RESEARCH ARTICLE


Lipid Profiles as Markers for the Severity of Liver Diseases in Cirrhotic Patients



Rehab Badawi1, Mohamed Zakaria Abu Rahma2, Haidi K. Ramadan2, Shaimaa Soliman3, Dina A. Mohareb4, Nehad Hawash1, Rania Elkafoury1, Sherief Abd-Elsalam1, *
1 Department of Tropical Medicine and Infectious Diseases, Faculty of Medicine, Tanta University, Tanta, Egypt
2 Department of Tropical Medicine and Gastroenterology, Faculty of Medicine, Assiut University, Assiut, Egypt
3 Public Health and Community Medicine, Menoufia University, Menoufia
4 Department of Clinical Pathology , Faculty of Medicine, Assiut University, Assiut, Egypt


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Creative Commons License
© 2021 Badawi et al.

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: (https://creativecommons.org/licenses/by/4.0/legalcode). This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

* Address correspondence to this author at the Department of Tropical Medicine and Infectious Diseases, Faculty of Medicine, Tanta University, El-Giash Street 31527, Tanta, Egypt; Tel: +2-01147773440;
E-mail: sherif.abdelbaky@med.tanta.edu.eg


Abstract

Background

Liver cirrhosis is a diffuse process in which the anatomical structure and function of the liver are disturbed. Lipid metabolism occurs mainly in the hepatocytes. In liver cirrhosis, it is expected to detect abnormal lipid profile and abnormal neutrophil to lymphocyte ratio due to necro-inflammation and hepatocyte dysfunction. This study aimed to estimate the lipid profile in patients with liver cirrhosis and to assess its relation to the severity of the liver disease based on Child-Pugh Turcotte score and Neutrophil to Lymphocyte Ratio (NLR).

Methods:

This study included 500 cirrhotic patients. All patients are subjected to history taking, clinical examination, liver and renal function tests, lipid profile, and also abdomino-pelvic ultrasound. Child -Pugh score, fibrosis-4 score (FIB4), and neutrophil and platelet lymphocyte ratio were calculated.

Results:

A total of 500 patients were enrolled in this study; 12 patients were excluded (two patients were on the immunosuppressive drug, three patients had body mass index (BMI) >30, and seven patients took lipid-lowering drugs). Cholesterol level was significantly higher in patients with Child- Score A than B and C. Cholesterol, Low-Density Lipoprotein (LDL), and very-low-density lipoprotein (VLDL) cholesterol were significantly higher in Child B than C. A significant negative correlation was found between cholesterol level and each of FIB4 and NLR ratios.

Conclusion:

There was a significant negative correlation between the severity of liver cirrhosis and lipid profiles (except triglyceride), FIB4 and NLR ratio.

Keywords: Liver, Cirrhosis, Lipids, Cholesterol, Triglycerides, Liver failure.



1. INTRODUCTION

Liver cirrhosis is a diffuse liver disease including fibrosis and disturbance of normal liver architecture with the formation of cirrhotic nodules [1].

The global prevalence of cirrhosis from autopsy studies ranges from 4.5% to 9.5% of the general population [ 1-32].

Multiple etiological factors contribute to the development of cirrhosis, as exemplified in epidemiological studies thatidentified regular (moderate) alcohol consumption, age above 50 years, and male gender as risk factors in chronic hepatitis C, or older age obesity, insulin resistance/type 2 diabetes, hypertension and hyperlipidemia (all features of the metabolic syndrome) in non-alcoholic steatohepatitis (NASH) [2, 27].

The most common important causes of liver cirrhosis are chronic hepatitis B, chronic hepatitis C, and alcoholic and (NASH) [2-4].

Several scoring systems have been developed to evaluate liver status as Child-Turcotte pugh score (CTP) and model for end-stage liver disease (MELD) [5, 6].

Neutrophil to lymphocyte ratio (NLR) test has been developed as a simple test to expect the presence of infection and to predict the severity of multiple malignancies [7-9]. NLR may be helpful in the prediction of liver disease severity because of the necroinflammatory changes occurring in different liver diseases and in liver cirrhosis [10-12].

Lipid metabolism and lipoprotein biosynthesis occur mainly in the hepatocytes; abnormal lipid profiles can be detected in patients with severe liver dysfunction. There is a prominent decrease in plasma cholesterol and triglyceride (TG) levels in patients with severe hepatitis and hepatic failure [13].

The preceding studies have reported that cirrhotic patients have abnormal metabolism of lipids, especially reduction in cholesterol level and hypobetalipoproteinemia, and the lipid profile may be considered a valuable method in assessing liver disease [33].

The aim of this study was to estimate the lipid profile in patients with liver cirrhosis and to assess its relation to the severity of the disease based on Child-Pugh Turcotte Score (CTP) and NLR

2. METHODS

It was a cross-section study. It included 500 subjects in the Department of Tropical Medicine and Infectious diseases in Tanta University Hospital and Assiut University Hospital from January 2017 to December 2018. Institutional ethical committee approval was obtained before the start of the study, and informed consent was signed by every patient before enrolment in the study; and by abiding the rules and regulations as per Helsinki Declaration. This study has been approved by the institutional review board of the, (registration number, 32382\06\18).

All authors had access to the study data, and reviewed and approved the final manuscript.

Patients more than 18 years old with chronic liver disease, etiologies were included in the study.

Diagnosis of liver cirrhosis was based on history, ultrasound, fibroscan and upper gastro-intestinal endoscopy. Patients are known to have dyslipidemia before detection of chronic liver disease, taking lipid-lowering drugs or immunosuppressive drugs, history of taking glucose, recent parenteral nutrition, patients with body mass index (BMI) >30, or patients unwilling to participate in the study were excluded.

A detailed history was taken. A clinical examination was made. Laboratory and radiological evaluations have been made, including complete blood count, fasting lipid profile (including cholesterol, triglycerides (TG), low- density lipoprotein(LDL), high- density lipoprotein (HDL) and very low - density lipoprotein (VLDL).

Serum cholesterol and triglyceride levels were analysed by in vitro enzymatic colorimetric kit method. HDL estimation was done by the enzymatic kit method after precipitation of serum by phosphotungstate and magnesium chloride [ 27].

Liver function tests, and renal function tests, and ultrasonography on the abdomen and pelvis were conducted. Child-Pugh Turcotte score [14], NLR and platelet to lymphocyte ratio, and FIB 4 were calculated for all patients.

A total Child-Pugh score of 5 to 6 is considered Child-Pugh class A (well-compensated disease), 7 to 9 is class B (significant functional compromise), and 10 to 15 is class C (decompensated disease).

Statistical Analysis: The normality of the different variables was tested by the Shapiro Wilks test. Statistical package for social science (IBM SPSS Statistics for Windows, version 23, IBM corp., Armonk, N.Y USA). V 23 was used to analyze the data. Quantitative data were compared using ANOVA for normally distributed data and Kruskal Wallis test for non-normally distributed data with LSD or Tamhane as post hoc test. Pearson and Spearman correlation coefficients were used. A two-sided P value <0.05 was considered statistically significant.

3. RESULTS

A total of 500 patients were enrolled in this study; 12 patients were excluded (two patients were on the immunosuppressive drug, three patients had BMI >30, and seven patients took lipid-lowering drugs). Four hundred and eighty-eight patients were analyzed during the period of the study. There were 338 (69.3%) males and 150 (30.7%) females. The mean age was 56.37 ± 11.13 years. Seventy patients had hypertension (14.3%) and 144 (29.5%) patients had Diabetes Mellitus (DM). The patients in this study were divided according to Child -Pugh Turcotte score, 96 patients (19.7%) were class A, 195 patients (40.0%) class B, and 197 patients (40.4%) class C. No significant difference in liver and kidney functions. Patients, characteristics and laboratory data are shown in Tables 1 and 2.

Table 1. Patients’ characteristics.
Variables No (%)
Gender
Male
Female:

338 (69.3)
150 (30.7)
Hypertension
No
Yes

418 (85.7)
70 (14.3)
Diabetes mellitus
No
Yes

344 (70.5)
144 (29.5)
Ascites
No
Mild
Moderate
Marked

151 (30.9)
104 (21.3)
143 (29.3)
90 (18.4)
Jaundice
No
Mild
Marked

266 (54.5)
55 (11.3)
167 (34.2)
Lower limb edema
No
Mild
Moderate
Marked

106 (21.7)
198 (40.6)
143 (29.3)
41 (29.3)
Hepatitis C 344 (70.5)
Hepatitis B 80 (16.4)
Others 64 (13.11)
Child-Pughclassification
A
B
C

96 (19.7)
195 (40.0)
197 (40.4)
A total Child-Pugh score of 5 to 6 is considered Child-Pugh class A (well-compensated disease), 7 to 9 is class B (significant functional compromise), and 10 to 15 is class C (decompensated disease).
Table 2. Laboratory characteristics of the patients.
Variables Mean ±SD, Range
Age 56.37 ± 11.13, 18092
FIB4 6.14 ± 6.16, 0.22-74.79
FBS (mg/dL) 131.45 ± 57.92, 65.0-568.0
Total bilirubin (mg/dl) 2.66 ± 3.30, 0.3-27.7
Albumin (gm/dl) 2.85 ± 1.09, 1.2-21.0
ALT (U/ml) 42.75 ± 47.22, 5.0-498.0
AST (U/ml) 67.92 ± 58.90, 10.0-402.0
INR 1.48 ± 0.40, 0.99-3.91
S creatinine (mg/dl) 1.07 ± 0.43, 0.21-3.20
HB (gm/dl) 10.32 ± 2.45, 0.0-17.3
WBCs (cells/mcL) 8.44 ± 14.46, 0.03-160.0
Platelets (1000/cmm) 134.29 ± 84.65, 7.5-860.0
Neutrophils (cells/mcL) 1.40 ± 2.35, 0.24-21.13
Lymphocytes (cells/mcL) 0.87 ± 6.07, 0.03-134.0

The mean total cholesterol level and triglyceride level were 110.38 ± 43.09 mg\dl, and 80.43 ± 37.59 mg\dl, respectively. The mean LDL cholesterol was 77.69 ± 12.40 mg\ dl. The mean VLDL cholesterol was 19.35 ± 2.35 mg \dl. The mean HDL cholesterol was 33.42 ± 4.58mg\dl (Table 3). Cholesterol level was significantly higher in patients with CTP class A than in other classes (P <0.001 for each). Also, it was significantly higher in patients with class B than in class C (P<0.001).

Table 3. Lipid profiles among the patients.
Variable
Normal Value
Mean ± SD
Total cholesterol (mg/dl)
>200 mg/dl
110.38 ± 43.09
LDL cholesterol (mg/dl)
>130 mg/dl
77.69 ± 12.40
VLDL cholesterol (mg/dl)
>30 mg/dl
19.35 ± 2.35
HDL cholesterol (mg/dl)
<40 mg/dl
33.42 ± 4.58
Triglycerides (mg/dl)
>150 mg/dl
80.43 ± 37.59
Table 4. Correlation of lipid profile with child grade.
A (n=96) B (n=195) C (n=197) P value Post Hoc
Cholesterol (mg/dl) 135.47 ± 46.66 111.89 ± 38.26 96.67 ± 40.12 <0.001 P1 <0.001
P2 <0.001
P3 <0.001
Triglyceride(mg/dl) 80.47 ± 34.10 80.33 ± 33.42 80.51 0.99 -
LDL cholesterol (mg/dl) 80.33 ± 13.31 79.37 ± 12.01 74.74 ± 11.75 <0.001 P1 0.528
P2 <0.001
P3 <0.001
VLDL cholesterol (mg/dl) 20.00 ± 2.56 19.69 ± 2.30 18.69 ± 2.14 <0.001 P1 0.699
P2 <0.001
P3 <0.001
HDL cholesterol (mg/dl) 34.58 ± 4.90 33.98 ± 4.25 32.30 ± 4.51 <0.001 P1 0.675
P2 0.001
P3 <0.001

No significant difference in triglyceride level among the different classes (P =0.99). However, LDL cholesterol, VLDL cholesterol and HDL cholesterol were significantly higher in CTP class B than class C (P <0.001 for each); however, there was (Table 4).

A significant negative correlation was found between each cholesterol level, LDL cholesterol, VLDL cholesterol and HDL cholesterol with CTP class (P <0.001 for each) (Table 5 ). Also, there was a significant negative correlation between cholesterol level and each of NLR ratio and FIB4 (P <0.001 and 0.005 respectively) (Table 6).

Table 5. spearman correlation of lipid profiles and CTP.
Variable Child Pugh Grade
R P value
Cholesterol (mg/dl) -0.326 <0.001
Triglyceride (mg/dl) 0.001 0.984
LDL cholesterol (mg/dl) -0.179 <0.001
VLDL cholesterol (mg/dl) -0.230 <0.001
HDL cholesterol (mg/dl) -0.208 <0.001
NLR 0.115 0.011

Table 6. Spearman correlation of cholesterol with liver disease severity markers.
- Cholesterol
R P Value
FIB 4 -0.280 <0.001
N/L ratio -0.126 0.005
P/L ratio 0.02 0.662

4. DISCUSSION

This study was conducted to reveal the relation between the severity of liver disease and the lipid profile. In our study, all of the lipid markers were considerably greater in Child-Pugh A, although they began to decline with the progression of liver cirrhosis. The total cholesterol level was significantly higher in patients with Child-score A than B and C. Cholesterol, LDL, and VLDL cholesterol were significantly higher in Child B than C. A significant negative correlation was found between cholesterol level and each of FIB4 and NLR ratios. This could be explained by a decrease in the synthetic function of the diseased liver [12].

These findings were in agreement with the previous studies; Muhammed and Jayaraj [15] stated that all parameters of lipid profile, including triglycerides, were significantly lower in cirrhotic patients and were inversely correlated with the severity of cirrhosis [15].

Tauseef et al. [ 29 ] also supported our results and concluded that the amount of decrements measured in the levels of serum total cholesterol, LDL, and HDL in patients with cirrhosis are related to the progress in cirrhosis [ 29].

However, a study in 2013 conducted by Mandel et al. compared the lipid profile in 150 cirrhotic patients with healthy control detected those lipid profile parameters, other than serum TG and HDL levels, were reduced with the severity of liver cirrhosis but without significant correlation between the severity of liver disease and lipid profile. This could be because the majority of patients had cirrhosis due to non-alcoholic fatty liver disease [16]. Also, Mohammad Reza Ghadir et al. revealed that serum lipid levels diminished linearly with the progression of liver damage except for serum triglyceride level [17].

Sen et al. concluded that HDL and TG were significantly elevated in the patients with grade III fatty liver [18].

Due to the major role of inflammation in the process of advanced cirrhosis [19-21], and NLR is an indicator of inflammation (neutrophils present the inflammation and lymphocytes regulatory immune response) [22], NLR can act as a marker of severity of liver fibrosis. Our study was similar to the previous studies which detected a significant positive correlation between Child- score and N/L ratio as NLR was higher in Child C patients [23-25].

Further studies are needed to confirm our results and to assess the predictive value of the lipid profile measurement in cirrhotic patients.

CONCLUSION

In conclusion, there was a significant negative correlation between the severity of liver cirrhosis and lipid profiles (except triglyceride), FIB4 and NLR ratio.

LIMITATION OF THE STUDY

It was a single-center study with a small number of patients. Further studies are needed.

ETHICS APPROVAL AND CONSENT TO PARTICIPATE

This study has been approved by the Institutional Review Board of the Faculty of Medicine, Tanta University, Tanta, Egypt (registration number,32382\06\18).

HUMAN AND ANIMAL RIGHTS

No animals were used in this research. All human research procedures were followed in accordance with the ethical standards of the committee responsible for human experimentation (institutional and national), and with the Helsinki Declaration of 1975, as revised in 2013.

CONSENT FOR PUBLICATION

Informed consent was signed by every patient before enrolment in the study.

AVAILABILITY OF DATA AND MATERIALS

Not applicable.

FUNDING

None.

CONFLICT OF INTEREST

The authors declare no conflict of interest, financial or otherwise.

ACKNOWLEDGEMENTS

Declared none.

REFERENCES

[1] Anthony PP, Ishak KG, Nayak NC, Poulsen HE, Scheuer PJ, Sobin LH. The morphology of cirrhosis. Recommendations on definition, nomenclature, and classification by a working group sponsored by the World Health Organization. J Clin Pathol 1978; 31(5): 395-414.
[2] Elgouhari HM, Abu-Rajab Tamimi TI, Carey WD. Hepatitis B virus infection: understanding its epidemiology, course, and diagnosis. Cleve Clin J Med 2008; 75(12): 881-9.
[3] Kwon YC, Ray RB, Ray R. Hepatitis C virus infection: establishment of chronicity and liver disease progression. EXCLI J 2014; 13: 977-96.
[4] Council G, Assembly G. Global burden of liver disease: A true burden on health sciences and economies. Available from: http://www.worldgastroenterology.org/ publications/ e-wgn/ e-wgn-expert-point-of-view-articles-collection/global-burden-of-liver-disease-a-true-burden-on-health-sciences-and-economies
[5] Aguiar MI, Braga VA, Almeida PC, Garcia JH, Lima CA. Severity of liver disease and quality of life in liver transplantation. Acta Paul Enferm 2016; 29(1): 107-14.
[6] Durand F, Valla D. Assessment of the prognosis of cirrhosis: Child-Pugh versus MELD. J Hepatol 2005; 42(1): S100-7.
[7] Biyik M, Ucar R, Solak Y, et al. Blood neutrophil-to-lymphocyte ratio independently predicts survival in patients with liver cirrhosis. Eur J Gastroenterol Hepatol 2013; 25(4): 435-41.
[8] Liu D, Huang Y, Li L, Song J, Zhang L, Li W. High neutrophil-to-lymphocyte ratios confer poor prognoses in patients with small cell lung cancer. BMC Cancer 2017; 17(1): 882.
[9] Sato Y, Gonda K, Harada M, et al. Increased neutrophil-to-lymphocyte ratio is a novel marker for nutrition, inflammation and chemotherapy outcome in patients with locally advanced and metastatic esophageal squamous cell carcinoma. Biomed Rep 2017; 7(1): 79-84.
[10] Chen SS, Yu KK, Ling QX, et al. Factors associated with significant liver necroinflammation in chronic hepatitis B patients with cirrhosis. Sci Rep 2016; 6: 33093.
[11] Zhang H, Sun Q, Mao W, Fan J, Ye B. Neutrophil-to-lymphocyte ratio predicts early mortality in patients with HBV-related decompensated cirrhosis. Gastroenterol Res Pract 2016; 2016: 4394650.
[12] Shah RM. Study of lipid profile in cirrhotic patients. Natl J Integr Res Med 2012; 3: 89-93.
[13] Halsted CH. Nutrition and alcoholic liver disease. Semin Liver Dis 2004; 24(3): 289-304.
[14] Schuppan D, Afdhal NH. Liver cirrhosis. Lancet 2008; 371(9615): 838-51.
[15] Muhammed HP, Jayaraj K. Correlation of lipid profile in patients with severity of liver disease: a cross sectional study in a tertiary care hospital. Int J Res Med Sci 2017; 5(1): 326-9.
[16] Mandal SK, Sil K, Chatterjee S, Ganguly J, Chatterjee K, Sarkar P, et al. A study on lipid profiles in chronic liver diseases. Natl J Med Res 2013; 3: 70-2.
[17] Ghadir MR, Riahin AA, Havaspour A, Nooranipour M, Habibinejad AA. The relationship between lipid profile and severity of liver damage in cirrhotic patients. Hepat Mon 2010; 10(4): 285-8.
[18] Sen A, Kumar J, Misra RP, Uddin M, Shukla PC. Lipid profile of patients having non-alcoholic fatty liver disease as per ultrasound findings in north Indian population: A retrospective observational study. J Med Appl Sci 2013; 3: 59.
[19] Biyik M, Ucar R, Solak Y, et al. Blood neutrophil-to-lymphocyte ratio independently predicts survival in patients with liver cirrhosis. Eur J Gastroenterol Hepatol 2013; 25(4): 435-41.
[20] Thabut D, Massard J, Gangloff A, et al. Model for end-stage liver disease score and systemic inflammatory response are major prognostic factors in patients with cirrhosis and acute functional renal failure. Hepatology 2007; 46(6): 1872-82.
[21] Cazzaniga M, Dionigi E, Gobbo G, Fioretti A, Monti V, Salerno F. The systemic inflammatory response syndrome in cirrhotic patients: relationship with their in-hospital outcome. J Hepatol 2009; 51(3): 475-82.
[22] Avanzas P, Quiles J, López de Sá E, et al. Neutrophil count and infarct size in patients with acute myocardial infarction. Int J Cardiol 2004; 97(1): 155-6.
[23] Sungkar T, Rozi MF, Dairi LB. Neutrophil-to-Lymphocyte Ratio (NLR) and its correlation with severity of decompensated liver cirrhosis based on Child-Turcotte Pugh (CTP) score. J Clin Diag Res 2019; 13(2): OC29-31.
[24] Probowati W, Bayupurnama P, Ratnasari N. Correlation between neutrophil to lymphocyte ratio with child turcottepugh in liver cirrhosis patients. ActaInterna. J Intern Med 2016; 6(1): 28-35.
[25] Biyik M, Ucar R, Solak Y, et al. Blood neutrophil-to-lymphocyte ratio independently predicts survival in patients with liver cirrhosis. Eur J Gastroenterol Hepatol 2013; 25(4): 435-41.
[26] Farrell GC, Larter CZ. Nonalcoholic fatty liver disease: from steatosis to cirrhosis. Hepatology 2006; 43(2)(Suppl. 1): S99-S112.
[27] Burstein M, Scholnick HR, Morfin R. Rapid method for the isolation of lipoproteins from human serum by precipitation with polyanions. J Lipid Res 1970; 11(6): 583-95.
[28] Lim YS, Kim WR. The global impact of hepatic fibrosis and end-stage liver disease. Clin Liver Dis 2008; 12(4): 733-746, vii.
[29] Tauseef A, Zafar M, Rashid B, et al. Correlation of fasting lipid profile in patients with chronic liver disease: A descriptive cross-sectional study in tertiary care hospital. Cureus 2020; 12(10): e11019.
[30] Hanafy AS, Soliman S, Abd-Elsalam S. Rescue therapy for chronic hepatitis C virus infection after repeated treatment failures: Impact on disease progression and risk of hepatocellular carcinoma. Hepatol Res 2019; 49(4): 377-84.
[31] Abdelmoemen G, Khodeir SA, Abou-Saif S, Kobtan A, Abd-Elsalam S. Prevalence of occult hepatitis C virus among hemodialysis patients in Tanta university hospitals: A single-center study. Environ Sci Pollut Res Int 2018; 25(6): 5459-64.
[32] Ahmed OA, Kaisar HH, Hawash N, et al. Efficacy of sofosbuvir plus ribavirin with or without peginterferon-alfa in treatment of a cohort of Egyptian patients with hepatitis C virus infection. Infect Disord Drug Targets 2017; 17(2): 95-100.
[33] Bassani L, Fernandes SA, Raimundo FV, Harter DL, Gonzalez MC, Marroni CA. Lipid profile of cirrhotic patients and its association with prognostic scores: A cross-sectional study. Arq Gastroenterol 2015; 52(3): 210-5.