Table 3

Demographic and clinical data of subjects bearing the [p.Ile148Thr;p.Ile1023_Val1024del] complex allele or the p.Ile148Thr mutation

GenderCurrent age (years)DiagnosisAge at diagnosis/enrolment (years/months)Cause of diagnosis/enrolmentAllele 1Allele 2SCL* (mmol/L)Current FEV1† (%)Pancreatic statusCFTR gating (%)Other complications
M31CF8 yearsRespiratoryp.[Ile148Thr;Ile1023_Val1024del]p.Phe508del6691PI7.7CFRD; Pa col.; nasal polyposis; bronchiectasis
FDied (34)CF6 yearsRespiratoryp.[Ile148Thr;Ile1023_Val1024del]p.Phe508del11224PI7.8CFRD; Pa col.
MDied (14)CF2 monthsNBSp.[Ile148Thr;Ile1023_Val1024del]p.Lys684SerfsX389169PIn.a.Cirrhosis; Pa col.
FDied (13)CF2 monthsNBSp.[Ile148Thr;Ile1023_Val1024del]p.Asn1303Lys10145PI6.5Cirrhosis; CFRD; Pa col.
F18CF6 monthsRespiratoryp.[Ile148Thr;Ile1023_Val1024del]p.Gly85Glu8067PIn.a.Recurrent pancreatitis; IGT; Pa col.; DIOS
F39Healthy37 yearsFamiliarityp.Ile148ThrP.Phe508del12n.a.PSn.a.
M46Healthy39 yearsFamiliarityp.Ile148ThrP.Phe508del11n.a.PS42.3
F41Healthy41 yearsFamiliarityp.Ile148ThrP.Phe508del15n.a.PS41.0
M50Healthy38 yearsFamiliarityp.Ile148Thrc.579+1G>T15n.a.PS56.0
M32Healthy32 yearsFamiliarityp.Ile148ThrNn.a.n.a.n.a.87.4
M28Healthy28 yearsFamiliarityp.Ile148ThrNn.a.n.a.n.a.86.3
  • *For patients with CF, we reported SCL at diagnosis while for healthy subjects we reported current SCL.

  • †For patients who had died, we reported the last FEV1 available.

  • CF, cystic fibrosis; CFRD, cystic fibrosis-related diabetes; DIOS, distal intestine obstruction syndrome; FEV1, forced expiratory volume in 1 second; IGT, impaired glucose tolerance; n.a., not assessed; N, wild-type allele; NBS, newborn screening; Pa col., Pseudomonas aeruginosa chronic colonisation; PI, pancreatic insufficiency; PS, pancreatic sufficiency; SCL, sweat chloride level.