Transcript Treatment of Cystic Fibrosis Lung Disease

Author: Richard H. Simon, M.D., 2008-2010
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Cystic Fibrosis
v
Fall 2008
Richard H. Simon
Pulmonary and Critical Care Medicine
Department of Internal Medicine
Objectives
Understand:
The genetic nature of cystic fibrosis (CF)
The pathophysiology of CF lung disease
Know how to diagnose CF
Learn the basic approach to treating CF
lung disease
Cystic Fibrosis
Inherited disease
Autosomal recessive
Gene cloned in 1989:
“CFTR”
Cystic Fibrosis
Transmembrane
conduction Regulator
1601 mutations in CFTR
known to cause CF
An extensive amount of
information is known
about CFTR
Science, September 1989
Schematic Representation of CFTR
Genetic Disorder Research Project Wiki Site
Pathophysiology of CF
Disease manifestations
?
CFTR Dysfunction
Lungs
Sinuses
Pancreas
Liver
Bones
Vas deferens
Airway Cross Sectional View
Mucus layer
Pericellular layer
with cilia
Epithelial cell layer
Knowles & Boucher 2002;109:571
Required Geometry for Effective
Mucociliary Clearance
Knowles & Boucher 2002;109:571
Pathophysiology of CF Lung Disease
Source Undetermined
Consequences of CFTR Deficiency on
Airway Clearance
Knowles & Boucher 2002;109:571
Pathophysiology of CF Lung Disease
CF Gene Mutation
Ion Transport Abnormalities
Altered Airway
Environment
Infection
Inflammation
Tissue
Damage
R. Simon
Pathophysiology of CF
Lung Disease
CF Gene Mutation
Recurrent Bronchitis
Bronchiectasis
Chronic Respiratory
Failure
Death
R. Simons
Source Undetermined
Prevalence of Infections in CF Patients
100
P. aeruginosa
Percent
80
60
S. aureus
40
H. influenza
MRSA
20
S. maltophilia
B. cepacia
0
0 to 1
2 to 5
6 to 10
11 to 17
18 to 24
Age (years)
Cystic Fibrosis Foundation Patient Registry Data. 2005
25 to 34
35 to 44
45+
Natural History of CF Lung Infections
Ps. aeruginosa or B. cepacia complex species
persist in the lung
True infection, not “colonization”
Difficulty in eradicating infection:
Intrinsic antibiotic resistance
Acquired antibiotic resistance
Poor antibiotic penetration into secretions
Alginate produced by mucoid Ps. (biofilms)
CF-related defects in mucosal (but not systemic)
defenses
Diagnostic criteria for cystic fibrosis
Part 1: Clinical Manifestation of Disease
At least one of the following:
1) One or more clinical manifestations of CF
Meconium ileus
Chronic bronchitis / bronchiectasis
Chronic infection of the paranasal sinuses
Pancreatic insufficiency
Salt loss syndromes
Male infertility due to congenital bilateral absence of the
vas deferens
2) Positive newborn screening test
3) History of CF in a sibling
Diagnostic Criteria for Cystic Fibrosis
Part 2: Laboratory evidence of CFTR abnormality
At least one of the following:
1)
Elevated sweat chloride test
2)
Identification of a mutation in each CFTR gene
known to cause CF
3)
In vivo demonstration of characteristic abnormalities
in ion transport across nasal epithelium (not widely
available)
Sweat Test for Diagnosis of CF
Controls
1500
n=4269
CF
1200
240
n=920
900
180
600
120
300
600
0
0
0
20
40
60
80
100
120
140
160
180
mEq/L
Shwachman H, Mahmoodian A. Mod Prob Pediatr 1967;10:158
Number of patients with CF
Number of normal controls
1800
Use of Genotyping to Diagnose CF
Population Frequency of Specific CFTR Mutations Causing CF
ΔF508
G542X
G551D
N1303K
W1282X
621+1G  T
R553X
1717-1G  A
R1162X
R117H
Δ I507
3849+10kbC  T
R347P
1601 CFTR
mutations known
to cause CF
Only 25
mutations have a
frequency > 0.1%
0
10
20
30
40
50
Frequency, %
CF Genetic Analysis Consortium
60
70
Genotyping for CF Diagnosis
Current commercial screening tests
Look for presence of between 25 - 100 mutations
These will detect a CF allele only ~90% of time
For a group of patients with known CF, genotyping
would be diagnostic in only ~81% of patients
 Screening for most common mutations is not as
sensitive as sweat testing (98%) to diagnose classic
CF
Genetic Diagnosis of CF
Tests becoming commercially available
for detecting mutations more broadly
PCR used to amplify all exons and
surrounding splice sites
Heteroduplex formation screening and/or
sequencing
Analysis for large deletions and duplications
Cost ~ $2,500
Acute Exacerbations of
CF Lung Disease
Symptoms
Increased cough with sputum production
Hemoptysis
Increased shortness of breath
Fever (not required)
Reduction in FEV1
Worsening infiltrates on chest x-ray (not
required)
Acute Exacerbations of
CF Lung Disease
Antibiotic treatment
Oral antibiotics
If symptoms are mild, and
Bacteria are susceptible
Intravenous antibiotics otherwise
Management of Chronic Lung Disease
in Cystic Fibrosis
Aerosolized Antibiotics
High dose tobramycin
proven for chronic
infection
TOBI® 300 mg in 5 ml bid
every other month
Ramsey B, et al. NEJM 1999;340:23-30
Mucolytic Therapy for CF
DNase
(Pulmozyme ®)
Chronic use
improves FEV1
and causes fewer
exacerbations
Fuchs HJ, et al. NEJM 1994;331:637-642
Bronchodilators in CF
No studies in acute exacerbations but
routinely given
Chronic use -- FEV1 improves acutely in
some patients
b-adrenergic agonists (e.g. albuterol,
salmeterol)
Anticholinergic agents (ipratroprium bromide,
tiotroprium)
Anti-Inflammatory Treatment in CF
Glucocorticoids
Oral (prednisone)
Preserves lung function, but too many adverse
effects
Inhaled
Used for subgroup of with bronchial hyperreactivity
(asthma) symptoms
Ibuprofen
Beneficial for young patients
No evidence for improvement in adults
Azithromycin in CF
Improved FEV1
Fewer exacerbations of
CF lung disease
Uncertain mechanism
of action
Anti-inflammatory?
Bacterial toxin or
biofilm production?
Change in FEV1 (% predicted)
Macrolide Therapy for CF
5
4
3
2
1
0
-1
-2
-3
-4
Azithromycin
Placebo
0
4
8
12
16
20
Study Week
Saiman L, et al. JAMA. 2003;290:1749-56
24
28
Nebulized Hypertonic Saline (7%)
Effect on FEV1
Randomized, doubleblind, placebo
controlled trial
N = 164
Inhalation of 4 ml of 7%
vs. 0.9% saline bid for
48 weeks
Elkins MR et al. N Engl J Med 2006;354:229-240
Effect of 7% Saline on Frequency of
Pulmonary Exacerbations
Elkins MR et al. N Engl J Med 2006;354:229-240
Physiotherapy for CF
No studies in acute exacerbations
But “standard of care” treatment
Beneficial for chronic management
Physiotherapy Options for CF
•Flutter
•Acapella
•PEP
•Vest
Supplemental Oxygen
Use same guidelines as COPD
Home Versus Hospital Therapy for
Acute Exacerbation
Home regimen must duplicate full hospital
program
IV drugs
Physiotherapy
Nutrition
Et cetera
Results from small studies showed mixed
results
Assisted Ventilation in CF
Past studies show very poor outcomes
Non-invasive ventilation being used as a
bridge to lung transplantation
Lung Transplantation CF
Bilateral lung transplantation
Outcome similar to non-CF
transplantation
Problems
Long waiting lists
Many exclusions
Living donor transplants
Number of Transplant Patients
Number of CF Patients With Lung
Transplants 1988 - 2005
200
178
180
153
146
137 135
160
140
120
92
100
161
151 142
134 141
131
104
80
55 53
60
40
20
13
5
6
0
88 89 90 91 92 93 94 95 96 97 98 99 00 01 02 03 04 05
Year
Source Undetermined
Median Predicted Survival for Cystic
Fibrosis
35
30
Age, yr
25
20
15
10
5
0
1940
Source Undetermined
1950
1960
1970
1980
Calendar Year
1990
2000
New Therapies for CF Under Development –
September 2007
Source Undetermined
Cystic Fibrosis 1989
Clip of Identification of the
Cystic Fibrosis Gene:
Chromosome Walking and
Jumping from Science,
September 1989, removed
Science, September 1989
Cystic Fibrosis Now
Image of
Dan Bessette, the child from
the September 1989 cover of
Science, a 19 year old college
sophomore in 2003
References
Simon RH. Treatment of CF lung disease.
UpToDate, 2008.
Davis P. Cystic Fibrosis Since 1938. Am J
Respir Crit Care Med 2006;173: 475-482.
Additional Source Information
for more information see: http://open.umich.edu/wiki/CitationPolicy
Slide 5: Science, September 1989
Slide 6: Genetic Disorder Research Project Wiki Site, http://runkle-science.wikispaces.com/Cystic+Fibrosis
Slide 8: Knowles & Boucher 2002;109:571
Slide 9: Knowles & Boucher 2002;109:571
Slide 10: Source Undetermined
Slide 11: Knowles & Boucher 2002;109:571
Slide 12: R. Simon
Slide 13: Source Undetermined; R. Simon
Slide 14: Cystic Fibrosis Foundation Patient Registry Data. 2005
Slide 18: Shwachman H, Mahmoodian A. Mod Prob Pediatr 1967;10:158
Slide 19: CF Genetic Analysis Consortium
Slide 25: Ramsey B, et al. NEJM 1999;340:23-30
Slide 26: Fuchs HJ, et al. NEJM 1994;331:637-642
Slide 29: Saiman L, et al. JAMA. 2003;290:1749-56
Slide 30: Elkins MR et al. N Engl J Med 2006;354:229-240
Slide 31: Elkins MR et al. N Engl J Med 2006;354:229-240
Slide 38: Source Undetermined
Slide 39: Source Undetermined
Slide 40: Source Undetermined
Slide 41: Science, September 1989