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A Quick Guide to the
Mutation1717-1G–›A
C F T R S C I E N C E
© 2016 Vertex Pharmaceuticals Incorporated | VXR-HQ-02-00045a(1) | 03/2016
Loss of CFTR activity is the underlying cause of cystic fibrosis (CF)1
• People with 2 CFTR mutations resulting in loss of CFTR activity generally have a CF phenotype, which may include1-3,6
– Elevated sweat chloride (>60 mmol/L)
– Pancreatic insufficiency
– CBAVD a
– Lung function decline over time
– Pseudomonas aeruginosa colonization
aCBAVD, congenital bilateral absence of the vas deferens.
References: 1. Davis PB et al. Am J Respir Crit Care Med. 1996;154(5):1229-1256. 2. Rowe SM et al. Proc Am Thorac Soc. 2007;4(4):387-398. 3. Zielenski J. Respiration. 2000;67(2):117-133. 4. Sheppard DN et al. Nature. 1993;362(6416):160-164. 5. Welsh MJ, Smith AE. Cell. 1993;73(7): 1251-1254. 6. Castellani C et al. J Cyst Fibros. 2008;7(3):179-196.
Some CFTR mutations result in little to no CFTR activity3-5
0% 100%
Total CFTR Activity
0% 100%
Total CFTR Activity
Some CFTR mutations result in residual or partial CFTR activity3-5
Spectrum of Phenotypes Associated With Total CFTR Activity1,2
Total CFTR Activity
% of Normal
No CF Disease
CFTR-relatedDisorders
Cystic Fibrosis
Individuals with 2 normal alleles and CFTR mutation carriers
Clinical entities associated with CFTR dysfunctionthat do not fulfill diagnostic criteria for CF, e.g., CBAVD, acute recurrent or chronic pancreatitis and bronchiectasis
Typical phenotype: sinopulmonary disease, sweatchloride >60 mmol/L, pancreatic insufficiency, appearing early in life. In some patients, progressionof disease is delayed or not all features are present
100%
0%
Clinical Phenotype
2
Levels of CFTR activity affect survival in CF1
References: 1. McKone EF et al. Chest. 2006;130(5):1441-1447. 2. The World Bank. http://data.worldbank.org/indicator/SP.DYN.LE00.IN?page=2. Accessed November 12, 2015. 3. MacKenzie T et al. Ann Int Med. 2014;161:233-241.
1.00
0.75
0.50
0.25
0.00
0 10 20
Risk Time (Age)
Surv
ival
Pro
babi
lity
30 40 50
Residual CFTR activity (Class IV, V): R117H, R334W, R347P, 3849+10KbC–›T, 2789+5G–›A, A455E
Severely reduced CFTR activity (Class I, II, III): G542X, R553X, W1282X, R1162X, 621-IG–›T, 1717-1G–›A, 1078delT, 3659delC, I507del, N1303K, S549N, G85E, F508del, G551D, R560T
n=1126
n=14,525
• Life expectancy in Western countries (general population born in 2000) is ~79 years2
• Between 1993 and 2002, median survival for US patients with genotypes associated with little to no CFTR activity was 36.3 years (95% CI, 35.5 to 37.6 years), while median survival for those having genotypes associated with residual CFTR activity was 50 years (95% CI, 47.1 to 55.9 years)1
– In this study, patients with the 1717-1G–›A mutation (Class I) were part of the severely reduced CFTR activity group
• More recent US data (2000-2010) suggest median survival across genotypes continues to improve3
Survival Curves by CFTR Activity During a 10-Year Follow-Up (1993-2002) of Patients From the US CFF Registrya
a Data are from a retrospective study of patients enrolled in the Cystic Fibrosis Foundation patient registry measuring risk of death over a 10-year observation period from 1993 to 2002. Patients were grouped as having a high-risk or low-risk genotype based on the functional effects of their class of CFTR mutation on phenotype and mortality. Patients having a Class I, II, or III mutation on both alleles were considered high-risk, while patients having at least 1 Class IV or V mutation were categorized as low-risk. A total of 15,651 patients had a CFTR genotype of a known functional class; 14,525 (93%) had a high-risk CFTR genotype and 1126 (7%) had a low-risk CFTR genotype.1
This survival curve represents population-based outcomes.1 Individual outcomes in cystic fibrosis are variable.
Adapted with permission from McKone EF et al. Chest. 2006;130(5):1441-1447.
3
Country registries listing the 1717-1G–›A mutation report 0.1% to 3% prevalence among patients with CF1-10
• In the CFTR2 global database, ~1% of patients with CF have at least 1 copy of the 1717-1G–›A mutation11
Aus9: 2%
Brazil2: 0.1%
US1: 2%
Prevalence of the 1717-1G–›A Mutation in Patients With Cystic Fibrosis (% of Patients With at Least 1 Allele)
2%
2%
2%
2%
0.4%
Switzerland12
Italy13
Hungary13
Poland13
Canada14
Country % of Alleles
Additional sources report frequency of the 1717-1G–›A mutation on CF alleles
References: 1. Cystic Fibrosis Foundation. Cystic Fibrosis Foundation Patient Registry 2013 Annual Data Report. Bethesda, MD. © 2014; Cystic Fibrosis Foundation. 2. The Brazilian Cystic Fibrosis Study Group. Brazilian Cystic Fibrosis Patient Registry. 2012 Annual Report. 3. Belgisch Mucoviscidose Register – Registre Belge de la Mucoviscidose. The Belgian Cystic Fibrosis Registry. Summary Report 2011. © 2014; Institute of Public Health (WIV-ISP), Brussels, Belgium. 4. French Cystic Fibrosis Registry. Annual Report 2013. © Vaincre la Mucoviscidose and Ined, 2015; Paris, France. 5. Cystic Fibrosis Trust. UK Cystic Fibrosis Registry Annual Data Report 2014. © 2015; Cystic Fibrosis Trust; London, UK. 6. The Cystic Fibrosis Registry of Ireland. 2013 Annual Report. © CFRI, 2015; Dublin, Ireland. 7. Nederlandse Cystic Fibrosis Stichting. Dutch Cystic Fibrosis Patient Regristry. Report on the Year 2014. © 2015 NCFS. 8. Mukoviszidose e.V. und Mukoviszidose Institut gemeinnützige Gesselschaft für Forschung und Therapienntwicklung mbH. Beriichtsband Qualitätssicherung Mukoviszidose 2012. © 2013, Bonn, Germany. 9. Cystic Fibrosis Australia. Australian Cystic Fibrosis Data Registry 2013–16th Annual Report. © 2015; Cystic Fibrosis Australia; Baulkham Hills NSW, Australia. 10. PORT CFNZ National Data Registry, 2014 Registry Report, Cystic Fibrosis New Zealand. Christchurch, New Zealand. 11. US CF Foundation, Johns Hopkins University, The Hospital for Sick Children. The Clinical and Functional TRanslation of CFTR (CFTR2). http://www.cftr2.org. Accessed November 12, 2015. 12. European Cystic Fibrosis Society. ECFS Patient Registry 2010 Annual Data Report. 2014. 13. Bobadilla JL et al. Hum Mutat. 2002;19(2):575-606. 14. World Health Organization. The molecular genetic epidemiology of cystic fibrosis: report of a joint meeting of WHO/ECFTN/ICF(M)A/ECFS; June 19, 2002; Genoa, Italy. © World Health Organization; 2004.
Europe:Belgium3: 3%France4: 2% UK5: 1%Ireland6: 1%Netherlands7: 1% Germany8: 0.7%
New Zealand10: 0.5%
4
The 1717-1G–›A mutation results in defective biosynthesis of the CFTR protein1-3
References: 1. Hull J et al. Hum Mol Genet. 1993;2(6):689-692. 2. Green DM et al. Respir Res. 2010;11:140. doi: 10.1186/1465-9921-11-140. 3. Zielenski J. Respiration. 2000;67(2):117-133.
• 1717-1G–›A is a splice mutation, which produces a premature stop codon1
• The cell cannot synthesize a full-length CFTR protein, a Class I mutation1-3
• As a result, few to no CFTR proteins are present at the apical cell surface3
CFTR Processing
CFTR Synthesis
CFTR Trafficking
Endoplasmicreticulum
Proteosome
Golgicomplex
T
T
T
T
T
T
A
A
A
G
C
C
C
C
C
Rest ofCFTRgene
CFTR gene(DNA)
EndoplasmicReticulum
mRNA
DNA
CFTR gene
mRNA Pre-mRNA
RNA processing
Splicingdefect
Chromosome 7
DNA
Transcription
Illustrative Example of Class I Defect
CFTR Turnover
CFTR Function
5
The 1717-1G–›A allele results in little to no total CFTR activity1-5
Defective Synthesis (Class I)
1717-1G–›A allele results in few to no CFTR channels at
apical surface
Channel-open Probability: N/A Conductance: N/A
Little to No1717-1G–›A–CFTR
Activity
CFTR Function
A virtual absence of 1717-1G–›A-CFTR protein quantity…
…regardless of function since few to no CFTR proteins reach the surface…
…results in little to no total CFTR activity
References: 1. Hull J et al. Hum Mol Genet. 1993;2(6):689-692. 2. Green DM et al. Respir Res. 2010;11:14. doi: 10.1186/1465-9921-11-140. 3. Zielenski J. Respiration. 2000;67(2):117-133. 4. Welsh MJ, Smith AE. Cell. 1993;73(7):1251-1254. 5. Sheppard DN et al. Nature. 1993;362(3):160-164.
1
1
2
2
3
3
Total CFTR activity can be defined as total ion transport mediated by CFTR protein channels at the cell surface, depending on CFTR protein quantity and function.5
x x =
Channel-openProbability
Conductance
CFTR FunctionTotal
CFTR ActivityxCFTR Quantity x =
N/A, not applicable.
6
Both CFTR alleles play a role in determining phenotype or disease severity1-6
• A 1717-1G–›A allele results in little to no CFTR activity. The phenotype of a particular patient is also influenced by the mutation on the other allele1-6
• 1717-1G–›A typically results in the indicated phenotypes
No CF DiseaseNormal individuals and CF carriers
Cystic Fibrosis
CFTR-related DisorderClinical entities associated with CFTR dysfunction that do not fulfill diagnostic criteria for CF
Normal Normal Normal
Normal Residual
Residual Residual
Residual
Littleto None
Littleto None
Littleto None
Littleto None
Allele 1Total CFTR Activity
Allele 2Total CFTR Activity
TotalCFTR
Activity
0%
100%
References: 1. US CF Foundation, Johns Hopkins University, The Hospital for Sick Children. The Clinical and Functional TRanslation of CFTR (CFTR2). http://www.cftr2.org. Accessed November 12, 2015. 2. deGracia J et al. Thorax. 2005;60(7):558-563. 3. Cystic Fibrosis Genotype-Phenotype Consortium. N Engl J Med. 1993;329(18):1308-1313. 4. Davis PB et al. Am J Respir Crit Care Med. 1996;154(5):1229-1256. 5. Castellani C et al. J Cyst Fibros. 2008;7(3):179-196. 6. Zielenski J. Respiration. 2000;67(2):117-133.
Adapted from Zielenski J. Respiration. 2000;67(2): 117-133.
7
1717-1G–›A in combination with another allele that produces little to no CFTR activity usually results in a CF phenotype1-5
References: 1. US CF Foundation, Johns Hopkins University, The Hospital for Sick Children. The Clinical and Functional TRanslation of CFTR (CFTR2). http://www.cftr2.org. Accessed Novemebr 12, 2015. 2. deGracia J et al. Thorax. 2005;60(7): 558-563. 3. Cystic Fibrosis Genotype-Phenotype Consortium. N Engl J Med. 1993;329(18):1308-1313. 4. Davis PB et al. Am J Respir Crit Care Med. 1996;154(5):1229-1256. 5. Castellani C et al. J Cyst Fibros. 2008;7(3):179-196.
CF Phenotype In patients registered in the CFTR2 database with a 1717-1G–›A mutation on 1 allele and a pancreatic insufficient mutation on the second allele1
• Elevated sweat chloride (average):103 mmol/L
• Lung function decline over time
• Pseudomonas colonization: 54% of patients
• Pancreatic insufficiency: 97% of patients
Little to NoTotal CFTR
Activity
EnvironmentalFactors
Modifier Genes
Little to NoCFTR Protein
Activity
CFTR Genotype
Allele #1: 1717-1G–›A
Little to NoCFTR Protein
Activity
Allele #2
8
Summary• Loss of CFTR activity is the underlying cause of CF
• Levels of CFTR activity affect survival in CF
• Country registries listing the 1717-1G–›A mutation report 0.1% to 3% prevalence among patients with CF
• The 1717-1G–›A mutation results in defective biosynthesis of the CFTR protein
• The 1717-1G–›A allele results in little to no total CFTR activity
• Both CFTR alleles play a role in determining phenotype or disease severity
• 1717-1G–›A in combination with another allele that produces little to no CFTR activity usually results in a CF phenotype
9
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