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International Journal of Chemistry, Mathematics and Physics (IJCMP)
[Vol-6, Issue-6, Nov-Dec, 2022]
https://dx.doi.org/10.22161/ijcmp.6.6.1
ISSN: 2456-866X
http://www.aipublications.com/ijcmp/ Page | 1
The Impacts of Viral Hepatitis on Liver Enzymes and
Bilrubin
Dr. Noaman Abdulateef Abdulrazzaq, Mustafa Mamon Ahmed, Farah Thamer Hasan
Al-Turath University, Iraq, Baghdad
Received: 16 Oct 2022; Received in revised form: 03 Nov 2022; Accepted: 08 Nov 2022; Available online: 12 Nov 2022
©2022 The Author(s). Published by AI Publications. This is an open access article under the CC BY license
(https://creativecommons.org/licenses/by/4.0/)
Abstract— Viral hepatitis is an infection that causes liver inflammation and damage. Several different
viruses cause hepatitis, including hepatitis A, B, C, D, and E. The hepatitis A and E viruses typically cause
acute infections. The hepatitis B, C, and D viruses can cause acute and chronic infections. Hepatitis A
causes only acute infection and typically gets better without treatment after a few weeks. The hepatitis A
virus spreads through contact with an infected person’s stool. Protection by getting the hepatitis A
vaccine. Hepatitis E is typically an acute infection that gets better without treatment after several weeks.
Some types of hepatitis E virus are spread by drinking water contaminated by an infected person’s stool.
Other types are spread by eating undercooked pork or wild game. Hepatitis B can cause acute or chronic
infection. Recommendation for screening for hepatitis B in pregnant women or in those with a high chance
of being infected. Protection from hepatitis B by getting the hepatitis B vaccine. Hepatitis C can cause
acute or chronic infection. Doctors usually recommend one-time screening of all adults ages 18 to 79 for
hepatitis C. Early diagnosis and treatment can prevent liver damage. The hepatitis D virus is unusual
because it can only infect those who have a hepatitis B virus infection. A coinfection occurs when both
hepatitis D and hepatitis B infections at the same time. A superinfection occurs already have chronic
hepatitis B and then become infected with hepatitis D. The aim of this study is to find the effect of each
type of viral hepatitis on the bilirubin (TB , DSB) , and liver enzymes; AST, ALT, ALP,GGT among
viral hepatitis patients. 200 patients were selected from the viral hepatitis units in the central public
health laboratory in Baghdad city, all the chosen cases were confirmed as a positive samples , they
are classified into four equal group each with fifty individual and with a single serological viral
hepatitis type either; anti-HAV( IgM ) , HBs Ag , anti-HCV ,or anti-HEV(IgM ). All patients were
tested for; serum bilirubin ( TB ,D.SB ) , AST , ALT , ALP , GGT. Another fifty quite healthy and normal
person was selected as a control group for comparison. . Liver enzymes and bilirubin changes are
more pronounced in HAV, HEV than HCV and HBVAST and ALT lack some sensitivity in detecting HCV
,HBV and mild elevations of ALT or AST in asymptomatic patients can be evaluated efficiently
by considering ,hepatitis B, hepatitis C. ALT is generally a more sensitive indicator of acute liver cell
damage than AST, It is relatively specific for hepatocyte necrosis with a marked elevations in viral
hepatitis. Liver enzymes and bilirubin changes are more pronounced in HAV, HEV than HCV and
HBV.AST and ALT lack some sensitivity in detecting HCV ,HBV and mild elevations of ALT or AST
in asymptomatic patients can be evaluated efficiently by considering ,hepatitis B, hepatitis C. ALT is
generally a more sensitive indicator of acute liver cell damage than AST, It is relatively specific for
hepatocyte necrosis with a marked elevations in viral hepatitis.
Keywords— viral hepatitis, liver enzyme.
Abdulrazzaq et al.
International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022)
http://www.aipublications.com/ijcmp/ Page | 2
I. INTRODUCTION
Hepatitis Inflammation of the liver that can be caused by
viruses , chemicals , drugs , alcohol , inherited diseases
,or the patient’s own immune system. Hepatitis may
occur with limited or no symptoms , but often leads
to jaundice, anorexia and malaise .Hepatitis is acute
when it lasts less than six months and chronic when it
persist longer.
Causes;
The most common cause of viral hepatitis are the five
unrelated hepatotropic viruses , A , B, C ,D , E, and
Other viruses which can also cause hepatitis includes
; Herpes simplex , Cytomegalo virus , Epstein
Barr virus , Yellow fever.
HDV
HCV
HBV
HEV
HAV
Parent-eral
Parent-eral
Parent-eral
Enteric
Enteric
Transmission
Delta virus
Hepacivirus
Hepadn-avirus
Hepe virus
Picornavirus
Classification
-ssRNA
+ssRNA
+dsDNA
+ssRNA
+ssRNA
Genome
Delta Ag
CoreAg
HBsAg,HBeAg
Antigen
30-60 days
15-150 days
45-160 days
15-60 days
15-45 days
Incubat-ion
period
YES with HBV
YES (com-mon)
YES (uncommon)
NO
NO
Chroni-city
Liver function tests;
Groups of clinical biochemistry laboratory blood assays
designed to give information about the state of a patient's
liver.
They are indicative of:
1) liver inflammation: ALT and AST.
2) Cholestasis or biliary obstruction bilirubin (total, direct),
ALP, GGT
3) synthetic function: albumin, PT.
Viral hepatitis with its different serotypes are known to
have various extent of effects on the liver function tests.
Aim of the study
The aim of this study is to find the effect of each type
of viral hepatitis whether A , B ,C , or E on the bilirubin
(TB , DSB) , and liver enzymes; AST, ALT, ALP,GGT
among viral hepatitis patients.
II. INDIVIDUALS AND METHODS
200 patients were selected from the viral hepatitis units
all the chosen cases were surveyed for different types
of viral hepatitis measured by ELISA and ELFA
methods which was confirmed as a positive samples
where they are classified into four equal group each with
fifty individual and with a single serological viral
hepatitis type either; anti-HAV( IgM ) , HBs Ag , anti-
HCV ,or anti-HEV(IgM ). All patients were tested for;
serum bilirubin ( TB ,D.SB ) , AST , ALT , ALP , GGT
, which are measured indirectly by using a
spectrophotometer method. Another fifty quite healthy
and normal person was selected as a control group.
III. RESULTS
Table (1). General descriptive statistics for the liver
enzymes and bilirubin, their number, mean± SD with the
maximum and minimum values.
ST.DEV.
MEAN
MAXIMUM
MINIMUM
N
Parameters
2.28672
2.2093
9.80
O.12
250
TSB
1.05555
.9220
5.10
O.O1
250
D.SB
67.38983
58.2234
450.00
3.00
250
ALT
64.35098
59.2780
291.00
4.00
250
AST
160.2512
166.7740
841.00
20.00
250
ALP
100.4452
82.3336
980.00
8.00
250
GGT
Abdulrazzaq et al.
International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022)
http://www.aipublications.com/ijcmp/ Page | 3
Tab.(2).mean for comparison of TSB and D.SB with the control group in different types of hepatitis.
Std.er.
Std.de.
mean
group
Parameters
.049
.284
.164
.203
.399
.349
2.013
1.163
1.438
2.828
.783
4.066
.836
1.466
3.893
Contr.
HAV
HBV
HCV
HEV
TSB
.029
.171
.087
.058
.128
.208
1.209
.260
.413
.909
.299
2.253
.362
.430
1.248
Contr.
HAV
HBV
HCV
HEV
D.SB
Tab (3).mean for comparison of AST and ALT with the control group in different types of hepatitis.
Std.er.
Std.de.
mean
group
parameter
1.353
7.101
4.859
1.849
11.874
9.569
50.212
34.360
13.075
83.966
23.314
90.660
33.740
17.567
131.10
Contro
HAV
HBV
HCV
HEV
AST
1.570
8.748
6.610
11.707
5.385
11.105
61.861
46.744
82.784
38.081
17.996
135.50
32.860
61.040
43.640
Contro
HAV
HBV
HCV
HEV
AlT
Tab(4).mean for comparison of ALP and GGT with the control group in different types of hepatitis.
Std.er.
Std.dev.
mean
group
parameter
2.172
25.374
7.003
9.984
17.498
19.178
179.427
49.520
70.601
123.731
64.078
194.840
71.800
122.792
180.300
Control
HAV
HBV
HCV
HEV
ALP
2.172
25.374
7.003
9.984
17.498
31.953
84.550
21.865
145.843
115.087
44.570
140.343
30.850
98.472
97.400
Control
HAV
HBV
HCV
HEV
GGT
Abdulrazzaq et al.
International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022)
http://www.aipublications.com/ijcmp/ Page | 4
ANOVA test;
It shows significant difference between the groups with a P-value ˂ 0.05 for all of the parameters.
Tab (5).Multiple Comparisons Dun net t-test with the Mean Difference and Significant P-values (˂ 0.05 ) between all
groups.
Significant P- values
Mean Difference
Group
Variable
.000
3.283*
3.110*
HAV
HEV
TSB
.000
1.954*
.948*
HAV
HEV
D.SB
.000
67.346*
107.786*
HAV
HEV
AST
.000
117.583*
43.043*
HAV
HCV
ALT
.000
330.762*
58.714*
116.222*
HAV
HCV
HEV
ALP
.000
95.922*
53.960*
52.888*
HAV
HCV
HEV
GGT
Abdulrazzaq et al.
International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022)
http://www.aipublications.com/ijcmp/ Page | 5
IV. DISCUSSION
A number of pitfalls can be encountered in the
interpretation of common blood liver function tests:
1. Normal LFTs do not always mean that the liver is
normal.
2. They often, but not always, indicate that something is
wrong with the liver.
3. They can provide clues to the nature of the problem.
4. Transaminases are the most sensitive indicators of
hepatic cell injury.
Unfortunately (85%) HCV people are free of any
symptoms , usually they are discovered because the liver
enzymes in their blood are above normal limits , and
their doctors do more blood tests to find the cause , or
they are discovered during their donation for blood in
blood bank and this is also true for HBV as (15%) of the
patients can easily passed unnoticed as some of them
have no outward signs or symptoms , and others do
experience just "flu-like" symptoms.
The present study illustrate the significant changes in
the values of the main hepatic markers in different
types of viral hepatitis which was noticed
mainly in HAV and HEV more than in the HCV
and HBV (Table5) , a hallmark results that can easily
be explained on the fact that the hepatocyte necrosis
results in the leakage of enzymes into the circulation .
While liver cell death with HBV and HCV occurs by
Abdulrazzaq et al.
International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022)
http://www.aipublications.com/ijcmp/ Page | 6
apoptosis (programmed cell death) as well as by
necrosis which presumably synthesize less AST and
ALT as they wither away. This probably explains why at
least one third of patients infected with hepatitis C
virus have persistently normal serum ALT, AST levels
despite the presence of inflammation on liver biopsy.
Thus, AST and ALT lack some sensitivity in detecting
HCV, HBV and mild elevations of ALT or AST in
asymptomatic patients can be evaluated efficiently by
considering , hepatitis B, hepatitis C.ALT is relatively
specific for hepatocyte necrosis with a marked elevations
in viral hepatitis (Table 2, Fig. B).
AlP and GGT levels typically rise to several times the
normal level after several days of bile duct obstruction or
intrahepatic cholestasis , Both AlP and GGT levels are
elevated in about 90% of patients with this study were
we found mildly to Moderately elevated ALP and GGT
due to hepatocyte necrosis in combination with some
intrahepatic cholestasis specifically in HAV and HEV
(Tab 4, Fig C ).
Viral hepatitis is one of the main causes of
hyperbilirubinemia whether it is direct or indirect fraction
of bilirubin. Actually, both categories of bilirubin was
elevated in all serotypes of viral hepatitis yet it
was also more prominent in HAV and HEV (Table 2,
Fig A).
V. CONCLUSION
1. Liver enzymes and bilirubin changes are more
pronounced in HAV, HEV than HCV and HBV.
2. AST and ALT lack some sensitivity in detecting HCV
,HBV and mild elevations of ALT or AST in
asymptomatic patients can be evaluated efficiently by
considering ,hepatitis B, hepatitis C.
3. ALT is generally a more sensitive indicator of acute
liver cell damage than AST, It is relatively specific for
hepatocyte necrosis with a marked elevations in viral
hepatitis.
REFERENCES
[1] Green RM, Flamm S. AGA technical review on the
evaluation of liver chemistry tests. Gastroenterology
2002;123(4):1367-84. [PubMed]
[2] Dufour DR, Lott JA, Nolte FS, Gretch DR, Koff RS, Seeff
LB. Diagnosis and monitoring of hepatic injury. I.
Performance characteristics of laboratory tests. Clin Chem
2000;46(12):2027-49. [PubMed]
[3] Fogden E, Neuberger J. Alternative medicines and the
liver. Liver Int 2003; 23 (4): 213-20. [PubMed]
[4] Lavanchy D. Hepatitis B virus epidemiology, disease
burden, treatment, and current and emerging prevention
and control measures. J Viral Hepat 2004; 11 (2): 97-107.
[PubMed]
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Hepatic viruses screening in multitransfused Egyptian
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The Impacts of Viral Hepatitis on Liver Enzymes and Bilrubin

  • 1. International Journal of Chemistry, Mathematics and Physics (IJCMP) [Vol-6, Issue-6, Nov-Dec, 2022] https://dx.doi.org/10.22161/ijcmp.6.6.1 ISSN: 2456-866X http://www.aipublications.com/ijcmp/ Page | 1 The Impacts of Viral Hepatitis on Liver Enzymes and Bilrubin Dr. Noaman Abdulateef Abdulrazzaq, Mustafa Mamon Ahmed, Farah Thamer Hasan Al-Turath University, Iraq, Baghdad Received: 16 Oct 2022; Received in revised form: 03 Nov 2022; Accepted: 08 Nov 2022; Available online: 12 Nov 2022 ©2022 The Author(s). Published by AI Publications. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/) Abstract— Viral hepatitis is an infection that causes liver inflammation and damage. Several different viruses cause hepatitis, including hepatitis A, B, C, D, and E. The hepatitis A and E viruses typically cause acute infections. The hepatitis B, C, and D viruses can cause acute and chronic infections. Hepatitis A causes only acute infection and typically gets better without treatment after a few weeks. The hepatitis A virus spreads through contact with an infected person’s stool. Protection by getting the hepatitis A vaccine. Hepatitis E is typically an acute infection that gets better without treatment after several weeks. Some types of hepatitis E virus are spread by drinking water contaminated by an infected person’s stool. Other types are spread by eating undercooked pork or wild game. Hepatitis B can cause acute or chronic infection. Recommendation for screening for hepatitis B in pregnant women or in those with a high chance of being infected. Protection from hepatitis B by getting the hepatitis B vaccine. Hepatitis C can cause acute or chronic infection. Doctors usually recommend one-time screening of all adults ages 18 to 79 for hepatitis C. Early diagnosis and treatment can prevent liver damage. The hepatitis D virus is unusual because it can only infect those who have a hepatitis B virus infection. A coinfection occurs when both hepatitis D and hepatitis B infections at the same time. A superinfection occurs already have chronic hepatitis B and then become infected with hepatitis D. The aim of this study is to find the effect of each type of viral hepatitis on the bilirubin (TB , DSB) , and liver enzymes; AST, ALT, ALP,GGT among viral hepatitis patients. 200 patients were selected from the viral hepatitis units in the central public health laboratory in Baghdad city, all the chosen cases were confirmed as a positive samples , they are classified into four equal group each with fifty individual and with a single serological viral hepatitis type either; anti-HAV( IgM ) , HBs Ag , anti-HCV ,or anti-HEV(IgM ). All patients were tested for; serum bilirubin ( TB ,D.SB ) , AST , ALT , ALP , GGT. Another fifty quite healthy and normal person was selected as a control group for comparison. . Liver enzymes and bilirubin changes are more pronounced in HAV, HEV than HCV and HBVAST and ALT lack some sensitivity in detecting HCV ,HBV and mild elevations of ALT or AST in asymptomatic patients can be evaluated efficiently by considering ,hepatitis B, hepatitis C. ALT is generally a more sensitive indicator of acute liver cell damage than AST, It is relatively specific for hepatocyte necrosis with a marked elevations in viral hepatitis. Liver enzymes and bilirubin changes are more pronounced in HAV, HEV than HCV and HBV.AST and ALT lack some sensitivity in detecting HCV ,HBV and mild elevations of ALT or AST in asymptomatic patients can be evaluated efficiently by considering ,hepatitis B, hepatitis C. ALT is generally a more sensitive indicator of acute liver cell damage than AST, It is relatively specific for hepatocyte necrosis with a marked elevations in viral hepatitis. Keywords— viral hepatitis, liver enzyme.
  • 2. Abdulrazzaq et al. International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022) http://www.aipublications.com/ijcmp/ Page | 2 I. INTRODUCTION Hepatitis Inflammation of the liver that can be caused by viruses , chemicals , drugs , alcohol , inherited diseases ,or the patient’s own immune system. Hepatitis may occur with limited or no symptoms , but often leads to jaundice, anorexia and malaise .Hepatitis is acute when it lasts less than six months and chronic when it persist longer. Causes; The most common cause of viral hepatitis are the five unrelated hepatotropic viruses , A , B, C ,D , E, and Other viruses which can also cause hepatitis includes ; Herpes simplex , Cytomegalo virus , Epstein Barr virus , Yellow fever. HDV HCV HBV HEV HAV Parent-eral Parent-eral Parent-eral Enteric Enteric Transmission Delta virus Hepacivirus Hepadn-avirus Hepe virus Picornavirus Classification -ssRNA +ssRNA +dsDNA +ssRNA +ssRNA Genome Delta Ag CoreAg HBsAg,HBeAg Antigen 30-60 days 15-150 days 45-160 days 15-60 days 15-45 days Incubat-ion period YES with HBV YES (com-mon) YES (uncommon) NO NO Chroni-city Liver function tests; Groups of clinical biochemistry laboratory blood assays designed to give information about the state of a patient's liver. They are indicative of: 1) liver inflammation: ALT and AST. 2) Cholestasis or biliary obstruction bilirubin (total, direct), ALP, GGT 3) synthetic function: albumin, PT. Viral hepatitis with its different serotypes are known to have various extent of effects on the liver function tests. Aim of the study The aim of this study is to find the effect of each type of viral hepatitis whether A , B ,C , or E on the bilirubin (TB , DSB) , and liver enzymes; AST, ALT, ALP,GGT among viral hepatitis patients. II. INDIVIDUALS AND METHODS 200 patients were selected from the viral hepatitis units all the chosen cases were surveyed for different types of viral hepatitis measured by ELISA and ELFA methods which was confirmed as a positive samples where they are classified into four equal group each with fifty individual and with a single serological viral hepatitis type either; anti-HAV( IgM ) , HBs Ag , anti- HCV ,or anti-HEV(IgM ). All patients were tested for; serum bilirubin ( TB ,D.SB ) , AST , ALT , ALP , GGT , which are measured indirectly by using a spectrophotometer method. Another fifty quite healthy and normal person was selected as a control group. III. RESULTS Table (1). General descriptive statistics for the liver enzymes and bilirubin, their number, mean± SD with the maximum and minimum values. ST.DEV. MEAN MAXIMUM MINIMUM N Parameters 2.28672 2.2093 9.80 O.12 250 TSB 1.05555 .9220 5.10 O.O1 250 D.SB 67.38983 58.2234 450.00 3.00 250 ALT 64.35098 59.2780 291.00 4.00 250 AST 160.2512 166.7740 841.00 20.00 250 ALP 100.4452 82.3336 980.00 8.00 250 GGT
  • 3. Abdulrazzaq et al. International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022) http://www.aipublications.com/ijcmp/ Page | 3 Tab.(2).mean for comparison of TSB and D.SB with the control group in different types of hepatitis. Std.er. Std.de. mean group Parameters .049 .284 .164 .203 .399 .349 2.013 1.163 1.438 2.828 .783 4.066 .836 1.466 3.893 Contr. HAV HBV HCV HEV TSB .029 .171 .087 .058 .128 .208 1.209 .260 .413 .909 .299 2.253 .362 .430 1.248 Contr. HAV HBV HCV HEV D.SB Tab (3).mean for comparison of AST and ALT with the control group in different types of hepatitis. Std.er. Std.de. mean group parameter 1.353 7.101 4.859 1.849 11.874 9.569 50.212 34.360 13.075 83.966 23.314 90.660 33.740 17.567 131.10 Contro HAV HBV HCV HEV AST 1.570 8.748 6.610 11.707 5.385 11.105 61.861 46.744 82.784 38.081 17.996 135.50 32.860 61.040 43.640 Contro HAV HBV HCV HEV AlT Tab(4).mean for comparison of ALP and GGT with the control group in different types of hepatitis. Std.er. Std.dev. mean group parameter 2.172 25.374 7.003 9.984 17.498 19.178 179.427 49.520 70.601 123.731 64.078 194.840 71.800 122.792 180.300 Control HAV HBV HCV HEV ALP 2.172 25.374 7.003 9.984 17.498 31.953 84.550 21.865 145.843 115.087 44.570 140.343 30.850 98.472 97.400 Control HAV HBV HCV HEV GGT
  • 4. Abdulrazzaq et al. International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022) http://www.aipublications.com/ijcmp/ Page | 4 ANOVA test; It shows significant difference between the groups with a P-value ˂ 0.05 for all of the parameters. Tab (5).Multiple Comparisons Dun net t-test with the Mean Difference and Significant P-values (˂ 0.05 ) between all groups. Significant P- values Mean Difference Group Variable .000 3.283* 3.110* HAV HEV TSB .000 1.954* .948* HAV HEV D.SB .000 67.346* 107.786* HAV HEV AST .000 117.583* 43.043* HAV HCV ALT .000 330.762* 58.714* 116.222* HAV HCV HEV ALP .000 95.922* 53.960* 52.888* HAV HCV HEV GGT
  • 5. Abdulrazzaq et al. International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022) http://www.aipublications.com/ijcmp/ Page | 5 IV. DISCUSSION A number of pitfalls can be encountered in the interpretation of common blood liver function tests: 1. Normal LFTs do not always mean that the liver is normal. 2. They often, but not always, indicate that something is wrong with the liver. 3. They can provide clues to the nature of the problem. 4. Transaminases are the most sensitive indicators of hepatic cell injury. Unfortunately (85%) HCV people are free of any symptoms , usually they are discovered because the liver enzymes in their blood are above normal limits , and their doctors do more blood tests to find the cause , or they are discovered during their donation for blood in blood bank and this is also true for HBV as (15%) of the patients can easily passed unnoticed as some of them have no outward signs or symptoms , and others do experience just "flu-like" symptoms. The present study illustrate the significant changes in the values of the main hepatic markers in different types of viral hepatitis which was noticed mainly in HAV and HEV more than in the HCV and HBV (Table5) , a hallmark results that can easily be explained on the fact that the hepatocyte necrosis results in the leakage of enzymes into the circulation . While liver cell death with HBV and HCV occurs by
  • 6. Abdulrazzaq et al. International Journal of Chemistry, Mathematics and Physics (IJCMP), Vol-6, Issue-6 (2022) http://www.aipublications.com/ijcmp/ Page | 6 apoptosis (programmed cell death) as well as by necrosis which presumably synthesize less AST and ALT as they wither away. This probably explains why at least one third of patients infected with hepatitis C virus have persistently normal serum ALT, AST levels despite the presence of inflammation on liver biopsy. Thus, AST and ALT lack some sensitivity in detecting HCV, HBV and mild elevations of ALT or AST in asymptomatic patients can be evaluated efficiently by considering , hepatitis B, hepatitis C.ALT is relatively specific for hepatocyte necrosis with a marked elevations in viral hepatitis (Table 2, Fig. B). AlP and GGT levels typically rise to several times the normal level after several days of bile duct obstruction or intrahepatic cholestasis , Both AlP and GGT levels are elevated in about 90% of patients with this study were we found mildly to Moderately elevated ALP and GGT due to hepatocyte necrosis in combination with some intrahepatic cholestasis specifically in HAV and HEV (Tab 4, Fig C ). Viral hepatitis is one of the main causes of hyperbilirubinemia whether it is direct or indirect fraction of bilirubin. Actually, both categories of bilirubin was elevated in all serotypes of viral hepatitis yet it was also more prominent in HAV and HEV (Table 2, Fig A). V. CONCLUSION 1. Liver enzymes and bilirubin changes are more pronounced in HAV, HEV than HCV and HBV. 2. AST and ALT lack some sensitivity in detecting HCV ,HBV and mild elevations of ALT or AST in asymptomatic patients can be evaluated efficiently by considering ,hepatitis B, hepatitis C. 3. ALT is generally a more sensitive indicator of acute liver cell damage than AST, It is relatively specific for hepatocyte necrosis with a marked elevations in viral hepatitis. REFERENCES [1] Green RM, Flamm S. AGA technical review on the evaluation of liver chemistry tests. Gastroenterology 2002;123(4):1367-84. [PubMed] [2] Dufour DR, Lott JA, Nolte FS, Gretch DR, Koff RS, Seeff LB. Diagnosis and monitoring of hepatic injury. I. Performance characteristics of laboratory tests. Clin Chem 2000;46(12):2027-49. [PubMed] [3] Fogden E, Neuberger J. Alternative medicines and the liver. Liver Int 2003; 23 (4): 213-20. [PubMed] [4] Lavanchy D. Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures. J Viral Hepat 2004; 11 (2): 97-107. [PubMed] [5] El Gawhary S, Omar N, Abdel Rahman L, Mahmoud M. Hepatic viruses screening in multitransfused Egyptian thalassemia patients. J Arab Child. 2009;20(3):193–202. [Google Scholar] [6] Ameli M, Besharati S, Nemati K, Zamani F. Relationship between elevated liver enzyme with iron overload and viral hepatitis in thalassemia major patients in Northern Iran. Saudi Med J. 2008;29(11):1611–5. [PubMed] [Google Scholar] [7] Ardalan FA, Osquei MR, Toosi MN, Irvanloo G. Synergic effect of chronic hepatitis C infection and beta thalassemia major with marked hepatic iron overload on liver fibrosis:a retrospective cross-sectional study. BMC Gastroenterol. 2004;4:17. [PMC free article] [PubMed] [Google Scholar] [8] Feld J, Lee JY, Locarnini S. New targets and possible new therapeutic approaches in the chemotherapy of chronic hepatitis B. Hepatology. 2003;38(3):545–53. [PubMed] [Google Scholar] [9] Khalifa AS, El-Sayed MH, Moustafa AO, Mohammed MM, Rady MS, Salama II. Hepatitis C virus infection in children with hematological diseases:risk factors and reliability of diagnosis assays. Egypt J Pediatr. 2002;19:293–308. [Google Scholar] [10] El-Faramawy A, El-Rashidy O, Tawfik P, Hussein G. Transfusion Transmitted Hepatitis:Where Do We Stand Now? A One Center Study in Upper Egypt. Hepat Mon. 2012;12(4):286–291. [PMC free article] [PubMed] [Google Scholar] [11] Angelucci E, Muretto P, Nicolucci A, Baronciani D, et al. Effects of iron overload and hepatitis C virus positivity in determining progression of liver fibrosis in thalassemia following bone marrow transplantation. Blood. 2002;100:17–21. [PubMed] [Google Scholar] [12] Di Marco V, Capra M, Gagliardotto F, Borsellino Z, et al. Liver disease in chelated transfusion-dependent thalassemics:the role of iron overload and chronic hepatitis C. Haematologica. 2008;93(8):1243–1246. [PubMed] [Google Scholar] [13] Edoardo G, Testa R, Savarino V. Liver enzyme alteration:a guide for clinicians. CMAJ. 2005;172(3):367–379. [PMC free article] [PubMed] [Google Scholar]