Fernando, Levy,Carlos Emílio
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Pediatria 2019
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572019000500443
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S0021-75572019000500443
record_format ojs
spelling oai:scielo:S0021-755720190005004432019-09-09Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosisGonçalves,Aline CristinaMarson,Fernando Augusto LimaMendonça,Regina Maria HolandaBertuzzo,Carmen SílviaPaschoal,Ilma AparecidaRibeiro,José DirceuRibeiro,Antônio FernandoLevy,Carlos Emílio CFTR protein CFTR mutation Cystic fibrosis Electrophysiology Ionic concentration Sweat test Abstract Objective: Cystic fibrosis diagnosis is dependent on the chloride ion concentration in the sweat test (≥ 60 mEq/mL - recognized as the gold standard indicator for cystic fibrosis diagnosis). Moreover, the salivary glands express the CFTR protein in the same manner as sweat glands. Given this context, the objective was to verify the correlation of saliva chloride concentration and sweat chloride concentration, and between saliva sodium concentration and sweat sodium concentration, in patients with cystic fibrosis and healthy control subjects, as a tool for cystic fibrosis diagnosis. Methods: There were 160 subjects enrolled: 57/160 (35.70%) patients with cystic fibrosis and two known CFTR mutations and 103/160 (64.40%) healthy controls subjects. Saliva ion concentration was analyzed by ABL 835 Radiometer® equipment and, sweat chloride concentration and sweat sodium concentration, respectively, by manual titration using the mercurimetric procedure of Schales & Schales and flame photometry. Statistical analysis was performed by the chi-squared test, the Mann -Whitney test, and Spearman's correlation. Alpha = 0.05. Results: Patients with cystic fibrosis showed higher values of sweat chloride concentration, sweat sodium concentration, saliva chloride concentration, and saliva sodium concentration than healthy controls subjects (p-value < 0.001). The correlation between saliva chloride concentration and sweat chloride concentration showed a positive Spearman's Rho (correlation coefficient) = 0.475 (95% CI = 0.346 to 0.587). Also, the correlation between saliva sodium concentration and sweat sodium concentration showed a positive Spearman's Rho = 0.306 (95% CI = 0.158 to 0.440). Conclusions: Saliva chloride concentration and saliva sodium concentration are candidates to be used in cystic fibrosis diagnosis, mainly in cases where it is difficult to achieve the correct sweat amount, and/or CFTR mutation screening is difficult, and/or reference methods for sweat test are unavailable to implement or are not easily accessible by the general population.info:eu-repo/semantics/openAccessSociedade Brasileira de PediatriaJornal de Pediatria v.95 n.4 20192019-08-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572019000500443en10.1016/j.jped.2018.04.005
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Gonçalves,Aline Cristina
Marson,Fernando Augusto Lima
Mendonça,Regina Maria Holanda
Bertuzzo,Carmen Sílvia
Paschoal,Ilma Aparecida
Ribeiro,José Dirceu
Ribeiro,Antônio Fernando
Levy,Carlos Emílio
spellingShingle Gonçalves,Aline Cristina
Marson,Fernando Augusto Lima
Mendonça,Regina Maria Holanda
Bertuzzo,Carmen Sílvia
Paschoal,Ilma Aparecida
Ribeiro,José Dirceu
Ribeiro,Antônio Fernando
Levy,Carlos Emílio
Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis
author_facet Gonçalves,Aline Cristina
Marson,Fernando Augusto Lima
Mendonça,Regina Maria Holanda
Bertuzzo,Carmen Sílvia
Paschoal,Ilma Aparecida
Ribeiro,José Dirceu
Ribeiro,Antônio Fernando
Levy,Carlos Emílio
author_sort Gonçalves,Aline Cristina
title Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis
title_short Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis
title_full Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis
title_fullStr Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis
title_full_unstemmed Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis
title_sort chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis
description Abstract Objective: Cystic fibrosis diagnosis is dependent on the chloride ion concentration in the sweat test (≥ 60 mEq/mL - recognized as the gold standard indicator for cystic fibrosis diagnosis). Moreover, the salivary glands express the CFTR protein in the same manner as sweat glands. Given this context, the objective was to verify the correlation of saliva chloride concentration and sweat chloride concentration, and between saliva sodium concentration and sweat sodium concentration, in patients with cystic fibrosis and healthy control subjects, as a tool for cystic fibrosis diagnosis. Methods: There were 160 subjects enrolled: 57/160 (35.70%) patients with cystic fibrosis and two known CFTR mutations and 103/160 (64.40%) healthy controls subjects. Saliva ion concentration was analyzed by ABL 835 Radiometer® equipment and, sweat chloride concentration and sweat sodium concentration, respectively, by manual titration using the mercurimetric procedure of Schales & Schales and flame photometry. Statistical analysis was performed by the chi-squared test, the Mann -Whitney test, and Spearman's correlation. Alpha = 0.05. Results: Patients with cystic fibrosis showed higher values of sweat chloride concentration, sweat sodium concentration, saliva chloride concentration, and saliva sodium concentration than healthy controls subjects (p-value < 0.001). The correlation between saliva chloride concentration and sweat chloride concentration showed a positive Spearman's Rho (correlation coefficient) = 0.475 (95% CI = 0.346 to 0.587). Also, the correlation between saliva sodium concentration and sweat sodium concentration showed a positive Spearman's Rho = 0.306 (95% CI = 0.158 to 0.440). Conclusions: Saliva chloride concentration and saliva sodium concentration are candidates to be used in cystic fibrosis diagnosis, mainly in cases where it is difficult to achieve the correct sweat amount, and/or CFTR mutation screening is difficult, and/or reference methods for sweat test are unavailable to implement or are not easily accessible by the general population.
publisher Sociedade Brasileira de Pediatria
publishDate 2019
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572019000500443
work_keys_str_mv AT goncalvesalinecristina chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
AT marsonfernandoaugustolima chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
AT mendoncareginamariaholanda chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
AT bertuzzocarmensilvia chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
AT paschoalilmaaparecida chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
AT ribeirojosedirceu chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
AT ribeiroantoniofernando chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
AT levycarlosemilio chlorideandsodiumionconcentrationsinsalivaandsweatasamethodtodiagnosecysticfibrosis
_version_ 1756375969005830144