Lab
Liver Function Test Abnormality
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Liver Function Test Abnormality
, LFT Abnormality, Transaminitis, Abnormal Hepatic Panel
See Also
Liver Function Test
Epidemiology
Mild asymptomatic transaminase elevations (<5x normal) are common
U.S.
Prevalence
may be as high as 10%
However, serious liver disease is found in only 5% of these cases
Approach
Focus of evaluation
Iatrogenic or Treatable disease
Communicable or Inheritable disease
True abnormality versus
False Positive
testing
History
Non-
Alcohol
ic
Fatty Liver
risk factors
Medications
Aminotransferase
Elevations (ALT, AST)
See
Hepatotoxin
Cholestatic Elevations (
Alkaline Phosphatase
, GGT)
Sulfonamide
s
Augmentin
Erythromycin
Captopril
Oral Hypoglycemic
s
Chlorpromazine
Imuran
Alcohol Abuse
(
Alcoholic Hepatitis
)
Contagious Contacts (
Viral Hepatitis
)
Sexually Transmitted Disease
Intravenous Drug Abuse
Transfusions
Needle Stick
s
Symptoms (mild elevations are usually asymptomatic)
Constitutional Symptoms
Fever
Weight loss
Fatigue
Malaise
Nausea
or
Vomiting
Pruritus
Arthralgia
s
Signs
Weight loss
Stigmata of
Chronic Liver Disease
or
Cirrhosis
Gynecomastia
Testicular atrophy
Spider Nevi
Finger nail
Clubbing
Asterixis
Abdominal exam
Hepatomegaly
Splenomegaly
Ascites
Differential Diagnosis (Transaminase elevation, Transaminitis)
Common hepatic causes
Alcoholic Liver Disease
(27%)
AST/ALT ration >2
GGT increased
Nonalcoholic Fatty Liver Disease
(25-51%)
Metabolic Syndrome
Increased
Serum Triglyceride
s and
Serum Glucose
and low
HDL Cholesterol
Uncommon hepatic causes
Hepatitis B
or
Hepatitis C
(18%)
Hemochromatosis
(3%)
Serum Iron
and
Ferritin
levels increased
Hepatotoxin
s (medications)
Rare hepatic causes
Autoimmune Hepatitis
(1%)
More common in young women with autoimmune disorders
Evaluation includes
SPEP
, ANA, SMA, LKM-1
Alpha-1 Antitrypsin Deficiency
(1%)
Associated with premature
COPD
Primary Biliary Cirrhosis
(0.3%)
Wilson Disease
Consider in liver disease at a young age (e.g. <30 years old)
Serum ceruplasmin abnormal
Extrahepatic causes
Celiac Disease
Hemolysis
Causes include
G6PD
,
Sickle Cell Anemia
, infection
Muscular disorders (e.g.
Polymyositis
)
Increased CPK and aldolase
Hypothyroidism
or
Hyperthyroidism
Labs
See
Liver Function Test
Markers of hepatocyte injury
Precautions
Liver
transaminases (ALT, AST) true normal ranges are <25 IU/L in women, <33 IU/L in men
For those with liver disease risk factors, the lab cut-offs (50-60 IU/L) are abnormal (not simply borderline)
Transaminase elevations are considered mild if <5 times normal
Elevations >5 times normal require extensive evaluation for cause
Alanine
transaminase (ALT)
Most specific for hepatocyte injury
Aspartate
transaminase (AST)
Less specific than ALT (present outside liver)
Non-liver causes include
Celiac Sprue
,
Hemolysis
,
Dermatomyositis
, tissue infarction,
Hyperthyroidism
AST to ALT Ratio
AST/ALT ratio <1 in Non-
Alcohol
ic
Fatty Liver
Disease (LR+ 80, LR- 0.2)
Sorbi (1999) Am J Gastroenterol 94(4): 1018-22 [PubMed]
AST/ALT ratio >2 in
Alcoholism
(LR+ 17, LR- 0.49)
AST/ALT ratio >4 in
Wilson's Disease
Lactate Dehydrogenase
(LDH)
Least specific for hepatocyte injury
Dramatically increased in ischemic hepatitis
Increased with alk phos in liver metastases
Markers of cholestasis
Serum Alkaline Phosphatase
Gamma glutamyl transferase
(GGT)
Serum Bilirubin
Marker of liver function and
Protein
synthesis
Serum Albumin
Prothrombin Time
Markers of advanced fibrosis
Platelet Count
(
Thrombocytopenia
)
Imaging
Abdominal Ultrasound
right upper quadrant
Preferred cost-effective evaluation
Abdominal CT
Consider if
Ultrasound
is non-diagnostic
Management
Increased serum transaminases (ALT, AST)
Criteria
Indicated in mild, asymptomatic liver transaminase (ALT, AST) elevations <5 times normal
Symptomatic or elevations >5 times normal should prompt more urgent, thorough evaluation
See
Alkaline Phosphatase
for cholestasis causes
Step 0: History and Physical
Lab and diagnostic evaluation as directed by history and physical
Avoid
Hepatotoxin
s including
Alcohol
Consider
Fastin
g lipid profile and
Serum Glucose
(or complete in step 1)
Plan repeat evaluation and labs in 2-4 weeks (see Step 2)
Step 1: Obtain initial lab work
Hepatic panel (as above)
Prothrombin Time
(INR)
Serum Albumin
Complete Blood Count
with
Platelet Count
Viral Hepatitis Serology
Consider
Hepatitis A Serology
Hepatitis B Serology
(
HBsAg
)
Hepatitis C Serology
Consider
Monospot
Serum Ferritin
,
Serum Iron
and
TIBC
(
Hemochromatosis
)
Fastin
g lipid profile and
Fastin
g
Glucose
(or
Hemoglobin A1C
)
Step 2: Evaluate labs, history and examination
Treat specific causes
Consider Non-
Alcohol
ic
Fatty Liver
disease (
NAFLD
) - most common
Step 3:
Gene
ral measures if no cause identified
Avoid
Hepatotoxin
s
Withdraw suspected medications
Abstain from
Alcohol
use
Reduce hepatic
Steatosis
risks
Weight loss if
Overweight
Improve
Blood Sugar
control in
Diabetes Mellitus
Treat
Hyperlipidemia
(esp.
Serum Triglyceride
s)
Repeat
Liver Function Test
s in 2-6 months
Obtain imaging as above if elevations persist
Liver Function Test
s often remain elevated on follow-up for longer than 2 years
Lilford (2013) Health Technol Assess 17(28): 1-307 [PubMed]
Step 4: Abnormal transaminases persist on recheck
Obtain
Ultrasound
of right upper quadrant
Obtain disease specific markers
Complete initial labs in Step 1 if not done
Ceruloplasmin (
Wilson's Disease
)
Antinuclear Antibody
Anti-
Smooth Muscle Antibody
Alpha-1-antitrypsin
Anti-tissue transglutaminase
Antibody
:
Celiac Sprue
Consider non-hepatic transaminase elevations
Peripheral Smear
,
Coombs
test (
Hemolysis
)
Rhabdomyolysis
or
Polymyositis
(
Creatine Kinase
, aldolase)
If testing as above is negative for specific cause
Obese patient: See
Steatosis
Non-obese Patient
Aminotransferase
s exceed twice normal
Refer to Gastroenterology for biopsy
Aminotransferase
s mildly elevated
Follow serial
Aminotransferase
s (AST, ALT)
Management
Increased
Alkaline Phosphatase
(marked) with normal transaminases
Confirm increase is due to gastrointestinal cause (e.g. as opposed to bone) with a fractionated
Alkaline Phosphatase
Cholestatic
Liver
Disease
Primary Sclerosing Cholangitis
Primary Biliary Cirrhosis
Infiltrative Conditions
Malignancy
Amyloidosis
Sarcoidosis
Infectious disease
References
Loftus (2012) Mayo POIM Conference, Rochester
References
(2002) Gastroenterology 123:1364-6 [PubMed]
Giboney (2005) Am Fam Physician 71(6):1105-10 [PubMed]
Oh (2011) Am Fam Physician 84(9): 1003-8 [PubMed]
Oh (2017) Am Fam Physician 96(11): 709-15 [PubMed]
Pratt (2000) N Engl J Med 342:1266-71 [PubMed]
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