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Celiac Crisis: A Life-Threatening Complication of Celiac Disease. 乳糜泻危象:乳糜泻危及生命的并发症。
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.393
Pooja Soni, Priya Gogia, Rajkumar Kundavaram

Celiac disease (CD) is an immune-mediated enteropathy with varied systemic involvement and association with increased morbidity and mortality. Strong clinical suspicion is the key, and diagnosis is made using histopathology and serology. Though the consumption of a strict gluten-free diet can improve symptoms and limit mucosal damage, curative therapy is still lacking. Significant clinical improvement can be seen after treatment with immunosuppressive therapy; however, there is no definitive role of immunosuppression in preventing complications. Celiac crisis (CC), a serious and life-threatening complication of CD, is characterized by acute onset and rapid progression of gastrointestinal manifestations associated with metabolic and electrolyte disturbances and neurological and renal dysfunction. Management comprises urgent hospitalization, fluid resuscitation, correction of electrolyte imbalance, and albumin infusion. Early identification and diagnosis of CD and timely initiation of a gluten-free diet with proper compliance are of paramount importance in preventing complications, including CC. Regular follow-up after diagnosis is a good approach to assessing adherence to the gluten-free diet, disease activity, and screening for complications. With the advent of improved diagnostic facilities and access to the health care system, timely diagnosis, and efficient management, prognosis has improved significantly in recent years.

乳糜泻(CD)是一种免疫介导的肠病,具有不同的全身累及,与发病率和死亡率增加有关。强烈的临床怀疑是关键,并通过组织病理学和血清学进行诊断。虽然食用严格的无麸质饮食可以改善症状并限制粘膜损伤,但仍然缺乏治疗方法。经免疫抑制治疗后临床改善明显;然而,免疫抑制在预防并发症方面没有明确的作用。乳糜泻危象(Celiac crisis, CC)是乳糜泻的一种严重且危及生命的并发症,其特点是急性发作和快速进展,伴有代谢和电解质紊乱以及神经和肾功能障碍。处理包括紧急住院、液体复苏、纠正电解质失衡和白蛋白输注。乳糜泻的早期识别和诊断以及及时开始无谷蛋白饮食的适当依从性对于预防并发症(包括CC)至关重要,诊断后定期随访是评估无谷蛋白饮食依从性、疾病活动和筛查并发症的好方法。近年来,随着诊断设备的改进和卫生保健系统的普及,及时的诊断和有效的管理,预后有了显著改善。
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引用次数: 0
Outcome of selective non-diverting low anterior resection after neoadjuvant chemoradiotherapy and curative surgery for proximal rectal cancer: A prospective case series. 直肠癌近端新辅助放化疗和根治性手术后选择性非转移低位前切除术的疗效:前瞻性病例系列。
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.396
Aidin Yaghoobi Notash, Ehsan Sadeghian, Ehsan Sobhanian, Behnam Behboudi, Seyed Mohsen Ahmadi Tafti, Zahra Moghimi, Amir Keshvari, Mohammad Sadegh Fazeli, Mohammad Reza Keramati

Background: Low anterior resection (LAR) is the gold standard for curative cancer treatment in the middle and upper rectum. In radically operated patients, the local recurrence rates with total mesorectal excision (TME) after 5 and 10 years was<10%, with 80% in 5 years survival. Anastomotic leakage (AL) affects 4%-20% of patients who underwent LAR. Based on some studies, there is a risk reduction of symptomatic AL after LAR and the need for reoperation in patients with a defunctioning stoma (DS), also known as diverting stoma. Ileostomy has many complications, such as skin irritation and leakage, dehydration, obstruction, and parastomal hernia. Considering the complications of defunctioning loop-ileostomy (DLI) we designed this study to evaluate noninserting stoma in a particular group of patients.

Methods: This retrospective cohort case series study utilized data of 20 patients with rectal adenocarcinoma with lesion>7 cm from anal verge in rectoscopy who underwent LAR after 28 sessions of chemoradiotherapy (CRT) and 6 weeks of rehabilitation. All of the patients matched our criteria, so DLI was not performed on any of them.

Results: Among our 20 patients, four AL were happened (20%). C-reactive protein (CRP) on post-operation day (POD) six was valuable. Computed tomography (CT) scan was not used as a reliable modality in our study. In all patients with positive AL, magnetic resonance imaging (MRI) was useful and reported correctly, and direct vision of the anastomosis site by rigid rectoscopy was not safe enough to make decisions about it.

Conclusion: The leakage rate was not far from the average leakage rate in other studies. Then it seems it is possible to forget about defunctioning loop stoma (DLS) in safe cases to reduce the stoma complications. Due to our restricted case selection and our close observation protocol, we had no significant complications compared to other studies. According to this study, not inserting stoma in suitable cases with restricted protocol selection is possible, and the leakage rate is not higher in comparison with patients with stoma.

背景:低位前切除术(LAR)是治疗中、上直肠肿瘤的金标准。在根治性手术患者中,5年和10年后全直肠系膜切除术(TME)的局部复发率分别为:方法:本回顾性队列病例系列研究利用了20例直肠镜检查中病灶距肛门边缘bbb70 cm的直肠腺癌患者的资料,这些患者在接受28次放化疗(CRT)和6周康复治疗后接受了LAR。所有的病人都符合我们的标准,所以没有对他们进行DLI。结果:20例患者中发生AL 4例(20%)。术后第6天(POD) c反应蛋白(CRP)检测有价值。在我们的研究中,计算机断层扫描(CT)不是一种可靠的方式。在所有AL阳性患者中,磁共振成像(MRI)是有用的,报告是正确的,刚性直肠镜直接看到吻合部位是不够安全的。结论:与其他研究的平均渗漏率相差不大。因此,在安全的情况下,似乎可以忘记功能失效的环形造口(DLS),以减少造口并发症。由于我们有限的病例选择和严密的观察方案,与其他研究相比,我们没有出现明显的并发症。根据本研究,在方案选择有限的情况下,合适的病例不插入造口是可能的,并且与有造口的患者相比,漏出率并不高。
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引用次数: 0
Efficacy of Methotrexate and Anti-TNF Combination Therapy in Adults with Refractory Crohn's Disease. 甲氨蝶呤联合抗肿瘤坏死因子联合治疗成人难治性克罗恩病的疗效观察
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.395
Paria Boustani, Anahita Sadeghi, Sina Khayatian, Sudabeh Alatab, Amir Anushiravani, Ali Reza Sima, Homayoon Vahedi

Background: Biological medications have played a significant role in maintenance therapy for Crohn's disease (CD), but some cases become refractory to these agents. Methotrexate (MTX) appears to be a cost-effective and readily available drug for enhancing the effectiveness of maintenance therapy when used in combination with anti-tumor necrosis factor (anti-TNF) therapy in such cases. However, its effectiveness is still to be established. We aimed to assess the efficacy of MTX and anti-TNF combination therapy in patients with refractory CD.

Methods: A retrospective cohort study was conducted on adult patients with CD who were refractory to anti-TNF therapy and were initiated on weekly intravenous MTX in addition to the anti-TNF therapy. These patients were then followed up for over a year. The primary outcome measured was the clinical response to treatment, based on the Harvey-Bradshaw Index. The secondary outcomes included assessing the adverse events and complications of MTX therapy.

Results: Of 70 patients, 44 were included in the final analysis. Among them, 30 patients (68.2%) achieved complete remission, four patients (9.1%) had a partial clinical response, and 10 patients (22.7%) required surgery. The adverse events and complications of MTX therapy were mild and infrequent (9.1%). None of the demographic or clinical factors were significantly associated with response to treatment (P>0.05).

Conclusion: Combining MTX with anti-TNF therapy appears to be an effective and safe treatment for patients with Crohn's disease, particularly those with severe disease who are less responsive to monotherapy. However, further studies are needed to confirm these findings.

背景:生物药物在克罗恩病(CD)的维持治疗中发挥了重要作用,但一些病例对这些药物变得难治。在这种情况下,甲氨蝶呤(MTX)与抗肿瘤坏死因子(anti-TNF)治疗联合使用时,似乎是一种具有成本效益且易于获得的药物,可提高维持治疗的有效性。然而,其有效性仍有待确定。我们的目的是评估MTX和抗tnf联合治疗难治性CD患者的疗效。方法:对抗tnf治疗难治性成年CD患者进行回顾性队列研究,这些患者在抗tnf治疗的基础上开始每周静脉注射MTX。然后对这些患者进行了一年多的随访。主要衡量指标是基于哈维-布拉德肖指数的临床治疗反应。次要结果包括评估MTX治疗的不良事件和并发症。结果:70例患者中,44例纳入最终分析。其中30例(68.2%)患者达到完全缓解,4例(9.1%)患者达到部分临床缓解,10例(22.7%)患者需要手术治疗。甲氨蝶呤治疗的不良事件和并发症轻微且少见(9.1%)。人口统计学或临床因素均与治疗反应无显著相关(P < 0.05)。结论:MTX联合抗肿瘤坏死因子治疗似乎是一种有效且安全的治疗克罗恩病患者,特别是那些对单一治疗反应较差的严重疾病患者。然而,需要进一步的研究来证实这些发现。
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引用次数: 0
Altered Cytokine Production in Patients with Helicobacter pylori Infection. 幽门螺杆菌感染患者细胞因子产生的改变。
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.398
Abdollah Safikhani Mahmoodzadeh, Elham Moazamian, Seyedeh Azra Shamsdin, Gholam Abas Kaydani

Background: Helicobacter pylori is a gram-negative pathogen. The infection caused by this pathogen may result in gastritis and can increase the risk of gastric cancer. This study investigated the relationship between H. pylori infection as the main risk factor for gastritis and changes in serum inflammatory cytokine levels.

Methods: Blood samples from 85 patients with stomach pain, including 46 H. pylori-positive (Hp+) and 39 H. pylori-negative (Hp-) cases, were collected and referred to a gastroenterologist. After isolation and identification of H. pylori, the severity of gastritis was determined for each patient based on the histopathological findings. Finally, the serum levels of cytokines were measured using the multiplex kit and flow cytometry methods.

Results: There were significant differences in the levels of interleukin-2 (IL-2), IL-4, IL-17A, IL-17F, IL-22, tumor necrosis factor-alpha (TNF-α), and interferon-gamma (IFN-γ) between the Hp- and the Hp+ specimens (P≤0.05). The levels of IL-2, IL-17A, IL-17F, IL-22, TNF-α, and IFN-γ were significantly higher in patients with mild and moderate gastritis than Hp- group (P≤0.05). In addition, IL-4 significantly increased in patients with moderate gastritis compared with Hp- individuals (P=0.008).

Conclusion: Among the inflammatory cytokines evaluated in this study, IL-17A, IL-17F, and IL-22 may play a crucial role in developing moderate gastritis in infected patients with H. pylori.

背景:幽门螺杆菌是一种革兰氏阴性病原体。这种病原体引起的感染可导致胃炎,并可增加胃癌的风险。本研究探讨了幽门螺杆菌感染作为胃炎的主要危险因素与血清炎症细胞因子水平变化的关系。方法:收集85例胃痛患者的血液样本,其中幽门螺杆菌阳性(Hp+) 46例,幽门螺杆菌阴性(Hp-) 39例。在分离和鉴定幽门螺杆菌后,根据组织病理学结果确定每位患者的胃炎严重程度。最后,使用多重检测试剂盒和流式细胞术检测血清细胞因子水平。结果:Hp-组与Hp+组血清白细胞介素-2 (IL-2)、IL-4、IL-17A、IL-17F、IL-22、肿瘤坏死因子α (TNF-α)、干扰素γ (IFN-γ)水平差异均有统计学意义(P≤0.05)。轻、中度胃炎患者血清IL-2、IL-17A、IL-17F、IL-22、TNF-α、IFN-γ水平均显著高于Hp-组(P≤0.05)。此外,与Hp-个体相比,中度胃炎患者IL-4显著升高(P=0.008)。结论:在本研究评估的炎症因子中,IL-17A、IL-17F和IL-22可能在幽门螺杆菌感染患者发生中度胃炎中起关键作用。
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引用次数: 0
Correlation between Autoimmune Hashimoto's Thyroiditis and Helicobacter pylori Infection: A Case-Control Study. 自身免疫性桥本甲状腺炎与幽门螺杆菌感染的相关性:一项病例对照研究
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.397
Mahla Shajari, Maryam Rezaei, Fereshteh Osmani, Ebrahim Shafaie, Zoya Tahergorabi

Background: Among environmental factors, infectious agents, including Helicobacter pylori, can act as triggers for autoimmune thyroid diseases. Therefore, this study aimed to investigate the correlation between autoimmune Hashimoto's thyroiditis with H. pylori infection.

Methods: The participants in this case-control study were 74 individuals 17-62 years who were divided into two groups, including 38 diagnosed Hashimoto's thyroiditis patients from an outpatient clinic of endocrinology and 36 apparently healthy individuals that were selected from family members of cases group age-matched and sex-matched. For individuals in two groups, a questionnaire was completed, including demographic information. Then, they were referred to the laboratory for thyroid stimulating hormone (TSH) and free T4 (FT4) in the control group and anti-thyroid peroxidase antibody (TPO-Ab) levels measurement in case and control groups. Stool samples were obtained from all individuals for H. pylori antigen detection using the ELIZA kit.

Results: There was no significant difference in the mean age of case and control groups (P=0.96), and 81.1% of individuals were female. 58.6% of patients with Hashimoto's thyroiditis and 41.4% of the control group had positive H. pylori, but there was no statistically significant difference between the two groups (P=0.34). Furthermore, there was a significant positive correlation between TPO-Ab levels and H. pylori infection (r=0.2, P=0.03).

Conclusion: TPO-Ab levels were associated with H. pylori infection diagnosed by H. pylori antigen.

背景:在环境因素中,感染因子,包括幽门螺杆菌,可以作为自身免疫性甲状腺疾病的触发因素。因此,本研究旨在探讨自身免疫性桥本甲状腺炎与幽门螺杆菌感染的相关性。方法:病例对照研究74例,年龄17-62岁,随机分为两组,其中38例为内分泌科门诊确诊的桥本甲状腺炎患者,36例为病例组家属中年龄匹配、性别匹配的表面健康个体。对于两组中的个人,完成了一份调查问卷,包括人口统计信息。对照组检测促甲状腺激素(TSH)和游离T4 (FT4),对照组和病例组检测抗甲状腺过氧化物酶抗体(TPO-Ab)水平。所有个体的粪便样本均采用ELIZA试剂盒进行幽门螺杆菌抗原检测。结果:病例组与对照组的平均年龄差异无统计学意义(P=0.96), 81.1%为女性。桥本甲状腺炎患者幽门螺杆菌阳性率为58.6%,对照组为41.4%,但两组比较差异无统计学意义(P=0.34)。TPO-Ab水平与幽门螺杆菌感染呈显著正相关(r=0.2, P=0.03)。结论:TPO-Ab水平与幽门螺杆菌抗原诊断的幽门螺杆菌感染相关。
{"title":"Correlation between Autoimmune Hashimoto's Thyroiditis and <i>Helicobacter pylori</i> Infection: A Case-Control Study.","authors":"Mahla Shajari, Maryam Rezaei, Fereshteh Osmani, Ebrahim Shafaie, Zoya Tahergorabi","doi":"10.34172/mejdd.2024.397","DOIUrl":"10.34172/mejdd.2024.397","url":null,"abstract":"<p><strong>Background: </strong>Among environmental factors, infectious agents, including <i>Helicobacter pylori</i>, can act as triggers for autoimmune thyroid diseases. Therefore, this study aimed to investigate the correlation between autoimmune Hashimoto's thyroiditis with <i>H. pylori</i> infection.</p><p><strong>Methods: </strong>The participants in this case-control study were 74 individuals 17-62 years who were divided into two groups, including 38 diagnosed Hashimoto's thyroiditis patients from an outpatient clinic of endocrinology and 36 apparently healthy individuals that were selected from family members of cases group age-matched and sex-matched. For individuals in two groups, a questionnaire was completed, including demographic information. Then, they were referred to the laboratory for thyroid stimulating hormone (TSH) and free T4 (FT4) in the control group and anti-thyroid peroxidase antibody (TPO-Ab) levels measurement in case and control groups. Stool samples were obtained from all individuals for <i>H. pylori</i> antigen detection using the ELIZA kit.</p><p><strong>Results: </strong>There was no significant difference in the mean age of case and control groups (<i>P</i>=0.96), and 81.1% of individuals were female. 58.6% of patients with Hashimoto's thyroiditis and 41.4% of the control group had positive <i>H. pylori</i>, but there was no statistically significant difference between the two groups (<i>P</i>=0.34). Furthermore, there was a significant positive correlation between TPO-Ab levels and <i>H. pylori</i> infection (<i>r</i>=0.2, <i>P</i>=0.03).</p><p><strong>Conclusion: </strong>TPO-Ab levels were associated with <i>H. pylori</i> infection diagnosed by <i>H. pylori</i> antigen.</p>","PeriodicalId":18517,"journal":{"name":"Middle East Journal of Digestive Diseases","volume":"16 4","pages":"230-234"},"PeriodicalIF":0.0,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11725020/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142979070","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
Evaluation of Hematological Parameters as Markers for Subclinical Inflammation in Adults with Familial Mediterranean Fever. 血液学参数作为成人家族性地中海热亚临床炎症标志物的评价。
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.399
Mohamed Gamal Abd Rabou, Ali Mahmoud Ramadan, Ahmed Mohamed Mohsen, Marwa Shawky

Background: Repeated polyserositis, another name for familial Mediterranean fever (FMF), is an autoimmune disorder with an autosomal recessive nature primarily characterized by short-lived repeated periods of peritonitis, pleuritis, and arthritis, generally accompanied by fever.

Methods: Our participants were divided into two groups. Group I (patients): 100 individuals who were diagnosed as patients with FMF and were monitored. Group II (control): matched- healthy individuals (100 controls). They were compared and followed up as regards demographic, clinical, and laboratory data: routine investigations, neutrophil/lymphocyte ratio (NLR), platelet lymphocyte ratio (PLR), and mean platelet volume (MPV), red cell distribution width (RDW), C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR).

Results: Group I: MPV mean was 12.03±2.89, whereas group II MPV mean was 7.74±0.57. MPV was significantly statistically greater in group I than in group II. RDW mean in group I was 17.07±1.39 and in group II was 12.92±0.63. RDW was also significantly statistically greater in group I compared with group II. Group I's NLR mean was 3.05±0.71, whereas group II's NLR mean was 1.75±0.2. PLR mean in group I was 164.8±122.8 and in group II was 111.26±29.16.

Conclusion: A statistically significant association was shown between the diagnosis of adult FMF and NLR, PLR, MPV, and RDW.

背景:重复性多浆液炎是家族性地中海热(FMF)的另一种名称,是一种常染色体隐性的自身免疫性疾病,主要特征为短时间反复发作的腹膜炎、胸膜炎和关节炎,通常伴有发烧。方法:研究对象分为两组。第一组(患者):100名确诊为FMF患者并进行监测的个体。第二组(对照组):匹配健康个体(100例对照)。比较并随访他们的人口学、临床和实验室数据:常规检查、中性粒细胞/淋巴细胞比率(NLR)、血小板淋巴细胞比率(PLR)、平均血小板体积(MPV)、红细胞分布宽度(RDW)、c反应蛋白(CRP)和红细胞沉降率(ESR)。结果:ⅰ组MPV平均值为12.03±2.89,ⅱ组MPV平均值为7.74±0.57。MPV在I组明显高于II组。组平均RDW为17.07±1.39,组平均RDW为12.92±0.63。与II组相比,I组的RDW也有显著的统计学差异。ⅰ组NLR平均值为3.05±0.71,ⅱ组NLR平均值为1.75±0.2。组平均PLR为164.8±122.8,组平均PLR为111.26±29.16。结论:成人FMF的诊断与NLR、PLR、MPV和RDW有统计学意义。
{"title":"Evaluation of Hematological Parameters as Markers for Subclinical Inflammation in Adults with Familial Mediterranean Fever.","authors":"Mohamed Gamal Abd Rabou, Ali Mahmoud Ramadan, Ahmed Mohamed Mohsen, Marwa Shawky","doi":"10.34172/mejdd.2024.399","DOIUrl":"10.34172/mejdd.2024.399","url":null,"abstract":"<p><strong>Background: </strong>Repeated polyserositis, another name for familial Mediterranean fever (FMF), is an autoimmune disorder with an autosomal recessive nature primarily characterized by short-lived repeated periods of peritonitis, pleuritis, and arthritis, generally accompanied by fever.</p><p><strong>Methods: </strong>Our participants were divided into two groups. Group I (patients): 100 individuals who were diagnosed as patients with FMF and were monitored. Group II (control): matched- healthy individuals (100 controls). They were compared and followed up as regards demographic, clinical, and laboratory data: routine investigations, neutrophil/lymphocyte ratio (NLR), platelet lymphocyte ratio (PLR), and mean platelet volume (MPV), red cell distribution width (RDW), C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR).</p><p><strong>Results: </strong>Group I: MPV mean was 12.03±2.89, whereas group II MPV mean was 7.74±0.57. MPV was significantly statistically greater in group I than in group II. RDW mean in group I was 17.07±1.39 and in group II was 12.92±0.63. RDW was also significantly statistically greater in group I compared with group II. Group I's NLR mean was 3.05±0.71, whereas group II's NLR mean was 1.75±0.2. PLR mean in group I was 164.8±122.8 and in group II was 111.26±29.16.</p><p><strong>Conclusion: </strong>A statistically significant association was shown between the diagnosis of adult FMF and NLR, PLR, MPV, and RDW.</p>","PeriodicalId":18517,"journal":{"name":"Middle East Journal of Digestive Diseases","volume":"16 4","pages":"242-249"},"PeriodicalIF":0.0,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11725023/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142979142","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
Developing Mobile Health Applications for Inflammatory Bowel Disease: A Systematic Review of Features and Technologies. 开发炎症性肠病的移动健康应用:特征和技术的系统回顾。
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.394
Parvin Akbarian, Farkhondeh Asadi, Azam Sabahi

Background: Patients with inflammatory bowel disease (IBD) require lifelong treatment, which significantly impacts their quality of life. Self-management of this disease is an effective factor in managing chronic conditions and improving patients' quality of life. The use of mobile applications is a novel approach to providing self-management models and healthcare services for patients with IBD. The present systematic review aimed to identify the features and technologies used in the development of IBD disease management applications.

Methods: This systematic review was conducted according to PRISMA guidelines in PubMed, Scopus, and Web of Sciences databases up to August 8, 2023, which included initial searches, screening studies, assessing eligibility and risk of bias, and study selection. The data extraction form was based on the study objectives, including bibliographic information from articles, such as the first author's name, year of publication, country of origin, and details related to mobile health applications, such as the name of the application, features and technologies used, advantages and disadvantages, main outcomes, and other results. The content of the research was analyzed according to the research objectives.

Results: In the initial review of four databases, a total of 160 articles were retrieved and subsequently entered into EndNote. After removing duplicates and irrelevant studies based on title, abstract, and full-text assessments, 12 articles were finally selected. The studies were conducted between the years 2015 and 2024. 100% of the applications designed for patients with IBD were aimed at treatment, 83% were for self-management of the disease, and 33% of the applications were intended for disease diagnosis. The features of IBD management applications were categorized into four groups: education, monitoring, counseling, and diagnosis and treatment.

Conclusion: Various mobile applications have been developed for the management of IBD, each differing in features and technologies used. While current IBD applications have limited capabilities in diagnosing disease severity, they still hold significant potential in empowering patients through education, counseling, and monitoring. The integration of artificial intelligence and decision support systems may enhance the effectiveness and reliability of these applications.

背景:炎症性肠病(IBD)患者需要终身治疗,这严重影响了他们的生活质量。这种疾病的自我管理是控制慢性疾病和改善患者生活质量的有效因素。使用移动应用程序是一种为IBD患者提供自我管理模式和医疗保健服务的新方法。本系统综述旨在确定IBD疾病管理应用开发中使用的特征和技术。方法:本系统综述根据PRISMA指南在PubMed、Scopus和Web of Sciences数据库中进行,截止到2023年8月8日,包括初始检索、筛选研究、评估合格性和偏倚风险以及研究选择。数据提取表基于研究目标,包括文章的书目信息,如第一作者姓名、出版年份、原产国,以及与移动医疗应用相关的详细信息,如应用名称、使用的功能和技术、优缺点、主要结果和其他结果。根据研究目标对研究内容进行了分析。结果:在4个数据库的初始审查中,共检索到160篇文章,并随后进入EndNote。在根据标题、摘要和全文评估去除重复和不相关的研究后,最终选择了12篇文章。这些研究是在2015年至2024年间进行的。为IBD患者设计的应用程序中,100%用于治疗,83%用于疾病的自我管理,33%用于疾病诊断。IBD管理应用的特点分为四组:教育、监测、咨询、诊断和治疗。结论:已经开发了各种用于IBD管理的移动应用程序,每种应用程序的特点和使用的技术不同。虽然目前IBD应用在诊断疾病严重程度方面的能力有限,但它们在通过教育、咨询和监测增强患者能力方面仍具有巨大潜力。人工智能和决策支持系统的集成可以提高这些应用的有效性和可靠性。
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引用次数: 0
Ulcerative and Cytomegalovirus Colitis Associated with Fournier's Gangrene: A Case Report. 溃疡性巨细胞病毒结肠炎合并富尼耶坏疽1例。
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.401
Ali Berkcan Bozdogan, Gamze Sonmez, Erke Baytok, Goksel Guven, Bengi Ozturk

Fournier gangrene is a rare but severe complication of ulcerative colitis, characterized by necrotizing fasciitis affecting the genital and perineal regions. We present a case of a 53-year-old man with a history of ulcerative colitis and cytomegalovirus (CMV) colitis who developed Fournier gangrene, an exceptionally uncommon occurrence in this patient population. The patient initially presented with intense pain, swelling, and skin discoloration in the genital area, accompanied by systemic symptoms, including fever. Prompt recognition and intervention are critical due to the aggressive nature of Fournier gangrene, which often results in significant morbidity and mortality. This case underscores the importance of vigilance for unusual presentations of necrotizing infections in patients with inflammatory bowel disease (IBD), particularly those with complicating factors such as immunosuppression and concurrent infections.

富尼尔坏疽是一种罕见但严重的溃疡性结肠炎并发症,其特征是坏死性筋膜炎影响生殖器和会阴区域。我们报告一例53岁男性溃疡性结肠炎和巨细胞病毒(CMV)结肠炎病史,并发富尼耶坏疽,这在该患者群体中非常罕见。患者最初表现为生殖器区域剧烈疼痛、肿胀和皮肤变色,并伴有全身症状,包括发烧。由于富尼耶坏疽的侵袭性,它经常导致显著的发病率和死亡率,因此及时识别和干预至关重要。本病例强调了对炎症性肠病(IBD)患者异常表现的坏死性感染保持警惕的重要性,特别是那些伴有免疫抑制和并发感染等并发症的患者。
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引用次数: 0
Multifocal Gastric Granular Cell Tumor: A Case Report. 胃多灶性颗粒细胞瘤1例报告。
Q3 Medicine Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI: 10.34172/mejdd.2024.400
Samira Saeian, Kamran B Lankarani, Mohammad Hossein Anbardar, Seyed Majid Ahmadi

Granular cell tumors (GCTs) of the gastrointestinal tract are rare neoplasms often detected incidentally as subepithelial lesions during endoscopic examination. The occurrence of GCTs in the gastric cavity is even rarer. So far, there have been only four reports of multifocal gastric GCTs. Our study presents the fifth case involving a middle-aged lady with incidental multifocal gastric GCT. It is the first such case reported in West Asia.

胃肠道颗粒细胞瘤(gct)是一种罕见的肿瘤,通常在内镜检查时被偶然发现为上皮下病变。胃腔gct的发生更为罕见。到目前为止,只有4例多灶胃gct的报道。我们的研究提出了第五例涉及一位中年妇女偶发多灶性胃GCT。这是西亚报告的首例此类病例。
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引用次数: 0
Circulating MicroRNAs and Cytokines Associated with Celiac Disease. 与乳糜泻相关的循环微RNA和细胞因子
Q3 Medicine Pub Date : 2024-07-01 Epub Date: 2024-07-31 DOI: 10.34172/mejdd.2024.388
Dargham Hammad, Fadyia Mahdi Muslim Alameedy

Background: The current research examines the molecular terrain of celiac disease (CD) through microRNA (miRNA) and cytokines as potential new diagnostic and therapeutic markers. Gluten-appropriate immune response is a key feature of an autoimmune clinical entity known as CD that leads to inflammation and degeneration of small intestine mucosa. However, the mechanisms responsible for this remain unclear.

Methods: Quantitative reverse transcription polymerase chain reaction (RT-qPCR ) was carried out on serum samples obtained from patients with CD and control groups to unravel their pathogenesis. Assessing miR-155, miR-15b, interleukin (IL)-2, IL-7, IL-35and IL-37 levels in expression might be useful in diagnosing or treating the disorder.

Results: A significant dysregulation of these molecular players in patients with CD compared with healthy controls has been evidenced by results from this study. For instance, miR-155 was up-regulated, whereas miR-15b was significantly down-regulated in CD, illustrating their roles in immune responses and inflammation-mediated processes. Besides, there was an over-expression of IL-2 and an under-expression of IL-37 in patients with CD, indicating these biomolecules' role in immuno-dysregulation and inflammatory process underlying CD. In addition, a positive correlation between IL-2 and miRNA 155 expression levels was observed in patients with CD, suggesting that they could be involved together with other cytokines, showing the interplay between immune response pathways and inflammatory cascades during CD pathogenesis.

Conclusion: These molecular signature discoveries might result in new and revolutionary diagnostic modalities and molecular-targeted therapies for CD pathogenesis. When used with the scientific understanding of miRNAs and cytokines associated with CD pathophysiology, it creates a basis for personalized medicine based on the individualized molecular profile of all patients. This will undoubtedly increase the efficacy of CD treatment strategies. In brief, more research on molecular pathways' workings should be done to harness their potential in CD diagnosis and treatment.

背景:目前的研究通过微小核糖核酸(miRNA)和细胞因子作为潜在的新诊断和治疗标记物,对乳糜泻(CD)的分子地形进行了研究。麸质适当的免疫反应是被称为 CD 的自身免疫性临床实体的一个关键特征,它会导致小肠粘膜的炎症和变性。然而,造成这种情况的机制仍不清楚:方法:对 CD 患者和对照组的血清样本进行定量反转录聚合酶链反应(RT-qPCR),以揭示其发病机制。评估 miR-155、miR-15b、白细胞介素(IL)-2、IL-7、IL-35 和 IL-37 的表达水平可能有助于诊断或治疗该疾病:结果:与健康对照组相比,CD 患者体内这些分子角色的表达明显失调。例如,在 CD 患者中,miR-155 上调,而 miR-15b 则显著下调,这说明了它们在免疫反应和炎症介导过程中的作用。此外,IL-2 在 CD 患者中表达过高,而 IL-37 则表达过低,这表明这些生物大分子在 CD 的免疫调节和炎症过程中起着重要作用。此外,在 CD 患者中观察到 IL-2 和 miRNA 155 的表达水平呈正相关,表明它们可能与其他细胞因子一起参与其中,显示了 CD 发病过程中免疫反应途径和炎症级联之间的相互作用:这些分子特征的发现可能会为 CD 的发病机制带来革命性的新诊断模式和分子靶向疗法。通过对与 CD 病理生理学相关的 miRNA 和细胞因子的科学认识,可为基于所有患者个体化分子特征的个性化医疗奠定基础。这无疑将提高 CD 治疗策略的疗效。简而言之,我们应该对分子通路的工作原理进行更多的研究,以挖掘其在 CD 诊断和治疗中的潜力。
{"title":"Circulating MicroRNAs and Cytokines Associated with Celiac Disease.","authors":"Dargham Hammad, Fadyia Mahdi Muslim Alameedy","doi":"10.34172/mejdd.2024.388","DOIUrl":"10.34172/mejdd.2024.388","url":null,"abstract":"<p><strong>Background: </strong>The current research examines the molecular terrain of celiac disease (CD) through microRNA (miRNA) and cytokines as potential new diagnostic and therapeutic markers. Gluten-appropriate immune response is a key feature of an autoimmune clinical entity known as CD that leads to inflammation and degeneration of small intestine mucosa. However, the mechanisms responsible for this remain unclear.</p><p><strong>Methods: </strong>Quantitative reverse transcription polymerase chain reaction (RT-qPCR ) was carried out on serum samples obtained from patients with CD and control groups to unravel their pathogenesis. Assessing miR-155, miR-15b, interleukin (IL)-2, IL-7, IL-35and IL-37 levels in expression might be useful in diagnosing or treating the disorder.</p><p><strong>Results: </strong>A significant dysregulation of these molecular players in patients with CD compared with healthy controls has been evidenced by results from this study. For instance, miR-155 was up-regulated, whereas miR-15b was significantly down-regulated in CD, illustrating their roles in immune responses and inflammation-mediated processes. Besides, there was an over-expression of IL-2 and an under-expression of IL-37 in patients with CD, indicating these biomolecules' role in immuno-dysregulation and inflammatory process underlying CD. In addition, a positive correlation between IL-2 and miRNA 155 expression levels was observed in patients with CD, suggesting that they could be involved together with other cytokines, showing the interplay between immune response pathways and inflammatory cascades during CD pathogenesis.</p><p><strong>Conclusion: </strong>These molecular signature discoveries might result in new and revolutionary diagnostic modalities and molecular-targeted therapies for CD pathogenesis. When used with the scientific understanding of miRNAs and cytokines associated with CD pathophysiology, it creates a basis for personalized medicine based on the individualized molecular profile of all patients. This will undoubtedly increase the efficacy of CD treatment strategies. In brief, more research on molecular pathways' workings should be done to harness their potential in CD diagnosis and treatment.</p>","PeriodicalId":18517,"journal":{"name":"Middle East Journal of Digestive Diseases","volume":"16 3","pages":"185-192"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11459281/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142391721","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}
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Middle East Journal of Digestive Diseases
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