Background and Objective: Osteoarthritis is the most common form of arthritis and joint disease and a major cause of disability among middle-aged and elderly people. The process of the progressive destruction of articular cartilage, causes pain and dysfunction of the joints involved. However, the main cause of this disease is not known. In several epidemiological studies from other countries, the problem was reported to be associated with cardiovascular disease. The aim of this study was to find the relationship between carotid artery atherosclerosis in elderly women and osteoarthritis of the joints. Materials and Methods: This cross-sectional study was done on 256 middle-aged and elderly women referred to the Vali-e-Asr Hospital in Zanjan. The patients were divided randomly into two groups of test and control following medical examination. The rate and severity of atherosclerosis and the presence or absence of atherosclerotic plaques were evaluated using Doppler Sono. The data were analyzed using the SPSS software. The mean values were subjected to student t-test and chi-square methods. Results: Of the total of 256 women who participated (mean age 56.79 years) in the study, 30.8% of women with osteoarthritis and 17.5% of the normal groups had carotid artery atherosclerotic plaque (P=0.009 OR=2.1). Even after normalization for age, osteoarthritis was still considered a risk factor for the carotid plaque. The mean carotid artery intima-media thickness was 0.975 mm in the test group compared with 0.910 mm in the control group (P<0.0001). Conclusion: Our findings are consistent with the outcome of some previous studies reporting a significant relationship between osteoarthritis and atherosclerotic disease. A proper drug treatment to reduce the severity of atherosclerosis in order to prevent the progress of osteoarthritis is recommended.
Background and Objective: As the main virulence factor of Helicobacter pylori, HP-NAP has an important role in immunoprotection against this pathogen. This antigen is a strong candidate as a part of multi-component vaccine in the clinical trial against this bacterium. Due to NAP importance, it was used in this study as a template for optimization of heterologous genes with a low A-T content and low expression in E. coli. Materials and Methods: A synthetic single gene that could reach the highest level of expression in the host was designed by using bioinformatics tools. Results: A number of factors that influence gene expression level were changed for HP-NAP gene optimizing: the codon usage bias in E. coli was changed the G+C content was upgraded from 38% to 45% and the stem-loop structure was broken. These could result to prolong of the half-life of the mRNA and overexpression of recombinant of HP-NAP protein up to 800 mg per liter. Conclusion: Applying of bioinformatics tools was appropriated to optimize of HP-NAP overexpression in E. coli. From our results, it appears that combination of In Silico and experimental approach is a logical approach for expression of heterologous genes in another host.
Background and objective: Association of 6q loci, where IGF2R gene is located, with insulin resistance has been well established. In this study, relationship between 3'UTR and type 2 diabetes and insulin resistance indices in non diabetic subjects was investigated. Materials and Methods: 350 participants (175 diabetic type 2 patient and 175 non-diabetic individuals) were entered in this study. Demographic data were collected. BMI and serum levels of glucose, lipid profiles and IGF2 of all participants were measured. Genotype polymorphism of studied participants was determined by PCR-RFLP method. Then, the relationship between genotypes and insulin resistance indices was measured and analyzed using statistical procedures of ANOVA and post hoc analysis. Results: The genotypes frequency comprised CC (6.85%), AA (33.45%), and CA (59.55%), indicating that the frequency of carrier with CA genotype polymorphism was significantly (P<0.05) higher in type 2 diabetic patients (80.6%) than in non-diabetic participants. Serum FBS levels of CA carriers were significantly (P=0.001) higher than carriers of other two genotypes (CC and AA). The mean levels of serum IGF2 in participants carrying CC and CA genotypes were significantly (P= 0.001) more than other participants carrying genotype AA. Conclusion: (C>A) IGF2R3′UTR polymorphism was associated with type 2 diabetes and some insulin resistance indices especially FBS. However, the A allele may have a protective effect on developing type 2 diabetes. References 1- Shaw JE, Sicree RA, Zimmet PZ. Global estimates of the prevalence of diabetes for 2010 and 2030. Diabetes Res Clin Pract. 2010 87: 4-14. 2- Pettitt DJ, Talton J, Dabelea D, et al. Prevalence of diabetes mellitus in U.S. youth in 2009: The search for diabetes in youth study. Diabetes Care. 2014 37: 402-8. 3- Hossain P, Kawar B, El Nahas M. Obesity and diabetes in the developing world — a growing challenge. N Engl J Med. 2007 18: 213-5. 4- Hegele RA, Pollex RL. Gentic and physiological insights into metabolic syndrome. Am J Physiol Regul Integr Comp Physiol. 2005 289: 663-9. 5- Tritos NA, Mantzoros CS. Clinical review 97: syndromes of severe insulin resistance. J Clin Endocrinol Metab. 1998 83: 3025-30. 6- Laureys G, Barton DE, Ullrich A, Francke U. Chromosomal mapping of the gene for the type II insulin-like growth factor receptor/cation-independent mannose 6-phosphate receptor in man and mouse. Genomics. 1988 3: 224-29. 7- Riesewijk AM, Xu YQ, Schepens MT, et al. Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Biochem Biophys Res Commun. 1998 245: 272-77. 8- Brown J, Gilbert R, Delanie C. Structure and functional analysis of the IGF-II/IGF2R interaction. EMBO J. 2008 27: 265-76. 9- Ong KK, Dunger DB. Developmental aspects in the pathogenesis of type 2 diabetes. Mol Cell Endocrinol. 2001 185: 145-49. 10- Müller MJ, Lagerpusch M, Enderle J, Schautz B, Heller M, Bosy-Westphal A. Beyond the body mass index: tracking body composition in the pathogenesis of obesity and the metabolic syndrome. Obes Rev. 2012 13: 6-13 11- Ludwig T, Eggenschwiler J, Fisher P, D’Ercole AJ, Davenport ML, Efstratiadis A. Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in IGF2 and IGF1R null backgrounds. Developmental Biology. 1996 177: 517-35. 12- Binici DN, Karaman A, Coşkun M, Oğlu AU, Uçar F. Genomic damage in patients with type-2 diabetes mellitus. Genet Couns. 2013 24:149-56. 13- Duggirala R, Blangero J, Almasy L, et al. A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans. Am J Hum Genet. 2001 68: 1149-64. 14- Villuendas G, Carretero JIB, Bermejo AL, et al. The ACAA-insertion/deletion polymorphism at the 30 UTR of the IGF-II receptor gene is associated with type 2 diabetes and surrogate markers of insulin resistance. Eur J Endocrin. 2006 155: 331-36. 15- Lv K, Guo Y, Zhang Y, Wang K, Jia K, Sun S. Allele-specific targeting of hsa-miR-657 to human IGF2R creates a potential mechanism underlying the association of ACAA-insertion/deletion polymorphism with type 2 diabetes. Biochem Biophys Res Commun. 2008 374: 101-5. 16- Alberti KG, Zimmet PZ. Definition, diagnosis and classification of diabetes mellitus and its complications. 1. Diagnosis and classification of diabetes mellitus, provisional report of a WHO consultation. Diabet Med 1998 15: 539-53. 17- Dalton M, Cameron AJ, Zimmet PZ, et al. Waist circumference, waist-hip ratio and body mass index and their correlation with cardiovascular disease risk factors in Australian adults. J Intern Med. 2005 254: 555-63. 18- Matsuda M, DeFronzo R. Insulin sensitivity indices obtained from oral glucose tolerance testing. Diabetes Care. 1999 22:1462-70. 19- Fridwald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972 18: 499-502. 20- Bloomgarden MD. Concepts of insulin resistance. Metab Synd Related Disord. 2005 3: 284-93. 21- Bouche C, Serdy S, Kahn CR, Goldfine AB. The cellular fate of glucose and its relevance in type 2 diabetes. Endocr Rev. 2004 25: 807-30. 22- San Millan JL, Corton M, Villuendas G, Sancho J, Peral B, Escobar-Morreale HF. 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Background and Objective: Non-alcoholic fatty liver disease has been identified as a major health -related problem.There is no proven therapy for NAFLD. However, a number of possible treatments have been proposed and studied. The aim of this study was to evaluate the therapeutic effects of both Chlorella Vulgaris and Artichoke leaf extracts on NAFLD.
Materials and Methods: In this clinical trial study, 90 patients with NAFLD participated and randomly allocated to three groups. After initial examination, lipids and liver enzymes were measured. The groups received Metformin, Chlorella supplements and Artichoke. After the therapeutic period, liver enzymes were measured again. All collected data were analyzed using SPSS software and independent T-Test, Mann-Whitney and Chi-Square tests.
Results: At baseline, mean age, systolic and diastolic blood pressure, BMI, ALT, AST, HDL, LDL, TG, CHOL and FBS showed no significant difference in three groups. But, after the completion of the treatment, serum ALT, AST, systolic and diastolic blood pressure and BMI significantly decreased in all three groups.
Conclusion: Our study showed the beneficial effects of Artichoke and Chlorella vulgaris in patients with NAFLD. We suggest future studies be performed with larger sample sizes for precise evaluation of the effects of Artichoke and Chlorella vulgaris on NAFLD.
Background and Aims:Colorectal cancer (CRC) poses a significant global health challenge, with elevated mortality rates. Previous research has implicated reduced SLC4A4 levels and increased expression of hsa-miR-223-3p and hsa-miR-106a-5p in CRC. This study explores the diagnostic potential of hsa-circRNA-001587 and hsa-circ-0004872 in CRC within a population-based framework. By focusing on these circRNAs, the investigation aims to contribute valuable insights into CRC diagnostics.
Methods: In this population-based study, tissue samples from 30 pairs of CRC and adjacent normal tissues were collected at Shahid Beheshti University of Medical Sciences and Valiasr Hospital in Birjand, Iran. Systematic patient recruitment, comprehensive data collection, and rigorous tissue sample procedures were employed. The focus of RNA extraction and analysis was on hsa-circRNA-001587 and hsa-circ-0004872, with validation carried out through reverse transcription qPCR and Sanger sequencing.
Results: Our results indicated a notable reduction in the expression of hsa-circRNA-001587 (downregulated by 1.34-fold) and hsa-circ-0004872 (downregulated by 2.19-fold) in CRC tissues compared to adjacent normal tissues (p-value > 0.05). Furthermore, our statistical analysis revealed a robust and significant association between hsa-circ-0004872 and hsa-circRNA-001587, suggesting that an increase in one corresponds consistently with an increase in the other (p-value ≤ 0.001, r = 0.81).
Conclusion: Hsa-circ-0004872 and hsa-circRNA-001587, which act as tumor suppressors in CRC through a novel hsa-circ-0004872/hsa-circRNA-001587/hsa-miR-223-3p/hsa-miR-106a-5p/SLC4A4 axis, could serve as potential biomarkers and therapeutic targets for CRC treatment. Further investigations in serum, plasma, and cell lines are needed for a comprehensive understanding.
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