Categories of ΔF508 homozygous cystic fibrosis twin and sibling pairs with distinct phenotypic characteristics
- 1 August 2000
- journal article
- Published by Cambridge University Press (CUP) in Twin Research
- Vol. 3 (04) , 277-293
- https://doi.org/10.1375/twin.3.4.277
Abstract
Cystic fibrosis (CF), the most common severe autosomal recessive trait among Caucasians, is caused by molecular lesions in the cystic fibrosis transmembrane conductance regulator gene (CFTR). The course of the multi-organ disease CF is highly variable, suggesting the influence of environmental factors and/or modulating genes other than CFTR on the disease phenotype. To evaluate the cause of CF disease variability, the European CF Twin and Sibling Study collected data on two clinical parameters most sensitive for the course and prognosis of CF, ie weight predicted for height (wfh)% (representative for the nutritional status) and FEVPerc (representative for the pulmonary status) for a cohort of 277 sibling pairs, 12 pairs of dizygous twins and 29 pairs of monozygous twins. Of these 318 CF twin and sib pairs, 114 were reported to be homozygous for the most frequent CF disease-causing lesion, ΔF508. Intra-pair discordance was assessed by the intra-pair differences with wfh% and FEVPerc and by DELTA, a composite parameter defined by linear combination of wfh% and FEVPerc in order to describe discordance with respect to the overall disease severity. Monozygous twins had a significantly lower DELTA than dizygous twins (P = 0.05) indicating that CF disease severity is modulated by an inherited component in addition to the CFTR gene itself. Extreme phenotypes are considered to be more informative for the analysis of any quantitative trait. Thus, we aimed to quantify disease severity and intra-pair discordance in order to select pairs with the extreme phenotypes DIS (discordant patient pairs), CON+ (concordant and mildy affected patient pairs) and CON− (concordant and severely affected patient pairs). The algorithm reliably discriminated between pairs DIS, CON+ and CON− among the cohort of ΔF508 homozygotes. The selected pairs from these categories demonstrated non-overlapping properties for wfh%, FEVPerc and the intra-pair difference of both parameters. Twin Research (2000) 3, 277–293.Keywords
This publication has 37 references indexed in Scilit:
- Distribution and heritability of BMI in Finnish adolescents aged 16 y and 17 y: A study of 4884 twins and 2509 singletonsInternational Journal of Obesity, 1999
- The influence of allotypes on the IgG subclass response to chromosomal β-lactamase of Pseudomonas aeruginosa in cystic fibrosis patientsClinical and Experimental Immunology, 1997
- Cystic fibrosis-related diabetes is associated with HLADQB1 alleles encoding Asp-57− moleculesJournal of Clinical Immunology, 1994
- Locating human quantitative trait loci: Guidelines for the selection of sibling pairs for genotypingBehavior Genetics, 1994
- Allotypes of α1‐antitrypsin in patients with cystic fibrosis, homozygous and heterozygous for deltaF508Pediatric Pulmonology, 1994
- Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutationThe Lancet, 1991
- Independent genetic determinants of pancreatic and pulmonary status in cystic fibrosisThe Lancet, 1990
- Gradient of distribution in Europe of the major CF mutation and of its associated haplotypeHuman Genetics, 1990
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and TorontoJournal of Clinical Epidemiology, 1988