Literature DB >> 22149546

Inflammatory markers in relation to nonalcoholic fatty liver disease in urban South Indians.

Gokulakrishnan Kuppan1, Ranjit Mohan Anjana, Mohan Deepa, Prabu Paramasivam, Sathishkumar Chandrakumar, Velmurugan Kaliyaperumal, Viswanathan Mohan.   

Abstract

OBJECTIVE: This study assessed the association of inflammatory markers, high-sensitivity C-reactive protein (hsCRP), and total leukocyte count with nonalcoholic fatty liver disease (NAFLD) in urban South Indians. SUBJECTS AND METHODS: We randomly selected subjects with and without NAFLD (n=100 each) from the Chennai Urban Rural Epidemiology Study conducted in Chennai in south India. NAFLD was diagnosed by ultrasonography. hsCRP was measured by nephelometry, and leukocyte count was measured by flow cytometry. Insulin resistance was analyzed by homeostasis assessment model using the following expression: fasting insulin (μIU/mL)×fasting glucose (mmol/L)/22.5.
RESULTS: Mean hsCRP values were significantly higher in subjects with NAFLD compared with those without (4.2±1.2 mg/L vs. 2.2±0.4 mg/L; P<0.001). Leukocyte count was also higher in subjects with NAFLD compared with those without (7.8±1.4×10(3)/μL vs 6.9±0.9×10(3)/μL, P<0.001). Both hsCRP (P<0.001) and leukocyte count (P<0.001) increased with increasing severity of NAFLD. Multiple logistic regression analysis was done using NAFLD as the dependent variable and hsCRP and leukocyte count as independent variables. Both hsCRP (odds ratio 1.293, 95% confidence interval 1.13-1.470, P<0.001) and leukocyte count (odds ratio 1.293, 95% confidence interval 1.069-1.564, P=0.008) had a significant association with NAFLD even after adjusting for waist circumference, insulin resistance, serum triglycerides, and presence of type 2 diabetes.
CONCLUSIONS: hsCRP and leukocyte count are associated with NAFLD after adjusting for conventional cardiometabolic risk factors.

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Year:  2011        PMID: 22149546     DOI: 10.1089/dia.2011.0213

Source DB:  PubMed          Journal:  Diabetes Technol Ther        ISSN: 1520-9156            Impact factor:   6.118


  9 in total

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Authors:  Jianjin Guo; Wei Ren; Aimei Li; Ying Ding; Wanhua Guo; Dongming Su; Cheng Hu; Kuanfeng Xu; Heng Chen; Xinyu Xu; Tao Yang; Weiping Jia
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2.  Nonalcoholic fatty liver disease in morbidly obese subjects: correlation among histopathologic findings, biochemical features, and ultrasound evaluation.

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3.  Hepatic Steatosis Is Associated with High White Blood Cell and Platelet Counts.

Authors:  Yu-Lin Chao; Pei-Yu Wu; Jiun-Chi Huang; Yi-Wen Chiu; Jia-Jung Lee; Szu-Chia Chen; Jer-Ming Chang; Shang-Jyh Hwang; Hung-Chun Chen
Journal:  Biomedicines       Date:  2022-04-13

4.  Association of Inflammatory Cytokines With Non-Alcoholic Fatty Liver Disease.

Authors:  Yamei Duan; Xiongfeng Pan; Jiayou Luo; Xiang Xiao; Jingya Li; Prince L Bestman; Miyang Luo
Journal:  Front Immunol       Date:  2022-05-06       Impact factor: 8.786

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6.  Associations between White Blood Cell Count and the Development of Incidental Nonalcoholic Fatty Liver Disease.

Authors:  Goh Eun Chung; Jeong Yoon Yim; Donghee Kim; Min-Sun Kwak; Jong In Yang; Su Jin Chung; Sun Young Yang; Joo Sung Kim
Journal:  Gastroenterol Res Pract       Date:  2016-12-13       Impact factor: 2.260

7.  High-normal levels of hs-CRP predict the development of non-alcoholic fatty liver in healthy men.

Authors:  Jieun Lee; Kijung Yoon; Seungho Ryu; Yoosoo Chang; Hyoung-Ryoul Kim
Journal:  PLoS One       Date:  2017-02-24       Impact factor: 3.240

Review 8.  Changes in the immune system - the key to diagnostics and therapy of patients with non-alcoholic fatty liver disease.

Authors:  Marcin Kosmalski; Łukasz Mokros; Piotr Kuna; Andrzej Witusik; Tadeusz Pietras
Journal:  Cent Eur J Immunol       Date:  2018-06-30       Impact factor: 2.085

9.  Association of high-sensitivity C-reactive protein (hs-CRP) with non-alcoholic fatty liver disease (NAFLD) in Asian Indians: A cross-sectional study.

Authors:  Rahul Kumar; Y C Porwal; Nishanth Dev; Priyadarshi Kumar; Sanjay Chakravarthy; Ashok Kumawat
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  9 in total

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