Methods— We retrospectively reviewed the medical records of all

Methods.— We retrospectively reviewed the medical records of all 1562 (male 724, female 838) new patients presenting with recurrent headaches to 9 Pediatric Neurology Clinics

of tertiary Hospitals. Data regarding age of onset, duration of symptoms before presentation, frequency, duration of each episode, intensity, location and quality of headache, associated neurologic symptoms and a comprehensive neurological examination were obtained for each patient. The International Classification of Headache Disorders, second edition, was used to classify headache types. Results.— Neuroimaging procedures were performed in 77.1% of the patients. Overall, 9.3% (112/1204) of the patients had abnormal findings from neuroimaging. The highest yield was ACP-196 manufacturer in patients with an abnormal neurological examination wherein abnormal findings on neuroimaging were seen in 50.0% (9/18) of patients (P < .001). The yield was low when imaging was carried out in view of

changes in the type of headache (12.9% [26/201]), neurologic dysfunction (10.8% [9/83]), recent onset of severe headaches (7.0% [12/171]), and demands of parent and physicians (10.1% [21/208]). Eleven patients underwent surgery based on neuroimaging results. There was no significant relation between abnormality on neuroimaging and age, sex, headache type, age of onset of CCI-779 cost headache, duration of symptoms before presentation, duration, frequency, location and intensity of headache (P > .05). Conclusions.— Neuroimaging procedures in children and adolescents

with headaches, although not always required, are very commonly performed. We suggest that more strict guidelines for rational use of neuroimaging are needed for pediatric headache patients. “
“(Headache 2010;50:176-184) Objective.— To investigate the effects of migraine and related pharmacotherapy on cognitive performance and cognitive change over time in a longitudinal population-based study. Methods.— Migraineurs (n = 99) and healthy controls (n = 1724) participating in the Maastricht Aging Study were cognitively tested at baseline and after 6 years. Scores on Mini Mental State Examination, immediate and delayed recall tests, and tests for simple and complex speed were compared for both groups. Generalized Estimating Equations analyses were performed to test the longitudinal effects of migraines on MCE公司 cognition. Effects of migraine medication use were also tested. Results.— Migraine headaches were found to have no effect on any of the cognitive measures. Medication use also had no effect on all cognitive measures. Conclusions.— No evidence was found that migraine headaches or migraine-related medication use are risk or protective factors for cognitive dysfunction or cognitive deterioration over time. “
“Recent genome-wide association studies (GWAS) have identified 3 loci in or near PRDM16 (1p36.32, rs2651899), LRP1 (12q13.3, rs11172113) and TRPM8 (2q37.

Second, treatment regimens were not uniform, although there were

Second, treatment regimens were not uniform, although there were no obvious differences according to recipient:donor MK 1775 genotype pairs. Finally, although the cohort is larger than most studies of HCV after OLT, power to detect smaller effects on survival was low. The data should therefore be considered limited to hypothesis generation. In conclusion, the data suggest that recipient IL28B TT genotype is associated with more rapid histological recurrence of HCV. Recipient and donor liver IL28B genotype are strongly and independently associated with IFN-based treatment response in patients after OLT. Treatment was generally safe and has previously been associated with improved

graft survival in this cohort. The data therefore support the preferential allocation of CC donor livers to patients with HCV infection. Prospective validation in larger multicenter cohorts is warranted. “
“Molecular analysis of hepatic fibrogenesis

has progressed with respect to both fibrosis progression and regression by using cell biological, PD-1/PD-L1 phosphorylation molecular biological and (epi)genetic approaches. Recent researches have revealed sources of collagen-producing cells other than hepatic stellate cells in the liver, and the involvement of the innate immune system and oxidative stress in the fibrotic process has attracted new attention. Together with these advancements in basic knowledge on the cellular and molecular biology of hepatic fibrosis, clinical researches have linked the clarification of the relationship between progression of the fibrosis stage and therapeutic efficacy for chronic viral hepatitis and non-alcoholic steatohepatitis and validation of the regression of advanced fibrosis, even cirrhosis, of appropriate therapies using modern medicines. Furthermore, non-invasive assessment of liver fibrosis using an ultrasound-based modality has become

a focus in the clinical diagnosis of liver fibrosis instead of liver biopsy. Taken together, liver fibrosis research has been evolving both basically and clinically in the past three decades. “
“It is unclear whether practice-related 上海皓元 aspects of antimicrobial therapy contribute to the high mortality from septic shock among patients with cirrhosis. We examined the relationship between aspects of initial empiric antimicrobial therapy and mortality in patients with cirrhosis and septic shock. This was a nested cohort study within a large retrospective database of septic shock from 28 medical centers in Canada, the United States, and Saudi Arabia by the Cooperative Antimicrobial Therapy of Septic Shock Database Research Group between 1996 and 2008. We examined the impact of initial empiric antimicrobial therapeutic variables on the hospital mortality of patients with cirrhosis and septic shock. Among 635 patients with cirrhosis and septic shock, the hospital mortality was 75.6%.

These articles reflect on the rationale behind the original recom

These articles reflect on the rationale behind the original recommendations and reviews. In addition, they give us valuable personal insights and projections by authors, principally those of the original articles—by definition authorities in their fields, as to where the future lies. As far as the liver is concerned, excellent reviews encompassing aspects of etiology, diagnosis, prevention and clinical management have been written on hepatitis E (R Aggarwal), acute liver failure in Japan (M Oketani and colleagues), gastric

varices (M Hashizume and colleagues), hepatitis B in Asia (H Chan, JD Jia), treatment of chronic hepatitis B (MF Yuen, CL Lai), NAFLD and NASH in Japan (T Okanoue and colleagues) Ridaforolimus and more generally in Asia-Pacific (S Chitturi, V Wong), terlipressin for hepatorenal syndrome (H Rakeja and Y Chawla), and radiofrequency ablation

for HCC (N Izumi). Such important clinical advances come from the expansion of knowledge about disease causation and pathogenic mechanisms, and articles describing the relevant science figure prominently among JGH most-cited articles.1 In this JGH Silver Jubilee Supplement, disease mechanisms are again a major component of reviews, those on Barrett’s (J Dent), gastric emptying with diabetes (J Chang and colleagues), hepatitis C virus (HCV) genotypic variability ITF2357 purchase (K Chayama, CN Hayes) and effects on and of steatosis (SJ Hwang, SD Lee), HBV genotypes (CL Lin, JH Kao), HBV X protein (MC Kew) and cell death (JM Schattenberg and colleagues) in hepatocarcinogenesis, reactive oxygen and inflammatory recruitment (H. Jaeschke) hepatic ischemia-reperfusion injury (N Teoh), hepatocyte growth factor (K Matsumoto and colleagues), and new concepts in liver regeneration (K Riehle and colleagues).

I hope you will enjoy reading these articles as much as I have, and be informed, MCE instructed and inspired by them. On behalf of the Editors and all involved with JGH, we hope that this high standard at the time of celebrating 25 years of JGH is a taste of the major contributions to knowledge and practice of gastroenterology and hepatology that will be published in these pages during the next 25 years. I am grateful to all the original authors of key articles published in JGH for their gracious acceptance to write again for us, and for keeping to a punishing set of time lines. Julia Ballard (Wiley-Blackwell, Melbourne) assisted with valuable research into the citation status of JGH articles. My personal assistant, Betty Rooney, as well as my wife and colleague, Narci Teoh, went well beyond the call of duty to assist in completing this project in a timely and efficient manner. “
“We read with interest the article by Sonneveld et al.

31,63,64 Endoscopy is currently the only method available for ma

.31,63,64 Endoscopy is currently the only method available for management of the EA risk in BE. Screening and surveillance with such a costly and invasive technique is far from optimal, so it is important that efforts are made to find more simple options suited to use in screening and surveying the great majority of individuals U0126 clinical trial at low absolute risk for development of EA. This method is not yet fully validated nor generally available.

It appears to be the only relatively low-cost, non-endoscopic screening method for which there are clinical data. A cytology sponge is compressed and encased in a gelatin capsule attached to a string. The capsule, but not the end of the string is swallowed.102 After a few minutes in the stomach, the liberated sponge is dragged back up the esophagus. This procedure would seem to score high on any “yuck” scale, but it is reported to be well-tolerated and suitable for use in primary care.103 The problem of a “needle in a haystack” search of the recovered exfoliated mucosal cells for esophageal columnar metaplastic cells is solved not by cell morphological criteria, but by molecular biological identification of cells in which trefoil Torin 1 in vitro factor 3 is strongly expressed, a feature unique to esophageal columnar metaplasia. A pilot study in 96 controls and 36 BE patients found this test to have a sensitivity of 78% and a specificity

of 94% for presence of BE.101 It is even possible that this technique, coupled with a panel of molecular markers, might be capable of screening for dysplasia or even EA. Watch

this space! Many studies have found specific changes in the esophageal mucosa that are associated with subsequent development of EA. None of these has yet achieved the 上海皓元医药股份有限公司 status of a validated biomarker,31 but there is still a good chance that this will occur (Fig. 2). Study of esophageal mucosal factors imposes the practical and financial burden of getting “a bit” of the esophagus. The level of participation in screening programs for colon cancer is strongly influenced by the characteristics of the screening test. The ideal screening method for BE would be a blood test or buccal smear that might be applied to assess risk for BE in those with reflux-induced symptoms. There is hope that systemic104 or genetic markers27 of risk for BE could become well-enough characterized that a non-invasive BE screening method could be devised. The author is grateful to AstraZeneca for their very long-term and continual support of the International Working Group for the Classification of Oesophagitis, which has made possible the development of the Los Angeles Classification of reflux oesophagitis, the Prague C&M criteria and the Barrett’s Oesophagus Related Neoplasia (BORN) project. The BORN project which will provide training on the diagnosis of early esophageal adenocarcinoma, is also facilitated by support from Olympus.

In these cases, whole exome or whole genome sequencing may be ben

In these cases, whole exome or whole genome sequencing may be beneficial, although at present, the costs associated with performing this routinely in a diagnostic laboratory and the extensive downstream bioinformatic analysis required may be prohibitive. “
“Background and Aims:  Proton pump inhibitors (PPI) have been

rarely used for prevention of upper gastrointestinal bleeding (UGIB) induced by non-steroidal anti-inflammatory drugs (NSAIDs) and/or aspirin in Japan. The increased incidence of UGIB in the aged society is becoming a serious problem. The aim of this study was to retrospectively evaluate whether PPI can prevent UGIB. Methods:  We examined records of 2367 patients (aged 67.9 ± 15.1 years, male 1271) attending the only hospital serving the rural area, with little population movement. We investigated the correlation between the check details frequency of usage of medicine (PPI, Target Selective Inhibitor Library histamine 2 receptor antagonists [H2RA], NSAIDs, aspirin) and incidence of UGIB over 12 years. UGIB was defined as cases with hematemesis and/or melena and definite bleeding at upper gastrointestinal endoscopy. The annual incidence of UGIB of inhabitants (16 065 ± 375.3 persons/year) was evaluated. The frequency of usage of medicine

was compared with the total number of patients prescribed any medication (1080 ± 33.2 persons/year). Results:  The frequency of PPI usage has increased significantly 4.6%30.8% (P < 0.05). NSAIDs and aspirin usage increased significantly in the latter half of the survey period (P < 0.05). The annual incidence of UGIB significantly decreased 160.8 23.6/100 000 inhabitants

per annum (P ≤ 0.05) due to widespread use of PPI. No patients died due to UGIB after 2006. The incidence of UGIB and the prevalence of PPI usage were found to have a negative correlation (r = −0.804, P = 0.0016). Conclusions:  By widespread use of PPI, UGIB and related death has declined significantly. This survey showed that continuous PPI treatment decreases UGIB and related death in community medicine. “
“Viral infections are often linked to altered drug metabolism in patients; however, the underlying molecular mechanisms remain 上海皓元医药股份有限公司 unclear. Here we describe a mechanism by which activation of antiviral responses by the synthetic double-stranded RNA ligand, polyinosinic-polycytidylic acid (polyI:C), leads to decreased acetaminophen (APAP) metabolism and hepatotoxicity. PolyI:C administration down-regulates expression of retinoic X receptor-α (RXRα) as well as its heterodimeric partner pregnane X receptor (PXR) in mice. This down-regulation results in suppression of downstream cytochrome P450 enzymes involved in conversion of APAP to its toxic metabolite. Although the effects of polyI:C on drug metabolism are often attributed to interferon production, we report that polyI:C can decrease APAP metabolism in the absence of the type I interferon receptor.

32, 34, 35 We previously reported36

32, 34, 35 We previously reported36 Sorafenib cost that more than 15% of small HCC nodules (1-3 cm) lack the typical contrast HCC pattern at imaging (hyperenhancement in the arterial phase followed by washout),1, 2 and these theoretically correspond

to nodules in which vascular derangement has not yet fully taken place; thus, the potential of TACE is limited. In light of these considerations, our finding that the smaller nodules in the present series were less efficiently treated by arterial chemoembolization than the larger ones is not unexpected. Furthermore, Alba and coworkers12 reported that tumors that were preoperatively detected by CT because of hypervascularity had more necrosis (mean = 67.8%) and were larger (2.58 cm) than those not detected preoperatively (mean necrosis level = 1.57%, diameter = 1.68 cm). Riaz and coworkers28 found instead that the highest rate of complete necrosis after TACE could be achieved in nodules in the intermediate size range of 3 to 5 cm in comparison with smaller and larger nodules. Our population and consequent findings are different from those patients undergoing TACE as a unique modality (usually

with HCCs at an intermediate stage) and their findings. These patients often have nodules > 5 cm and rarely have tumors < 2 cm; in this case, an increase in the rate Venetoclax purchase of necrosis in the larger ones would be completely unexpected. Our multivariate logistic regression analysis showed that the independent predictors of complete tumor necrosis were the selective/superselective TACE procedure (P = 0.049) and a single nodule treatment (P = 0.008), whereas the nodule size played a minor role (P = 0.089). In the setting of a locoregional bridge treatment for LT, the rate of complete necrosis according to a pathological analysis after percutaneous radiofrequency ablation was reported to be approximately 50%, but it was 61% to 63% in nodules < 3 cm and 15% in HCCs > 3 cm (usually 3-5 cm).37 The rate of complete necrosis in the entire series was fully

comparable to that achieved after selective/superselective TACE in our present population of transplant patients (53.8%). These data, together with our finding MCE that HCCs 3 to 5 cm in size had a higher rate of necrosis than smaller tumors after TACE, support the strategy (commonly used in many centers) of using a bridge treatment involving percutaneous ablation for smaller nodules (<3 cm) and selective/superselective TACE for larger nodules (>3 cm). Combined treatment might also be an option. As for the post-TACE CT assessment, dense Lipidol uptake proved to be a poorly specific marker of a complete histological response. Dedicated trials are warranted to identify the best strategy for post-TACE evaluations.

An Asian-specific questionnaire to investigate the impact of envi

An Asian-specific questionnaire to investigate the impact of environmental factors, particularly in childhood, on disease development is lacking. We aimed to (i) translate the International Organisation for study of Inflammatory Bowel Disease (IOIBD) environmental questionnaire from English to Chinese, and (ii) develop a Chinese self-administered environmental questionnaire for IBD patients in Asia. Methods: (i) Forward translation was independently performed by two bilingual translators, and checked by a bilingual gastroenterologist. A reconciliated version was backward translated and verified. Forward-backward translation was repeated for any major revision. Pilot testing was conducted in

5 patients and test-retest reliability was assessed in 32 IBD HDAC inhibitor patients. (ii) A modified Chinese questionnaire was developed after literature review and the content was verified by 2 gastroenterologists. Results: In 32 IBD patients (median age 44, IQR 33-56), test-retest reliability of the translated questionnaire showed moderate to strong agreement in 85 of 87 questions (98%) (kappa or ICC, 0.5-1.0). Modifications were made to 2 questions with low kappa coefficient based on consensus. Subsequently, a Chinese version 39-item environmental questionnaire was developed. The items were grouped into 5 areas (childhood immunizations, hygiene conditions, dietary habits, smoking and lifestyle

factors). Test-retest reliability of this new questionnaire on 49 subjects showed moderate agreement in most questions. Conclusion: The INCB024360 purchase Chinese version of Environmental Factor questionnaire MCE公司 is valid and reliable. Further validation in other Asian populations may improve our understanding on environmental exposure in

IBD aetiology. Key Word(s): 1. inflammatory bowel disease; 2. questionnaire; 3. environmental factor Presenting Author: WHITNEY WING YAN TANG Additional Authors: SIEW CHIEN NG, MARTIN CHI SANG WONG Corresponding Author: WHITNEY WING YAN TANG Affiliations: The Chinese University of Hong Kong, The Chinese University of Hong Kong Objective: Patients with Inflammatory Bowel Disease (IBD) are primarily managed with medical treatment. However, for patients with severe disease, many required bowel resection eventually. This study aims to evaluate the risk factors associated with bowel resection among patients with IBD. Methods: This study was a retrospective cohort study. Prevalent cases were identified from hospital record in Prince of Wales Hospital. Data were collected by reviewing medical notes. Results: Four hundred ninety-nine IBD cases [234 Crohn's disease (CD), 259 ulcerative colits (UC), mean age 33, disease duration 8 years] were identified. Stricturing (Hazard ratio, 5.38; 95% CI, 2.76-10.48; P < 0.001) and penetrating disease behavior (HR, 13.151; 95% CI, 6.54-26.46; P < 0.

Helicobacter pylori may be considered as the most common infectio

Helicobacter pylori may be considered as the most common infectious pathogen of the gastroduodenal tract, but it is also one of the best models of infectious disease. This is mainly due to the fact that determinants of virulence and pathogenicity have been largely studied and this allowed researchers to correlate their expression not only with different diseases of the gastroduodenal tract but also with disorders outside of the stomach [1]. Indeed, this bacterium produces a low-grade inflammatory state, induces molecular mimicry mechanisms, and interferes with the absorbance of nutrients and drugs, possibly influencing the occurrence

and/or the evolution of many diseases [2]. In this article, the most recent findings on the role of H. pylori infection in different extragastric CB-839 diseases will be reviewed. Despite the great number of studies published so far in this field, the role of H. pylori infection and/or CagA-positive strains still remains controversial. In a recent study on 433 patients, Eskandarian et al. [3] showed that seropositivity

for H. pylori was significantly associated with a risk of short-term adverse outcome in patients with acute coronary syndromes. On the other hand, Schöttker et al. [4] found an inverse relationship of CagA-positive H. pylori strains with fatal cardiovascular events. Similarly, Grub et al. [5] did not find an association between selleck chemical chronic infections and coronary artery disease in patients with inflammatory rheumatic diseases. Based on these results, the association between H. pylori infection and ischemic heart disease remains uncertain, as some studies support the previously demonstrated hypothesis, while others show no relationship [6, 2]. Concerning ischemic stroke, Chen et al. [7] reported a positive association between H. pylori MCE公司 infection, interleukine (IL)-18, and carotid intima-media thickness, while Longo-Mbenza et al. [8] demonstrated an association between known cardiovascular risk factors, carotid plaque, stroke, and H. pylori infection. Finally, a study

by Izadi et al. [9] showed that Helicobacter species may replicate in the coronary arterial wall, and so, H. pylori may increase levels of total cholesterol and LDL. In a recent study, Zhou et al. [10] found a high prevalence of H. pylori infection in patients with diabetes mellitus (DM), especially Type 2. Similar results were reported by Jeon et al. [11] who analyzed sera from 782 individuals over age 60 years. Interestingly, some authors such as Shin et al. [12] also proposed a role of H. pylori in the occurrence of the metabolic syndrome. On this subject, a recent study by Chen et al. [13] reported the presence of a synergistic interaction between H. pylori and higher body mass index (BMI) in increasing the level of glycosylated hemoglobin, while Akanuma et al. [14] demonstrated that H. pylori eradication significantly increased BMI but not glycosylated hemoglobin. Moreover, H.

13 The effects of EFV observed in our experiments were reversible

13 The effects of EFV observed in our experiments were reversible, but bearing in mind the prolonged plasmatic half-life and long-term daily administration of this drug,19 our results draw attention to the fact that patients are potentially exposed to sustained mitochondrial EPZ-6438 dysfunction. NNRTIs induce more liver toxicity than other antiretrovirals, and up to 10% of HIV patients treated with EFV exhibit increases in liver enzymes that sometimes require discontinuation of therapy.9 Furthermore, the risk of hepatotoxicity is much greater when HIV coexists with the HBV or HCV infection,8 both of which are characterized by

increases in mediators known to undermine mitochondrial function.20 Therefore, we can speculate that low doses of EFV induce levels of dysfunction below those necessary to generate direct damage, whereas higher doses or the presence of stimuli that further compromise the mitochondria exacerbate these effects AZD2014 in vitro to a point that becomes clinically relevant. Of the concentrations studied, only that of 10 μM is within usual therapeutic plasma levels, but given the high rate of interindividual variability in the pharmacokinetics of EFV, we believe that the higher doses employed in our experiments are also relevant. In fact, clinical studies report supratherapeutic plasma concentrations of

EFV (up to 30-50 μM) in as many as 20% of HIV-1–infected patients,21, 22 and the relationship between plasma concentration and the adverse effects of EFV, in particular those related to the liver23 and central nervous system,7 is well established. Our results with isolated mitochondria from rat livers point to inhibition of complex I as the mechanism responsible for the effects of EFV on cell respiration. The rapidness of the actions described in our

experiments rules out any interference with mitochondrial DNA replication, which until now was considered to be the principal mechanism of the mitochondrial toxicity of antiretroviral drugs, because a much longer MCE公司 time frame is necessary for its effects to be manifested.24 If not too intense or prolonged, a reduced cell respiration is not in itself a sign of mitochondrial malfunction, and could be considered a form of cellular adaptation to changes in environmental factors or oxygen availability/redistribution.14, 25 However, in light of our previous observations of a decreased mitochondrial membrane potential with similar concentrations of EFV,26 the increased ROS production and the drop in ATP levels detected in the current study point to a certain level of dysfunction within the respiratory chain that compromises the functioning of the mitochondria. This is a novel area of research that has been the focus of little attention, but one recent study of HIV-1–infected patients undergoing EFV-based treatment has reported an increased lymphocyte mitochondrial depolarization and other signs of dysfunction unrelated to mitochondrial DNA replication.

High FDG uptake of extraabdominal L/N was found on 2 patients (in

High FDG uptake of extraabdominal L/N was found on 2 patients (inguinal and supraclavicular L/N). They were diagnosed as benign L/N enlargement. High FDG uptake on bone was found at 4 patients. 3 patients of them showed bone metastasis in liver CT and 1 patient who had metastasis to mandible diagnosed as both adrenal metastasis without

staging change. 1 patient showed high uptake on prostate and confirmed http://www.selleckchem.com/products/Roscovitine.html as benign nodule on biopsy. 1 patient with abdominal muscle metastasis was detected on both liver CT and 18F-FDG PET-CT. Skin metastasis was suspected on 1 patient and was confirmed as false positive high uptake of FDG. Conclusion: 27 patients of 160 patients were suspected as extrahepatic metastasis on 18F-FDG PET-CT. However there was no change on staging and treatment after 18F-FDG PET-CT because most of them were already suspected on liver CT or confirmed as false positive on biopsy and on other confirmative examinations. Key Word(s): 1. 18F-FDG PET-CT; 2. HCC; 3. metastasis; 4. stage; Presenting Author: CHEN WU Additional Authors: YUXIU YANG Corresponding Author: CHEN WU, YUXIU YANG Affiliations: Henan Provincial Hospital Objective: It has been found that cyclindepenr Kinase 5 (CDK5) has high correlation with kinds of nerve system diseases, lung cancer, prostatic carcinoma, and hepatic tumor. By analyzing the abnormal

expression of CDK5 in blood plasma of patients with hepatocellular carcinoma (HCC), we can make a study of the relativity between CDK5 and HCC, and then explore the clinical significance of this relativity in diagnosis of HCC. Methods: The selleck sample collected included the plasma of 60 patients with hepatocellular carcinoma, 40 patients with cirrhosis and 60 healthy controls. In the experiment, the enzyme linked immunosorbent assay (ELISA) and MCE PCR techniques with SYBR Green I fluorescent quantization can be used respectively

to measure the expression levels of CDK5 protein and mRNA of the sample. Then the sensitivity and specificity could be calculated, and the relationship between the expression of CDK5 and clinical pathological parameters was analyzed. In addition, data were analyzed by SPSS 17.0 software. Results: The expression level of CDK5 protein in plasma of patients with HCC was higher than those in patients with cirrhosis and healthy controls (p < 0.05), and it had no-relationship with sex, age, size, the value of AFP, the size of the tumor and the TMN stages (p > 0.05). At the same time, compared with hepatocirrhosis patients and healthy controls, the expression level of mRNA of CDK5 in plasma of HCC patients was found higher (p < 0.05), and it had no-relationship with sex, age, the value of AFP, the size of the tumor and the TNM stage (p > 0.05). Conclusion: CDK5 showed high relative with hepatocellular carcinoma, and CDK5 in plasma can be considered as an assistant sign of tumor to diagnose hepacellular carcinoma. Key Word(s): 1. HCC; 2. CDK5; 3. ELISA; 4.