Background: CARD4/NOD1 is a member of the Caterpiller (CLR) gene family and is involved in the recognition of entero-invasive bacteria, such as Helicobacter pylori and ensures immunity responses. As a consequence, gene variability can influence the gastric inflammatory response to Helicobacter pylori. Objectives: The study was conducted to investigate the frequency of the E266K CARD4/NOD1 gene polymorphism and its relationship with Helicobacter pylori infection as well as the outcome on upper gastrointestinal endoscopy. Methods: Consecutive patients who underwent gastrointestinal endoscopy were eligible for the study. DNA was isolated from whole blood and polymerase chain reaction followed by restriction fragment length polymorphism procedure was used for genotyping. The link between endoscopic diagnosis, Helicobacter pylori infection status and genotype data was analyzed using Pearson\u2019s chi-square test and regression analysis. Results: A total of 186 patients were studied (mean age of 43 years with SD = 12.6, male was 37%). Helicobacter pylori infection rate is indifferent between patients with different variants of E266K (wildtype (n=80) 54%, heterozygotes (n=71) 65% and homozygotes (n=35) 43%; p=0.09). In patients infected with Helicobacter pylori, the prevalence of peptic ulcer identified by endoscopy was 19%, 17% and 47% for the E266K wildtype, heterozygote and homozygote variants, respectively (p=0.049). Conclusion: The E266K CARD4/NOD1 gene polymorphism carriers are at increased risk of peptic ulcer in the presence of Helicobacter pylori.
Peptic ulcer ; gene ; Helicobacter pylori

Background: Some researchers indicated that investigating MUC5AC is necessary for H.pylori infection because H.pylori is easy to locate in MUC5AC. However, there is no publication about the effect of variable number tandem repeat polymorphism of MUC5AC on H.pylori infection. Objective: To investigate the relationship between mucin 5AC variable number tandem repeated polymorphism and H.pylori infection. Subject and Method: 170 patients were studied, mean age: 43, male: 35%. Blood samples were collected from patients, who visited Can Tho General Hospital for upper gastrointestinal endoscopy. DNA was isolated from whole blood; the repeated section of the MUC5AC alleles was not cut out with a restriction enzyme (SacI). H.pylori infection was diagnosed with 14 C urea breath test. Distributions of allele fragment length were compared to H.pylori positive and negative patients. Results: 52% of patients were H.pylori infected. MUC5AC SacI-restricted allele fragment lengths ranged from 6.2 to 11.2 kbp (mean 7.9), the calculated number of repeated ranged from 170 to 380 (mean 243). Mean allele length was identical for H.pylori positive and negative patients were 7.9 kbp, and the distribution of allele fragment lengths was also similar for both groups (p=0.7). Conclusion: The number of repeats in the MUC5AC gen was highly polymorphic, but the variation in allele length was limited. The variable number tandem repeat polymorphism of MUC5AC was not associated with H.pylori infection.
H.pylori infection ; MUCSAC

Background: Several studies reported a high prevalence of vitamin B12 deficiency in some Asian countries and in Asian immigrants living in Western countries. However, there is no data regarding the prevalence of vitamin B12 deficiency in Viet Nam.\r\n', u'Objectives: The aim of this study was to determine the prevalence of vitamin B12 deficiency in patients with upper gastrointestinal symptoms in the Mekong Delta and to investigate the risk factors for vitamin B12 deficiency. \r\n', u'Methods: Blood samples were collected from patients visiting Can Tho General Hospital for upper gastrointestinal endoscopy. Serum vitamin B12 concentration was measured at the University Medical center St Radboud Nijmegen, Netherlands. \r\n', u'Results: Between September and December 2003, 216 patients (80 male, 136 female, mean age 43.2 years) were studied. Ten patients had gastric cancer, 28 peptic ulcer disease/ and 178 gastritis only or no visible pathology. Only 2 patients (0.9%) had clinical vitamin B12 deficiency (<160 pmol/l, whereas 15 patients (7.0%) had sub-clinical vitamin 812 deficiency (160-250 pmol/l). H. pylori positive patients (n=111) were more likely to have para-clinical vitamin B12 deficiency than H. pylori negative patients (odds ratio 3.7~ 95%CI 1.10-12.76). \r\n', u'Conclusions: Vitamin B12 deficiency is uncommon in the Mekong Delta. Helicobacter pylori infection is a risk factor for vitamin B12 deficiency. \r\n', u'
Vitamin B12 deficiency ; gastroenterologic symptoms

Background: Dementia is a common pathological condition that affects older people. Most causes of dementia are Alzheimer\u2019s disease and vascular dementia. Diagnosing these conditions mostly relied on clinical patterns, but some biomarkers have been mentioned as the indicators of this condition. Objectives: 1) To evaluate the alteration of some biomarkers in cerebrospinal fluid (CSF) samples from Alzheimer\u2019s patients. 2) To compare the concentration of biomarkers in CSF samples from patients with vascular dementia and Alzheimer\u2019s disease. Subjects and method: Case group involved 41 patients who were diagnosed as AD and vascular dementia based on DSM-IV criteria. 31 matched healthy people were included in control group. All subjects were given neuro-psychological tests and thorough clinical examination. Brain CT scan and MRI were done for both groups. CSF samples were taken from patients in the study group to measure levels of some biomarkers. Results. The levels of total taurine (T-tau) and phosphorylated taurine (P-tau) 181 proteins are higher in the dementia group. The concentration of Abeta-42 is significantly different between case and control groups, but similar between vascular dementia and Alzheimer\u2019s disease patients. Conclusion: Changes in biomarkers are valuable in different diagnosis of Alzheimer\u2019s disease and other types of dementia. However, findings of CSF studies have to be considered with findings from imaging studies and clinical examination.
Biomarker ; Dementia ; Alzheimer\u2019s disease

Background: Recently, microplate almar blue assay has been used commonly in detecting gen related to tuberculosis drug resistance, which provides results after 5-7 days with lower cost compared to traditional methods. Objective: To evaluate the application of microplate almar blue assay for rapid detection of drug resistance of M. tuberculosis strains. Subject and Method: A microplate-based assay which uses Alamar blue reagent - an oxidation reduction dye (MABA), was used for the determination of the anti-tuberculosis drug (isoniazid-INH, rifampicine-RIF, streptomycine-STR and ethabuton=EMB) resistance of 96 M. tuberculosis strains isolated from Vietnamese patients in comparison to those obtained by conversional method. Result: MABA showed to have high sensitivity and specificity in testing the sensitivity to individual anti-tuberculosis drugs (from 82.4% for STR to 93.3% for - INH and from 82.5% for EMB to 98.4% for STR; respectively), as well as for the multi-drug resistant M.tuberculosis (86.4% of sensitivity), highly correlated with the result determined by proportion method. Conclusion: MABA reveals the advantage in shortening test time, in simple performance and lower cost compared with the conversional culture based methods.
Microplate almar blue assay ; M. tuberculosis ; drug resistance

Background: Hepatocellular carcinoma (HCC) is the most common primary hepatic tumor and one of the most common cancers worldwide. HCC is a primary malignancy of hepatocellular origin. Objectives:The aim of study is to combinate therapy of transarterial chemoembolization and percutaneousethanol injection afterward emerging metatasis caused by fine needle aspiration cytology. Subjects and method: A 50 years old male patient with hepatocellular carcinoma having a diameter of tumor more than 5 cm was treated by combination of transarterial chemoembolization and percutaneous ethanol injection from December 2000. Results & Conclusion: Results of study showed that: Transarterial chemoembolization and percutaneous ethanol injection are the two of non-surgical methods for treatment of hepatocellular carcinoma which are most commonly available in applied clinical activities at present. Up to now, the patient's life expectancy after therapy is more than 6 years that means the result of treatment is very good. However, the emerging metatasis into the anterior-right-Iower chest wall that was caused by fine needle aspiration cytology should be reviewed for further evaluating clinical experience, especially in cases with quite clear imaging features of untrasonography and significantly elevated AFP level higher than 200 ng/rnl.
Carcinoma ; Hepatocellular/ pathology ; therapy

The liver is commonly injured after blunt abdominal trauma. The choice of treatment for liver trauma depends not only on injury severity but also on the patient’s hemodynamic status. Most minor- and moderate-grade liver injuries in hemodynamically stable patients allow for conservative treatment or minimal intervention, while emergency laparotomy is indicated for patients with severe-grade liver trauma and hypotensive shock.We describe a 19-year-old male patient with traumatic shock due to grade IV liver injury and multiple fractures. An emergency laparotomy was performed, but the bleeding could not be controlled, and the patient remained hemodynamically unstable. Hyperacute transarterial embolization was successfully performed. In this case report, we emphasize the importance of transarterial embolization in cases of residual bleeding after initial damage-control surgery, even in hemodynamically unstable patients.

The liver is commonly injured after blunt abdominal trauma. The choice of treatment for liver trauma depends not only on injury severity but also on the patient’s hemodynamic status. Most minor- and moderate-grade liver injuries in hemodynamically stable patients allow for conservative treatment or minimal intervention, while emergency laparotomy is indicated for patients with severe-grade liver trauma and hypotensive shock.We describe a 19-year-old male patient with traumatic shock due to grade IV liver injury and multiple fractures. An emergency laparotomy was performed, but the bleeding could not be controlled, and the patient remained hemodynamically unstable. Hyperacute transarterial embolization was successfully performed. In this case report, we emphasize the importance of transarterial embolization in cases of residual bleeding after initial damage-control surgery, even in hemodynamically unstable patients.

The liver is commonly injured after blunt abdominal trauma. The choice of treatment for liver trauma depends not only on injury severity but also on the patient’s hemodynamic status. Most minor- and moderate-grade liver injuries in hemodynamically stable patients allow for conservative treatment or minimal intervention, while emergency laparotomy is indicated for patients with severe-grade liver trauma and hypotensive shock.We describe a 19-year-old male patient with traumatic shock due to grade IV liver injury and multiple fractures. An emergency laparotomy was performed, but the bleeding could not be controlled, and the patient remained hemodynamically unstable. Hyperacute transarterial embolization was successfully performed. In this case report, we emphasize the importance of transarterial embolization in cases of residual bleeding after initial damage-control surgery, even in hemodynamically unstable patients.

The RET gene point mutation is the main molecular alteration involved in medullary thyroid carcinoma (MTC) tumorigenesis. Previous studies in Vietnam mainly consisted of case reports, with limited data on larger sample sizes. In this study, we investigated RET gene mutations in exons 10, 11, and 16 and analyzed clinicopathological features of a series of Vietnamese MTC patients. Methods: We collected 33 tissue samples from patients with MTC and analyzed RET mutations using the Sanger sequencing method. The relationship between hotspot RET mutations (exons 10, 11, 16) and clinicopathological features were investigated. Results: Among the 33 analyzed cases, 17 tumors (52%) harbored RET mutations in exon 10, 11, or 16. A total of 10 distinct genetic alterations were identified, including eight missense mutations and two short indels. Of these, seven were classified as pathogenic mutations based on previous publications, with p.M918T being the most frequent (4 cases), followed by p.C634R (3 cases) and p.C618R (3 cases). Mutations were significantly associated with specific histological patterns, such as the nested/insular pattern (p=.026), giant cells (p=.007), nuclear pleomorphism (p=.018), stippled chromatin (p=.044), and amyloid deposits (p=.024). No mutations were found in germline analyses, suggesting these were somatic alterations. Conclusions: Our results provided the first comprehensive analysis of RET mutations in Vietnamese MTC patients. The most frequent mutation was p.M918T, followed by p.C634R and p.C618R. Mutations in these three exons were linked to specific histopathological features. Information on mutational profiles of patients with MTC will further aid in the development of targeted therapeutics to ensure effective disease management.