Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

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Dr. Mamta Gupta,
"It gives me great pleasure to be associated with JCDR, since last 2-3 years. Since then I have authored, co-authored and reviewed about 25 articles in JCDR. I thank JCDR for giving me an opportunity to improve my own skills as an author and a reviewer.
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Reviewing articles is no less a pain staking process and requires in depth perception, knowledge about the topic for review. It requires time and concentration, yet I enjoy doing it. The JCDR website especially for the reviewers is quite user friendly. My suggestions for improving the journal is, more strict review process, so that only high quality articles are published. I find a a good number of articles in Obst. Gynae, hence, a new journal for this specialty titled JCDR-OG can be started. May be a bimonthly or quarterly publication to begin with. Only selected articles should find a place in it.
An yearly reward for the best article authored can also incentivize the authors. Though the process of finding the best article will be not be very easy. I do not know how reviewing process can be improved. If an article is being reviewed by two reviewers, then opinion of one can be communicated to the other or the final opinion of the editor can be communicated to the reviewer if requested for. This will help one’s reviewing skills.
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Aug 2018

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Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
On May 11,2011

Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
Strengths of the journal: The journal has an online first facility in which the accepted manuscripts may be published on the website before being included in a regular issue of the journal. This cuts down the time between their acceptance and the publication. The journal is indexed in many databases, though not in PubMed. The editorial board should now take steps to index the journal in PubMed. The journal has a system of notifying readers through e-mail when a new issue is released. Also, the articles are available in both the HTML and the PDF formats. I especially like the new and colorful page format of the journal. Also, the access statistics of the articles are available. The prepublication and the manuscript tracking system are also helpful for the authors.
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Overall, the publishing process with JCDR has been smooth, quick and relatively hassle free and I can recommend other authors to consider the journal as an outlet for their work."

Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
On April 2011

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.

Dr. Anuradha
On Jan 2020

Important Notice

Original article / research
Year : 2022 | Month : September | Volume : 16 | Issue : 9 | Page : BC01 - BC04 Full Version

Quantification of Microsomal Triglyceride Transfer Protein in Non Alcoholic Fatty Liver Disease Patients: A Cross-sectional Study

Published: September 1, 2022 | DOI:
Mayuri Shukla, Mamatha Kunder, Prabhakar Kamarthy, Sharath Balakrishna

1. PhD Scholar, Department of Cell Biology and Molecular Genetics, Sri Devaraj Urs Academy of Higher Education and Research, Kolar, Karnataka, India. 2. Assistant Professor, Department of Biochemistry, Sri Devaraj Urs Medical College, Kolar, Karnataka, India. 3. Professor, Department of Medicine, Sri Devaraj Urs Medical College, Kolar, Karnataka, India. 4. Associate Professor and Head, Department of Cell Biology and Molecular Genetics, Sri Devaraj Urs Academy of Higher Education and Research, Kolar, Karnataka, India.

Correspondence Address :
Dr. Mamatha Kunder,
Department of Biochemistry, Sri Devaraj Urs Medical College, Tamaka, Kolar-563101, Karnataka, India.


Introduction: Non Alcoholic Fatty Liver Disease (NAFLD) is one of the common liver disease characterised by fat accumulation in hepatocytes. NAFLD is a broad spectrum of simple steatosis, Non Alcoholic Steatohepatitis (NASH), cirrhosis and hepatocellular carcinoma. Triglycerides (TG) are exported in the form of Very Low Density Lipoprotein (VLDL). VLDL are formed by incorporation of TG into apo-B by Microsomal Triglyceride transfer Protein (MTP). Therefore, MTP is a key protein for lipid transport. Estimation of MTP protein levels and its correlation with simple steatosis and steatohepatitis can be helpful in understanding its role in NAFLD progression.

Aim: To estimate the serum levels of MTP in simple steatosis and steatohepatitis and also to check its correlation with TG and VLDL in NAFLD patients with and without co-morbidities.

Materials and Methods: The present cross-sectional study was carried out in Department of Cell Biology and Molecular Genetics, Sri Devaraj Urs Academy of Higher Education and Research, Kolar, Karnataka, India, between November 2019 to January 2021. Study participants included 60 NAFLD subjects which were divided into simple steatosis (group 1, n=10) and steatohepatitis (group 2, n=50). These subjects were further subdivided into cases with co-morbidities and cases without co-morbidities. Serum levels of MTP, high sensitivity C Reactive Protein (hs-CRP), Fasting Blood Sugar (FBS), liver enzymes, lipid profile were assessed. Statistical analysis was done by using unpaired Student’s t-test and Pearson’s correlation.

Results: The mean age was 46.5 years in steatosis group and 48.85 years in steatohepatitis group. In steatosis group, there were 5 (50%) males and 5 (50%) females, whereas in steatohepatitis group 32 (64%) were females and 18 (36%) were males. The serum levels of MTP were significantly decreased in simple steatosis cases with co-morbidities as compared to cases without co-morbidities (p=0.006). A significant negative correlation was observed between MTP v/s TG and MTP v/s VLDL (r=-0.665, p=0.036) in simple steatosis cases with and without co-morbidities. Same trend was observed in steatohepatitis cases but the correlation was insignificant (r=-0.08, p=0.563).

Conclusion: The serum levels of MTP decreases as the NAFLD progresses. A significant decrease in serum levels of MTP was also observed in cases with co-morbidities as compared to cases without co-morbidities. Serum levels of MTP showed negative correlation with TG and VLDL in simple steatosis cases.


Co-morbidities, Hyperlipidaemia, Lipid transportation, Non alcoholic steatohepatitis, Very low density lipoprotein

NAFLD is the most common liver disease with a prevalence of 9-32% in India and 25% of global adult population (1). NAFLD is characterised by the accumulation of excessive fat in the liver in absence of alcohol intake (2). NAFLD includes different stages, where simple fat accumulation without any inflammation of hepatocytes is termed as Simple steatosis or Non Alcoholic Fatty Liver (NAFL). Simple steatosis if left untreated further progresses to inflammation of hepatocytes and this stage is termed as NASH, followed by fibrosis and hepatocellular carcinoma (3).

Fat accumulation in liver can be a result of either lack of breakdown of fatty acids or lack of fatty acid export from liver to peripheral tissues (4),(5). TG are exported from liver in the form of VLDL particles. TG rich VLDL particles represent the mechanism by which fatty acids are exported from the liver and delivered to muscle for oxidation and adipose tissue for storage, respectively (6).

VLDL are formed by incorporation of TG into apolipoprotein B (apoB) by MTP (7),(8),(9). MTP was identified as a major cellular protein capable of transferring neutral lipids and is localised to endoplasmic reticulum in hepatocytes. MTP is a heterodimer with two distinct subunits. A unique large α-subunit (97kDa) and a multifunctional Protein Disulfide Isomerase (PDI) β-subunit (55kDa). The 97kDa subunit confers all of the lipid transfer activity to the heterodimer (10). VLDL assembly is a two-step process that begins in the endoplasmic reticulum lumen. In the first step, MTP acts to incorporate a small amount of TG in apoB100 as it is being translated by ribosomes and translocated across the endoplasmic reticulum membrane (6). In the second step, additional TG is packaged into the nascent apoB100-containing particles as they traverse from the endoplasmic reticulum to the golgi apparatus to form VLDL particles (11).

In-vitro studies have shown that lipid transfer by the MTP is most efficient with TG and cholesterol although MTP transfers polar lipids also along with the neutral lipids (8),(12). According to several lines of evidence, MTP polymorphisms have been linked to lipid homeostasis and, in turn, to a higher risk of NAFLD (13),(14). Lower hepatic expression of MTP plays a crucial role in NAFLD development and is one of the potential gene found to be associated with NAFLD susceptibility (15). The most common and widely investigated polymorphism in MTP gene is -493 G>T (rs1800591) (16),(17).

Therefore, aim was to study MTP in simple steatosis and steatohepatitis, which can be helpful in assessing the disease progression. Simple steatosis is asymptomatic and steatohepatitis is an advanced stage which further progresses to irreversible conditions like fibrosis and cirrhosis. Usually many patients are diagnosed only at advanced stage of NAFLD (18). Therefore, assessment of NAFLD is essential at early stages to prevent the further complications and progression of the disease. Hence, simple steatosis and steatohepatitis were selected in this study, to stratify before NAFLD progresses to advanced stages. However, to the best of our knowledge, till date no study measured the serum levels of MTP. Thus, this study was aimed to measure the serum levels of MTP and also to check its correlation with the stages of NAFLD in patients with or without co-morbidities in order to understand its role in disease progression.

Material and Methods

The present-cross sectional study was carried out in Department of Cell Biology and Molecular Genetics, Sri Devaraj Urs Academy of Higher Education and Research, Kolar, Karnataka, India between November 2019 to January 2021. Study was approved by the Institutional Ethics Committee (IEC) of Sri Devaraj Urs Medical College (DMC/KLR/IEC/657/2021-22). The written informed consent was obtained prior to the recruitment of the subjects.

Inclusion criteria: NAFLD patients, aged between 25-60 years and with or without complications (diagnosed by laboratory tests, Ultrasonography) such as obesity, hyperlipidaemia, hypertension, diabetes and cardiovascular diseases, were included in the study.

Exclusion criteria: Subjects with other chronic liver diseases like hepatitis, chronic obstructive pulmonary disease, alcohol consumption, smoking history were excluded from the study.

Sample size calculation: Total 60 patients were enrolled in present study by convenient sampling.

Subjects and Study Design

The study participants included 60 NAFLD patients. The patients were broadly categorised into two groups; group 1 (simple steatosis) and group 2 (steatohepatitis). National Cholesterol Education Program Adult Treatment Panel (NCEP ATPIII) guidelines (19) and ultrasonography were followed to differentiate the stages. Cases with high serum levels of liver enzymes like Alanine transaminase (ALT) (<35 mg/dL), Aspartate aminotransferase (AST) (<45 mg/dL) and TG (>150 mg/dL) along with impression of hepatomegaly with fatty infiltration were considered as steatohepatitis or NASH. In addition to above, cases without inflammation (hs-CRP within the normal range: <10 mg/L) were considered as simple steatosis and with inflammation (hs-CRP >10 mg/L) were considered as steatohepatitis in the present study (19).

Simple steatosis (Group 1): Characterised by increased fat accumulation without inflammation included 10 patients. Further patients with simple steatosis were subdivided based on co-morbidities into- 1A (cases with co-morbidities- five patients) and 1B (cases without co-morbidities-five patients).

Steatohepatitis (Group 2): Characterised by increased fat accumulation with inflammation included 50 patients. Patients with steatohepatitis were subdivided based on co-morbidities into- 2A (cases with co-morbidities- 25 patients) and 2B (cases without co-morbidities- 25 patients).

The co-morbidities like obesity, hyperlipidaemia, hypertension, diabetes and cardiovascular diseases were considered. Body Mass Index (BMI) was calculated to confirm obesity, FBS was measured for diabetic patients, and blood pressure for hypertension. Patients with any three of the above mentioned co-morbidities were considered in cases with co-morbidities group.

Sample Collection

Five mL venous blood was collected from all the subjects in tubes containing sodium fluoride for FBS estimation. For investigations like hs-CRP, Liver Function Tests (LFT) and lipid profile blood was collected in tube without anticoagulant. Blood samples were centrifuged at 3000rpm for 10 minutes at room temperature within 2 hours. of collection. Basic parameters were analysed immediately and serum for MTP estimation was aliquoted and stored at -70°C until further analysis.

Biochemical Evaluation

The biochemical parameters were analysed by standard methods using Vitros 5.1 FS clinical chemistry analyser (Table/Fig 1). VLDL was calculated using Friedwald’s formula. Serum levels of MTP were estimated by Enzyme Linked Immunosorbent Assay (ELISA) using a commercial kit. (Catalogue no. SEC641Hu, Cloud clone corp., USA).

Statistical Analysis

Statistical analysis was carried out using Graph Pad Prism V.9. Shapiro-Wilk test was used to assess the normality of data. Statistical difference between the two groups were analysed using unpaired t-test. Results are represented as Mean±Standard Deviation (SD). Pearson’s correlation was used to determine the relationship between variables. The p-value <0.05 was considered statistically signi?cant and p-value <0.0001 as highly significant.


Simple steatosis had 5 (50%) females and 5 (50%) males and there were 32 (64%) females and 18 (36%) males in steatohepatitis. No statistical differences (p<0.05) were observed between Simple steatosis and Steatohepatitis, with respect to age, BMI, FBS and Lipid profile. The hs-CRP levels showed a significant increase in Steatohepatitis (group 2) as compared to Simple steatosis (group 1) (p<0.0001). Steatohepatitis subjects had higher serum levels of TG and VLDL (217.71±97.16) (43.54±19.43) respectively as compared to serum levels of triglyceride and VLDL Simple steatosis subjects (193.2±80.30) (38.64±16.06) respectively, but did not show any statistically significant difference (p=0.071).Serum MTP levels were measured and analysed in Simple steatosis (1.93±0.61) and Steatohepatitis (1.48±1.02) patients of NAFLD subjects and no statistical significant difference was observed (p=0.995) (Table/Fig 2).

Mean VLDL and TG levels were significantly higher in NAFLD patient with co-morbidities as compared to NAFLD without co-morbidities in Steatohepatitis patients and this difference was significant (p<0.0001), but non-significant in Simple steatosis patients (p=0.107). Mean MTP levels were significantly lower in NAFLD cases with co-morbidities as compared to NAFLD cases without co-morbidities in Simple steatosis patients (p=0.006), but non-significant in Steatohepatitis patients (p=0.532) (Table/Fig 3).

Correlation analysis was done between serum levels of MTP versus TG and MTP versus VLDL. A negative correlation was observed in both the cases with co-morbidities (group 1A and 2A), suggesting inverse relation between MTP and TG as well as VLDL. However, a significant negative correlation was observed between MTP and TG, VLDL in simple steatosis cases with and without co-morbidities (1A+1B) (r=-0.665, p=0.036) (Table/Fig 4).


MTP as the name suggests is involved in transfer of TG from hepatocytes to the peripheral tissues. Therefore, if MTP is dysfunctional it may contribute to TG accumulation in hepatocytes which eventually results in fatty liver (20),(21). Present study measured and compared the serum levels of MTP in NAFLD subjects with Simple steatosis (Group 1) and Steatohepatitis (Group 2). Present study results showed that levels of MTP were decreased in Steatohepatitis as compared to Simple steatosis. As Steatohepatitis of NAFLD is associated with inflammation and is the advanced stage of NAFLD, decreased levels of MTP in Steatohepatitis indicates impact of its association with NAFLD and its stages.

Studies have associated NAFLD with co-morbidities like obesity, diabetes mellitus, cardiovascular disease and hyperlipidaemia (22),(23),(24),(25),(26). These co-morbidities with NAFLD carries an increased risk of liver related morbidity and mortality (27). Therefore, in this study authors wanted to investigate whether MTP levels are affected by the presence of co-morbidities in NAFLD patients. In the present study, when MTP levels were compared between cases with co-morbidities and cases without co-morbidities in both the stages, subjects with co-morbidities had decreased levels of MTP as compare to subjects without co-morbidities. This further supports the role of MTP in pathogenesis and progression of NAFLD stages.

NAFLD is a multifactorial disease that results from complicated interactions among dietary components, lifestyle choices and genetic determinants (28). Several research have been looked into gene-expression based NAFLD staging in order to better understand disease progression and find the effective treatment (29),(30),(31). An interaction between MTP and NAFLD is also been identified with the help of genetic studies. A polymorphism at promoter region (-493G/T) of MTP is associated in NASH with type 2 Diabetes Mellitus. The G allele is associated with decreased MTP transcription and is prone to increased TG content in hepatocytes (30),(32),(33). Transversion of base guanine to thymine at 493 position in the promoter region of MTP is found to be associated with decreased transcription level of MTP and failure in TG secretion from hepatocytes which increases the susceptibility to NAFLD (17),(20). The -493 allele is also considered as a risk factor in pathogenesis of metabolic syndromes (34). The polymorphism in MTP gene is also been suggested to be a useful and practical biomarker for early diagnosis of NAFLD (35). Therefore, decreased serum levels of MTP observed in advanced stage of NAFLD in present study thus could be linked to altered gene expression.


The study was limited firstly by small sample size due to inadequate number of patients who met the inclusion criteria and secondly due to lack of genetic analysis.


The decreased serum levels of MTP in advanced NAFLD stage suggests that MTP can be a complementary marker in differentiating simple steatosis from steatohepatitis. As MTP also shows a negative correlation with TG and VLDL when compared between cases with co-morbidities and cases without co-morbidities, therefore MTP can be considered as complementary marker in subjects with co-morbidities as well. For further prospects, studies involving all stages of NAFLD in a larger population are required. The genetic analysis and increased sample size might show significant results which can be helpful in identifying MTP as a complementary marker for differentiating the simple steatosis from steatohepatitis and assessing the disease progression.


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DOI and Others

DOI: 10.7860/JCDR/2022/56386.16811

Date of Submission: Mar 15, 2022
Date of Peer Review: Apr 08, 2022
Date of Acceptance: May 27, 2022
Date of Publishing: Sep 01, 2022

• Financial or Other Competing Interests: None
• Was Ethics Committee Approval obtained for this study? Yes
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. NA

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