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The link between gluten intake and the risk of cancers. 麸质食品摄入量与癌症风险之间的联系。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i2.2945
Sajjad Bakhtiari, Nastaran Asri, Sepehr Maleki, Saba Rahimi, Amirreza Jabbari, Alireza Ahmadzadeh, Somayeh Jahani-Sherafat, Masoumeh Farahani, Ehsan Nazemalhosseini Mojarad, Mohammad Rostami-Nejad

Gluten is a complex mixture of hundreds of related proteins, with the two major groups being gliadin and glutenin. Gliadin primarily affects the viscosity of dough, while glutenin contributes to its strength. Nowadays, there is evidence suggesting an increase in gluten exposure due to advancements in cereal technology. Consumption of gluten can lead to development of gluten-related disorders (GRDs) in susceptible individuals. Some GRDs have been strongly associated with an increased risk of developing certain types of cancer. Colorectal cancer and lymphoma are among the most commonly reported malignancies associated with GRDs. Dietary factors, including gluten intake, have been recognized as significant modifiable risk factors for the development of digestive system cancers. The present study aimed to collect current information on the effect of gluten on the incidence of cancer in the general population and among GRDs patients. Protein-Protein Interaction (PPI) Network analysis of common genes between celiac disease (CD) and cancer was also conducted.

麸质蛋白是由数百种相关蛋白质组成的复杂混合物,其中主要的两类是胶adin 和麸质蛋白。胶蛋白主要影响面团的粘度,而谷朊蛋白则增强面团的强度。如今,有证据表明,由于谷物技术的进步,人们接触麸质的机会越来越多。食用麸质食品会导致易感人群患上麸质相关疾病(GRDs)。某些麸质相关疾病与罹患某些类型癌症的风险增加密切相关。结肠直肠癌和淋巴瘤是最常报道的与麸质相关疾病有关的恶性肿瘤。包括麸质摄入量在内的饮食因素已被认为是消化系统癌症发病的重要可改变风险因素。本研究旨在收集有关麸质对普通人群和 GRDs 患者癌症发病率影响的最新信息。本研究还对乳糜泻(CD)与癌症之间的常见基因进行了蛋白质-蛋白质相互作用(PPI)网络分析。
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引用次数: 0
Evaluation strategy of anti-mitochondrial antibodies M2-negative: the role of multiplex rodent tissues and related clinical implications. 抗线粒体抗体 M2- 阴性的评估策略:多重啮齿动物组织的作用及相关临床意义。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i1.2879
Chiara Tolassi, Roberto Assandri

Indirect immunofluorescence on HEp-2 cell line (HEp-2-IIF) remains "gold standard" method for the detection of antinuclear antibodies (ANA). ANA is an operative definition, showing the possibility of autoantibodies (Aab) to bind nuclear, and cytoplasmic antigens. One of the major examples is represented by anti-mitochondrial antibodies (AMAs), which target proteins of the inner and outer mitochondrial membranes, located into the cytoplasm. The standard IIF on rat kidney/stomach/liver tissue sections, with the combined use of other commercial assays, may all be used in ordinary lab life to validate the AC-21 pattern on Hep-2 cells. The routine lab experience teaches that commercial kits cannot always be detected and define specific AMAs. In these cases the literature proposes the use of other homemade assays to detect AMAs as immunoprecipitation (IP) and Western blot (IP-WB). However, using IP or IP-WB is difficult to apply in a routine laboratory, because of numerous cases to process and the related troubles. Where find confirmation of the AC-21 pattern if line-immunoblot and other routine methods (ELISA, CLIA/FEIA assays) fail? We review AC-21 AMA-like sera from our patients (year 2022) and propose a revised diagnostic algorithm based on the combined use of IIF on Hep-2 cells, line immunoblot and IIF on rodent tissue as a third line method. We demonstrated that, particularly in cases where the second level test was unsuccessful, the application of IFI on rodent tissues became indispensable to verify the existence of AMAs.

HEp-2 细胞系(HEp-2-IIF)间接免疫荧光法仍是检测抗核抗体(ANA)的 "金标准 "方法。ANA 是一个有效的定义,表明自身抗体(Aab)可与核和细胞质抗原结合。其中一个主要例子是抗线粒体抗体(AMA),它针对位于细胞质中的线粒体内膜和外膜蛋白质。大鼠肾/胃/肝组织切片上的标准 IIF,结合使用其他商业检测方法,都可以在普通实验室生活中用来验证 Hep-2 细胞上的 AC-21 模式。常规实验室经验表明,商业试剂盒并不总能检测和确定特定的 AMA。在这种情况下,文献建议使用免疫沉淀(IP)和 Western 印迹(IP-WB)等其他自制检测方法来检测 AMA。然而,由于需要处理的病例众多且相关麻烦,IP 或 IP-WB 难以在常规实验室中应用。如果线-免疫印迹和其他常规方法(ELISA、CLIA/FEIA 检测)失败,到哪里去确认 AC-21 模式?我们回顾了患者的 AC-21 AMA 样血清(2022 年),并提出了一种修订的诊断算法,该算法基于肝-2 细胞上的 IIF、线免疫印迹和啮齿动物组织上的 IIF 作为三线方法的联合使用。我们证明,特别是在第二级检测不成功的情况下,在啮齿类动物组织上应用 IFI 已成为验证是否存在 AMA 的不可或缺的方法。
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引用次数: 0
Abdominal pain in a young lady with inverted Meckel's diverticulum: a case report. 一名患有倒置梅克尔憩室的年轻女性的腹痛:病例报告。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i1.2815
Seyed Mohammad Reza Nejatollahi, Keihan Mostafavi, Fariba Ghorbani

Meckel diverticulum is the most common congenital anomaly of the gastrointestinal tract which is located in small bowel within 2 feet of the ileocecal valve. Nevertheless, an inverted Meckel's diverticulum is an uncommon condition believed to result from aberrant peristalsis in that specific area. This article showed signs, symptoms, and possible clinical presentations using CARE guidelines in a case of inverted Meckel's diverticulum and reviews other possible features lastly, definitive treatment, results, and case follow-up were shown to refresh, and raise surgeons' awareness of this rare disorder.

梅克尔憩室是胃肠道最常见的先天性畸形,位于回盲瓣2英尺以内的小肠中。然而,倒置的梅克尔憩室是一种不常见的疾病,据信是由于该特定区域的异常蠕动造成的。本文介绍了一例倒置梅克尔憩室患者的体征、症状和可能的临床表现,采用了 CARE 指南,并回顾了其他可能的特征,最后还介绍了明确的治疗方法、结果和病例随访,让人耳目一新,并提高了外科医生对这种罕见疾病的认识。
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引用次数: 0
Design and development of a self-care application for patients with liver cirrhosis. 设计和开发肝硬化患者自我护理应用程序。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i1.2846
Zahra Asadzadeh, Elham Maserat, Leila Alizadeh, Zeinab Mohammadzadeh

Aim: Due to the capabilities of the mobile application in the self-care of patients, the present study was conducted to design and evaluate a mobile-based self-care application for patients with liver cirrhosis.

Background: Liver cirrhosis is a progressive and chronic disease that, if left untreated, leads to liver cancer and, finally, the death of the patient.

Methods: This study was conducted in six phases, including determining and confirming the validity of the minimum data set and capabilities for the application, designing a conceptual and logical model and determining the technical capabilities, designing the application, evaluating the prototype usability in a laboratory environment by technical experts, evaluation of the application usability in a real environment by 30 patients with QUIS (Questionnaire of User Interface Satisfaction) questionnaire.

Results: The designed application has capabilities such as calculating the patient's MELD score (Model for End-Stage Liver Disease), medication reminder, location in emergency, and conversation with the physician. The results showed that the patients evaluated the application with a score of 7.94 (out of 9 points) at a good level.

Conclusion: The self-care application can help patients with liver cirrhosis and their families access the necessary information related to the special care of the patient at any time and place; it also helps better manage the patient's life, improve the quality of life, and monitor the patient. These applications can effectively manage chronic diseases by reducing the burden of referrals and costs.

目的:鉴于移动应用在患者自我护理方面的功能,本研究旨在为肝硬化患者设计和评估基于移动的自我护理应用:背景:肝硬化是一种进展性慢性疾病,如果不及时治疗,会导致肝癌,最终导致患者死亡:本研究分六个阶段进行,包括确定和确认应用程序最低数据集和功能的有效性、设计概念和逻辑模型并确定技术能力、设计应用程序、由技术专家在实验室环境中评估原型的可用性、由 30 名患者在真实环境中使用 QUIS(用户界面满意度问卷)问卷评估应用程序的可用性:设计的应用程序具有计算患者的 MELD 评分(终末期肝病模型)、用药提醒、急诊定位和与医生对话等功能。结果显示,患者对该应用程序的评价为 7.94 分(满分 9 分),处于良好水平:自我护理应用程序可以帮助肝硬化患者及其家属随时随地获取与患者特殊护理相关的必要信息,还有助于更好地管理患者的生活,提高生活质量,并对患者进行监测。这些应用可有效管理慢性疾病,减少转诊负担和费用。
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引用次数: 0
Investigation of GNB1 derivative circular RNAs hsa_circ_0009361 and hsa_circ_0009362 expressions in colorectal cancer patients: potential new diagnostic factors. 研究结直肠癌患者中 GNB1 衍生物环状 RNA hsa_circ_0009361 和 hsa_circ_0009362 的表达:潜在的新诊断因素。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i1.2863
Zahra Mozooni, Nafiseh Golestani, Hossein Sadeghi

Aim: We aim to investigate the relationship between hsa_circ_0009361 plus hsa_circ_0009362 expression levels and the clinicopathological features of colorectal cancer (CRC) patients.

Background: Circular RNAs (circRNAs) are implicated in the progression and development of CRC. CircRNAs have been recognized as diagnostic and prognostic biomarkers, opening up a new window to comprehend the molecular basis of CRC. Given the significance of circRNAs and the G protein subunit b1 (GNB1) gene in malignancies, the goal of the current investigation was to determine the expression levels of GNB1 derivative circular RNAs circGNB1 (hsa_circ_0009361 and hsa_circ_0009362) in CRC and adjacent control tissues.

Methods: The expression levels of the GNB1 derivative circular RNAs (hsa_circ_0009361 and hsa_circ_0009362) were evaluated using the quantitative real-time PCR (qRT-PCR) method in 45 CRC tissues and adjacent control tissues. Furthermore, we analyzed the diagnostic power of the mentioned circRNAs by plotting the receiver operating characteristic (ROC) curve. The association between the expression levels of hsa_circ_0009361 and hsa_circ_0009362 was evaluated using correlation analysis.

Results: Our results revealed that the expression levels of hsa_circ_0009361 and hsa_circ_0009362 were significantly down-regulated in CRC tissues compared to the adjacent control group. Analysis of patients' clinicopathological features indicated that expressions of hsa_circ_0009361 and hsa_circ_0009362 were differently related to lymph vascular invasion (P<0.001). ROC curve results showed that these circRNAs are good candidate diagnostic biomarkers in CRCs. Pearson's correlation test revealed a positive correlation between hsa_circ_0009361 and hsa_circ_0009362 expression levels (P<0.0001).

Conclusion: These results demonstrated that hsa_circ_0009361 and hsa_circ_0009362 expression levels may be used as possible diagnostic biomarkers for CRC.

目的:我们旨在研究 hsa_circ_0009361 和 hsa_circ_0009362 表达水平与结直肠癌(CRC)患者临床病理特征之间的关系:背景:环状 RNA(circRNA)与 CRC 的进展和发展有关。循环 RNA 被认为是诊断和预后的生物标志物,为了解 CRC 的分子基础打开了一扇新窗口。鉴于循环RNA和G蛋白亚基b1(GNB1)基因在恶性肿瘤中的重要作用,本研究旨在确定GNB1衍生物循环RNA circGNB1(hsa_circ_0009361和hsa_circ_0009362)在CRC和邻近对照组织中的表达水平:方法:采用实时定量 PCR(qRT-PCR)方法评估了 GNB1 衍生物循环 RNA(hsa_circ_0009361 和 hsa_circ_0009362)在 45 例 CRC 组织和邻近对照组织中的表达水平。此外,我们还通过绘制接收者操作特征曲线(ROC)分析了上述 circRNAs 的诊断能力。通过相关分析评估了hsa_circ_0009361和hsa_circ_0009362表达水平之间的关联:结果表明:与邻近对照组相比,hsa_circ_0009361和hsa_circ_0009362在CRC组织中的表达水平明显下调。对患者临床病理特征的分析表明,hsa_circ_0009361和hsa_circ_0009362的表达与淋巴管侵犯(Phsa_circ_0009361和hsa_circ_0009362表达水平(PConclusion:这些结果表明,hsa_circ_0009361和hsa_circ_0009362的表达水平可作为诊断CRC的生物标记物。
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引用次数: 0
Use of stool color card as screening tool for biliary atresia in resource-constraint country. 在资源有限的国家使用粪便色卡作为胆道闭锁的筛查工具。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i2.2931
Rubaiyat Alam, Khan Lamia Nahid, Md Omar Faruk, Elena Haque Rasna, Md Rukunuzzaman

Aim: The study was aimed to find out the efficacy of a stool color card (SCC) in differentiating biliary atresia (BA) from non-BA in resource-limited countries.

Background: stool color screening system was introduced in 2004 which lead to marked improvement in sensitivity of detecting BA.

Methods: This cross-sectional observational study was conducted from January, 2019 through July, 2022 on purposively sampled infants who developed jaundice before three months of age, had direct bilirubin of > 20 % of total with pale stool and dark urine.

Results: 144 cases (male, 96) were included in the study and their mean age at admission was 87.3±37.2 days and mean age at onset of jaundice was 6.1±7.7 days. BA was confirmed in 106 (73.6%) cases and 38 (26.4%) children were in non-BA group. Frequency of persistent pale stool between BA and non- BA were 88 vs 8 (83.0 % Vs 21.0 %) which was highly significant (p=0.000). Mean difference of total and direct serum bilirubin, median alanine transferase and alkaline phosphatase were not statistically significant between two groups. Median of serum gamma glutamyl transpeptidase (GGT) in BA was 570 U/L and in non-BA it was 138.0 U/L which was statistically significant (p=0.000). The sensitivity, specificity, positive predictive value, negative predictive value and accuracy of SCC were 83%, 78.9%, 91.7%, 62.5% and 81.9% respectively.

Conclusion: SCC has good sensitivity to diagnose BA but failed to prove better specificity to rely simply on it. SCC may be used as early screening tool for prompt referral to appropriate medical care centers for final evaluation of BA.

目的:该研究旨在了解粪便色卡(SCC)在资源有限的国家区分胆道闭锁(BA)和非BA的有效性。背景:2004年引入粪便色卡筛查系统,显著提高了检测BA的灵敏度:这项横断面观察性研究于2019年1月至2022年7月进行,研究对象为特意抽取的3个月大前出现黄疸、直接胆红素>总胆红素的20%、大便颜色浅且尿液颜色深的婴儿:144 例病例(男,96 例)入院时的平均年龄为(87.3±37.2)天,黄疸发病时的平均年龄为(6.1±7.7)天。106例(73.6%)确诊为黄疸型肝炎,38例(26.4%)为非黄疸型肝炎。黄疸型胆汁淤积症与非黄疸型胆汁淤积症患儿大便颜色持续苍白的比例分别为 88 vs 8 (83.0 % vs 21.0 %),差异非常显著(P=0.000)。两组间血清总胆红素和直接胆红素、丙氨酸转移酶和碱性磷酸酶中位数的平均差异无统计学意义。BA 组血清γ谷氨酰转肽酶(GGT)中位数为 570 U/L,非 BA 组为 138.0 U/L,差异有统计学意义(P=0.000)。SCC的敏感性、特异性、阳性预测值、阴性预测值和准确性分别为83%、78.9%、91.7%、62.5%和81.9%:SCC在诊断BA方面具有良好的灵敏度,但未能证明其具有更好的特异性。SCC可作为早期筛查工具,以便及时转诊到适当的医疗中心,对BA进行最终评估。
{"title":"Use of stool color card as screening tool for biliary atresia in resource-constraint country.","authors":"Rubaiyat Alam, Khan Lamia Nahid, Md Omar Faruk, Elena Haque Rasna, Md Rukunuzzaman","doi":"10.22037/ghfbb.v17i2.2931","DOIUrl":"10.22037/ghfbb.v17i2.2931","url":null,"abstract":"<p><strong>Aim: </strong>The study was aimed to find out the efficacy of a stool color card (SCC) in differentiating biliary atresia (BA) from non-BA in resource-limited countries.</p><p><strong>Background: </strong>stool color screening system was introduced in 2004 which lead to marked improvement in sensitivity of detecting BA.</p><p><strong>Methods: </strong>This cross-sectional observational study was conducted from January, 2019 through July, 2022 on purposively sampled infants who developed jaundice before three months of age, had direct bilirubin of > 20 % of total with pale stool and dark urine.</p><p><strong>Results: </strong>144 cases (male, 96) were included in the study and their mean age at admission was 87.3±37.2 days and mean age at onset of jaundice was 6.1±7.7 days. BA was confirmed in 106 (73.6%) cases and 38 (26.4%) children were in non-BA group. Frequency of persistent pale stool between BA and non- BA were 88 vs 8 (83.0 % Vs 21.0 %) which was highly significant (p=0.000). Mean difference of total and direct serum bilirubin, median alanine transferase and alkaline phosphatase were not statistically significant between two groups. Median of serum gamma glutamyl transpeptidase (GGT) in BA was 570 U/L and in non-BA it was 138.0 U/L which was statistically significant (p=0.000). The sensitivity, specificity, positive predictive value, negative predictive value and accuracy of SCC were 83%, 78.9%, 91.7%, 62.5% and 81.9% respectively.</p><p><strong>Conclusion: </strong>SCC has good sensitivity to diagnose BA but failed to prove better specificity to rely simply on it. SCC may be used as early screening tool for prompt referral to appropriate medical care centers for final evaluation of BA.</p>","PeriodicalId":12636,"journal":{"name":"Gastroenterology and Hepatology From Bed to Bench","volume":"17 2","pages":"146-150"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11234486/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141590137","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
All-cause mortality of hospitalized inflammatory bowel disease patients: a multicenter study from Iran. 住院炎症性肠病患者的全因死亡率:一项来自伊朗的多中心研究。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i3.2962
Sulmaz Ghahramani, Babak Tamizifar, Vahid Rajabpour, Seyedeh-Zeynab Hosseinian, Samira Saeian, Hassan Shahoon, Kamran Bagheri Lankarani

Aim: In this multicenter study, we investigated all causes of mortality in hospitalized inflammatory bowel disease (IBD) patients.

Background: The widespread use of biologics and immune suppressive treatments, along with the longer lifespan of patients with IBD, may have changed the cause of death in this population. Knowing this may lead to better preventive and therapeutic strategies for IBD patients.

Methods: This cross-sectional study reviewed records of 1926 IBD patients hospitalized in referral hospitals in Isfahan and Shiraz during 2013-2021. In nine years, 84 patients, 39 from Isfahan and 45 from Shiraz, died. We retrospectively gathered data on demographic, clinical, and laboratory information, as well as the cause of death. We extracted the cause of death from the death sheets and classified it using the International Classification of Diseases (ICD-10). Using the Kaplan-Meier model, we estimated the median survival time from disease diagnosis to death.

Results: Males accounted for 47 (55%) of the deceased patients. The mean age of the patients was 48.63 ± 18.7 years. The mortality rates among hospitalized UC and CD patients were 7.2% and 7.8%, respectively. The median duration of admission to death was 8 days, with 19 (22.6%) of IBD patients dying on the first day of their hospital admission. Half of the cohort of deceased IBD patients had survived for 8 years following their disease diagnosis. 32.7% of all recorded causes of death were due to certain infectious diseases. The second and third most common causes of death were diseases of the digestive system and diseases of the circulatory system, including pulmonary embolism, accounting for 30.1% and 14.2%, respectively.

Conclusion: According to this study from Iran, infectious diseases are the leading cause of death among hospitalized IBD patients. Prevention and clinical management of pulmonary embolism in IBD patients require more careful consideration. We strongly encourage population-based cohort studies to enhance the findings.

目的:在这项多中心研究中,我们调查了住院炎症性肠病(IBD)患者的所有死因:背景:生物制剂和免疫抑制治疗的广泛使用,以及 IBD 患者寿命的延长,可能改变了这一人群的死亡原因。了解这一点可能有助于为 IBD 患者制定更好的预防和治疗策略:这项横断面研究回顾了 2013-2021 年期间在伊斯法罕和设拉子转诊医院住院的 1926 名 IBD 患者的记录。九年中,有 84 名患者死亡,其中 39 人来自伊斯法罕,45 人来自设拉子。我们回顾性地收集了有关人口统计学、临床和实验室信息以及死亡原因的数据。我们从死亡表中提取了死因,并使用国际疾病分类(ICD-10)进行了分类。我们使用 Kaplan-Meier 模型估算了从疾病诊断到死亡的中位生存时间:男性占死亡患者的 47%(55%)。患者的平均年龄为(48.63 ± 18.7)岁。住院的 UC 和 CD 患者的死亡率分别为 7.2% 和 7.8%。从入院到死亡的中位时间为8天,其中19名(22.6%)IBD患者在入院第一天死亡。半数已故 IBD 患者在确诊疾病后存活了 8 年。在所有记录的死亡原因中,32.7%是由某些传染病引起的。第二和第三大常见死因是消化系统疾病和循环系统疾病,包括肺栓塞,分别占30.1%和14.2%:根据伊朗的这项研究,感染性疾病是导致住院 IBD 患者死亡的主要原因。IBD患者肺栓塞的预防和临床治疗需要更仔细的考虑。我们强烈鼓励开展基于人群的队列研究,以加强研究结果。
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引用次数: 0
Advances in blood DNA methylation-based assay for colorectal cancer early detection: a systematic updated review. 基于血液 DNA 甲基化的结直肠癌早期检测方法的进展:系统性最新综述。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i3.2978
Milad Khabbazpour, Masoud Tat, Ashraf Karbasi, Mohammad Ali Abyazi, Ghazal Khodadoustan, Zohreh Heidary, Majid Zaki-Dizaji

Aim: A systematic review was conducted to summarize the methylated circulating tumor DNA (ctDNA) markers reported over the last decade for early detection of colorectal cancer (CRC) and to identify the main technical challenges that are impeding their clinical implementation.

Background: CRC is a major cause of cancer deaths worldwide, but early detection is key for successful treatment. Non-invasive methods such as methylated ctDNA testing show promise for improving detection and monitoring of CRC.

Methods: A comprehensive search was performed using Web of Science, PubMed, and Scopus up to December 30, 2023, limited to articles published in the last 10 years (after 2012), while including advanced adenoma/stage 0 or stage I/II samples in biomarker validation.

Results: After identifying 694 articles, removing duplicates and screening titles, abstracts, and full texts, a total of 62 articles were found to meet the inclusion criteria. Among the single biomarkers, MYO1-G, SEPT9, SDC2, and JAM3 revealed the highest sensitivity for polyps and stage I/II CRC. For multi-biomarkers with suitable sensitivity, combinations of SFRP1, SFRP2, SDC2, PRIMA1, or ALX4, BMP3, NPTX2, RARB, SDC2, SEPT9, VIM or ZFHX4, ZNF334, ELOVL2, UNC5C, LOC146880, SFMBT2, GFRA1 were identified for polyps and stage I/II CRC.

Conclusion: Enhancing sensitivity and specificity of molecular screening methods is crucial for improving CRC detection. Identifying a select few valuable biomarkers is key to reducing costs, despite challenges posed by low ctDNA levels in plasma, particularly in early-stage cancers.

目的:我们进行了一项系统性综述,总结了过去十年间报道的用于早期检测结直肠癌(CRC)的甲基化循环肿瘤 DNA(ctDNA)标记物,并确定了阻碍其临床应用的主要技术挑战:背景:结直肠癌是全球癌症死亡的主要原因,但早期检测是成功治疗的关键。甲基化ctDNA检测等非侵入性方法有望改善对CRC的检测和监测:方法:使用 Web of Science、PubMed 和 Scopus 对截至 2023 年 12 月 30 日的文章进行了全面检索,仅限于过去 10 年(2012 年之后)发表的文章,同时将晚期腺瘤/0 期或 I/II 期样本纳入生物标记物验证:在识别了 694 篇文章、去除重复文章并筛选了标题、摘要和全文后,发现共有 62 篇文章符合纳入标准。在单一生物标记物中,MYO1-G、SEPT9、SDC2 和 JAM3 对息肉和 I/II 期 CRC 的敏感性最高。对于具有合适灵敏度的多生物标志物,SFRP1、SFRP2、SDC2、PRIMA1 或 ALX4、BMP3、NPTX2、RARB、SDC2、SEPT9、VIM 或 ZFHX4、ZNF334、ELOVL2、UNC5C、LOC146880、SFMBT2、GFRA1 的组合被确定为息肉和 I/II 期 CRC 的灵敏度:结论:提高分子筛查方法的灵敏度和特异性对改进 CRC 检测至关重要。尽管ctDNA在血浆中的含量较低,尤其是在早期癌症中,但找出少数有价值的生物标志物是降低成本的关键。
{"title":"Advances in blood DNA methylation-based assay for colorectal cancer early detection: a systematic updated review.","authors":"Milad Khabbazpour, Masoud Tat, Ashraf Karbasi, Mohammad Ali Abyazi, Ghazal Khodadoustan, Zohreh Heidary, Majid Zaki-Dizaji","doi":"10.22037/ghfbb.v17i3.2978","DOIUrl":"10.22037/ghfbb.v17i3.2978","url":null,"abstract":"<p><strong>Aim: </strong>A systematic review was conducted to summarize the methylated circulating tumor DNA (ctDNA) markers reported over the last decade for early detection of colorectal cancer (CRC) and to identify the main technical challenges that are impeding their clinical implementation.</p><p><strong>Background: </strong>CRC is a major cause of cancer deaths worldwide, but early detection is key for successful treatment. Non-invasive methods such as methylated ctDNA testing show promise for improving detection and monitoring of CRC.</p><p><strong>Methods: </strong>A comprehensive search was performed using Web of Science, PubMed, and Scopus up to December 30, 2023, limited to articles published in the last 10 years (after 2012), while including advanced adenoma/stage 0 or stage I/II samples in biomarker validation.</p><p><strong>Results: </strong>After identifying 694 articles, removing duplicates and screening titles, abstracts, and full texts, a total of 62 articles were found to meet the inclusion criteria. Among the single biomarkers, MYO1-G, SEPT9, SDC2, and JAM3 revealed the highest sensitivity for polyps and stage I/II CRC. For multi-biomarkers with suitable sensitivity, combinations of SFRP1, SFRP2, SDC2, PRIMA1, or ALX4, BMP3, NPTX2, RARB, SDC2, SEPT9, VIM or ZFHX4, ZNF334, ELOVL2, UNC5C, LOC146880, SFMBT2, GFRA1 were identified for polyps and stage I/II CRC.</p><p><strong>Conclusion: </strong>Enhancing sensitivity and specificity of molecular screening methods is crucial for improving CRC detection. Identifying a select few valuable biomarkers is key to reducing costs, despite challenges posed by low ctDNA levels in plasma, particularly in early-stage cancers.</p>","PeriodicalId":12636,"journal":{"name":"Gastroenterology and Hepatology From Bed to Bench","volume":"17 3","pages":"225-240"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11413380/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142284248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dynamic thiol/disulfide homeostasis and myeloperoxidase levels in Gilbert's syndrome with mild hyperbilirubinemia. 伴有轻度高胆红素血症的 Gilbert's 综合征的动态硫醇/二硫化物稳态和髓过氧化物酶水平。
Q3 Medicine Pub Date : 2024-01-01 DOI: 10.22037/ghfbb.v17i3.2968
Burak Furkan Demir, Canan Topcuoglu, Turan Turhan, Emin Altıparmak, Nisbet Yılmaz, İhsan Ateş

Aim: This study aimed to compare dynamic thiol/disulfide homeostasis and myeloperoxidase (MPO) levels in patients with Gilbert's syndrome (GS) and healthy controls.

Background: Thiol/disulfide homeostasis and MPO levels are both associated with increased progression of atherosclerosis.

Methods: The study included a total of 130 voluntary participants comprising 65 patients with GS and 65 healthy controls. These patients were selected randomly and dynamic thiol/disulfide homeostasis, MPO, complete blood count results, and biochemistry and lipid parameters were evaluated. Patients with known chronic diseases, medication usage, and acute infections were excluded from the study. Serum total thiol and native thiol levels were measured using the fully automated colorimetric method, while serum MPO levels were measured using the sandwich ELISA method.

Results: We found that patients with GS had significantly higher total thiol (352.3±38.6 vs. 317.9±47.9, p<0.001) and native thiol (386.6±42.6 vs. 348.0±51.1, p<0.001) and significantly lower disulfide (15.7±4.0 vs. 17.3±4.0, p=0.022) and MPO (130.7 vs. 166.3, p=0.006). In patients with bilirubin of <1 mg/dL, total thiol and native thiol levels were lower and disulfide, disulfide/native thiol (DNT) and disulfide/total thiol (DTT) ratios, and MPO levels were higher. Patients with bilirubin of <1 mg/dL also had higher total cholesterol.

Conclusion: In these patients with GS, the thiol/disulfide balance shifted towards thiols and proinflammatory MPO levels were lower. When bilirubin was <1 mg/dL, disulfide, DNT and DTT ratios, and MPO were higher. Bilirubin levels affected all parameters of thiol/disulfide homeostasis and MPO levels independently of other risk factors. In light of our results, we suggest that mild hyperbilirubinemia in cases of GS has an anti-inflammatory and antioxidant effect and may be protective against atherosclerosis.

目的:本研究旨在比较吉尔伯特综合征(GS)患者和健康对照组的动态硫醇/二硫化物稳态和髓过氧化物酶(MPO)水平:背景:硫醇/二硫化物稳态和MPO水平均与动脉粥样硬化的进展有关:该研究包括 65 名 GS 患者和 65 名健康对照者,共 130 名自愿参与者。研究人员随机挑选了这些患者,并对他们的动态硫醇/二硫平衡、MPO、全血细胞计数结果以及生化和血脂参数进行了评估。已知患有慢性疾病、服用药物和急性感染的患者不在研究范围内。采用全自动比色法测量血清总硫醇和原生硫醇水平,采用夹心酶联免疫吸附法测定血清MPO水平:结果:我们发现,GS 患者的总硫醇水平明显更高(352.3±38.6 vs. 317.9±47.9,p):在这些 GS 患者中,硫醇/二硫化物平衡向硫醇转移,促炎性 MPO 水平较低。当胆红素
{"title":"Dynamic thiol/disulfide homeostasis and myeloperoxidase levels in Gilbert's syndrome with mild hyperbilirubinemia.","authors":"Burak Furkan Demir, Canan Topcuoglu, Turan Turhan, Emin Altıparmak, Nisbet Yılmaz, İhsan Ateş","doi":"10.22037/ghfbb.v17i3.2968","DOIUrl":"10.22037/ghfbb.v17i3.2968","url":null,"abstract":"<p><strong>Aim: </strong>This study aimed to compare dynamic thiol/disulfide homeostasis and myeloperoxidase (MPO) levels in patients with Gilbert's syndrome (GS) and healthy controls.</p><p><strong>Background: </strong>Thiol/disulfide homeostasis and MPO levels are both associated with increased progression of atherosclerosis.</p><p><strong>Methods: </strong>The study included a total of 130 voluntary participants comprising 65 patients with GS and 65 healthy controls. These patients were selected randomly and dynamic thiol/disulfide homeostasis, MPO, complete blood count results, and biochemistry and lipid parameters were evaluated. Patients with known chronic diseases, medication usage, and acute infections were excluded from the study. Serum total thiol and native thiol levels were measured using the fully automated colorimetric method, while serum MPO levels were measured using the sandwich ELISA method.</p><p><strong>Results: </strong>We found that patients with GS had significantly higher total thiol (352.3±38.6 vs. 317.9±47.9, p<0.001) and native thiol (386.6±42.6 vs. 348.0±51.1, p<0.001) and significantly lower disulfide (15.7±4.0 vs. 17.3±4.0, p=0.022) and MPO (130.7 vs. 166.3, p=0.006). In patients with bilirubin of <1 mg/dL, total thiol and native thiol levels were lower and disulfide, disulfide/native thiol (DNT) and disulfide/total thiol (DTT) ratios, and MPO levels were higher. Patients with bilirubin of <1 mg/dL also had higher total cholesterol.</p><p><strong>Conclusion: </strong>In these patients with GS, the thiol/disulfide balance shifted towards thiols and proinflammatory MPO levels were lower. When bilirubin was <1 mg/dL, disulfide, DNT and DTT ratios, and MPO were higher. Bilirubin levels affected all parameters of thiol/disulfide homeostasis and MPO levels independently of other risk factors. In light of our results, we suggest that mild hyperbilirubinemia in cases of GS has an anti-inflammatory and antioxidant effect and may be protective against atherosclerosis.</p>","PeriodicalId":12636,"journal":{"name":"Gastroenterology and Hepatology From Bed to Bench","volume":"17 3","pages":"270-278"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11413386/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142284253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Opium use and gastrointestinal cancers: a systematic review and meta-analysis study. 吸食鸦片与胃肠道癌症:一项系统回顾和荟萃分析研究。
Q3 Medicine Pub Date : 2024-01-01
Mahsa Mohammadi, Philippe Tadger, Amir Sadeghi, Niloufar Salehi, Mohsen Rajabnia, Elham Paraandavaji, Sasan Shafiei, Ahmad Pirani, Mohammad Reza Hatamnejad, Erfan Taherifard, Fatemeh Kheshti, Arman Naderilordejani, Forough Honarfar, Khaled Rahmani, Majid Soruri, Hamed Kord Varkaneh, Omid Dadras, Ali Jahanian, Sara Rasta, Mohammad Reza Zali

Aim: The current systematic review and meta-analysis aimed to assess the association between Gastrointestinal (GI) cancers and opium use.

Background: GI malignancies are a global public health issue and are associated with many risk factors including genetic and lifestyle factors.

Methods: PubMed, Web of Science, Embase and Scopus and the Google Scholar search engine in addition to Persian databases including Magiran and SID were searched using relevant keywords. The associations of opium use, long duration of opium use, high daily amount opium use and high cumulative opium use and GI cancer and various subtypes of GI cancers were estimated and pooled in format of odds ratios (OR) and their corresponding 95% confidence intervals (CI) with a random effects model.

Results: 22 articles that were published between 1983 and 2022 entered the analyses. There were significant relationships between opium use based on crude effect sizes (OR: 2.53, 1.95-3.29) and adjusted effect sizes (OR: 2.64, 1.99-3.51), high daily opium use (or: 3.41, 1.92-6.06), long duration of opium use (OR: 3.03, 1.90-4.84) and high cumulative opium use (OR: 3.88, 2.35-6.41), all compared to never opium use, and GI cancer. The results were not sensitive to sensitivity analyses and no influential publication biases were found in these analyses.

Conclusion: Our meta-analysis showed that opium use could be associated with increased risk of overall and some particular GI cancers including oropharyngeal, gastric, pancreatic and colorectal cancers. Opium use as a potentially modifiable factor, therefore, should be more emphasized.

目的:本系统综述和荟萃分析旨在评估胃肠道(GI)癌症与鸦片使用之间的关联:背景:胃肠道恶性肿瘤是一个全球性的公共卫生问题,与许多风险因素有关,包括遗传和生活方式因素:方法:使用相关关键词搜索了 PubMed、Web of Science、Embase、Scopus 和 Google Scholar 搜索引擎,以及包括 Magiran 和 SID 在内的波斯语数据库。采用随机效应模型,以几率比(OR)及其相应的 95% 置信区间(CI)的形式对鸦片吸食、长期吸食鸦片、每日大量吸食鸦片和大量累积吸食鸦片与消化道癌症及各种亚型消化道癌症的关系进行了估计和汇总。根据粗效应量(或然比:2.53,1.95-3.29)和调整效应量(或然比:2.64,1.99-3.51),每天吸食大量鸦片(或然比:3.41,1.92-6.06)、吸食鸦片持续时间长(或然比:3.03,1.90-4.84)和累积吸食大量鸦片(或然比:3.88,2.35-6.41)与消化道癌症之间存在明显关系,所有这些都与从未吸食鸦片相比。这些结果对敏感性分析不敏感,在这些分析中也没有发现有影响的发表偏差:我们的荟萃分析表明,吸食鸦片可能会增加罹患胃肠道癌症(包括口咽癌、胃癌、胰腺癌和结直肠癌)的风险。因此,鸦片的使用作为一种潜在的可改变因素,应受到更多重视。
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Gastroenterology and Hepatology From Bed to Bench
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