Alpha1-register in Lithuania - Alfa-1 Sverige · 2016-07-07 · in different Lithuanian regions....

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Alpha1-register in Lithuania

Brigita Sitkauskiene, MD, PhDAssoc.Professor and Head

Division for Clinical Immunology and AllergologyKaunas University of Medicine, Lithuania

Malmö 2008

Kaunas Universityof Medicine

Kaunas MedicalUniversity Hospital

Sydney Burwell, DeanHarward Medical School 1900

“… half of what you are taught as medical students will in 10 years be shown to be wrong.

And the trouble is none of your teachers knows which half…”

ASTHMA COPD

Chronic persistent inflammation + airflow obstruction

EosinophilsCD4+ cellsMacrophages+Mast cellsNeutrophils?

NeutrophilsCD8+ cellsMacrophages++Eosinophils ?

Linden M 1993, Saetta M 1994Villar MTA 1995, Chanez P 1997

COPDAsthma

60-80% 80-90%

Li JT et al. 2006Boulet LP et al. Chest 2006

Weiss ST et al. Am J Respir Crit Care Med 2000Sitkauskiene B et al. Respir Med 2003

Adapted from Wood et al. Respir Res 2006

Activation of macrophages

Neutrophil

Neutrophilic inflammation

Activation of epithelial cells

Proteases

LTB4IL-8etc.

IL-8

Concentration of IL-8 in BAL fluid

Stravinskaite K et al. Lung 2008

0

50

100

150

200

250

300

COPDsmokers

COPD ex-smokers

‘Healthy’smokers

Healthy neversmokers

IL-8

(pg/

ml)

*

*

#p<0.05

*p<0.05 compared to healthy never-smokers

#p<0.05 compared to ‘healthy’ smokers

Correlation between BALf IL-8and smoking history

Pac

k-ye

ars

0

10

20

30

40

50

100 200 300 400IL-8 (pg/ml), BAL

COPD smokers Rs=0.81

COPD ex-smokers Rs=0.83

‘Healthy’ smokers Rs=0.80

12

BAL cells staining (ICC) positively for MMP-12

1- MMP12+ macrophage; 2- MMP12- macrophage

• Metalloproteinases (MMPs) mediate airway inflammation and remodelling• Indirect effect of smoke induced increase of MMP-12 is inactivation of α1-antitrypsin and emphysema

• MMP-12 mediates recruitment of neutrophils to the lung in response tocigarette smoke Gronski et al. 1997

Churg et al. 2003

COPD smokers

COPD ex-smokers

'Healthy' smokers

Healthy never- smokers

0

10

20

30

40

50

60

70

Induced sputum BAL

80

* #

* #

*

* #

* #

p<0.05

*

MMP-12+ macrophages (ICC) in different tissue compartments

MM

P-12

+ -m

acro

phag

es(%

of t

otal

mac

roph

ages

)

Babusyte A et al. Respir Res 2007

Asthma smokers

Asthma never- smokers

Pack-years

0

10

20

30

40

50

60

70

80

10 20 30 40 50 60

MM

P-12

+ -m

acro

phag

esin

BAL

(%)

100 COPD smokers (Rs=0.86*)

COPD ex-smokers (Rs=0.68*)

‘Healthy’ smokers (Rs=0.63*)

Babusyte A et al. Respir Res 2007

Correlation between smoking history andBAL MMP12+ macrophages

*p<0.05

γδ TCR+ lymphocytes in BAL

Urboniene D et al. ERS 2007

γδTC

R+

lym

phoc

ytes

(%)

COPD Asthma Control

p<0.001 NS

p<0.001

0123456789

10

γδ cell-deficient mice are fatally defective in their immune response to a gram-positive bacterium, have low mucosal IgA synthesis Fujihashi KJ et al. 1996

Smoking induces variety of inflammatory

responses;

modulates respiratory defense mechanisms

Many immunological changes in smokers are

not completely reversible after quitting smoking

Only 15-30% of smokers develop COPD

The risk results from a gene-environment interaction

• Severe hereditary deficiency of alpha1-antitrypsin (AAT) is the best described genetic risk factor for COPD

• AAT deficiency is most commonly seen in Caucasians

• AAT deficiency is an under-diagnosed condition world-wide

Blanco I et al. Eur Respir J 2006Sitkauskiene B et al. Respir Med 2008

WHO and ATS/ERS guidelines recommend

Establishment of screening programs for the detection of AAT deficiency in patients with COPD

• Family screening

• Appropriate management (including lifestyle changes

such as quitting smoking and replacement therapy)

• Specific counseling for these patients and families

ATS/ERS Statement. Am J Respir Crit Care Med 2003De Serres FJ et al. COPD 2006

Lithuanian Alpha-1 Research Association

Objective

• To estimate the AAT (mainly S and Z) gene frequencyand prevalence in a large cohort of Lithuanian patients with COPD

• To identify AAT deficiency cases in COPD patients

COPD patients (n=1580→1167) from the different Lithuanian regions

GOLD spirometric criteria for COPD

• FEV1/FVC < 0.7

• FEV1 < 80% pred.

Serum concentrations of AAT -by means of nephelometry

AAT phenotyping - by means of isoelectric-focusing

Presence of PI*Z allele by ELISA, qualitative method

EVALUATIONSPATIENTS

RESULTS

Sitkauskiene B et al. Respir Med 2008

Demographic characteristics and AAT genotypes Lithuanian cohort of COPD patients

P-value (ZZ vs other groups) 0.06 0.54

AAT N Sex Age (SD) Cumulativegenotypes % M pack-years (SD)

MM 1076 84 66 (10.4) 22.4 (12.4)MS 39 56 64 (7.8) 20.4 (11.6)MZ 40 65 67 (11.2) 21.3 (12)SS 1 0 61 22 (-)SZ 3 66 63 (2.8) 18 (2.8)ZZ 8 62 54 (11.3) 19 (11)

Total 1167 82 62 (10.3) 22.1 (12.2)

Smoking habits in Lithuania

Finbalt Health Monitor programGrabauskas V et al. Publication of National Public Health Institute 2003

Lithuanian Statistics 2007

Females FemalesMales MalesIn cities In villages

Occasionalsmokers

Everyday smokers

%

Smoking among males and femalesin different Lithuanian regions

Finbalt Health Monitor programGrabauskas V et al. Publication of National Public Health Institute 2003

Lithuanian statistics 2007

Males

Females

Total Alytus Kaunas Klaipeda Marijam- Paneve- Šiauliai Taurage Telšiai Utena Vilniuspole žys

%

Sitkauskiene B et al. Respir Med 2008

AAT genotypes and spirometric values Lithuanian cohort of COPD patients

P-value (ZZ vs other groups) 0.01 0.31 0.00

AAT N FEV1/FVC FEV1% pred. AAT serumgenotypes (CD) concentration

MM 1076 54.8 (10.5) 46 (15.8) 164.7 (39.8)MS 39 55.7 (11.2) 50.8 (16.1) 102 (11)MZ 40 58.6 (9.5) 51.5 (14.5) 99 (14)SS 1 65 48 88SZ 3 56.5 (6.3) 70 (4.2) 77 (19.7)ZZ 8 36.2 (18.6) 38.5 (18.1) 30 (12.4)

Total 1167 54.7 (10.9) 46.5 (15.9) 158 (43.6)

Beckman L et al. Hum Hered 1999Stakisaitis D et al. Med Sci Monit 2001Sitkauskiene B et al. Respir Med 2008

Calculated PI*S and PI*Z gene frequencyin COPD patients and healthy unrelated people

Samples Gene frequency per 1000 (95% Cl)

PI*S PI*Z

COPD N: 1167 18.8 (13.9-25.4) 25.3 (19.4-32.7)

Healthy unrelated 15.6 (12.5-19.6) 13.6 (10.7-17.4)

people N: 2491

Case control studies in other countries

Spain ZZ among COPD 0.37%

Italy 6.4%

Germany ZZ / chr. respir.diseases 0

Germany 14.7%

Denmark ZZ among COPD 0.8%

De la Roza C et al. Eur Respir J 2005

Luisetti M et al. Respir Med 1999

Wencker M et al. Eur Respir J 2002

Bals R et al. Respir Med 2007

Dahl M et al. Ann Intern Med 2002

021

14

2519

1725

19

27

28

22

12

27

23

2645 35

4

25

6 11

13

4

1 4

00

4

5

3

4

0

0

0

128

16

31

20 17

13 8

9

30

0

0

11

17

15

175

1213

31 20

2111

16

7

16

14

7

0

0

0

24 23

14 8

117 4

4 0

11

12 1011 11

18

2930

33

29

19

21

0

04

5 0

RUSSIA

RUSSIABELARUS

DEMMARK

NORWAY

SWEDEN

FINLAND

Gotland

Aland Arch.

ICELAND

LITHUANIA

LATVIA

ESTONIA

24 23

Beckman L et al. Hum Hered 1999De Serres F et al. Monaldi Arch Chest Dis 2007

Distribution of PI*S and PI*Z gene frequencies in Northern Europe countries

Z values are showed in grey circles

The highest incidence of PI*S:• South of the Scandinavian

Peninsula• Latvia• Denmark

The highest incidence of PI*Z:• Latvia• Southern Norway• Denmark• Southern Sweden• Estonia

Estimated number of subjects for each AAT genotype in COPD Lithuanian population

Estimated number of COPD patients over 40 yrs in the Lithuanian population

Calculated number of normal (MM) and deficiency genotypes in COPD (95% CI)

MM MS SS MZ SZ ZZ

159 829146 034

(143 193-148 428)

5 760(4 202-7 842)

57(31-104)

7 724(5 888-10 076)

152(86-266)

102(61-171)

Statistics Lithuania [accessed 08.07]Sitkauskiene B et al. Respir Med 2008

Alpha-1 antitrypsin augmentation therapy

Candidates

Young patients with severe hereditary AAT deficiencyand established emphysema

However, this therapy is very expensive, is not available in most countries

GOLD updated 2007

Therapy at each stage of COPD

GOLD updated 2007

Lung transplantation

Criteria for referral for lung transplantation:

• FEV1 < 35% predicted• PaO2 < 7.3-8.0 kPa (55-60 mmHg)• PaCO2 > 6.7 kPa (50 mmHg)• Secondary pulmonary hypertension

GOLD updated 2007

A case of lung transplantation in patient with hereditary AAT deficiency

Male, 52 yrs oldAlpha1- antitrypsin concentration 0.33 g/l

FVC 3.12 L – 70 %FEV1 1.12 L – 31 %FEV1/FVC 36 %

III° bronchial obstruction

Lung transplantation was performed 14 Oct 2008

III° decrease of gas diffusion,DLCO – 29% predicted

Pi MZ Pi MZ

Pi ZZ Pi ZZ

Pi MZ Pi MZ

Pi MZ

A case of lung transplantation in patient with hereditary AAT deficiency

-inheritance of AAT deficiency-

The OR for each genotypic class demonstrated a significant increase of MZ, SZ and ZZ genotypes in COPD patients.

The results of our study, with a significant number of ZZ individuals detected, support the general concept of targeted screening for AAT deficiency in countries like Lithuania, with a large population of COPD patients and low awareness among care-givers about this genetic condition.

Conclusions

Sabina Janciauskiene

Raimundas SakalauskasDanielius Serapinas

Agne BabusyteKristina Stravinskaite

Acknowledgements

Millennium Lithuaniae 2009

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