University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Seattle Children's Hospital, Seattle, WA, United States.
J Cyst Fibros. 2024 Jul;23(4):676-684. doi: 10.1016/j.jcf.2024.02.001. Epub 2024 Feb 15.
Sweat chloride (SC) concentrations in people with cystic fibrosis (PwCF) reflect relative CF transmembrane conductance regulator (CFTR) protein function, the primary CF defect. Populations with greater SC concentrations tend to have lesser CFTR function and more severe disease courses. CFTR modulator treatment can improve CFTR function within specific CF genotypes and is commonly associated with reduced SC concentration. However, SC concentrations do not necessarily fall to concentrations seen in the unaffected population, suggesting potential for better CFTR treatment outcomes. We characterized post-modulator SC concentration variability among CHEC-SC study participants by genotype and modulator.
PwCF receiving commercially approved modulators for ≥90 days were enrolled for a single SC measurement. Clinical data were obtained from chart review and the CF Foundation Patient Registry (CFFPR). Variability of post-modulator SC concentrations was assessed by cumulative SC concentration frequencies.
Post-modulator SC concentrations (n = 3787) were collected from 3131 PwCF; most (n = 1769, 47 %) were collected after elexacaftor/tezacaftor/ivacaftor (ETI) treatment. Modulator use was associated with lower SC distributions, with post-ETI concentrations the lowest on average. Most post-ETI SC concentrations were <60 mmol/L (79 %); 26 % were <30 mmol/L. Post-ETI distributions varied by genotype. All genotypes containing at least one F508del allele had individuals with post-ETI SC ≥60 mmol/L, with the largest proportion being F508del/minimal function (31 %).
Post-modulator SC concentration heterogeneity was observed among all genotypes and modulators, including ETI. The presence of PwCF with post-modulator SC concentrations within the CF diagnostic range suggests room for additional treatment-associated CFTR restoration in this population.
囊性纤维化(CF)患者的汗液氯化物(SC)浓度反映了相对 CF 跨膜电导调节剂(CFTR)蛋白功能,这是 CF 的主要缺陷。SC 浓度较高的人群往往 CFTR 功能较低,疾病过程更为严重。CFTR 调节剂治疗可改善特定 CF 基因型的 CFTR 功能,通常与 SC 浓度降低相关。然而,SC 浓度不一定降至未受影响人群的浓度,表明 CFTR 治疗的潜在效果更好。我们根据基因型和调节剂对 CHEC-SC 研究参与者的调节剂后 SC 浓度变异性进行了特征描述。
接受 ≥90 天商业批准调节剂治疗的 CF 患者入组进行单次 SC 测量。临床数据通过病历回顾和 CF 基金会患者登记处(CFFPR)获得。通过累积 SC 浓度频率评估调节剂后 SC 浓度的变异性。
从 3131 名 CF 患者中收集了调节剂后的 SC 浓度(n=3787);其中大多数(n=1769,47%)是在接受 elexacaftor/tezacaftor/ivacaftor(ETI)治疗后收集的。调节剂的使用与较低的 SC 分布相关,平均而言,ETI 后的浓度最低。大多数 ETI 后 SC 浓度均<60mmol/L(79%);26%<30mmol/L。ETI 后的分布因基因型而异。所有含有至少一个 F508del 等位基因的基因型都有 ETI 后 SC≥60mmol/L 的个体,其中以 F508del/最小功能型的比例最大(31%)。
所有基因型和调节剂,包括 ETI,都观察到调节剂后 SC 浓度的异质性。在该人群中,调节剂后 SC 浓度处于 CF 诊断范围内的 CF 患者的存在表明,在该人群中还可以通过治疗来恢复 CFTR。