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1.
Pan Afr Med J ; 38: 279, 2021.
Article in English | MEDLINE | ID: mdl-34122706

ABSTRACT

INTRODUCTION: drug-resistant tuberculosis is a major global health problem and a threat to health security given the increase in the number of cases and the challenges associated with care. Besides, the relationship between poor nutritional status and tuberculosis is clearly established. For relevant and evidence-based public health decision-making regarding the management of malnutrition in patients with drug-resistant tuberculosis in the initial phase, it is essential to estimate the prevalence of malnutrition and understand the risk factors associated with it. METHODS: we performed a retrospective cohort study in drug-resistant tuberculosis patients aged 18 years and older, among which the nutritional status was assessed through BMI. All predictors were included in a prediction model using the multivariate logistic model according to the lowest Akaike criterion. Discrimination and model calibration was evaluated using receiver performance analysis, and the Hosmer and Lemeshow test. RESULTS: this study revealed a prevalence of malnutrition of 64.7% in drug-resistant tuberculosis patients in our 218-patient series. The factors associated with malnutrition were: unsuccessful treatment, the active presence of mycobacterium tuberculosis, increased bacteriological conversion time, increased serum creatinine, increased transaminase SGPT of the liver, and anaemia. Some of the factors not associated with malnutrition included the history of anti-tuberculosis treatment, vomiting, hepatic SGPT, initial AFB count, smear and culture conversion time, depression, and chest X-ray. CONCLUSION: malnutrition remains a concern among drug-resistant tuberculosis patients in Guinea as it affects more than half of them with a negative impact on the outcome of treatment. Implementing specific interventions for these high-risk patients, including nutritional supplementation, psychosocial support, and treatment for tuberculosis, can improve management for better treatment outcomes.


Subject(s)
Antitubercular Agents/administration & dosage , Malnutrition/epidemiology , Tuberculosis, Multidrug-Resistant/epidemiology , Adult , Cohort Studies , Female , Guinea/epidemiology , Humans , Male , Malnutrition/etiology , Middle Aged , Mycobacterium tuberculosis/isolation & purification , Prevalence , Retrospective Studies , Risk Factors , Tuberculosis, Multidrug-Resistant/complications , Tuberculosis, Multidrug-Resistant/drug therapy , Young Adult
2.
J Huazhong Univ Sci Technolog Med Sci ; 36(3): 295-304, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27376795

ABSTRACT

Over the past decades, cancer has become one of the toughest challenges for health professionals. The epidemiologists are increasingly directing their research efforts on various malignant tumor worldwide. Of note, incidence of cancers is on the rise more quickly in developed countries. Indeed, great endeavors have to be made in the control of the life-threatening disease. As we know it, pancreatic cancer (PC) is a malignant disease with the worst prognosis. While little is known about the etiology of the PC and measures to prevent the condition, so far, a number of risk factors have been identified. Genetic factors, pre-malignant lesions, predisposing diseases and exogenous factors have been found to be linked to PC. Genetic susceptibility was observed in 10% of PC cases, including inherited PC syndromes and familial PC. However, in the remaining 90%, their PC might be caused by genetic factors in combination with environmental factors. Nonetheless, the exact mechanism of the two kinds of factors, endogenous and exogenous, working together to cause PC remains poorly understood. The fact that most pancreatic neoplasms are diagnosed at an incurable stage of the disease highlights the need to identify risk factors and to understand their contribution to carcinogenesis. This article reviews the high risk factors contributing to the development of PC, to provide information for clinicians and epidemiologists.


Subject(s)
Gene-Environment Interaction , Genetic Predisposition to Disease , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/genetics , ABO Blood-Group System/genetics , Alcohol Drinking/physiopathology , Diabetes Mellitus/genetics , Diabetes Mellitus/pathology , Humans , Incidence , Obesity/genetics , Obesity/pathology , Pancreas/metabolism , Pancreas/pathology , Pancreatic Neoplasms/mortality , Pancreatic Neoplasms/pathology , Pancreatitis, Chronic/genetics , Pancreatitis, Chronic/pathology , Precancerous Conditions/genetics , Precancerous Conditions/pathology , Prognosis , Risk Factors , Smoking/physiopathology , Survival Analysis , Pancreatic Neoplasms
3.
Oncotarget ; 7(24): 37192-37204, 2016 Jun 14.
Article in English | MEDLINE | ID: mdl-27177084

ABSTRACT

As the standard therapy for pancreatic cancer, gemcitabine shows limited efficacy in pancreatic cancer patients because of chemoresistance. Aberrant expression of Bmi1 has been reported to activate multiple growth-regulatory pathways and confer anti-apoptotic abilities to many cancer cells. However, the role of Bmi1 in response of pancreatic cancer cells towards gemcitabine resistance remains elusive. In this study, we found that certain dose of gemcitabine treatment induced Bmi1 expression in pancreatic cancer cells. Knockdown of Bmi1 enhanced ROS production and promoted the cytotoxic effect of gemcitabine. The increased oxidative stress upon gemcitabine treatment could disrupt mitochondrial membrane and decrease mitochondrial membrane potential, eventually leading to apoptosis. Bmi1 inhibition also suppressed the activation of NF-κB signaling and the expressions of downstream molecules in pancreatic cancer cells treated with gemcitabine. Moreover, we observed Bmi1 inhibition sensitized the pancreatic xenograft tumors to gemcitabine in vivo. Taken together, our study demonstrated that Bmi1 could decrease the sensitivity of pancreatic cancer cells to gemcitabine through increasing oxidative stress and inhibiting NF-κB signaling, thus Bmi1 may serve as a promising target for sensitizing pancreatic cancer cells to chemotherapy.


Subject(s)
Antimetabolites, Antineoplastic/pharmacology , Deoxycytidine/analogs & derivatives , Drug Resistance, Neoplasm , NF-kappa B/metabolism , Pancreatic Neoplasms/drug therapy , Polycomb Repressive Complex 1/metabolism , Animals , Antimetabolites, Antineoplastic/therapeutic use , Apoptosis , Cell Line, Tumor , Deoxycytidine/pharmacology , Deoxycytidine/therapeutic use , Down-Regulation , Enzyme-Linked Immunosorbent Assay , Fluorescent Antibody Technique , Gene Knockdown Techniques , Humans , Intracellular Membranes/drug effects , Membrane Potential, Mitochondrial/drug effects , Mice, Nude , Mitochondria/drug effects , Oxidative Stress , Pancreas/pathology , Pancreatic Neoplasms/pathology , Polycomb Repressive Complex 1/genetics , RNA, Small Interfering/genetics , Reactive Oxygen Species/metabolism , Signal Transduction , Treatment Outcome , Xenograft Model Antitumor Assays , Gemcitabine
4.
J Huazhong Univ Sci Technolog Med Sci ; 35(3): 384-389, 2015 Jun.
Article in English | MEDLINE | ID: mdl-26072078

ABSTRACT

The purpose of this study was to investigate the etiology, pathological characteristics, management and prognosis of chronic pancreatitis in the Chinese population. The clinical data of 142 patients with chronic pancreatitis were retrospectively studied. All patients were of Chinese nationality and hospitalized from January 2008 to December 2011. Their ages ranged from 14 to 76 years, with a mean of 43 years. Of 142 patients, there were 72 cases of obstructive chronic pancreatitis (50.70%), 19 cases of alcoholic chronic pancreatitis (13.38%), 14 cases of autoimmune pancreatitis (9.86%) and 37 cases of undetermined etiology (26.06%). Pathologically, the average inflammatory mass diameter was 3.8 ± 3.3 cm, biliary obstruction occurred in 36 cases, gall stones in 70 cases, calcification in 88 cases, ductal dilatation in 61 cases, side branch dilatation in 32 cases, ductal irregularity in 10 cases, lymphocytic inflammation in 23 cases, obliterative phlebitis in 14 cases, extra pancreatic lesion in 19 cases and fibrosis in 142 cases. Location of pancreatic lesion in the region of head (n=97), neck (n=16), body (n=12), tail (n=15) and whole pancreas (n=2) influenced the choice of surgical procedures. Ninety-four patients (66.20%) received surgical treatment and 33.80% received other treatments. After operation, 80.85% of 94 patients experienced decreased pain, and 8.51% of 94 showed recovery of endocrine function but with a complication rate of 12.77%. All the operations were performed successfully. According to the pain scale of European Organization for Research and Treatment of Cancer (QLQ-C30) a decrease from 76 ± 22 to 14 ± 18 was observed. Etiology, pathological characteristics, management and prognosis of chronic pancreatitis in the Chinese population vary from others.


Subject(s)
Autoimmune Diseases/epidemiology , Cholestasis/epidemiology , Pancreatitis, Alcoholic/epidemiology , Pancreatitis, Chronic/pathology , Pancreatitis, Chronic/therapy , Adolescent , Adult , Aged , Autoimmune Diseases/therapy , China/epidemiology , Cholestasis/therapy , Female , Humans , Male , Middle Aged , Pancreatitis, Alcoholic/therapy , Pancreatitis, Chronic/etiology , Prognosis , Retrospective Studies , Treatment Outcome , Young Adult
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