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. Author manuscript; available in PMC: 2018 Dec 1.
Published in final edited form as: Pediatr Pulmonol. 2017 Oct 30;52(12):1550–1557. doi: 10.1002/ppul.23884

Table 3.

Ethnic Differences In FEV1 Percent Predicted By PERT Use, F508del copies, and CFTR Mutation Class

FEV1 In
Hispanic
Patients
FEV1 In
Non-Hispanic
White Patients
Difference In
FEV1 Percent
Predicted
95% CI p-value
Pancreatic Enzyme Replacement

Yes 79.3% 85.3% −6.0% −6.6% to −5.3% <0.001
No 87.7% 91.8% −4.1% −5.0% to −3.2% <0.001

F508del Copies

Homozygote 79.8% 85.1% −5.3% −7.0% to −5.6% <0.001
Heterozygote 80.8% 86.3% −5.7% −6.5% to −4.6% <0.001
No Copies 81.1% 88.7% −7.6% −8.3% to −7.0% <0.001

CFTR Mutation Class

Class I–III 79.0% 85.1% −6.1% −7.0% to −5.3% <0.001
Class IV–V 87.8% 93.7% −5.9% −7.7% to −4.0% <0.001
Unclassified 81.8% 87.5% −5.7% −6.5% to −5.0% <0.001
a)

F508del copies were defined as homozygotes, heterozygotes, or no copies. CFTR mutation class was defined as CFTR class I–III, CFTR class IV–V, and unclassified.

b)

Models included the variable of interest (PERT use, F508del copies, or CFTR mutation class) with ethnicity interaction, adjusted for age, sex, PERT, BMI, sweat chloride concentration, MRSA, Pseudomonas aeruginosa, maternal education level, insurance type, tobacco exposure, age at diagnosis, CF-related diabetes, CFTR mutation class, and location in U.S.