Postek Magdalena, Zybert Katarzyna, Wozniacki Lukasz, Woynarowski Marek, Sands Dorota
Cystic Fibrosis Department, Institute of Mother and Child, 01-211 Warsaw, Poland.
Cystic Fibrosis Centre, Pediatric Hospital, 05-092 Dziekanow Lesny, Poland.
J Clin Med. 2025 Aug 26;14(17):6020. doi: 10.3390/jcm14176020.
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. : Forceps rectal biopsies were taken from 40 patients (CF; = 17 mean age 9.10 ± 4.18 (0.7-17.20); CRMS/CFSPID: = 16, mean age 6.66 ± 4.83 (0.6-18.0); healthy controls (HC): = 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), 3-isobutyl-1-methylxanthine with forskolin (ΔIsc), and histamine (Δisc) stimulation. Cumulative secretion was calculated for each study group. : We obtained statistically significant differences in cumulative chloride secretory response between CF and CRMS/CFSPID (CF ΔIsc 15.32 ± 15.47 µA/cm vs. CRMS/CFSPID ΔIsc 86.84 ± 37.84 µA/cm; < 0.001), and between CF and healthy controls (CF ΔIsc 15.32 ± 15.47 µA/cm vs. HC ΔIsc 80.16 ± 48.54 µA/cm; = 0.005). No differences in cumulative chloride secretion were observed between the CRMS/CFSPID and HC groups. : The conducted study suggests that ICM may offer diagnostic value, especially in cases where sweat test results are equivocal.
术语“囊性纤维化跨膜传导调节因子相关代谢综合征/囊性纤维化筛查阳性、诊断不确定(CRMS/CFSPID)”指筛查试验呈阳性但最终未确诊为囊性纤维化(CF)的患者。肠道电流测量(ICM)是一种新型诊断技术,可记录囊性纤维化跨膜传导调节因子的异常功能。我们的研究旨在比较波兰CF患者、CRMS/CFSPID人群以及对照组在ICM研究中的累积氯化物分泌反应。:对40名患者进行直肠活检钳取组织(CF组:n = 17,平均年龄9.10 ± 4.18岁(0.7 - 17.20岁);CRMS/CFSPID组:n = 16,平均年龄6.66 ± 4.83岁(0.6 - 18.0岁);健康对照组(HC):n = 7,平均年龄23.7 ± 9.5岁(7.8 - 34.6岁)。根据欧洲囊性纤维化协会诊断网络工作组的标准方案版本2.7在尤斯灌流小室中进行ICM测试。在使用卡巴胆碱(ΔIsc)、3 - 异丁基 - 1 - 甲基黄嘌呤与福斯可林(ΔIsc)以及组胺(Δisc)刺激后测量短路电流变化量(ΔIsc)。计算每个研究组的累积分泌量。:我们发现CF组与CRMS/CFSPID组之间在累积氯化物分泌反应上存在统计学显著差异(CF组ΔIsc为15.32 ± 15.47 μA/cm,CRMS/CFSPID组ΔIsc为86.84 ± 37.84 μA/cm;P < 0.001),CF组与健康对照组之间也存在差异(CF组ΔIsc为15.32 ± 15.47 μA/cm,HC组ΔIsc为80.16 ± 48.54 μA/cm;P = 0.005)。CRMS/CFSPID组与HC组之间未观察到累积氯化物分泌的差异。:所进行的研究表明,ICM可能具有诊断价值,尤其是在汗液试验结果不明确的情况下。