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 Table of Contents  
ORIGINAL ARTICLE
Year : 2016  |  Volume : 3  |  Issue : 1  |  Page : 11-15

Study of atherosclerotic risk markers in patients with nonalcoholic fatty liver disease


Department of Medicine, ERA's Lucknow Medical College, Lucknow, Uttar Pradesh, India

Date of Submission07-Jun-2015
Date of Decision19-Feb-2016
Date of Acceptance24-Feb-2016
Date of Web Publication16-Jun-2016

Correspondence Address:
Ritu Karoli
Department of Medicine, ERA's Lucknow Medical College, Sarfarazganj, Hardoi Road, Lucknow - 226 003, Uttar Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2347-9906.184100

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  Abstract 

Introduction: Nonalcoholic fatty liver disease (NAFLD) is described as hepatic component of metabolic syndrome as close association exists between the two. It has gained lots of importance in midst of rising epidemic of obesity worldwide in recent times as one of the predisposing risk factors of cardiovascular events. Study Design: The study design was a cross-sectional hospital-based study. Materials and Methods: Forty-eight patients diagnosed to have NAFLD were assessed for insulin resistance (IR) and noninvasive markers of subclinical atherosclerosis and compared with age, gender, and body mass index-matched controls. Results: The patients with NAFLD had significantly higher waist circumference, diastolic blood pressure, fasting insulin, homeostasis model assessment-IR, and significantly lower levels of high-density lipoprotein-cholesterol. They also had significantly higher carotid intima media thickness (CIMT) than controls. Mean CIMT was 0.76 ± 0.12 mm in patients with NAFLD and 0.54 ± 0.18 mm in controls. This difference was statistically significant (P = 0.001). The mean increase in brachial artery diameter was 0.26 ± 0.13 mm in patients and 0.48 ± 0.09 mm in controls. Conclusion: Patients with NAFLD have greater propensity to develop cardiovascular disease in view of the presence of subclinical atherosclerotic markers compared to controls.

Keywords: Atherosclerosis, carotid intima media thickness, nonalcoholic fatty liver disease


How to cite this article:
Karoli R, Fatima J, Shukla V, Khan AA, Pandey M, Mishra R. Study of atherosclerotic risk markers in patients with nonalcoholic fatty liver disease. J Obes Metab Res 2016;3:11-5

How to cite this URL:
Karoli R, Fatima J, Shukla V, Khan AA, Pandey M, Mishra R. Study of atherosclerotic risk markers in patients with nonalcoholic fatty liver disease. J Obes Metab Res [serial online] 2016 [cited 2017 May 24];3:11-5. Available from: http://www.jomrjournal.org/text.asp?2016/3/1/11/184100


  Introduction Top


Nonalcoholic fatty liver disease (NAFLD) is described as a hepatic component of metabolic syndrome as close association exists between the two. It has gained lots of importance in the midst of rising epidemic of obesity worldwide in recent times. The prevalence of fatty liver in general population of India [1],[2],[3] has been shown to be similar to the estimates reported from the Western countries. [4],[5] It is emerging as the most common chronic liver disease in Western countries [6] with higher prevalence in obese and patients with Type 2 diabetes mellitus. NAFLD being asymptomatic in most of the patients encompasses a histological spectrum ranging from steatosis to steatohepatitis, advanced fibrosis, and cirrhosis in the absence of consumption of significant alcohol. Subsets of NAFLD which progress to cirrhosis are being increasingly recognized as a major cause of liver-related morbidity and mortality with the potential to progress to liver failure. [7]

NAFLD is also now believed to be an integral part of metabolic syndrome which comprises a cluster of abnormalities such as abdominal obesity, atherogenic dyslipidemia, hypertension, elevated plasma glucose, and a prothrombotic and a proinflammatory state that greatly increases individual's probability of developing atherosclerotic cardiovascular disease (CVD) and Type 2 diabetes mellitus. [8],[9],[10] Insulin resistance (IR) is a key pathogenic factor in both NAFLD and metabolic syndrome. [11],[12]

In recent times, certain surrogate markers of atherosclerosis have been devised which can help to assess the cardiovascular risk noninvasively. Assessment of carotid intima media thickness (CIMT) [13] and endothelial dysfunction [14] is considered as a potential tool for predicting coronary atherosclerosis and future cardiovascular events. Hepatic steatosis being a common incidental finding in subjects undergoing abdominal ultrasonography for any other reason has been shown to be associated with carotid plaques and increased CIMT by several cross-sectional studies. [15],[16],[17] Targher et al. [18] reported in a prospective nested case-control study that NAFLD is a strong predictor of future cardiovascular events among Type 2 diabetes mellitus. Targher et al. in another study also showed a correlation between higher CIMT and severity of liver disease assessed by histological grades. [19]

Assessment of endothelial dysfunction by measuring flow-mediated dilatation (FMD) of the brachial artery is being considered as a potential tool for predicting coronary artery disease with recent data showing it to be a predictor of cardiovascular events. [20],[21] There are not much published data regarding the association between NAFLD and subclinical atherosclerosis in our patient population, so the present study was designed to characterize various causes of hepatomegaly in medical outpatient department (OPD) and wards, prevalence of NAFLD, various metabolic covariates including IR, obesity, dyslipidemia, hypertension, endothelial dysfunction, and CIMT in patients with NAFLD.


  Materials and methods Top


In a cross-sectional study, all consecutive patients >18 years old with hepatomegaly detected on clinical [22] and/or ultrasonographic examination [23] attending as OPD or admitted in medical wards of the of ERA's Lucknow Medical College between January 2010 to December 2010 were enrolled. Exclusion criteria included pregnancy or patients who were not willing to participate. A written informed consent was taken from all the participants and study protocol was approved by the Institutional Ethics Committee.

Each patient of the study population had been subjected to detailed history that included symptoms, history of alcohol consumption, drug history, high-risk behavior (illicit/intravenous drug abuse, sexual promiscuity, and tattooing), blood/blood product transfusion, needle prick or other modes of blood-borne transmission, history of travel, consumption of contaminated food and water, systemic illness, and detailed family history of significant systemic illnesses. Detailed general examination including anthropometric measurements and systemic examination was done in each patient.

Depending on the clinical diagnosis based on detailed history and clinical examination, patients were subjected to hematological and biochemical investigations as required and when feasible. Hematological parameters included hemoglobin, complete blood counts, coagulation profile, peripheral blood smear for parasites, stool examination, Widal test, viral markers for hepatitis, serology for dengue and amebiasis, and blood, urine, sputum cultures were done. Abdominal ultrasonography was performed in all the patients whereas chest skiagram, electrocardiography, and echocardiography were done when required. Biochemical tests comprised plasma glucose, electrolytes, lipid profile, renal and liver function tests.

The diagnosis of NAFLD was based on the presence of hepatic steatosis as bright/echogenic liver on abdominal ultrasound after exclusion of alcohol consumption, smoking, positive hepatic markers of viral hepatitis, autoimmune hepatitis, Wilson's disease, hemochromatosis alpha-1 anti-trypsin deficiency, and medications known to cause fatty liver (methotrexate, estrogens, amiodarone, and tamoxifen). Ultrasonography was performed by the same radiologist who was blinded for subject's medical history and diagnosis. A high-resolution B-mode scanner of General Electric Logic 5 with a 3.5 MHz convex-array probe was used. Hepatic steatosis was defined as diffuse increase in fine echoes in liver parenchyma with impaired visualization of intrahepatic vessels and the diaphragm. [24]

The patients who were diagnosed to have NAFLD were evaluated for fasting insulin, flow-mediated vasodilatation of brachial artery, and CIMT, and compared with controls. The controls were age, sex, and body mass index (BMI) matched healthy individuals who had ultrasonographically normal liver echogenicity and normal liver function tests enrolled from the hospital staff and their relatives. Homeostasis model assessment (HOMA) method for IR was calculated by the formula: Fasting serum insulin (microunits/ml) fasting serum glucose (mmol/L)/22.5.

Metabolic syndrome was diagnosed in patients with NAFLD and controls based on the presence of three or more of the following: (i) Waist circumference >102 cm for men and >88 cm for women (ii) serum triglyceride >150 mg/dl (iii) high-density lipoprotein (HDL) cholesterol <50 mg/dl (iv) serum fasting glucose >100 mg/dl (v) blood pressure ≥ 130/85 mmHg according to National Cholesterol Education Program/Adult Treatment Panel III, 2001 criteria. [25]

Flow-mediated dilatation measurement

Endothelial function was measured noninvasively by ultraonographic assessment of right brachial artery dimensions. [26] The diameter of the right brachial artery was measured twice, first at rest then after inducing reactive hyperemia with the help of pneumatic cuff. It was carried out by a blinded sonologist after an overnight fast in a cool, quiet room with B-mode ultrasound scanner (Siemens, Germany) using 10 MHz linear transducer. The diameter of right brachial artery was measured 2-8 cm above the antecubital space in the end diastolic phase from one media-adventitia interface to the other at the clearest part 3 times and an average was taken. After the detection of the right transducer position, skin was marked and arm was kept in the same position. The blood pressure cuff was tied on the upper arm and inflated to suprasystolic levels kept inflated for 4 min. Sixty seconds after the cuff was released, brachial artery dimensions were again measured. The maximum diameter measurement was defined as the average of three consecutive diameters measurements.

CIMT - It was measured by B-mode ultrasound using linear probe at a frequency of 10 MHz. The common carotid arteries were scanned at the level of bifurcation on either sides and mean value was used for analysis. The CIMT was measured in the far wall of the arteries at sites identified as diffuse and continuous projections with the greatest distance between the luminal intimal interface and media adventitial interface but without atherosclerotic plaques. Localized lesions >2 mm thickness were considered to be atherosclerotic plaques. CIMT was assessed by single observer who was blinded for the diagnosis.

Statistical analysis

The Statistical Package for the Social Sciences (SPSS version 13.0, SPSS Inc., Chicago, IL) was used for statistical analysis. Data were expressed as percentages, mean values (with standard deviations), or differences between groups were analyzed with Chi-square test for proportions and the Student's t-test for means. Results were defined as statistically significant when the P value (two-sided) was <0.05. Chi-square test of goodness of fit has been applied for seasonal variation. Analysis of correlations between parameters was performed by using Pearson's correlation coefficient and regression analysis was done to predict FMD and CIMT. Multiple regression analysis with CIMT as the dependent variable was used for adjustment of predictor variables that had been shown to have P < 0.05 in univariate analysis.


  Results Top


Forty-eight patients with NAFLD were compared with age-, sex- and BMI-matched healthy controls [Table 1]. The patients with NAFLD had significantly higher waist circumference, diastolic blood pressure, fasting insulin, HOMA-IR, and significantly lower levels of HDL-cholesterol. They also had significantly higher CIMT than controls.
Table 1: Clinical and biochemical characteristics of patients with nonalcoholic fatty liver disease and controls


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Mean CIMT was 0.76 ± 0.12 mm in patients with NAFLD and 0.54 ± 0.18 mm in controls. This difference was statistically significant (P = 0.001). The mean increase in brachial artery diameter was 0.26 ± 0.13 mm in patients and 0.48 ± 0.09 mm in controls. This difference was statistically significant (P = 0.001), indicating an increase in diameter with ischemia. Mean brachial artery diameter at baseline was 3.8 ± 1.9 mm in patients and 3.67 ± 2.3 mm in controls. The difference was not statistically significant (P = 0.5). Mean FMD was 8.12 ± 2.56% and 13.26 ± 2.8% in patients with NAFLD and in controls, respectively [Table 2]. The difference was statistically significant (P = 0.01). In univariate analysis, CIMT was positively correlated with age (r = 0.36, P = 0.03), BMI (r = 0.46, P = 0.01), waist circumference (r = 0.52, P = 0.001), and HOMA (r = 0.31, P = 0.04).

In multivariate analysis with CIMT as dependent variable, presence of NAFLD, waist circumference, and HOMA retained a significant association. Similarly for FMD, NAFLD and HOMA were the independent predictors.
Table 2: Atherosclerosis markers in patients with nonalcoholic fatty liver disease and control subjects


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  Discussion Top


Nonalcoholic steatohepatitis emerged from an anecdotal disease which was first described by Ludwig et al. [27] in 1980 to the most common cause of incident chronic liver disease at the end of the current decade. It was thought to be a benign condition, but is now increasingly recognized as a major cause of liver-related morbidity and mortality. NAFLD is commonly associated with components of the metabolic syndrome. This strongly supports the notion that NAFLD is the hepatic manifestation of the syndrome. Mishra et al. [28] found the prevalence of metabolic syndrome and NAFLD to be 24% and 14.8%, respectively, in nonalcoholic North Indian men. The prevalence of NAFLD in the general population has been reported by Mohan et al. [2] as 22% in normal glucose tolerance to 55% in patients with Type 2 diabetes.

Increasing recognition of the importance of NAFLD and its strong relationship with the metabolic syndrome has stimulated an interest in the possible role of NAFLD in the development of CVD. [29]

In the present study, all the patients with NAFLD were evaluated for the presence of components of metabolic syndrome and IR. We observed 25% prevalence of metabolic syndrome in patients with NAFLD as compared to 6% in controls. The patients with NAFLD had significantly higher waist circumference, diastolic blood pressure, fasting insulin, HOMA-IR, and significantly lower levels of HDL-cholesterol. We also made an attempt to assess the markers of subclinical atherosclerosis in them. They also had significantly higher CIMT and endothelial dysfunction than age-, sex- and BMI-matched controls.

The possible mediators linking NAFLD and CVD include the release of pro-atherogenic factors from the liver (C-reactive protein, fibrinogen, plasminogen activator inhibitor-1, and other inflammatory cytokines) as well as the contribution of NAFLD per se, IR, and atherogenic dyslipidemia, in turn favoring CVD progression. The clinical impact of NAFLD on CVD risk deserves particular attention in view of the implications for screening and surveillance strategies in the growing number of patients with NAFLD. Theoretically, the increased risk of cardiovascular events in patients with NAFLD is due to coexistence of this entity with metabolic syndrome.

One of the early processes in the pathophysiology of atherosclerosis is impaired endothelial function. Impaired endothelial function quantified by FMD is a marker of increased cardiovascular risk, due to its correlation with impaired endothelial function in the coronary arteries. The basic mechanism for FMD is to observe vasodilation by sonography after provoking ischemia by inflating blood pressure cuff. After brachial artery occlusion, endothelial nitric oxide is released and vascular smooth muscle relaxation occurs. The results of the present study are similar to those of Vlachopoulos et al. [30] and Villanova et al., [31] who also showed that NAFLD is associated with arterial stiffness and impaired endothelial function.

In recent years, several studies have shown the association between hepatic steatosis and carotid atherosclerosis. Manco et al. [32] have also observed a significant association between increased CIMT levels and NAFLD, although in a case-control study, they could not derive a suitable cutoff. We could demonstrate that atherosclerosis can affect vascular anatomy and physiology in NAFLD patients, independent of other risk factors. Given that age, gender, and BMI, as well as other cardiovascular risk factors, can influence the pathogenesis of atherosclerosis and its major determinants, i.e., FMD and CIMT, we matched cases and controls to eliminate as far as possible these effects on FMD and CIMT.

There are not much published data regarding the association between NAFLD and subclinical atherosclerotic risk markers in our population, which is the novelty of our study. The limitations of our study are small sample size and its cross-sectional design, so causative nature of the associations could not be established. Hence, large-scale prospective studies are needed to show the time sequence of events and also the association of NAFLD and incident cardiovascular events. Priorities for future research are the optimization of noninvasive screening, the identification of patients at risk of liver disease progression, future cardiovascular events, and management intervention strategies at the earliest.


  Conclusion Top


NAFLD is a hepatic manifestation of metabolic syndrome. It has an association with subclinical atherosclerosis that increases the risk for future cardiovascular events.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
  References Top

1.
Singh SP, Nayak S, Swain M, Rout N, Mallik RN, Agrawal O, et al. Prevalence of nonalcoholic fatty liver disease in coastal Eastern India: A preliminary ultrasonographic survey. Trop Gastroenterol 2004;25:76-9.  Back to cited text no. 1
    
2.
Mohan V, Farooq S, Deepa M, Ravikumar R, Pitchumoni CS. Prevalence of non-alcoholic fatty liver disease in urban South Indians in relation to different grades of glucose intolerance and metabolic syndrome. Diabetes Res Clin Pract 2009;84:84-91.  Back to cited text no. 2
    
3.
Amarapurkar D, Kamani P, Patel N, Gupte P, Kumar P, Agal S, et al. Prevalence of non-alcoholic fatty liver disease: Population based study. Ann Hepatol 2007;6:161-3.  Back to cited text no. 3
    
4.
Bellentani S, Saccoccio G, Masutti F, Crocè LS, Brandi G, Sasso F, et al. Prevalence of and risk factors for hepatic steatosis in Northern Italy. Ann Intern Med 2000;132:112-7.  Back to cited text no. 4
    
5.
Clark JM, Brancati FL, Diehl AM. The prevalence and etiology of elevated aminotransferase levels in the United States. Am J Gastroenterol 2003;98:960-7.  Back to cited text no. 5
    
6.
Farrell GC, Larter CZ. Nonalcoholic fatty liver disease: From steatosis to cirrhosis. Hepatology 2006;43 2 Suppl 1:S99-112.  Back to cited text no. 6
    
7.
Clark JM, Diehl AM. Nonalcoholic fatty liver disease: An underrecognized cause of cryptogenic cirrhosis. JAMA 2003;289:3000-4.  Back to cited text no. 7
    
8.
Angulo P. Nonalcoholic fatty liver disease. N Engl J Med 2002;346:1221-31.  Back to cited text no. 8
    
9.
Targher G. Non-alcoholic fatty liver disease, the metabolic syndrome and the risk of cardiovascular disease: The plot thickens. Diabet Med 2007;24:1-6.  Back to cited text no. 9
    
10.
Bellentani S, Bedogni G, Tiribelli C. Liver and heart: A new link? J Hepatol 2008;49:300-2.  Back to cited text no. 10
    
11.
Ahima RS. Insulin resistance: Cause or consequence of nonalcoholic steatohepatitis? Gastroenterology 2007;132:444-6.  Back to cited text no. 11
[PUBMED]    
12.
Bloomgarden ZT. Nonalcoholic fatty liver disease and insulin resistance in youth. Diabetes Care 2007;30:1663-9.  Back to cited text no. 12
    
13.
O'Leary DH, Polak JF. Intima-media thickness: A tool for atherosclerosis imaging and event prediction. Am J Cardiol 2002;90:18L-21L.  Back to cited text no. 13
    
14.
Verma S, Buchanan MR, Anderson TJ. Endothelial function testing as a biomarker of vascular disease. Circulation 2003;108:2054-9.  Back to cited text no. 14
    
15.
Targher G, Bertolini L, Padovani R, Zenari L, Zoppini G, Falezza G. Relation of nonalcoholic hepatic steatosis to early carotid atherosclerosis in healthy men: Role of visceral fat accumulation. Diabetes Care 2004;27:2498-500.  Back to cited text no. 15
    
16.
Brea A, Mosquera D, Martín E, Arizti A, Cordero JL, Ros E. Nonalcoholic fatty liver disease is associated with carotid atherosclerosis: A case-control study. Arterioscler Thromb Vasc Biol 2005;25:1045-50.  Back to cited text no. 16
    
17.
Volzke H, Robinson DM, Kleine V, Deutscher R, Hoffmann W, Ludemann J, et al. Hepatic steatosis is associated with an increased risk of carotid atherosclerosis. World J Gastroenterol 2005;11:1848-53.  Back to cited text no. 17
    
18.
Targher G, Bertolini L, Padovani R, Poli F, Scala L, Zenari L, et al. Non-alcoholic fatty liver disease is associated with carotid artery wall thickness in diet-controlled type 2 diabetic patients. J Endocrinol Invest 2006;29:55-60.  Back to cited text no. 18
    
19.
Targher G, Bertolini L, Padovani R, Rodella S, Zoppini G, Zenari L, et al. Relations between carotid artery wall thickness and liver histology in subjects with nonalcoholic fatty liver disease. Diabetes Care 2006;29:1325-30.  Back to cited text no. 19
    
20.
Kazmierski M, Michalewska-Wludarczyk A, Krzych LJ, Tendera M. Diagnostic value of flow mediated dilatation measurement for coronary artery lesions in men under 45 years of age. Cardiol J 2010;17:288-92.  Back to cited text no. 20
    
21.
Shimbo D, Grahame-Clarke C, Miyake Y, Rodriguez C, Sciacca R, Di Tullio M, et al. The association between endothelial dysfunction and cardiovascular outcomes in a population-based multi-ethnic cohort. Atherosclerosis 2007;192:197-203.  Back to cited text no. 21
    
22.
Glynn M. Gastrointestinal system. In: Swash M, Glynn M, editors. Hutchison's Clinical Methods. 22 nd ed. London, UK: Saunders Elsevier; 2007. p. 117-46.  Back to cited text no. 22
    
23.
Rumack CM, Wilson SR, Charbonean JW. The liver. In: Johnson JA, editor. Diagnostic Ultrasound. 3 rd ed. London, UK: Elsevier Mosby; 2005 p. 77-145.  Back to cited text no. 23
    
24.
Saadeh S, Younossi ZM, Remer EM, Gramlich T, Ong JP, Hurley M, et al. The utility of radiological imaging in nonalcoholic fatty liver disease. Gastroenterology 2002;123:745-50.  Back to cited text no. 24
    
25.
Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive summary of the third report of the national cholesterol education program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). JAMA 2001;285:2486-97.  Back to cited text no. 25
[PUBMED]    
26.
Corretti MC, Anderson TJ, Benjamin EJ, Celermajer D, Charbonneau F, Creager MA, et al. Guidelines for the ultrasound assessment of endothelial-dependent flow-mediated vasodilation of the brachial artery: A report of the international brachial artery reactivity task force. J Am Coll Cardiol 2002;39:257-65.  Back to cited text no. 26
    
27.
Ludwig J, Viggiano TR, McGill DB, Oh BJ. Nonalcoholic steatohepatitis: Mayo clinic experiences with a hitherto unnamed disease. Mayo Clin Proc 1980;55:434-8.  Back to cited text no. 27
[PUBMED]    
28.
Mishra S, Yadav D, Gupta M, Mishra H, Sharma P. Hyperinsulinemia predisposes to NAFLD. Indian J Clin Biochem 2008;23:130-5.  Back to cited text no. 28
    
29.
Targher G, Arcaro G. Non-alcoholic fatty liver disease and increased risk of cardiovascular disease. Atherosclerosis 2007;191:235-40.  Back to cited text no. 29
    
30.
Vlachopoulos C, Manesis E, Baou K, Papatheodoridis G, Koskinas J, Tiniakos D, et al. Increased arterial stiffness and impaired endothelial function in nonalcoholic fatty liver disease: A pilot study. Am J Hypertens 2010;23:1183-9.  Back to cited text no. 30
    
31.
Villanova N, Moscatiello S, Ramilli S, Bugianesi E, Magalotti D, Vanni E, et al. Endothelial dysfunction and cardiovascular risk profile in nonalcoholic fatty liver disease. Hepatology 2005;42:473-80.  Back to cited text no. 31
    
32.
Manco M, Bedogni G, Monti L, Morino G, Natali G, Nobili V. Intima-media thickness and liver histology in obese children and adolescents with non-alcoholic fatty liver disease. Atherosclerosis 2010;209:463-8.  Back to cited text no. 32
    



 
 
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