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Dive into the research topics where Jain Ak is active.

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Featured researches published by Jain Ak.


Helicobacter | 2008

Evaluation of Nested PCR in Detection of Helicobacter pylori Targeting a Highly Conserved Gene: HSP60

Varsha Singh; Shrutkirti Mishra; GRKoteswar Rao; Jain Ak; Vk Dixit; Anil Kumar Gulati; Divya Mahajan; Michael McClelland; Gopal Nath

Objective:  To comparatively evaluate a new nested set of primers designed for the detection of Helicobacter pylori targeting a highly conserved heat shock protein gene (Hsp60).


Renal Failure | 2011

Clinical Spectrum of Renal Disorders in Patients with Cirrhosis of Liver

Jai Prakash; Amit Kumar Mahapatra; Biplab Ghosh; Puneet Arora; Jain Ak

Background: There are limited studies describing various renal disorders and their prognostic impact in patients with cirrhosis of liver. The aim of this work was to study the clinical spectrum of renal disorders in patients with cirrhosis of liver and their prognostic impact. Methods: Patients with diagnosis of cirrhosis of liver were included in this study. Cirrhosis was diagnosed using standard clinical criteria. The cirrhotic patients were prospectively analyzed for the presence of renal diseases during the study period from January 2008 to April 2009. Results: Four hundred and four patients were included in this study and renal diseases were present in 44% (n = 178) patients. The spectrum of renal diseases were acute kidney injury (AKI; 24.5%), chronic kidney disease (CKD; 15.6%), acute on chronic renal failure (1.5%), nephritic syndrome (1.5%), and nephrotic syndrome (1%). The types of AKI were acute tubular necrosis (ATN; 44.4%), prerenal failure (36.4%), and hepatorenal syndrome (19.2%). The incidence of renal diseases was 15.7% in class A, 50% in class B, and 54.8% in class C cirrhosis. There was significant increase in mortality in patients with class C cirrhosis versus without renal disease (78.1% vs. 53.2%; p < 0.001). Conclusions: Renal diseases were present in a significant proportion (44%) of cirrhotic patients. ATN was the commonest form of AKI and we noted that the prevalence of CKD was 15.6% in our cirrhotic patients. The incidence of renal disease increased with increase in severity of cirrhosis of liver. The presence of renal disease seems to have adverse prognostic impact on class C cirrhosis.


Antiviral Research | 2013

Predictors of survival in hepatitis B virus related decompensated cirrhosis on tenofovir therapy: an Indian perspective.

Manjita Srivastava; Sumit Rungta; Vinod Kumar Dixit; Sunit K. Shukla; T.B. Singh; Jain Ak

Decompensated cirrhosis has low survival rate compared to compensated state. Effective viral suppression due to antiviral therapy (tenofovir) has been shown to slow disease progression and may delay the burden of liver transplantation. We aimed to evaluate the usefulness of various prognostic indicators in predicting the 24-months survival in HBV related decompensated cirrhosis after tenofovir therapy and to evaluate the post-treatment outcome. Ninety-six HBV related decompensated patients on antiviral (tenofovir) therapy were prospectively studied for 24months survival and mortality. Cutoff levels for several prognostic indicators were generated by ROC. Prediction of overall probability of mortality was also calculated. The overall probability of survival observed at 12months was 0.947 whereas at 24months it was found to be 0.833. According to Cox proportional hazards model, the univariate analysis revealed cutoff of >7.4logcopies/ml for HBV DNA, >1.2mg/dl for serum creatinine, >3.7mg/dl for total bilirubin, ⩽0.75 for platelets count, >10 for CTP and >20 for MELD as predictors of poor survival. Multivariate analysis showed MELD score of >20 was the most robust predictor of mortality, with 58 times higher risk (HR: 58.73, p<0.001). Post-treatment response with tenofovir for 24months significantly improved the hepatic functions and reverses decompensation and showed incredible efficacy in improvement of hepatic functional status with reduced viremia in a great majority of decompensated cirrhosis subjects having high MELD and HBV DNA level.


Journal of clinical and experimental hepatology | 2014

Hydatid Cyst of Liver Presented as Obstructive Jaundice in Pregnancy; Managed by PAIR.

Jayant Kumar Ghosh; Sundeep K. Goyal; Manas K. Behera; Vinod Kumar Dixit; Jain Ak

Incidence of Hydatid disease in pregnancy ranges from 1in 20,000 to 1 in 30,000. The most common site of hydatid cysts is the liver. The diagnosis of liver hydatid cysts is not difficult but the management during pregnancy is problematic. Both medical and surgical treatments are available but there is no consensus and each case has to be individualized. We present a case of liver hydatid cyst presented with obstructive jaundice during pregnancy which was managed by Puncture of the cyst under USG guidance; Aspiration of the cystic fluid, Injection of hypertonic saline, and Re-aspiration of solution without drainage (PAIR) and albendazole therapy. Very few cases of liver hydatosis were reported previously which had been managed by PAIR.


Interdisciplinary Perspectives on Infectious Diseases | 2016

Ulcerative Colitis and Its Association with Salmonella Species

Manish Kumar Tripathi; Chandra Bhan Pratap; Vinod Kumar Dixit; Tej Bali Singh; Sunit K. Shukla; Jain Ak; Gopal Nath

Ulcerative colitis (UC) is characterized by presence of ulcer in colon and bloody diarrhea. The present study explores the possibility of association between Salmonella and ulcerative colitis. The present study comprised 59 cases of UC, 28 of colon cancer (CC), 127 of irritable bowel syndrome (IBS), and 190 of healthy control. The serological study was done by Widal and Indirect Haemagglutination Assay (IHA) for ViAb. Nested PCR was performed targeting fliC, staA, and stkG gene for Typhi and Paratyphi A, respectively. A total of 15.3% patients were positive for Salmonella “O” antigen among them 18.6% UC, 35.5% CC, 12.6% IBS, and 15.3% healthy control. A total of 36.9% patients were positive for “H” antigen including 39.0%, 57.1%, and 67.7% UC, CC, and IBS, respectively. About 1.73% show positive agglutination for AH antigen including 3.4%, 3.6%, and 1.6%, UC, CC, and IBS. A total of 10.89% were positive for ViAb. While 6.8% of UC, 10.7% of CC, 11.0% of IBS, and 12.1% of healthy subjects were positive for the antibody, the PCR positivity rates for Salmonella specific sequences were 79.7% in UC, 53.6% in CC, 66.1% in IBS, and 16.3% in healthy controls. The present study suggested that higher prevalence of Salmonella might play important role in etiopathogenesis of UC, IBS, and CC.


Indian Journal of Medical Research | 2016

Comparative evaluation of long-term monotherapies & combination therapies in patients with chronic hepatitis B: A pilot study

Manjita Srivastava; Neha Singh; Vinod Kumar Dixit; Gopal Nath; Jain Ak

BACKGROUND & OBJECTIVES Reduction of viraemia in patients with chronic hepatitis B virus (HBV) infection using nucleoside/nucleotide analogues reduces fatal liver disease-related events, but development of resistance in virus presents serious clinical challenge. Therefore, comparative evaluation of prolonged antiviral monotherapy and combination therapies was prospectively studied to assess their influence on viral suppression, rapidity of response, development of drug resistance and surfacing mutants in chronic liver disease (CLD) patients. METHODS A total of 158 (62eAg-ve) chronic hepatitis B patients were prospectively studied for 24 months. Final analysis was performed on patients treated with lamivudine (LAM, n = 28), adefovirdipivoxil (ADV, n = 24), tenofovir disoproxil fumarate (TDF, n = 26), entecavir (ETV, n = 25), LAM + ADV (n = 28) and LAM + TDF (n = 27). Quantitative hepatitis B virus DNA was detected using real-time polymerase chain reaction. Multiple comparisons among drugs and genotypic mutations were analyzed. RESULTS Progressive biochemical and virological response were noted with all the regimens at 24 months except LAM and ADV which were associated with viral breakthrough (VBT) in 46.4 and 25 per cent, respectively. Mutations: rtM204V (39.3%), M204V+L180M (10.7%) while rtA181V (8.1%) and rtN236T (8.3%) were observed with LAM and ADV regimen, respectively. LAM + ADV combination therapy revealed VBT in seven per cent of the cases without mutations whereas TDF, ETV and LAM + TDF therapies neither showed VBT nor mutations. INTERPRETATION & CONCLUSIONS LAM was the least potent drug among all therapeutic options followed by ADV. TDF and ETV were genetically stable antivirals with a strong efficacy. Among newer combination therapies, LAM + TDF revealed more efficacy in virological remission and acted as a profound genetic barrier on long term. Hence, newer generation molecules (TDF, ETV) and effective combination therapy should be a certain choice.


Indian Journal of Medical Research | 1989

Irritable bowel syndrome : therapeutic evaluation of indigenous drugs

Yadav Sk; Jain Ak; Tripathi Sn; Gupta Jp


Journal of Association of Physicians of India | 1993

Evaluation of Manning's criteria in the diagnosis of irritable bowel syndrome.

Rao Kp; Siddhartha Datta Gupta; Jain Ak; Agrawal Ak; Gupta Jp


Journal of Infection in Developing Countries | 2008

Association of carcinoma of the gallbladder with typhoid carriage in a typhoid endemic area using nested PCR

Gopal Nath; Yogesh Kumar Singh; Kailash Kumar; Anil Kumar Gulati; Vijay K. Shukla; Ajay Kumar Khanna; Sunil Kumar Tripathi; Jain Ak; Mohan Kumar; Tej Bali Singh


Tropical gastroenterology : official journal of the Digestive Diseases Foundation | 1997

Needle aspiration in large amoebic liver abscess.

Tandon A; Jain Ak; Vinod Kumar Dixit; Agarwal Ak; Gupta Jp

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Vinod Kumar Dixit

Institute of Medical Sciences

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Gopal Nath

Institute of Medical Sciences

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Manish Kumar Tripathi

Institute of Medical Sciences

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Arttrika Ranjan

Institute of Medical Sciences

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Neha Singh

Institute of Medical Sciences

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Anil Kumar Gulati

Institute of Medical Sciences

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Neha Gupta

Institute of Medical Sciences

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Smita Verma

Institute of Medical Sciences

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