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1.
Pediatr Pulmonol ; 56(7): 2023-2028, 2021 07.
Article in English | MEDLINE | ID: mdl-33822490

ABSTRACT

Sweat chloride (Cl- ) concentration is the gold standard for diagnosing cystic fibrosis (CF). This is, however, challenging among patients with borderline values. Previous studies have reported that the sweat Cl- /Na+ ratio may be useful for diagnosing CF; however, little is known about Cl- /K+ and (Cl- + Na+ )/K+ ratios. This study aimed to retrospectively define the most appropriate outcome of the sweat test. Samples of sweat were collected using the Gibson and Cooke method. Cl- , Na+ , and K+ were further quantified in 2084 participants-1283 CF and 801 non-CF-based on clinical diagnosis. Among those with borderline sweat Cl- values (n = 502), 34.8% had CF. In the receiver operating characteristic curve analysis, the area under the curve was calculated to evaluate the diagnostic value of the ion ratios. In the overall population, all the ratios significantly discriminated CF from non-CF, whereas in the borderline group, only Cl- /Na+ significantly discriminated CF and non-CF subjects, regardless of age.


Subject(s)
Cystic Fibrosis , Sweat , Chlorides , Cystic Fibrosis/diagnosis , Cystic Fibrosis Transmembrane Conductance Regulator , Humans , Retrospective Studies , Sodium
2.
J Cyst Fibros ; 15(5): 579-82, 2016 09.
Article in English | MEDLINE | ID: mdl-27423539

ABSTRACT

BACKGROUND: When cystic fibrosis (CF) is suspected Nasal Potential Difference (NPD) measurements are proposed to support controversial diagnosis: we investigated appropriate outcomes at the CF Centre of Verona. SUBJECTS/METHODS: NPD were measured in 196 subjects: 50 non-CF, 65 classical CF (the reference group) and 81 with uncertain CF (case group). Discriminating power was determined by comparison between several outcomes from the CF reference group versus non-CF: basal, amiloride, 0Cl, isoproterenol, ATP, Delta-amiloride, Delta-0Cl, Delta-isoproterenol, Delta-ATP, Delta-isoproterenol+Delta-0Cl, Wilschanski Index (WI) and Sermet score (SS). The most appropriate cut-off values for variables with the best discriminating power were then applied to the case group. Descriptive statistics, logistic regression models and ROC curve analysis were applied. RESULTS: WI and SS were the most powerful in discriminating CF from non-CF subjects. In the reference group sensitivity of the 0.82 WI cut-off was 98%, specificity 96%; both sensitivity and specificity of the -0.44 SS cut-off value were 100%. For the case group, WI and SS were, respectively, consistent with CF diagnosis in 94% and 92% of the cases. CONCLUSIONS: Formulae have the highest discriminating power and can support the diagnosis in uncertain cases; they should be utilized for standardized interpretation of NPD for diagnosis and possibly for clinical research.


Subject(s)
Amiloride/pharmacology , Cystic Fibrosis/diagnosis , Electric Conductivity , Isoproterenol/pharmacology , Mucus/metabolism , Sweat , Adrenergic beta-Agonists/pharmacology , Adult , Cystic Fibrosis Transmembrane Conductance Regulator/genetics , Diagnosis, Differential , Discriminant Analysis , Epithelial Sodium Channel Blockers/pharmacology , Female , Genetic Testing/methods , Humans , Male , Membrane Potentials , Nasal Mucosa/drug effects , Nasal Mucosa/metabolism , ROC Curve , Sensitivity and Specificity , Sweat/chemistry , Sweat/metabolism
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