Journée d’Hépatologie du Centre Hépato-Biliaire – 13 juin 2014 - Paris 
DDuu « bbiinnggee ddrriinnkkiinngg » 
àà ll’’hhééppaattiittee aallccoooolliiqquuee 
Pr. Philippe Mathurin 
Hôpital Universitaire Claude Huriez 
Lille, France
Alcohol-attributable deaths as a percentage of total 
deaths
Important variations iinn lliivveerr cciirrrrhhoossiiss 
mmoorrttaalliittyy aaccrroossss EEuurrooppee 
HHiigghheerr rraatteess iinn EEaasstteerrnn ccoouunnttrriieess tthhaann iinn WWeesstteerrnn 
EEuurrooppeeaann ccoouunnttrriieess
Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
COUNTRIES WWIITTHH IIMMPPRROOVVEEMMEENNTTSS 
OOVVEERR PPAASSTT 
1100--2200 YYEEAARRSS
Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
AAllccoohhooll ccoonnssuummppttiioonn iinn EEuurrooppee
Cirrhosis in Europe: AA ppuubblliicc hheeaalltthh iissssuuee 
Age-adjusted (world population) mortality rates from cirrhosis per 
100,000 men 
Bosetti C, J Hepat 2007
COUNTRIES WWIITTHH IINNCCRREEAASSIINNGG 
RRAATTEESS OOVVEERR PPAASSTT 1100--2200 
YYEEAARRSS
Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
Alcohol and mortality in Russia: prospective 
observational study of 151 000 adults 
David Zaridze, …. Peto R. Lancet 2014
Alcohol and mortality in Russia: prospective 
observational study of 151 000 adults 
David Zaridze, …. Peto R. Lancet 2014
TTHHEE EEMMEERRGGIINNGG IISSSSUUEESS:: 
BBiinnggee ddrriinnkkiinngg,, ““tthhee uunnsseettttlleedd 
ddaaiillyy ddoossee ooff aallccoohhooll iinnttaakkee”” iinn 
tthhee ccoonntteexxtt ooff oobbeessiittyy
Prevalence of NAFLD in EEuurroopp:: lleessssoonnss ffrroomm tthhee 
DDiioonnyyssooss ssttuuddyy 
PPrreevvaalleennccee ooff NNAAFFLLDD aasssseesssseedd bbyy 
uullttrraassoonnooggrraapphhyy == 2200%% 
Bedogni G, Hepatology 2005
PPrrooggrreessssiioonn ooff oobbeessiittyy oovveerr tthhee ttiimmee 
11999977 :: 88..22 %% 
22000000 :: 99..66 %% 
22000033 :: 1111..33 %% 
22000066 :: 1122..44 %% 
+ 17% 
+ 17,7 % 
+ 9,7% 
Data from Obepi Survey 2009
Excess weight risk factor for 
Alcoholic Liver Disease 
60% 
Overweight Patients 
Non-Overweight Patients 
35% 
80% 
70% 
60% 
50% 
40% 
30% 
20% 
10% 
0% 
Alcoholic Cirrhosis 
Naveau S, Hepatology 1997
Effect of binge drinking on the liver: 
An alarming public health issue? 
• 3 questions on the potential impact of binge drinking in terms of liver disease: 
1. Do experimental data suggest a deleterious impact of binge drinking on liver tissue? 
→ Answer: YES 
2. Do behavioral studies suggest that adolescent binge drinkers are at higher risk of being 
heavy drinkers in adulthood, with the consequent risk of alcoholic liver disease? 
→ Answer : YES 
Probability of becoming a chronic drinker at an adult age was higher in male and female 
adolescent binge drinkers than in non-bingers: 6.7 % vs 2.3% and 9.6 vs 4.8 % 
3. Do epidemiological data support a future increase in the risk of cirrhosis related to binge 
drinking? 
→ Answer Likely 
Drastic increase in liver cirrhosis and mortality rates in the UK is particularly alarming 
Mathurin Gut 2009; McCarty CA Pediatrics 2004
Effect of binge drinking on the liver: 
An alarming public health issue? 
Binge drinking is a major public heath issue that 
can no longer be considered simply a 
momentary risk factor of behavioral concerns, 
but must now be viewed in light of long-term 
consequences, such as alcohol-induced liver 
disease 
Mathurin Gut 2009 
McCarty CA Pediatrics 2004
Effect of binge drinking on the liver: 
An alarming public health issue? 
Leon DL, Lancet 2006
Alcohol a major ppuubblliicc hheeaalltthh iissssuuee 
TThhee bbiinnggee ddrriinnkkiinngg PPhheennoommeennoonn 
11..22 bbiilllliioonnss 
11..55 bbiilllliioonnss 
↑ 25% 
Naimi TS, Jama 2003
How to reduce the burden of 
alchohol-attributable deaths: 
The most efficient public 
health policies
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique
EASL call for EU action – on liver 
disease 
• Recognise alcohol consumption as one of the cross-cutting 
risk factors for non-communicable diseases, including liver 
disease 
• Acknowledge liver disease as a public health priority in 
the EU’s public health and research policies and funding 
programmes 
• Ensure liver disease is addressed in future policy 
developments in the field of non-communicable diseases
Public health policy need to use the 
same concept than type II diabetes 
 Primary prevention: 
● For type II diabetes: 
- reduction of overweight in general population 
- modification of lifestyle at population level 
→ Physical activity 
→ behavior changes in terms of alimentation 
● For alcoholic liver disease 
- Decrease of alcohol consumption per inhabitant per year 
 Like type II diabetes there is a need to promote resarch program on 
● better understanding of how cirrhosis develops in people at risk 
● how to prevent or delay the development of cirrhosis and its complications
Disease progression non-iinnvvaassiivvee mmaarrkkeerrss iinn AALLDD 
Fibrotest 
< 0.32 
0.32-0.58 
>0.58 
Naveau S, Hepatology 2009
Alcoholic liver disease aanndd bbiioollooggiiccaall mmaarrkkeerrss 
FFiibbrrootteesstt 
Naveau S et al., Clin Gastroenterol Hepatol. 2005
Le Dépistage améliore la survie 
CHC sur VHC % des patients à 
un stade précoce 
Taux d’accès au 
dépistage 
Accès aux traitements 
curatifs (%) 
Pas de dépisgge 19% 0% 14,5% 
Dépistage actuel 
42% 57% 25,0% 
[Observatoire ANGH Chang] 
97 % Taux dépistage 42% 97% 32,5% 
Efficacité CHC 2000 87% 57% 40,5% 
CHC 2000 + 97% Accès 
87% 97% 58,5% 
dépistage 
Mourad A, Hepatology 2014
O’Shea RS, Hepatology 2010 
Journal of Hepatology 2012 
• First-line therapy in patients with severe ASH includes 
corticosteroids or pentoxifylline especially if there are 
contraindications to steroid therapy
MMoovviinngg ttoowwaarrdd tthhee RReessppoonnssee 
GGuuiiddeedd tthheerraappyy
LLiillllee mmooddeell:: aa ttooooll ffoorr nneeww ssttrraatteeggiieess 
EEvvaalluuaattiioonn ooff LLiillllee mmooddeell oonn oovveerraallll ppaattiieennttss ((nn==443388)) 
100 % 
75 % 
50 % 
25 % 
hhttttpp::////wwwwww..lliilllleemmooddeell..ccoomm 
Lille score < 0.45 85±2.5% 
p<0.00001 
Lille score ≥ 0.45 25±3.8% 
50 days 100 days 150 days 180 days 
Louvet A et al, Hepatology 2007
Complete responders 
Lille score ≤0.16 [≤35th percentile] 
Partial responders 
Lille score 0.16-0.56 [35-70th percentile] 
P Mathurin, Gut 2011 
Null responders 
Lille score ≥0.56 [≥ 70th percentile]
• Current management 
• Near Future 
• Distant Future : Arbitrary selection of novel molecules 
already tested in human beings 
• Transplantation for non-responders to medical 
therapy 
• Future Requirements
N-acetylcysteine aanndd ccoorrttiiccoosstteerrooiiddss :: 
TThhee nneeaarr ffuuttuurree ?? 
NNAACC aalloonnee iiss iinneeffffiicciieenntt 
Stewart S, J Hepatol 2007; Moreno C, J Hepatol 2010 
Nguyen-Khac E,New Engl J Med 2011
Prednisolone With vvss WWiitthhoouutt PPeennttooxxiiffyylllliinnee 
15.3% 
Steroids + pentoxifylline 
n=133 
Steroids + Placebo 
n=137 
EEnndd ppooiinntt == 66 mmoonntthh--ssuurrvviivvaall 
227700 ppaattiieennttss iinncclluuddeedd 
AH biopsy proven 
Madddrey ≥ 32 
Jaundice < 3 months 
n=270 
Mathurin P et al, JAMA 2013 
p=0.07 
8.4% 
11.7% 
p=0.007 
3.1%
• Current management 
• Near Future 
• Distant Future : Arbitrary selection of novel 
molecules already tested in human beings 
• Transplantation for non-responders to medical 
therapy 
• Future Requirements
PPootteennttiiaall tthheerraappeeuuttiicc ttaarrggeettss iinn tthhee ffuuttuurree 
Unsuitable molecule 
↓ 
RReeccoovveerryy 
↑↑ LLiivveerr FFuunnccttiioonn 
DDiisseeaassee 
↓↓ LLiivveerr FFuunnccttiioonn 
IInnffllaammmmaattiioonn 
NNeeccrroossiiss 
AAppooppttoossiiss 
↓ 
↑ 
Infection 
SSuurrvviivvaall PPrroobbaabbiilliittyy 
Survival Time
What can we learn from anti-TNF-a story 
TNF-a and ALD 
McClain CJ, Hepatology 1989 
Kamimura Hepatology 1995 
Yin M, Gastroenterology 1999 
Chang J, Hepatology 2004 
Yamada Y et al, PNAS 1997 
TNF alpha 
TTNNFF--a aanndd LLiivveerr RReeggeenneerraattiioonn
What can we learn from anti-TNF-a story? 
Tilg H , J Hepatol 2003 
Spahr L J hepatol 2002* 
SSttuuddyy DDeessiiggnn 
Mookerjee Gut 2003 
SSiinnggllee DDoossee 
Sharma P, J Hepatol 2009 
Inclusion criterion : Meld ≥15 Inclusion criterion : Maddrey 
SSttuuddyy DDeessiiggnn OOff RRCCTTSS 
MMuullttiippllee DDoosseess 
NC Boetticher, Gastroenterology 2008 
≥32 
Naveau S Hepatology 2004 
↑risk of Infections
- 
RReeccoovveerryy 
↑↑ LLiivveerr FFuunnccttiioonn 
DDiisseeaassee 
↓↓ LLiivveerr FFuunnccttiioonn 
Ideal molecule 
IInnffllaammmmaattiioonn 
NNeeccrroossiiss 
AAppooppttoossiiss 
+ 
- 
Infection 
SSuurrvviivvaall 
PPootteennttiiaall tthheerraappeeuuttiicc ttaarrggeettss iinn tthhee ffuuttuurree 
SSuurrvviivvaall PPrroobbaabbiilliittyy
Potential therapeutic ttaarrggeettss iinn tthhee ffuuttuurree 
IL-1 receptor antagonist (IL-1Ra) 
human IL-1ra [Anakinra®] 
↓↓ AAllccoohhooll lliivveerr iinnjjuurryy 
Petrasek J, J Clin Invest 2012 
BBRRDDUU IInnccoorrppoorraattiioonn 
human IL-1ra [Anakinra®] 
↑↑ LLiivveerr rreeggeenneerraattiioonn 
Sgroi A, PlosOne 2011 Boulton Ra, Hepatology 1997
Potential therapeutic ttaarrggeettss iinn tthhee ffuuttuurree 
Interleukin 22 [F-652] 
in phase I study 
↓↓ AAllccoohhooll lliivveerr iinnjjuurryy 
Ki SH, Hepatology 2010 
↑↑ LLiivveerr rreeggeenneerraattiioonn 
Feng D, Gastroenterology 2012 Park O, Hepatology 2010
Potential therapeutic ttaarrggeettss iinn tthhee ffuuttuurree 
Eculizumab [Soliris®] 
Antibody against C5 
↓↓ AAllccoohhooll lliivveerr iinnjjuurryy 
Pritchard MT, Gastroenterology 2007 
Cohen JI, Gastroenterology 2010 
BBlloocckkiinngg CC55 iimmpprroovveess oouuttccoommee iinn SSeeppssiiss 
Woehrl B, J Clin Invest 2011
• Current management 
• Near Future 
• Distant Future : Arbitrary selection of novel 
molecules already tested in human beings 
• Transplantation for non-responders to medical 
therapy 
• Future Requirements
SSeevveerree AAllccoohhoolliicc HHeeppaattiittiiss 
LLiivveerr TTrraannssppllaannttaattiioonn:: aa lloonngg wwaayy ttoo ggoo 
WWhheerree DDoo WWee AAllll CCoommee FFrroomm ?? 
• RReecceenntt ffoorrmmaall rreeccooggnniittiioonn tthhaatt AAHH iiss aann aabbssoolluuttee ccoonnttrraaiinnddiiccaattiioonn bbyy UUKK ttrraannssppllaanntt 
cceennttrreess ((BBaatthhggaattee AAJJ,, LLaanncceett 2000066)) 
• AAbbssttiinneennccee pprree--ttrraannssppllaanntt iiss nneecceessssaarryy ttoo eexxcclluuddee tthhoossee wwhhoo wwiillll iimmpprroovvee aanndd nnoott 
nneeeedd ttrraannssppllaannttaattiioonn 
• AAbbssttiinneennccee iiss uusseeffuull ttoo aallllooww ttiimmee ffoorr aasssseessssiinngg aanndd vveerriiffyyiinngg aallccoohhooll aaddddiiccttiivvee 
bbeehhaavviioouurr bbuutt « 6-month rule » is not a robust criterion 
Foster PF, Hepatology 1997 
Liver transplantation for alcoholic liver disease: bias, beliefs, 6-month rule, 
and relapse- but where are the data. 
Beresford TP, Everson GT Liver Transpl 2000
Where Do We Come From ? 
SSEEVVEERREE AALLCCOOHHOOLLIICC HHEEPPAATTIITTIISS 
LLIIVVEERR TTRRAANNSSPPLLAANNTTAATTIIOONN 
Where Do I Come From ? 
• Atterbury CE. The alcoholic in the lifeboat. Should drinkers be candidates for liver 
transplantation? J Clin Gastroenterol 1986 
The Jury stated: 
- wait-and-watch strategy using the 6-month criterion 
may be unfair for some non-responders with 70- 80% 
probability of dying during this period 
- recommended pilot studies evaluating early liver 
transplantation in non-responders 
• Lucey MR J Hepatol 2002; Is liver transplantation an appropriate treatment for acute 
alcoholic hepatitis?
Early liver transplantation: 
The French and Belgium Experience 
Philippe Mathurin1, Christophe Moreno2, Didier Samuel3, Jérôme 
Dumortier4, Julia Salleron5, François Durand6, Hélène Castel1, 
Alain Duhamel5, Georges-Philippe Pageaux7, Vincent Leroy8, 
Sébastien Dharancy1, Alexandre Louvet1, Emmanuel Boleslawski1, 
Valerio Lucidi2, Thierry Gustot2, Claire Francoz6, Christian 
Letoublon8, Denis Castaing3, Jacques Belghiti6, Vincent Donckier2, 
François-René Pruvot1, Jean-Charles Duclos-Vallée3 
Brussels, Grenoble, Lille, Lyon, Montpellier, Beaujon, 
Villejuif 
New EnglJ Med 2011
EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss 
• Early liver transplantation in non-responders undergoing 
their ffiirrsstt event of liver disease 
• Non responders were identified using Lille score ≥0.45 or 
worsening of liver function by day 7.
Early LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss 
SSeelleeccttiioonn pprroocceessss== 44 TTeeaamm cciirrcclleess 
Family structure 
Patient 
Time toward complete consensus 
= nurses, i.e. one resident and one fellow 
specialist in addiction 
= senior hepatologists 
senior anesthetist and surgeons
EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss 
Transplanted non responders N=26 
Male gender no. [%] 15 [57.7%] 
Age (years) median [95%CI] 47.4 [42.7-52.4] 
Duration of corticosteroids treatment (days) 
Median [95%CI] 
11.5 [7-18] 
Hepatorenal syndrome, no. [%] 15 [57.7%] 
Hemodiafiltration or MARS® system no. [%] 10 [38.5 %] 
Infection before transplantation no [%] 18 [69.2%] 
Mechanical ventilation no [%] 4 [15.4%]
Median [95%CI] 
Lille score 0.88 [0.76 – 0.95] 
MELD on first day of therapy 30.1 [27.7 - 33.4] 
MELD day 7 28.5 [26.2 – 33.7] 
MELD at listing 34.2 [29 – 37] 
MELD day 0 - MELD Listing - 5.44 [-7.3 – 2] 
MELD day 7 - MELD Listing - 1.9[-6 – 0] 
Time (days) from end of therapy to 
13 [6 – 17] 
listing 
Time (days) from listing to LT 8.5 [3 – 11] 
* MMaaxxiimmuumm ooff LLiillllee ssccoorree iiss 11 
** 
EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss
Early Transplantation sshhiifftt ssuurrvviivvaall ooff 
uunnrreessppoonnssiivvee ttoo rreessppoonnddeerrss 
• Final combined database included a total of 651 patients. Matching was 
performed using the global optimal algorithm 
• For matching criteria, we used the following pre-established ranges: age (+/- 10 
years), gender, Maddrey function (<60; 60-90 and >90) and Lille score (+/-0.15) 
• The overall optimal algorithm was able to select 3 unresponsive matched controls 
for 20 transplanted patients, 2 unresponsive matched controls for 3 transplanted 
patients and only 1 unresponsive matched control for 3 transplanted patients. 
• The overall optimal algorithm was able to select 4 responsive matched controls for 
21 transplanted patients, 2 responsive matched controls for 3 transplanted 
patients and only 1 responsive matched control for 2 transplanted patients
EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss
EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss 
• No alcohol relapse within the 6 month period 
• 3 patients resumed alcohol consumption during data collection 
- at 720, 740 and 1140 days 
[2 daily consumers and 1 had occasional consumption (approximately 
10g/week)] 
• 2 centers have prospective data base of severe alcoholic hepatitis only 4 
(1.83%) were directly selected by the 2 centers from their own recruitment 
• Proportions of eLT among the total number of procedures, and number 
of procedures for alcoholic liver disease, were 26/891 [2.92%]) and 26/315, 
[8.25%], respectively
Outcomes After Liver Transplantation for Alcoholic 
Hepatitis Are Similar to Alcoholic Cirrhosis 
Graft Survival Patient Survival 
Singal AK et al., Hepatology 2011
1. In patients with severe ASH not responding to medical therapy, 
early LT need to be further evaluated in carefully-selected 
patients 
Journal of Hepatology 2012
PPHHRRCC QQuuiicckkTTrraannss--HHAAAA 
AAHH nnoott rreessppoonnddiinngg ttoo mmeeddiiccaall tthheerraappyy 
AAllggoorriitthhmm bbaasseedd oonn oobbjjeeccttiivvee ccrriitteerriiaa 
RRaannggee ooff SSccoorree ffrroomm 00 ttoo 225500 GO 
AAllggoorriitthhmm ssccoorree ≥≥ 222200 GO 
AAllggoorriitthhmm ssccoorree << 222200GO 
Not selected 
SSeelleecctteedd 
CCoonnttrrooll ggrroouupp 
AAllccoohhoolliicc ccaannddiiddaatteess ffoorr 
lliivveerr ttrraannssppllaannttaattiioonn 
Classical selection 
6-month criteria 
Primary objective 
Non inferiority in terms of alcohol relapse 
Secondary endpoint survival benefit 
Non responders 
Not Transplanted
• Current management 
• Near Future 
• Distant Future : Arbitrary selection of novel 
molecules already tested in human beings 
• Transplantation for non-responders to medical 
therapy 
• Future Requirements
Better KKnnoowwlleeddggee ooff tthhee NNaattuurraall HHiissttoorryy 
66 mmoonntthhss Deaths due to liver injury in > 90 % of cases 
No impact of alcoholism behavior 
66--MMOONNTTHH PPEERRIIOODD 
SSUURRVVIIVVIINNGG TTHHEE 66 MMOONNTTHH PPEERRIIOODD 
OOPPTTIIMMAALL PPEERRIIOODD FFOORR SSTTUUDDIIEESS TTEESSTTIINNGG DDRRUUGG 
PPRREEVVEENNTTIINNGG LLIIVVEERR IINNJJUURRYY 
AAlliivvee RReessppoonnddeerrss ttoo mmeeddiiccaall tthheerraappyy 
GGoooodd LLiivveerr FFuunnccttiioonn 
Abstainers during 5 years 
Risk of Liver-Related death ≈ 15% 
Relapsers during 5 years 
Risk of Liver-Related death ≈ 50% 
AAFFTTEERR 66 MMOONNTTHHSS 
AAVVOOIIDD SSTTUUDDIIEESS TTEESSTTIINNGG DDRRUUGG PPRREEVVEENNTTIINNGG LLIIVVEERR IINNJJUURRYY 
AAlliivvee NNoonn--RReessppoonnddeerrss ttoo mmeeddiiccaall 
tthheerraappyy 
IInntteerrmmeeddiiaattee LLiivveerr ddyyssffuunnccttiioonn 
Abstainers during 5 years 
Risk of Liver-Related death ≈ 50% 
Relapsers during 5 years 
Risk of Liver-Related death ≈ 90% 
Louvet A, AASLD 2010
UUnnmmeett nneeeeddss 
• Animal models mimicking better liver Injury in human beings (liver 
dysfunction and regeneration) 
• Better network between basic and clinician researchers 
• Official recommendations from experts of scientific societies on the 
criteria that need to be fulfilled for an optimal study design 
• Development and validation of surrogate markers of survival (like the 
RECIST criteria in cancers) for testing of new molecules in phase I 
and/or II 
• Bring pharmaceutical companies to test and develop molecules
NIAAA Announces Request for Applications oonn AAllccoohhoolliicc HHeeppaattiittiiss 
“Integrated Approaches for Identifying 
Molecular Targets in Alcoholic Hepatitis”
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique
From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique

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From Binge Drinking to Alcoholic Liver Disease - Du Binge Drinking à l'Hépatite Alcoolique

  • 1. Journée d’Hépatologie du Centre Hépato-Biliaire – 13 juin 2014 - Paris DDuu « bbiinnggee ddrriinnkkiinngg » àà ll’’hhééppaattiittee aallccoooolliiqquuee Pr. Philippe Mathurin Hôpital Universitaire Claude Huriez Lille, France
  • 2. Alcohol-attributable deaths as a percentage of total deaths
  • 3. Important variations iinn lliivveerr cciirrrrhhoossiiss mmoorrttaalliittyy aaccrroossss EEuurrooppee HHiigghheerr rraatteess iinn EEaasstteerrnn ccoouunnttrriieess tthhaann iinn WWeesstteerrnn EEuurrooppeeaann ccoouunnttrriieess
  • 4. Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
  • 5. Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
  • 6. COUNTRIES WWIITTHH IIMMPPRROOVVEEMMEENNTTSS OOVVEERR PPAASSTT 1100--2200 YYEEAARRSS
  • 7. Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
  • 9. Cirrhosis in Europe: AA ppuubblliicc hheeaalltthh iissssuuee Age-adjusted (world population) mortality rates from cirrhosis per 100,000 men Bosetti C, J Hepat 2007
  • 10. COUNTRIES WWIITTHH IINNCCRREEAASSIINNGG RRAATTEESS OOVVEERR PPAASSTT 1100--2200 YYEEAARRSS
  • 11. Courtesy from D Leon. EASL 2010 Monothematic conference on ALD
  • 12. Alcohol and mortality in Russia: prospective observational study of 151 000 adults David Zaridze, …. Peto R. Lancet 2014
  • 13. Alcohol and mortality in Russia: prospective observational study of 151 000 adults David Zaridze, …. Peto R. Lancet 2014
  • 14. TTHHEE EEMMEERRGGIINNGG IISSSSUUEESS:: BBiinnggee ddrriinnkkiinngg,, ““tthhee uunnsseettttlleedd ddaaiillyy ddoossee ooff aallccoohhooll iinnttaakkee”” iinn tthhee ccoonntteexxtt ooff oobbeessiittyy
  • 15. Prevalence of NAFLD in EEuurroopp:: lleessssoonnss ffrroomm tthhee DDiioonnyyssooss ssttuuddyy PPrreevvaalleennccee ooff NNAAFFLLDD aasssseesssseedd bbyy uullttrraassoonnooggrraapphhyy == 2200%% Bedogni G, Hepatology 2005
  • 16. PPrrooggrreessssiioonn ooff oobbeessiittyy oovveerr tthhee ttiimmee 11999977 :: 88..22 %% 22000000 :: 99..66 %% 22000033 :: 1111..33 %% 22000066 :: 1122..44 %% + 17% + 17,7 % + 9,7% Data from Obepi Survey 2009
  • 17. Excess weight risk factor for Alcoholic Liver Disease 60% Overweight Patients Non-Overweight Patients 35% 80% 70% 60% 50% 40% 30% 20% 10% 0% Alcoholic Cirrhosis Naveau S, Hepatology 1997
  • 18. Effect of binge drinking on the liver: An alarming public health issue? • 3 questions on the potential impact of binge drinking in terms of liver disease: 1. Do experimental data suggest a deleterious impact of binge drinking on liver tissue? → Answer: YES 2. Do behavioral studies suggest that adolescent binge drinkers are at higher risk of being heavy drinkers in adulthood, with the consequent risk of alcoholic liver disease? → Answer : YES Probability of becoming a chronic drinker at an adult age was higher in male and female adolescent binge drinkers than in non-bingers: 6.7 % vs 2.3% and 9.6 vs 4.8 % 3. Do epidemiological data support a future increase in the risk of cirrhosis related to binge drinking? → Answer Likely Drastic increase in liver cirrhosis and mortality rates in the UK is particularly alarming Mathurin Gut 2009; McCarty CA Pediatrics 2004
  • 19. Effect of binge drinking on the liver: An alarming public health issue? Binge drinking is a major public heath issue that can no longer be considered simply a momentary risk factor of behavioral concerns, but must now be viewed in light of long-term consequences, such as alcohol-induced liver disease Mathurin Gut 2009 McCarty CA Pediatrics 2004
  • 20. Effect of binge drinking on the liver: An alarming public health issue? Leon DL, Lancet 2006
  • 21. Alcohol a major ppuubblliicc hheeaalltthh iissssuuee TThhee bbiinnggee ddrriinnkkiinngg PPhheennoommeennoonn 11..22 bbiilllliioonnss 11..55 bbiilllliioonnss ↑ 25% Naimi TS, Jama 2003
  • 22. How to reduce the burden of alchohol-attributable deaths: The most efficient public health policies
  • 29. EASL call for EU action – on liver disease • Recognise alcohol consumption as one of the cross-cutting risk factors for non-communicable diseases, including liver disease • Acknowledge liver disease as a public health priority in the EU’s public health and research policies and funding programmes • Ensure liver disease is addressed in future policy developments in the field of non-communicable diseases
  • 30. Public health policy need to use the same concept than type II diabetes  Primary prevention: ● For type II diabetes: - reduction of overweight in general population - modification of lifestyle at population level → Physical activity → behavior changes in terms of alimentation ● For alcoholic liver disease - Decrease of alcohol consumption per inhabitant per year  Like type II diabetes there is a need to promote resarch program on ● better understanding of how cirrhosis develops in people at risk ● how to prevent or delay the development of cirrhosis and its complications
  • 31. Disease progression non-iinnvvaassiivvee mmaarrkkeerrss iinn AALLDD Fibrotest < 0.32 0.32-0.58 >0.58 Naveau S, Hepatology 2009
  • 32. Alcoholic liver disease aanndd bbiioollooggiiccaall mmaarrkkeerrss FFiibbrrootteesstt Naveau S et al., Clin Gastroenterol Hepatol. 2005
  • 33. Le Dépistage améliore la survie CHC sur VHC % des patients à un stade précoce Taux d’accès au dépistage Accès aux traitements curatifs (%) Pas de dépisgge 19% 0% 14,5% Dépistage actuel 42% 57% 25,0% [Observatoire ANGH Chang] 97 % Taux dépistage 42% 97% 32,5% Efficacité CHC 2000 87% 57% 40,5% CHC 2000 + 97% Accès 87% 97% 58,5% dépistage Mourad A, Hepatology 2014
  • 34. O’Shea RS, Hepatology 2010 Journal of Hepatology 2012 • First-line therapy in patients with severe ASH includes corticosteroids or pentoxifylline especially if there are contraindications to steroid therapy
  • 35. MMoovviinngg ttoowwaarrdd tthhee RReessppoonnssee GGuuiiddeedd tthheerraappyy
  • 36. LLiillllee mmooddeell:: aa ttooooll ffoorr nneeww ssttrraatteeggiieess EEvvaalluuaattiioonn ooff LLiillllee mmooddeell oonn oovveerraallll ppaattiieennttss ((nn==443388)) 100 % 75 % 50 % 25 % hhttttpp::////wwwwww..lliilllleemmooddeell..ccoomm Lille score < 0.45 85±2.5% p<0.00001 Lille score ≥ 0.45 25±3.8% 50 days 100 days 150 days 180 days Louvet A et al, Hepatology 2007
  • 37. Complete responders Lille score ≤0.16 [≤35th percentile] Partial responders Lille score 0.16-0.56 [35-70th percentile] P Mathurin, Gut 2011 Null responders Lille score ≥0.56 [≥ 70th percentile]
  • 38. • Current management • Near Future • Distant Future : Arbitrary selection of novel molecules already tested in human beings • Transplantation for non-responders to medical therapy • Future Requirements
  • 39. N-acetylcysteine aanndd ccoorrttiiccoosstteerrooiiddss :: TThhee nneeaarr ffuuttuurree ?? NNAACC aalloonnee iiss iinneeffffiicciieenntt Stewart S, J Hepatol 2007; Moreno C, J Hepatol 2010 Nguyen-Khac E,New Engl J Med 2011
  • 40. Prednisolone With vvss WWiitthhoouutt PPeennttooxxiiffyylllliinnee 15.3% Steroids + pentoxifylline n=133 Steroids + Placebo n=137 EEnndd ppooiinntt == 66 mmoonntthh--ssuurrvviivvaall 227700 ppaattiieennttss iinncclluuddeedd AH biopsy proven Madddrey ≥ 32 Jaundice < 3 months n=270 Mathurin P et al, JAMA 2013 p=0.07 8.4% 11.7% p=0.007 3.1%
  • 41. • Current management • Near Future • Distant Future : Arbitrary selection of novel molecules already tested in human beings • Transplantation for non-responders to medical therapy • Future Requirements
  • 42. PPootteennttiiaall tthheerraappeeuuttiicc ttaarrggeettss iinn tthhee ffuuttuurree Unsuitable molecule ↓ RReeccoovveerryy ↑↑ LLiivveerr FFuunnccttiioonn DDiisseeaassee ↓↓ LLiivveerr FFuunnccttiioonn IInnffllaammmmaattiioonn NNeeccrroossiiss AAppooppttoossiiss ↓ ↑ Infection SSuurrvviivvaall PPrroobbaabbiilliittyy Survival Time
  • 43. What can we learn from anti-TNF-a story TNF-a and ALD McClain CJ, Hepatology 1989 Kamimura Hepatology 1995 Yin M, Gastroenterology 1999 Chang J, Hepatology 2004 Yamada Y et al, PNAS 1997 TNF alpha TTNNFF--a aanndd LLiivveerr RReeggeenneerraattiioonn
  • 44. What can we learn from anti-TNF-a story? Tilg H , J Hepatol 2003 Spahr L J hepatol 2002* SSttuuddyy DDeessiiggnn Mookerjee Gut 2003 SSiinnggllee DDoossee Sharma P, J Hepatol 2009 Inclusion criterion : Meld ≥15 Inclusion criterion : Maddrey SSttuuddyy DDeessiiggnn OOff RRCCTTSS MMuullttiippllee DDoosseess NC Boetticher, Gastroenterology 2008 ≥32 Naveau S Hepatology 2004 ↑risk of Infections
  • 45. - RReeccoovveerryy ↑↑ LLiivveerr FFuunnccttiioonn DDiisseeaassee ↓↓ LLiivveerr FFuunnccttiioonn Ideal molecule IInnffllaammmmaattiioonn NNeeccrroossiiss AAppooppttoossiiss + - Infection SSuurrvviivvaall PPootteennttiiaall tthheerraappeeuuttiicc ttaarrggeettss iinn tthhee ffuuttuurree SSuurrvviivvaall PPrroobbaabbiilliittyy
  • 46. Potential therapeutic ttaarrggeettss iinn tthhee ffuuttuurree IL-1 receptor antagonist (IL-1Ra) human IL-1ra [Anakinra®] ↓↓ AAllccoohhooll lliivveerr iinnjjuurryy Petrasek J, J Clin Invest 2012 BBRRDDUU IInnccoorrppoorraattiioonn human IL-1ra [Anakinra®] ↑↑ LLiivveerr rreeggeenneerraattiioonn Sgroi A, PlosOne 2011 Boulton Ra, Hepatology 1997
  • 47. Potential therapeutic ttaarrggeettss iinn tthhee ffuuttuurree Interleukin 22 [F-652] in phase I study ↓↓ AAllccoohhooll lliivveerr iinnjjuurryy Ki SH, Hepatology 2010 ↑↑ LLiivveerr rreeggeenneerraattiioonn Feng D, Gastroenterology 2012 Park O, Hepatology 2010
  • 48. Potential therapeutic ttaarrggeettss iinn tthhee ffuuttuurree Eculizumab [Soliris®] Antibody against C5 ↓↓ AAllccoohhooll lliivveerr iinnjjuurryy Pritchard MT, Gastroenterology 2007 Cohen JI, Gastroenterology 2010 BBlloocckkiinngg CC55 iimmpprroovveess oouuttccoommee iinn SSeeppssiiss Woehrl B, J Clin Invest 2011
  • 49. • Current management • Near Future • Distant Future : Arbitrary selection of novel molecules already tested in human beings • Transplantation for non-responders to medical therapy • Future Requirements
  • 50. SSeevveerree AAllccoohhoolliicc HHeeppaattiittiiss LLiivveerr TTrraannssppllaannttaattiioonn:: aa lloonngg wwaayy ttoo ggoo WWhheerree DDoo WWee AAllll CCoommee FFrroomm ?? • RReecceenntt ffoorrmmaall rreeccooggnniittiioonn tthhaatt AAHH iiss aann aabbssoolluuttee ccoonnttrraaiinnddiiccaattiioonn bbyy UUKK ttrraannssppllaanntt cceennttrreess ((BBaatthhggaattee AAJJ,, LLaanncceett 2000066)) • AAbbssttiinneennccee pprree--ttrraannssppllaanntt iiss nneecceessssaarryy ttoo eexxcclluuddee tthhoossee wwhhoo wwiillll iimmpprroovvee aanndd nnoott nneeeedd ttrraannssppllaannttaattiioonn • AAbbssttiinneennccee iiss uusseeffuull ttoo aallllooww ttiimmee ffoorr aasssseessssiinngg aanndd vveerriiffyyiinngg aallccoohhooll aaddddiiccttiivvee bbeehhaavviioouurr bbuutt « 6-month rule » is not a robust criterion Foster PF, Hepatology 1997 Liver transplantation for alcoholic liver disease: bias, beliefs, 6-month rule, and relapse- but where are the data. Beresford TP, Everson GT Liver Transpl 2000
  • 51. Where Do We Come From ? SSEEVVEERREE AALLCCOOHHOOLLIICC HHEEPPAATTIITTIISS LLIIVVEERR TTRRAANNSSPPLLAANNTTAATTIIOONN Where Do I Come From ? • Atterbury CE. The alcoholic in the lifeboat. Should drinkers be candidates for liver transplantation? J Clin Gastroenterol 1986 The Jury stated: - wait-and-watch strategy using the 6-month criterion may be unfair for some non-responders with 70- 80% probability of dying during this period - recommended pilot studies evaluating early liver transplantation in non-responders • Lucey MR J Hepatol 2002; Is liver transplantation an appropriate treatment for acute alcoholic hepatitis?
  • 52. Early liver transplantation: The French and Belgium Experience Philippe Mathurin1, Christophe Moreno2, Didier Samuel3, Jérôme Dumortier4, Julia Salleron5, François Durand6, Hélène Castel1, Alain Duhamel5, Georges-Philippe Pageaux7, Vincent Leroy8, Sébastien Dharancy1, Alexandre Louvet1, Emmanuel Boleslawski1, Valerio Lucidi2, Thierry Gustot2, Claire Francoz6, Christian Letoublon8, Denis Castaing3, Jacques Belghiti6, Vincent Donckier2, François-René Pruvot1, Jean-Charles Duclos-Vallée3 Brussels, Grenoble, Lille, Lyon, Montpellier, Beaujon, Villejuif New EnglJ Med 2011
  • 53. EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss • Early liver transplantation in non-responders undergoing their ffiirrsstt event of liver disease • Non responders were identified using Lille score ≥0.45 or worsening of liver function by day 7.
  • 54. Early LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss SSeelleeccttiioonn pprroocceessss== 44 TTeeaamm cciirrcclleess Family structure Patient Time toward complete consensus = nurses, i.e. one resident and one fellow specialist in addiction = senior hepatologists senior anesthetist and surgeons
  • 55. EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss Transplanted non responders N=26 Male gender no. [%] 15 [57.7%] Age (years) median [95%CI] 47.4 [42.7-52.4] Duration of corticosteroids treatment (days) Median [95%CI] 11.5 [7-18] Hepatorenal syndrome, no. [%] 15 [57.7%] Hemodiafiltration or MARS® system no. [%] 10 [38.5 %] Infection before transplantation no [%] 18 [69.2%] Mechanical ventilation no [%] 4 [15.4%]
  • 56. Median [95%CI] Lille score 0.88 [0.76 – 0.95] MELD on first day of therapy 30.1 [27.7 - 33.4] MELD day 7 28.5 [26.2 – 33.7] MELD at listing 34.2 [29 – 37] MELD day 0 - MELD Listing - 5.44 [-7.3 – 2] MELD day 7 - MELD Listing - 1.9[-6 – 0] Time (days) from end of therapy to 13 [6 – 17] listing Time (days) from listing to LT 8.5 [3 – 11] * MMaaxxiimmuumm ooff LLiillllee ssccoorree iiss 11 ** EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss
  • 57. Early Transplantation sshhiifftt ssuurrvviivvaall ooff uunnrreessppoonnssiivvee ttoo rreessppoonnddeerrss • Final combined database included a total of 651 patients. Matching was performed using the global optimal algorithm • For matching criteria, we used the following pre-established ranges: age (+/- 10 years), gender, Maddrey function (<60; 60-90 and >90) and Lille score (+/-0.15) • The overall optimal algorithm was able to select 3 unresponsive matched controls for 20 transplanted patients, 2 unresponsive matched controls for 3 transplanted patients and only 1 unresponsive matched control for 3 transplanted patients. • The overall optimal algorithm was able to select 4 responsive matched controls for 21 transplanted patients, 2 responsive matched controls for 3 transplanted patients and only 1 responsive matched control for 2 transplanted patients
  • 58. EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss
  • 59. EEaarrllyy LLTT iinn AAllccoohhoolliicc hheeppaattiittiiss • No alcohol relapse within the 6 month period • 3 patients resumed alcohol consumption during data collection - at 720, 740 and 1140 days [2 daily consumers and 1 had occasional consumption (approximately 10g/week)] • 2 centers have prospective data base of severe alcoholic hepatitis only 4 (1.83%) were directly selected by the 2 centers from their own recruitment • Proportions of eLT among the total number of procedures, and number of procedures for alcoholic liver disease, were 26/891 [2.92%]) and 26/315, [8.25%], respectively
  • 60. Outcomes After Liver Transplantation for Alcoholic Hepatitis Are Similar to Alcoholic Cirrhosis Graft Survival Patient Survival Singal AK et al., Hepatology 2011
  • 61. 1. In patients with severe ASH not responding to medical therapy, early LT need to be further evaluated in carefully-selected patients Journal of Hepatology 2012
  • 62. PPHHRRCC QQuuiicckkTTrraannss--HHAAAA AAHH nnoott rreessppoonnddiinngg ttoo mmeeddiiccaall tthheerraappyy AAllggoorriitthhmm bbaasseedd oonn oobbjjeeccttiivvee ccrriitteerriiaa RRaannggee ooff SSccoorree ffrroomm 00 ttoo 225500 GO AAllggoorriitthhmm ssccoorree ≥≥ 222200 GO AAllggoorriitthhmm ssccoorree << 222200GO Not selected SSeelleecctteedd CCoonnttrrooll ggrroouupp AAllccoohhoolliicc ccaannddiiddaatteess ffoorr lliivveerr ttrraannssppllaannttaattiioonn Classical selection 6-month criteria Primary objective Non inferiority in terms of alcohol relapse Secondary endpoint survival benefit Non responders Not Transplanted
  • 63. • Current management • Near Future • Distant Future : Arbitrary selection of novel molecules already tested in human beings • Transplantation for non-responders to medical therapy • Future Requirements
  • 64. Better KKnnoowwlleeddggee ooff tthhee NNaattuurraall HHiissttoorryy 66 mmoonntthhss Deaths due to liver injury in > 90 % of cases No impact of alcoholism behavior 66--MMOONNTTHH PPEERRIIOODD SSUURRVVIIVVIINNGG TTHHEE 66 MMOONNTTHH PPEERRIIOODD OOPPTTIIMMAALL PPEERRIIOODD FFOORR SSTTUUDDIIEESS TTEESSTTIINNGG DDRRUUGG PPRREEVVEENNTTIINNGG LLIIVVEERR IINNJJUURRYY AAlliivvee RReessppoonnddeerrss ttoo mmeeddiiccaall tthheerraappyy GGoooodd LLiivveerr FFuunnccttiioonn Abstainers during 5 years Risk of Liver-Related death ≈ 15% Relapsers during 5 years Risk of Liver-Related death ≈ 50% AAFFTTEERR 66 MMOONNTTHHSS AAVVOOIIDD SSTTUUDDIIEESS TTEESSTTIINNGG DDRRUUGG PPRREEVVEENNTTIINNGG LLIIVVEERR IINNJJUURRYY AAlliivvee NNoonn--RReessppoonnddeerrss ttoo mmeeddiiccaall tthheerraappyy IInntteerrmmeeddiiaattee LLiivveerr ddyyssffuunnccttiioonn Abstainers during 5 years Risk of Liver-Related death ≈ 50% Relapsers during 5 years Risk of Liver-Related death ≈ 90% Louvet A, AASLD 2010
  • 65. UUnnmmeett nneeeeddss • Animal models mimicking better liver Injury in human beings (liver dysfunction and regeneration) • Better network between basic and clinician researchers • Official recommendations from experts of scientific societies on the criteria that need to be fulfilled for an optimal study design • Development and validation of surrogate markers of survival (like the RECIST criteria in cancers) for testing of new molecules in phase I and/or II • Bring pharmaceutical companies to test and develop molecules
  • 66. NIAAA Announces Request for Applications oonn AAllccoohhoolliicc HHeeppaattiittiiss “Integrated Approaches for Identifying Molecular Targets in Alcoholic Hepatitis”