Transcript Lung

Sarcoidosis Overview
Kenneth S. Knox, MD
Assistant professor of medicine
Division of Pulmonary & Critical Care Medicine
Indiana University
What is Sarcoidosis ?
Nobody knows
• Systemic inflammatory/immunologic disorder
• Hallmark is granulomatous (noncaseating)
inflammation and a CD4+ T cell alveolitis in the
lung
• Thought to be in response to something
– Occupational exposure or Environment
– Bacteria or virus
– Autoantigen (much like lupus and rheumatoid)
Epidemiology
** ACCESS trial– A Case Controlled Etiologic Study of Sarcoidosis
1) Rybicki BA, Iannuzzi MC, Frederick MM, Familial aggregation of sarcoidosis. A case-control
etiologic study of sarcoidosis (ACCESS). Am J Respir Crit Care Med. 2001 Dec 1;164(11):2085-91.
2) Baughman RP, Teirstein AS, Judson MA, Clinical characteristics of patients in a case control study
of sarcoidosis. Am J Respir Crit Care Med. 2001 Nov 15;164(10 Pt 1):1885-9.
3) Freemer M, King TE Jr. The ACCESS study: characterization of sarcoidosis in the United States. Am
J Respir Crit Care Med. 2001 Nov 15;164(10 Pt 1):1754-5.
4) Rossman M, Thompson B, Frederick M,. Sarcoidosis: association with human leukocyte antigen class
II amino acid epitopes and interaction with environmental exposures. Chest. 2002 Mar;121(3)supl.
5) Pandey JP, Frederick M; ACCESS Research Group. A Case Control Etiologic Study of Sarcoidosis.
TNF-alpha, IL1-beta, and immunoglobulin (GM and KM) gene polymorphisms in sarcoidosis. Hum
Immunol. 2002 Jun;63(6):485-91.
6) Judson MA, Baughman RP, Thompson BW, Two year prognosis of sarcoidosis: the ACCESS
experience. Sarcoidosis Vasc Diffuse Lung Dis. 2003 Oct;20(3):204-11.
7) Rossman MD, Thompson B, Frederick M, HLA-DRB1*1101: a significant risk factor for sarcoidosis
in blacks and whites. Am J Hum Genet. 2003 Oct;73(4):720-35.
Sarcoidosis- background
Second most common lung disease
in young adults (second only to
asthma)
• Lifetime risk .85% for US whites
• Lifetime risk 2.4% for US blacks
• 21.6 females and 15.3 males per 100,000 per yr
ACCESS
ACCESS defined, Historical
IU sarcoid data
• 398 patients with sarcoidosis (Wishard
and Clarian visited in past 2 years)
• Over 700 in database
• Support group
• Sarcoidosis and Immunologic lung disease
program
Epidemiology
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Typically 20-40 yo, 35-45 with a third > 50
Women > Men
Blacks > Whites 7:1 in U.S.,4:1 in Detroit
Familial risk
– sibs, aunts, uncles, grandparents OR 5.2-5.8
and parents OR= 3.8, whites > blacks
ACCESS defined, Historical
Epidemiology- prognosis
Better prognosis
Unfavorable prognosis
• Lofgren syndrome
• Older (over 40) F
• Stage II ?, III, IV X-ray
• Black –pernio (puerto rican), eye,
-E nodosum F, arthritis, nodes,
+/- uveitis
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•
•
•
Stage 1 X-ray
Younger
White -calcium, nodosum
Anterior uveitis F
ACCESS defined, Historical
liver, periph nodes, BM
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•
Posterior uveitis- Asian
Unresponsive to steroid
Neuro F, Cardiac- Asian
Elevated calcium M
Environmental Hypothesis
(+) Associations
(-) Associations
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Agriculture
Insecticides/pesticides
Mold/Mildew
Musty odors
ACCESS defined
Tobacco
Children
Cat/Animal dust
Feather/down pillows
Environmental Hypothesis
Uncertain
Likely not associated
• Beryllium- similar disease
• “Clustering” many reports,
(ie: navy, Isle of Man)
• Firefighting- anecdotes
• School teachers- my
experience
• Geographical (“farther from
the equator”)
• Wood dust and pine
pollen
• Metals
• Silica
• Talc
• Health-care workers
• Pets
– Seasonal (“cool summer,
mild winter”) “springtime dz”
– cases reported worldwide.
Infection Hypothesis
Bacteria
– Mycobacteria
– Propionibacteria
– Borrelia
Virus
– Epstein-Barr
– Human herpesvirus 8
– CMV, Coxsackie B
Review: Current Opinion in Pulmonary Medicine 2002,8, 413-476
ATS/ERS/WASOG statement on sarcoidosis: Sarc Vasc Diff Lung Dis 1999,16
Infection Hypothesis
Notable, recent infectious
possibilities
• Tuberculosis (PCR study, Drake 2002)
• Propionibacteria (Ishigi, Lancet, 1999)
• Histoplasmosis (IU experience)
Autoimmune Hypothesis
You react to “privileged selfantigens”
• Infection
• Injury
** Many exposures, infections, and “injury”
can be associated with “granulomatous inflammation”
Recent etiologies
Associated with therapy “Immunemodulating”
• HIV reconstitution syndrome
– Foulon et al. Sarcoidosis in HIV-infected patients in the era of
highly active antiretroviral therapy. Clin Infect Dis. 2004 Feb
1;38(3):418-25.
• IFN therapy for hepatitis
– Pietropaoli A et al. Interferon-alpha therapy associated with the
development of sarcoidosis. Chest. 1999 Aug;116(2):569-72.
Genetics
• Genetic background
– Familial risk (monozygotic twin studies,
siblings and parents)
– Race, ethnicity
• Genetic background
– HLA (DR17, DRB1*1101)
– Other polymorphisms (TNF, Ig-KM)
– BTNL2 truncating splice site mutation
ACCESS defined
Who gets Sarcoidosis ?
Infectious
Sarcoidosis =
OR
X Genetic X ??
Environment
Organ involvement
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Lung
Eye
Skin
Brain/spinal cord
Lymph nodes
Heart
** Heterogeneous disease!
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Kidneys
Liver/spleen
Muscles/nerves
Joints/bones
Hematologic
Metabolic
Symptoms
• Nonspecific
– Fever, sweats
– Weakness,
– Weight loss
– Aches and pains
• Psychological issues
• Organ specific symptoms
Specific Symptoms
• Lung: cough, short of breath, chest pain
• Eye: blurred vision, pain, redness
• Skin: flat rash, nodules, lupus pernio, E.
nodosum
• Heart: palpitations, skipped beats, dizziness,
death
• Central nervous system/nerves: headache,
pain, weakness, memory difficulties, vision
loss, hormone abnormalities
Specific Symptoms
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Muscles: pain
Bones/joints: arthritis, pain, joint swelling
Liver/GI: pain, diarrhea, nausea, jaundice
Vocal cords/salivary glands: hoarseness,
swelling
• Kidneys: kidney stones, failure, polyuria if
calcium and hormone problems
Laboratory Testing
• Bloodwork
– Blood counts (CBC)
• Lymphopenia (45%); leukopenia (30%)
• Anemia up to 20%; low platelets < 2%
– Liver (AST, GGT, Alk phos) and kidney (Cr)
function, Calcium (Ca) and other
chemistries
– Proteins (IgG, albumin)
– Tests of muscle (CK) and inflammation
(ESR,CRP)
• Urine analysis/collection
More Directed Testing
• Tuberculin skin test (PPD)
• Fungal blood work (Histoplasmosis in Indiana)
 Angiotensin Converting Enzyme (ACE)
 Lysozyme
Diagnosis- Ocular
• Eye: anterior or posterior uveitis, mass
• Testing: Slit-lamp eye exam, MRI
• Diagnosis: can biopsy lid if small
lesions
– Reluctant if no visible lesion (yield < 2050%)
25% of patients
Diagnosis and Derm
• Skin: many rashes
– Lupus pernio (biopsy)
– Nodules, flat patches (biopsy)
– Erythema Nodosum (biopsy non-specific)
• Diagnosis: Appearance can be classic,
biopsy to support
20% of patients
Diagnosis- cardiac
• Heart: dysrhythmia, pericardial, pulm htn
if severe, causing shortness of breath
• Testing: EKG, thallium, echo, gallium,
MRI
• Diagnosis:
– Can biopsy heart, but not typical
– Presumed if sarcoidosis affecting other
organs
– “Cold spots” on stress test that improve,MRI
5% symptomatic, 30% incidental
Diagnosis- musculoskeletal
• Bone: pain, arthritis
• Testing: X-ray
• Diagnosis:
– Can have classic features
< 5% have bone involvement; less than 1% have chronic
muscle involvement
IU Liver disease
• Hepatobiliary disease in sarcoidosis is rarely
clinically overt.
• When present, it can range from asymptomatic
liver test abnormalities to cirrhosis.
• Can be first manifestation of sarcoidosis.
• Granulomatous hepatitis, with varying degrees
of fibrosis, most common pathologic finding.
• Male gender and splenomegaly are significantly
associated with sarcoid-related liver disease.
• Gender difference persisted after reanalysis with
N=340 (Liver test abnormality group, p=0.0006).
Diagnosis of Neurosarcoidosis
CNS: headache, memory loss, palsy,
weakness, dizziness, visual, stroke
• Testing: EEG and EMG, muscle/nerve
biopsy, MRI brain and spinal cord, CSF
ACE
• Features: can be presenting sign, can
occur during course of Rx, spontaneous
remission
• Diagnosis: biopsy CNS or other. Clinical…
5% symptomatic, 15% overall
IU neurosarcoid data
AFRICAN AMERICAN
n=19
CAUCASIAN
n=20
Cranial nerve
11 (58%)
7 (35%)
•lesions
39 with documented
neurosarcoidosis
Peripheral
– “Neuropathy” most
common
8 (42.1%)
14 (70%)
neuropathy
Brain lesions
10 (53%)
7 (35%)
Spinal cord
lesions
Brain+Spinal
cord (CNS)
> than 1 part of
nervous
system
4 (21%)
2 (10%)
14 (74%)
9 (45%)
8 (42.1%)
8 (40%)
Pulmonary Diagnosis of Sarcoid
Lung:
cough, short of breath, chest pain
• Testing: PFTs, chest x-ray and CT scan
• Diagnosis: usually requires biopsy
– to exclude other things that look like sarcoid
• (TB, lymphoma, histo, malignancy)
– to support the diagnosis of sarcoid
• The lung and lung lymph nodes are the most
common site for biopsy (90% have thoracic at Dx)
– Bronchoscopy (BAL, Biopsy), Mediastinoscopy
Lung
PFTs
• Restrictive pattern most common (scarred
lung)
– Diffusing capacity first, then Lung capacity
• Can have obstruction (asthma-like)
• ACCESS >13%
• Low Oxygen levels at rest, with exercise or
sleep
Lung
Staging disease by Chest X-ray:
Stage 0 Normal (5%, ACCESS 8%)
Stage 1 Large chest lymph nodes only
(50%,40%)
Stage 2 Chest nodes and lung infiltrate
(25%,37%)
Stage 3 Lung infiltrates only (15%, 10%)
Stage 4 Fibrosis (5%, 5%)
IU clinical BAL Lab
TNF
IFN
Lymphocyte
subsets
Tissue- granuloma shuffle
(Classically, a “Non-necrotizing granuloma without necrosis”)
BEST
• TBBx
• Whole LN, chest
WORST
• Peripheral node
• Skin in non-specific site
DDx: TB, Endemic fungal infection,
Malignancy, GLUS, Wegner’s, HP
foreign body reaction
** Many times supportive evidence and clinical context
Endobronchial biopsy for sarcoidosis: a prospective
study. Shorr AF, Torrington KG, Hnatiuk OW. Chest. 2001 Jul;120(1):109-14.
Six TBB specimens were obtained, as were six EBB samples. For
patients with abnormal-appearing airways, four specimens were
obtained from the abnormal-appearing airways and two specimens
were obtained from the main carina. In patients with normalappearing airways, four specimens were obtained from a secondary
carina and two specimens were obtained from the main carina. EBB
findings were positive in 61.8% of patients, while TBB showed
nonnecrotizing granulomas in 58.8% of subjects. The addition of
EBB increased the yield of FOB by 20.6%. Although EBB findings
were more frequently positive in abnormal-appearing airways (p =
0.014), EBB provided diagnostic tissue in 30.0% of patients with
normal-appearing endobronchial mucosa.
CONCLUSION: EBB has a yield comparable to TBB and
can safely increase the diagnostic value of FOB.
Pulmonologists should consider routinely performing EBB
in cases of suspected sarcoidosis.
Diagnostic value of transbronchial needle aspiration by
Wang 22-gauge cytology needle in intrathoracic
lymphadenopathy.
Cetinkaya E, Yildiz P, Altin S, Yilmaz V. Chest. 2004 Feb;125(2):527-31.
Diagnostic material was obtained from 16 of 21 patients
with sarcoidosis (76%). In sarcoidosis, TBNA provided
the only diagnostic specimen in 13 of 21 patients (62%).
CONCLUSION: TBNA performed with a Wang 22-gauge
cytology needle is an effective and safe way of obtaining
cytologic specimens from intrathoracic lymph nodes and can
rapidly provide diagnosis, both in malignant and benign
mediastinal diseases. Hopefully, this technique will reduce
further need for more invasive surgical procedures.
Treatment options- first line
CONSIDER NOT TREATING!
– Can wait up to 6 months to see if
spontaneous remission occurs (especially
pulmonary)
– Side effects- weight gain, glucose,
cataracts, bone loss, insomnia, infection,
ulcer, adrenal
– Old dogma- early treatment alters natural
course of disease unfavorably…
Early Treatment of Stage II Sarcoidosis Improves 5Year Pulmonary Function*
Anne Pietinalho, MD, PhD; et al. the Finnish Pulmonary Sarcoidosis Study Group†
Study objective: To evaluate the 5-year prognosis of patients with stage I and stage II newly
detected (< 3 months) pulmonary sarcoidosis treated immediately after diagnosis with
prednisolonefor 3 months followed by inhaled budesonide for 15 months. 79 patients with
initial stage I disease and 70 patients with stage II disease.
Treatment: Oral prednisolone for 3 months followed by inhaled budesonide for 15 months
(800mg bid), or placebo tablets followed by placebo inhaler therapy. Thereafter, treatment
only on anindividual basis in the case of clinical deterioration.
Results: Placebo-treated patients more frequently required treatment with corticosteroids
during the 5-year follow-up (p < 0.05). Steroid-treated patients with initial stage II(-III) disease
improved more in FVC and DLCO (p < 0.05). No differences in reported adverse events or in
SACE, serum calcium, or urinary calcium values were seen.
Conclusion: Immediate treatment of pulmonary stage
II(-III) sarcoidosis but not stage I disease improved the
5-year prognosis with regard to lung function
variables. (CHEST 2002; 121:24–31)
Treatment options- first line
Topical steroids as primary therapy
MILD DISEASE
– Eyedrops
– Creams/ointments
– Intralesional
– Inhaled
• Alone
• After oral therapy for maintenance
Treatment options- first line
Steroids are the mainstay of treatment
– Start 20-40mg prednisone a day, need to
follow closely.
– May need more or intravenous if severe,
difficulty expected, or acute disease
– May be able to taper over first 3 months to a
lower dose or every other day dosing
Treatment options- second line
If prednisone failure, intolerance, or need
another controller agent
Methotrexate (5-20mg/week)
– Liver toxicity, lung toxicity, mouth sores, abortion
– Blood counts, Cr, and liver function monthly, biopsy?
– Baughman RP et al. Methotrexate is steroid sparing in acute
sarcoidosis: results of a double blind, randomized trial.
Sarcoidosis Vasc Diffuse Lung Dis. 2000 Mar;17(1):60-6.
Azathioprine (Imuran- 200 max per day)
– Low blood counts, diarrhea, small increase in malignancy
– Blood counts and liver function monthly
– Muller-Quernheim et al. Treatment of chronic sarcoidosis with an
azathioprine/prednisolone regimen.
Eur Respir J. 1999 Nov;14(5):1117-22.
New Treatment options- second line
If prednisone failure, intolerance, or
need another controller agent
Leflunomide (+/- MTX)
– Liver toxicity, Blood counts, Cr, and liver
function monthly
Mycophenolate
– Low blood counts, diarrhea, small increase in
malignancy
– Blood counts, Cr and liver function monthly
Treatment options- second line
If prednisone failure, intolerance, or
need another agent
• Hydroxychloroquine- 200mg-400mg per
day
– Eye, skin, calcium, neuro, occ pulm
– Ophthalmology every 6 months
– ** immunomodulator (Ag processing)
Baughman, et al. Seminars in Respiratory Infections;1998
Jones and Callen, J Am Acad Derm; 1990
Toxic, out of favor therapies
• CSA -Stern BJ et al. Arch Neurol. 1992;49(10):1065-72
– Kidney, CNS, hypertension, hair growth, gingival
hypertrophy
– Monitor: kidney function, lipids, electrolytes, blood
pressure
• Chlorambucil
• Cytoxan- IV (neuro, still used)
– 90% response (after MTX failure)
– Lower et al. Arch Intern Med. 1997; 157:1864-68
– Myelodysplasia, low blood counts, bladder, lung
toxicity, fetal, hair loss
– Blood counts and urinalysis.
Treatment options
Unclear role, adjunctive, third line
• Antibiotics
– Minocycline
– Clofazamine
• Other
– Captopril
– Allopurinol
– Other immunosuppressives
Treatment options
Web-based medicine- risky!
• http://www.gethealthyagain.com/
• http:// www.ivillagehealth.com
• Chelation
• Supplements??
Melatonin, Lancet 1995
Fish oil??
Antioxidants??
“Enzyme therapy”
• Marshall Plan?
• Carcinosin
• Euphrasia
• Graphites
• Leuticum (Syphilinum)
• Bacillinum
• Sepia
• Phosphorus
• Arsenicum album
Promising therapies
• Anti-TNF therapy
– Thalidomide- skin (Baughman, Chest; 2002)
– Pentoxifylline- trial stopped, too few patients
(Zabel, AJRCCM 1997)
– Etanercept- no benefit stage II/III pulmonary
(Utz, Chest; 2003), little in uveitis (Baughman, WASOG;
2002), OK for skin and arthritis (Khanna, J
Rheumatol; 2003)
– Infliximab- end of enrollment, pulmonary,
promising (Yee, Ann Int Med; 2001; AJRCCM 2006)
– Adalimumab
Treatment guided by prognosis
Better prognosis
Unfavorable prognosis
• Lofgren syndrome
• Older (over 40) F
• Stage II ?, III, IV X-ray
• Black –pernio (puerto rican), eye,
-E nodosum F, arthritis, nodes,
+/- uveitis
•
•
•
•
Stage 1 X-ray
Younger
White -calcium, nodosum
Anterior uveitis F
liver, periph nodes, BM
•
•
•
•
Posterior uveitis- Asian
Unresponsive to steroid
Neuro F, Cardiac- Asian
Elevated calcium M
Quality of life- Psychosocial
• Sarcoidosis patients showed a lower overall QOL
and general health, and suffered from more
fatigue and sleeping problems than the healthy
control group
• The health status of sarcoidosis patients
assessed by the Sickness Impact Profile (SIP),
was impaired compared to the health status of
healthy controls especially in the areas of sleep,
ability to work, recreation, and social interactions.
• Sarcoidosis patients with bodily symptoms
suffered from more depressive symptoms