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1.
Clin J Sport Med ; 31(1): 86-90, 2021 Jan.
Article in English | MEDLINE | ID: mdl-30371534

ABSTRACT

OBJECTIVE: Liver cancer is the second most common cause of death from cancer. Physical activity (PA) was found to be associated with lower risks of several types of cancer. However, the association between PA and the risk of liver cancer is still inconclusive. This systematic review and meta-analysis was aiming to summarize the association between PA and liver cancer risk. METHODS: Literatures related were identified by searching PubMed, EMBASE, and Chinese Biomedical literature database from 1965 to 2017 without language limitation. Meta-analyses were performed using random effect model. RESULTS: A total of 5 cohort studies involving 2 513 975 subjects were identified. The pooled relative risk of leisure-time PA with liver cancer risk was 0.92 [95% confidence interval (CI), 0.84-1.01]. There is no significant association between leisure-time PA and liver cancer risk. However, leisure-time PA significantly reduced liver cancer risk in never smokers. The pooled hazard ratio of daily total PA with liver cancer risk was 0.75 (95% CI, 0.66-0.86). CONCLUSIONS: Daily total PA significantly reduces liver cancer risk, whereas leisure-time PA significantly reduces liver cancer risk only in never smokers.


Subject(s)
Exercise , Liver Neoplasms/epidemiology , Liver Neoplasms/prevention & control , Humans , Non-Smokers , Risk Factors
2.
Clin Exp Med ; 20(2): 241-248, 2020 May.
Article in English | MEDLINE | ID: mdl-32052245

ABSTRACT

Alanine aminotransferase (ALT) levels between 1 and 2 times the upper limit of normal (ULN) are common in patients with chronic hepatitis B (CHB) infection. There are few clinical studies focused on this group of patients because of the poorer treatment outcomes compared to those with more than 2 × ULN ALT level. However, treatments are necessary to reduce liver damage for patients with minimally elevated ALT levels. And biomarkers are needed in predicting the treatment response. In this study, a total of 106 patients with CHB were enrolled and treated with entecavir, telbivudine or tenofovir disoproxil fumarate. Liver stiffness was measured by transient elastography, and quantitative levels of hepatitis B core antibody (HBcAb) were detected by ELISA. At week 96, 31 (29.25%) patients achieved hepatitis B e antigen (HBeAg) seroconversion. Notably, baseline HBcAb levels and liver stiffness measurements (LSM) were higher in patients who achieved HBeAg seroconversion. The multivariate analysis showed that the baseline HBcAb levels and LSM were independent predictors for HBeAg seroconversion. The area under receiver operating characteristic curve of baseline HBcAb, LSM and the combination of them for HBeAg seroconversion was 0.714, 0.720 and 0.717, respectively. In addition, we discovered that the patients with baseline HBcAb levels ≥ 4.15 log10 IU/mL and LSM ≥ 9.85 kPa had higher rates of HBeAg seroconversion. Therefore, the measurement of HBcAb and liver stiffness might be good approaches for the optimization of antiviral therapy for HBeAg-positive CHB patients with minimally elevated ALT levels.


Subject(s)
Alanine Transaminase/blood , Hepatitis B Antibodies/blood , Hepatitis B, Chronic/drug therapy , Seroconversion/drug effects , Adult , Antiviral Agents/therapeutic use , Biomarkers/blood , Elasticity Imaging Techniques , Female , Guanine/analogs & derivatives , Guanine/therapeutic use , Hepatitis B, Chronic/immunology , Hepatitis B, Chronic/virology , Humans , Liver/drug effects , Liver/pathology , Male , Prospective Studies , Telbivudine/therapeutic use , Tenofovir/therapeutic use
3.
Clin Res Hepatol Gastroenterol ; 42(6): 553-563, 2018 12.
Article in English | MEDLINE | ID: mdl-30104170

ABSTRACT

BACKGROUND: Laparoscopic surgery in patients with liver cirrhosis (CL) is considered to be challenging. Recent studies have shown that laparoscopic liver resection (LLR) is more beneficial of reduced operative stress and postoperative complications in patients with CL. AIM: A meta-analysis was done to review the currently available published data comparing LLR for patients with CL versus those non-cirrhosis of the liver (NCL). METHODS: The electronic databases of PubMed, Wiley, Web of Science, Embase, and the Cochrane Library were searched from date of inception to January 29, 2018. Studies reporting a comparison of outcomes and methods of LLR in CL and NCL groups were included. The studies were evaluated using the modified Newcastle-Ottawa Scale. RESULTS: A total of 1573 patients from six cohort studies were included in final analysis. The CL group had a slightly shorter operative time compared with the NCL group (weighted mean difference [WMD], 18.78min shorter; 95% confidence interval [CI], -43.54-5.98; P=0.14) and delayed hospital stay (WMD, 1.26 days longer; 95% CI, -0.05-2.56; P=0.06). Blood loss, blood transfusion rate, mortality, and conversion rate did not differ significantly between the groups. CONCLUSIONS: LLR is safe and feasible in the CL compared with the NCL groups. Our present review indicates that LLR should be considered when selecting surgery for patients with CL.


Subject(s)
Hepatectomy , Laparoscopy , Liver Cirrhosis/complications , Blood Loss, Surgical/statistics & numerical data , Blood Transfusion/statistics & numerical data , Conversion to Open Surgery/statistics & numerical data , Humans , Length of Stay/statistics & numerical data , Operative Time , Postoperative Complications
4.
Accid Anal Prev ; 115: 41-52, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29544136

ABSTRACT

Longitudinal speed reduction markings (LSRMs) are designed to alert drivers to an upcoming change in roadway geometry (e.g. direct connectors with smaller radii). In Beijing, LSRMs are usually installed on direct connectors of urban expressways. The objective of this paper is to examine the influence of LSRMs on vehicle operation and driver behavior, and evaluate the decelerating effectiveness of LSRMs on direct connectors with different radii. Empirical data were collected in a driving simulator, and indicators representing vehicle operation status and driving behavior were proposed. To examine the influence of LSRMs, an analysis segment was defined, which begins 500 m prior to the entering point of the connector and ends at the exiting point of the connector. Furthermore, the analysis segment was evenly divided into a series of subsections; the length of each subsection is 50 m. This definition is introduced based on the assumption that drivers would decelerate smoothly in advance of the connector. The analysis results show that drivers tend to decelerate earlier when the radii were 200 m or 300 m. When approaching the connector, drivers tend to decelerate at 500 m thru 250 m in advance of the connector with a 200 m radius; deceleration happens at 300 m-0 m in advance of the connector with a 300 m radius. On the connector, drivers controlled the throttle pedal use at 100 thru 300 m after the entering point when the radius was 200 m; deceleration occurred in two regions when the radius was 300 m: 0 m-900 m from the entering point, and the last 1,000 m of the connector. The analytical results further revealed that LSRMs would be effective at reducing speeds when the radius of the direct connector was 300 m.


Subject(s)
Accidents, Traffic/prevention & control , Automobile Driving , Deceleration , Environment Design , Adolescent , Adult , Beijing , Computer Simulation , Female , Foot , Humans , Male , Young Adult
5.
Arch Virol ; 153(9): 1677-84, 2008.
Article in English | MEDLINE | ID: mdl-18668195

ABSTRACT

Multiple studies have established that GTPase activity is critical for MxA to act against RNA viruses. Recently, it was shown that MxA can also restrict the replication of hepatitis B virus (HBV), a DNA virus, but the requirements for GTPase activity in inhibition of HBV by MxA remain unknown. Here, we report that GTPase-defective mutants (K83A, T103A, and L612K) can downregulate extracellular HBsAg and HBeAg and reduce the expression of extra- and intracellular HBV DNA in HepG2 cells to levels similar to that achieved by wild-type MxA. Furthermore, TMxA and T103, two nuclear forms of wild-type MxA and a GTPase-defective mutant (T103A) could only slightly decrease the expression of extra- and intracellular HBV DNA in HepG2 cells. In conclusion, GTPase activity is not essential for MxA protein to inhibit HBV replication, and MxA may have only a minimal effect on the replicative cycle of HBV in the nucleus.


Subject(s)
GTP Phosphohydrolases/metabolism , GTP-Binding Proteins/metabolism , Hepatitis B virus/physiology , Hepatitis B/enzymology , Virus Replication , Cell Line , Cell Nucleus/enzymology , Cell Nucleus/virology , GTP Phosphohydrolases/genetics , GTP-Binding Proteins/genetics , Gene Expression Regulation, Viral , Hepatitis B/virology , Hepatitis B virus/genetics , Humans , Mutation , Myxovirus Resistance Proteins , Protein Transport
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