Work

Pilot Evaluation of Intestinal Current Measurement in Cystic Fibrosis and CRMS/CFSPID Patients in Poland

Year: 2025

Type: article

Abstract: Background/Objectives: The term ‘cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID)’ refers to patients with positive screening tests but without a final diagnosis of Cystic Fibrosis (CF). Intestinal Current Measurement (ICM) is a novel diagnostic technique that may document the abnormal function of the cystic fibrosis transmembrane conductance regulator. Our study aims to compare the cumulative chloride secretory response in the ICM study in the Polish population of CF patients, CRMS/CFSPID, and in a control group. Methods: Forceps rectal biopsies were taken from 40 patients (CF; n = 17 mean age 9.10 ± 4.18 (0.7–17.20); CRMS/CFSPID: n = 16, mean age 6.66 ± 4.83 (0.6–18.0); healthy controls (HC): n = 7, mean age 23.7 ± 9.5 (7.8–34.6). ICM tests were performed in the Ussing Chamber according to standard protocol version 2.7 of the European Cystic Fibrosis Society Diagnostic Network Working Group. Delta short circuit-current (ΔIsc) was measured after carbachol (ΔIsccarbachol), 3-isobutyl-1-methylxanthine with forskolin (ΔIscIBMX/forskolin), and histamine (Δischistamine) stimulation. Cumulative secretion was calculated for each study group. Results: We obtained statistically significant differences in cumulative chloride secretory response between CF and CRMS/CFSPID (CF ΔIsccarbachol+IBMX/forskolin+histamine 15.32 ± 15.47 µA/cm2 vs. CRMS/CFSPID ΔIsccarbachol+IBMX/forskolin+histamine 86.84 ± 37.84 µA/cm2; p < 0.001), and between CF and healthy controls (CF ΔIsccarbachol+IBMX/forskolin+histamine 15.32 ± 15.47 µA/cm2 vs. HC ΔIsccarbachol+IBMX/forskolin+histamine 80.16 ± 48.54 µA/cm2; p = 0.005). No differences in cumulative chloride secretion were observed between the CRMS/CFSPID and HC groups. Conclusions: The conducted study suggests that ICM may offer diagnostic value, especially in cases where sweat test results are equivocal.

Source: Journal of Clinical Medicine

DOI: 10.3390/jcm14176020

Authors: Magdalena Postek, Katarzyna Zybert, Lukasz Wozniacki, Marek Woynarowski, Dorota Sands

Institutions: Instytut Matki i Dziecka, Jan Kochanowski University

Language: English

Topic: Cystic Fibrosis Research Advances

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $3,137