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Alcoholic liver disease

Alcoholic liver disease. Sadie T. Velásquez , M.D. Case presentation.

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Alcoholic liver disease

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  1. Alcoholic liver disease Sadie T. Velásquez, M.D.

  2. Case presentation 48 yo female with Cirrhosis presenting with increasing abdominal pain and girth for two days with worsening jaundice, LEE. Pt was treated two weeks prior at an OSH for the same symptoms and found to have low Hct and transfused 2 units. Labs from the OSH included Na of 130, BUN/Cr 26/ 0.9 T bili 10.8 AST/ALT/ALP 69/31/186 and INR 3.27, pt was also treated for an UTI. Pt with h/o EtOH abuse, last drink this month. ROS: +SOB, no wheezes, + dark stools x 1 week, no BRBPR. + early satiety. No n/v, HA, f/c, night sweats, GU/GI changes, rashes, muscle/joint aches. PMH: Cirrhosis (2 year) PSH: cholecystecotmy, tubal ligation Meds: lactulose, lasix, spirololactone (all from last hospital 2 weeks ago) Social: Lives in SA with husband, unemployed. Denied D, T; EtOH 6 beers q 2 days/prior heavy EtOH; 6 kids all uncomplicated vaginal deliveries FamilyHx: mom with DM

  3. Vitals: T AF R 20s HR 75 BP 104/56 02Sat 98% Physical: General: Alert and oriented x3, Lethargic Cardiac: regular, normal rate, 3/6 systolic murmur; no rubs or gallops Lungs: clear to auscultation bilaterally, no wheezes, rales, or rhonchi Abdomen/GI: soft, tender to palpation, distended, no rebound/guarding, + abd wall edema Ext: 3+ LE edema up thighs bilaterally Neuro: no asterixis, no nystagmus, CN 2-12 grossly intact

  4. Labs: CHEM 123/ 5.6/95/21/60/2.9 CBC 6.5 >8.4/24<60 LFT 108/47/213, GGT 15 INR 2 NH3 78 Lipase 57 Tbili 12.3 D bili 6.5, Lipase 78  negative hep panel, ANA, ALMK, HIV, alpha 1 antitrypsin (MELD 34) Imaging: CXR: Cardiomegaly with a mild degree of pulmonary vascular congestion. Patchy opacities within left lower lobe may represent superimposed pneumonia. AbdSono: 1. Heterogeneous echotexture of liver may represent steatosis versus fibrosis. No focal liver lesion is seen. 2. Extensive subcutaneous soft tissue edema involving the lower abdominal wall. No free fluid is visualized

  5. Alcoholic liver disease AASLD Practice Guidelines

  6. Objectives • Metabolism of Alcohol • Genetics of Alcohol abuse • Risk factors for Alcoholic Liver Disease • Screening • Diagnosis • Prognosis • Treatment

  7. At last, Britain's a world leader again (unfortunately it's in drinking alcohol) . http://www.dailymail.co.uk/news/article-1357865/Britain-countries-drink-alcohol-world-new-figures-show.html

  8. Male deaths and alcohol http://www.dailymail.co.uk/news/article-1357865/Britain-countries-drink-alcohol-world-new-figures-show.html

  9. How does alcohol damage the liver?

  10. Pathophysiologyof Alcohol-Induced Liver Injury

  11. ROS= Reactive oxygen species

  12. Why do some get alD and others don’t?

  13. Genetics of alcohol abuse/ALD • In the 70s, they found that up to a third of confirmed alcoholics have completely normal liver histology. • In the 1980s, Hrubec and Omenn found evidence supporting a genetic component to predisposition from a large study of 15924 male twin pairs. The concordance rate for alcoholic cirrhosis was 14.6% in monozygotic twins and 5.4% in dizygotic twins. • In 1992, Day noted that ‘why only a few alcoholics develop significant liver disease remains largely a mystery’ and also discusses the idea of a ‘polygenic’ disorder and the using a molecular genetic approach to identify those at ‘high risk’ for ALD. • Uhl maps out genes in 2001 in drug abusers supporting polygenic contributions of common allelic variants to polysubstance abuse vulnerability.

  14. Risk factors • *Dose, duration of alcohol • Type of alcohol • Drinking patterns • Sex • Ethnicity • Protein calorie malnutrition • Genetic factors • Polymorphisms of genes • Concomitant viral hepatitis

  15. What is a unit of alcohol?

  16. Screening for alcohol abuse • CAGE Questionnaire • Have you ever felt you should CUT down on your drinking? • Have people ANNOYED you by criticizing your drinking? • Have you ever felt GUILTY about your drinking? • Have you ever had a drink first thing in the morning to steady your nerves or to get rid of a hangover (EYE-OPENER)? • (EACH REPSONSE 0 OR 1 → ≥ 2 IS SIGNIFICANT) • Sensitivity of 71% and specificity of 90%

  17. AUDIT Questionnaire • WHO • ≥8 for men up to age 60, or ≥ 4 for women, adolescents or men > 60 is positive • Sensitivity 51-97% and specificity 78-96%

  18. Disease spectrum Standard drink is 12g in the USA • Spectrum of injury varies from simple steatosis to cirrhosis • Three histologic stages of ALD • Fatty liver or simple steatosis • In ~90% of those who drink > 60g/day of alcohol • Alcoholic hepatitis • Mild to severe, life-threatening injury • Chronic hepatitis with hepatic fibrosis or cirrhosis • Associated histologic changes including the presence of Mallory’s hyaline, megamitochondria or perivenular and perisinusoidal fibrosis

  19. Diagnosis • History of significant alcohol intake • Clinical evidence of liver disease • Supporting laboratory abnormalities • May have elevated GGT, macrocytosis • AST typically 2-6x normal • AST/L ratio >2 in 70%, but greater value in patients without cirrhosis • Need to rule-out other etiologies of liver disease

  20. Diagnosis • Physical exam may be normal or suggest advanced cirrhosis • Exam findings most common with ALD: • Parotid enlargement • Dupuytren’s contracture • Feminization • HE • Ascites • Spider nevi • Weakness • Edema

  21. Diagnosis • Hepatic imaging: Ultrasound, CT or MRI • Value is to exclude other causes of abnormal liver tests • Higher volume index of the caudate lobe, more frequent visualization of the R posterior hepatic notch and smaller size of regenerative nodules of the liver are suggestive findings • Liver biopsy • Confirm the diagnosis • Convey prognostic importance • If no treatment for ALD or AH is contemplated, it usually is not necessary to make a histologic diagnosis

  22. Alcoholic hepatitis

  23. Cirrhosis

  24. prognosis • Maddrey’sdiscriminant function (MDF) • MELD score • Glasgow Alcoholic Hepatitis score

  25. prognosis • Maddrey’sdiscriminant function (MDF) • 4.6 (Patient’s prothrombin time – control prothrombin time) + total bilirubin • ≥32 have the highest risk of dying with 30 day mortality of 30-50% • HE and elevated MDF were at the highest risk • Sensitivity ~ 83-86%, specificity 48-60%

  26. prognosis • MELD score • 3.8 x log(bilirubin in mg/dL) + 11.2 x log(INR) + 9.6 x log(creatinine) + 6.4 • Poor prognosis if >18 • Change of ≥2 in the first week independently predicts in-hospital mortality • Sensitivity ~85%, specificity ~ 84%

  27. prognosis • Glasgow Alcoholic Hepatitis score • 5 variables: Age, WBC, BUN, PT ratio, bilirubin on day 1 or on day 7 • Poor prognosis if >8

  28. Treatment • Abstinence • Naltrexone or acamprosate may be considered in combination with counseling • Nutritional therapy • Steroids • Anticytokine Therapy • Combination therapy • Liver transplantation

  29. Treatment- Steroids • MDF ≥ 32 +/- HE without contraindications • Prednisolone 40mg/day for 4 weeks then tapered over 2-4 weeks • Recent study in NEJM on NAC + prednisolone • If steroids contraindicated, consider pentoxifylline therapy

  30. Liver transplantation • ALD is the second most common indication for liver transplantation in the Western world • 95% of those with ESLD related to alcohol are never formally evaluated for LT • 6-month period of abstinence is recommended for listing • Overall survival rates similar between alcohol-related and other LT recipients • Transplant recipients for alcoholic liver disease are highly likely to drink after transplantation (11-49%), but only a small fraction revert to heavy use or abuse

  31. Summary • Screen for alcohol use and evaluate those with evidence of liver disease • Rule-out other etiologies of liver disease • Consider liver biopsy if contemplating tx or uncertainty of the dx • Risk stratify using MDF and MELD • Encourage abstinence +/- medical therapy • Assess for nutritional, vitamin, mineral deficiencies in AH or advanced ALD and treat aggressively • Steroids for severe disease, MDF ≥ 32, or pentoxifylline • Frequent interval feedings to improve nitrogen balance in patients with alcoholic cirrhosis • Consider appropriate patients for LT

  32. References • O'Shea RS, Dasarathy S, McCullough AJ; Practice Guideline Committee of the American Association for the Study of Liver Diseases; Practice Parameters Committee of the American College of Gastroenterology. Alcoholic liver disease. Hepatology. 2010 Jan;51(1):307-28. • Uhl GR, Liu QR, Walther D, Hess J, Naiman D. Polysubstanceabusevulnerabilitygenes: genome scans for association, using 1,004 subjects and 1,494 single-nucleotide polymorphisms. Am J Hum Genet 2001;69: 1290-1300.  • Brown K. Alcohol hepatotoxicity: a genotypic predisposition? Am J Gastroenterol 1992;87:677-678. • Day CP, Bassendine MF. Genetic predisposition to alcoholic liver disease. Gut 1992;33:1444-1447.  • Goodwin DW, Schulsinger F, Hermansen L, Guze SB, Winokur G. Alcohol problems in adoptees raised apart from alcoholic biological parents. Arch Gen Psychiatry 1973;28:238-243.  • Glucocorticoids plus N-acetylcysteine in Severe Alcoholic Hepatitis. NEJM 2011 Nov 10; 365;19: 1781-1789. • Reed T, Page WF, Viken RJ, Christian JC. Genetic predisposition to organ-specific endpoints of alcoholism. Alcohol Clin Exp Res 1996;20: 1528-1533.  • Mathurin P, Abdelnour M, Ramond MJ, Carbonell N, Fartoux L, Serfaty L, et al. Early change in bilirubin levels is an important prognostic factor in severe alcoholic hepatitis treated with prednisolone. HEPATOLOGY 2003;38:1363-1369.  • Schuckit. New Findings in the Genetics of Alcoholism. JAMA 1999;281:1875-1876. • Michael R. Lucey, M.D., Philippe Mathurin, M.D., Ph.D., and Timothy R. Morgan, M.D. Alcoholic Hepatitis. N Engl J Med 2009; 360:2758-2769

  33. Questions?

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