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

<b>Background/Objectives:</b> 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. <b>Methods</b>: Forceps rectal biopsies were taken from 40 patients (CF; <i>n</i> = 17 mean age 9.10 ± 4.18 (0.7-17.20); CRMS/CFSPID: <i>n</i> = 16, mean age 6.66 ± 4.83 (0.6-18.0); healthy controls (HC): <i>n</i> = 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 (ΔIsc<sub>carbachol</sub>), 3-isobutyl-1-methylxanthine with forskolin (ΔIsc<sub>IBMX/forskolin</sub>), and histamine (Δisc<sub>histamine</sub>) stimulation. Cumulative secretion was calculated for each study group. <b>Results</b>: We obtained statistically significant differences in cumulative chloride secretory response between CF and CRMS/CFSPID (CF ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 15.32 ± 15.47 µA/cm<sup>2</sup> vs. CRMS/CFSPID ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 86.84 ± 37.84 µA/cm<sup>2</sup>; <i>p</i> < 0.001), and between CF and healthy controls (CF ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 15.32 ± 15.47 µA/cm<sup>2</sup> vs. HC ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 80.16 ± 48.54 µA/cm<sup>2</sup>; <i>p</i> = 0.005). No differences in cumulative chloride secretion were observed between the CRMS/CFSPID and HC groups. <b>Conclusions</b>: The conducted study suggests that ICM may offer diagnostic value, especially in cases where sweat test results are equivocal.

Authors

Institutions

Publication Details

Journal
Journal of Clinical Medicine
Published
2025-08-26
DOI
https://doi.org/10.3390/jcm14176020
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

K. Zybert, Łukasz Woźniacki, Marek Woynarowski, Magdalena Postek et al.
Journal of Clinical Medicine
Cystic Fibrosis Research Advances
article

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

K. Zybert, Łukasz Woźniacki, Marek Woynarowski, Magdalena Postek, Dorota Sands
article en

Abstract

<b>Background/Objectives:</b> 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. <b>Methods</b>: Forceps rectal biopsies were taken from 40 patients (CF; <i>n</i> = 17 mean age 9.10 ± 4.18 (0.7-17.20); CRMS/CFSPID: <i>n</i> = 16, mean age 6.66 ± 4.83 (0.6-18.0); healthy controls (HC): <i>n</i> = 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 (ΔIsc<sub>carbachol</sub>), 3-isobutyl-1-methylxanthine with forskolin (ΔIsc<sub>IBMX/forskolin</sub>), and histamine (Δisc<sub>histamine</sub>) stimulation. Cumulative secretion was calculated for each study group. <b>Results</b>: We obtained statistically significant differences in cumulative chloride secretory response between CF and CRMS/CFSPID (CF ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 15.32 ± 15.47 µA/cm<sup>2</sup> vs. CRMS/CFSPID ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 86.84 ± 37.84 µA/cm<sup>2</sup>; <i>p</i> < 0.001), and between CF and healthy controls (CF ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 15.32 ± 15.47 µA/cm<sup>2</sup> vs. HC ΔIsc<sub>carbachol+IBMX/forskolin+histamine</sub> 80.16 ± 48.54 µA/cm<sup>2</sup>; <i>p</i> = 0.005). No differences in cumulative chloride secretion were observed between the CRMS/CFSPID and HC groups. <b>Conclusions</b>: The conducted study suggests that ICM may offer diagnostic value, especially in cases where sweat test results are equivocal.

Journal of Clinical MedicineVol. 14(17)
Jan Kochanowski University (PL)
Openalex Percentile: Top 67%
Cystic Fibrosis Research Advances
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.