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Intra- and peri-meniscal polynucleotide injections for the treatment of symptomatic degenerative meniscus of the knee: 1-year findings from a prospective clinical trial. 半月板内和半月板周围注射多核苷酸治疗膝关节症状性退行性半月板:1年前瞻性临床试验结果
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-06-01 DOI: 10.26355/eurrev_202506_37273
G Anzillotti, P Conte, E M Bertolino, A Ferrero, B Di Matteo, M Vacca, M Di Martino, D Altomare, N Magarelli, E Lanza, P Verdonk, E Kon

OBJECTIVE: Degenerative meniscal lesions consist of an alteration of the meniscal structure, eventually leading to pain and dysfunction. In the absence of mechanical symptoms, meniscectomy should be considered the last resort. Polynucleotides represent a novel treatment option which have shown promising results in different fields, including knee osteoarthritis. Hence, this study aimed to evaluate the safety and efficacy of a cycle of intra- and peri-meniscal polynucleotide injections for the treatment of degenerative meniscus. MATERIALS AND METHODS: This prospective study included 30 patients aged 25-65 with degenerative meniscal tears confirmed by MRI. Eligible patients were treated with three intra- and peri-meniscal injections of polynucleotides, administered with a two-week time interval under ultrasound guidance. The primary outcome was improvement in the overall Knee Injury and Osteoarthritis Outcome Score (KOOS) by at least 10 points from baseline to 12-month follow-up. Secondary outcomes included Visual Analog Scale (VAS) for pain, the International Knee Documentation Committee (IKDC) score, and the Tegner Activity Scale. Safety was assessed through the monitoring of adverse events. RESULTS: Twenty-four patients completed the 12-month follow-up. KOOS scores showed a statistically significant improvement from a mean of 61.99 at baseline to 84.32 at 12 months [95% CI: (79.25, 89.4); p<0.001]. VAS mm scores also decreased significantly, from 62.68 at baseline to 20.63 at 12 months [95% CI, (12.84, 28.41), p<0.001]. Improvements in IKDC and Tegner scores were observed but plateaued after 6 months. No adverse events were reported throughout the entire study period. CONCLUSIONS: A cycle of three intra- and peri-meniscal poly-nucleotides injections is able to provide statistically significant improvements in clinical scores up to 1 year of follow-up in patients affected by symptomatic degenerative meniscus of the knee.

Graphical abstract: https://www.europeanreview.org/wp/wp-content/uploads/Graphical-abstract-1-2.jpg.

目的:退行性半月板病变包括半月板结构的改变,最终导致疼痛和功能障碍。在没有机械症状的情况下,半月板切除术应被认为是最后的手段。多核苷酸代表了一种新的治疗选择,在不同的领域显示出有希望的结果,包括膝关节骨关节炎。因此,本研究旨在评估半月板内和半月板周围注射周期多核苷酸治疗退行性半月板的安全性和有效性。材料和方法:这项前瞻性研究包括30例年龄在25-65岁之间,经MRI证实患有退行性半月板撕裂的患者。符合条件的患者接受三次半月板内和半月板周围注射多核苷酸,在超声引导下间隔两周给药。主要结局是总体膝关节损伤和骨关节炎结局评分(oos)从基线到12个月随访至少改善10分。次要结果包括疼痛的视觉模拟量表(VAS)、国际膝关节文献委员会(IKDC)评分和Tegner活动量表。通过监测不良事件来评估安全性。结果:24例患者完成了12个月的随访。KOOS评分从基线时的平均61.99分改善到12个月时的平均84.32分[95% CI:(79.25, 89.4);图形摘要:https://www.europeanreview.org/wp/wp-content/uploads/Graphical-abstract-1-2.jpg。
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引用次数: 0
Expression of Concern. 表达关心。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-06-01 DOI: 10.26355/eurrev_202506_37270
N Authors Listed
<p><p>The Publisher, in agreement with the Editor-in-Chief, is issuing this Expression of Concern to inform readers that a formal investigation is currently underway regarding a set of published articles. Despite multiple attempts to contact the corresponding authors, we have not received any response to date. Further editorial actions, such as retraction or correction, will be taken as appropriate in due course. The articles under investigation fall into the following categories. These studies report extended follow-up periods, yet were published prior to the actual conclusion of the declared follow-up. This discrepancy raises serious concerns about the validity of the timeline and outcome reporting: Liao Y, Cheng S, Xiang J, Luo C. lncRNA CCHE1 increased proliferation, metastasis and invasion of non-small lung cancer cells and predicted poor survival in non-small lung cancer patients. Eur Rev Med Pharmacol Sci. 2018 Mar;22(6):1686-1692. doi: 10.26355/eurrev_201803_14581. PMID: 29630113. Yao N, Sun JQ, Yu L, Ma L, Guo BQ. LINC00968 accelerates the progression of epithelial ovarian cancer via mediating the cell cycle progression. Eur Rev Med Pharmacol Sci. 2019 Jun;23(11):4642-4649. doi: 10.26355/eurrev_201906_18043. PMID: 31210289. Hao XZ, Yang K. LncRNA MAGI2-AS3 suppresses the proliferation and invasion of non-small cell lung carcinoma through miRNA-23a-3p/PTEN axis. Eur Rev Med Pharmacol Sci. 2019 Sep;23(17):7399-7407. doi: 10.26355/eurrev_201909_18848. PMID: 31539127. Jiang J, Wu RH, Zhou HL, Li ZM, Kou D, Deng Z, Dong M, Chen LH. TGIF2 promotes cervical cancer metastasis by negatively regulating FCMR. Eur Rev Med Pharmacol Sci. 2020 Jun;24(11):5953-5962. doi: 10.26355/eurrev_202006_21488. PMID: 32572908. These articles have been questioned as they appear to reuse identical or similar graphical elements and images from a shared library across multiple unrelated studies: Xu CF, Liu P, Tan J, Hu DF. Long noncoding RNA LINC00052 suppressed the proliferation, migration and invasion of glioma cells by upregulating KLF6. Eur Rev Med Pharmacol Sci. 2019 Jun;23(11):4822-4827. doi: 10.26355/eurrev_201906_18068. PMID: 31210314. Zheng FX, Wang XQ, Zheng WX, Zhao J. Long noncoding RNA HOXA-AS2 promotes cell migration and invasion via upregulating IGF-2 in non-small cell lung cancer as an oncogene. Eur Rev Med Pharmacol Sci. 2019 Jun;23(11):4793-4799. doi: 10.26355/eurrev_201906_18064. PMID: 31210310.Liao J, Xie N. Long noncoding RNA DSCAM-AS1 functions as an oncogene in non-small cell lung cancer by targeting BCL11A. Eur Rev Med Pharmacol Sci. 2019 Feb;23(3):1087-1092. doi: 10.26355/eurrev_201902_16998. PMID: 30779076. Lu J, Xu FQ, Guo JJ, Lin PL, Meng Z, Hu LG, Li J, Li D, Lu XH, An Y. Long noncoding RNA GAS5 attenuates cardiac fibroblast proliferation in atrial fibrillation via repressing ALK5. Eur Rev Med Pharmacol Sci. 2019 Sep;23(17):7605-7610. doi: 10.26355/eurrev_201909_18883. PMID: 31539152. Shi JQ, Wang B, Cao XQ, Wang YX, Cheng
在主编的同意下,出版商发布此关注声明,通知读者,目前正在对一系列已发表的文章进行正式调查。尽管我们多次尝试联系通讯作者,但至今未收到任何回复。我们将在适当的时候采取进一步的编辑行动,如撤回或更正。被调查的物品可分为以下几类。这些研究报告了较长的随访期,但在宣布的随访实际结束之前发表。这一差异引起了人们对时间线和结果报告有效性的严重关注:廖莹,程生,向杰,罗超。lncRNA CCHE1增加非小细胞肺癌细胞的增殖、转移和侵袭,并预测非小细胞肺癌患者的生存率较差。中华医学杂志,2018;22(6):1686-1692。doi: 10.26355 / eurrev_201803_14581。PMID: 29630113。姚宁,孙建强,于磊,马磊,郭宝强。LINC00968通过介导细胞周期进程加速上皮性卵巢癌的进展。中华医学杂志,2019;23(11):4642-4649。doi: 10.26355 / eurrev_201906_18043。PMID: 31210289。郝晓贞,杨凯。LncRNA MAGI2-AS3通过miRNA-23a-3p/PTEN轴抑制非小细胞肺癌的增殖和侵袭。医药科学进展,2019;23(17):7399-7407。doi: 10.26355 / eurrev_201909_18848。PMID: 31539127。姜军,吴荣荣,周海龙,李志明,寇东,邓志,董明,陈丽玲。TGIF2通过负调控FCMR促进宫颈癌转移。中华医学杂志,2014;24(11):5953-5962。doi: 10.26355 / eurrev_202006_21488。PMID: 32572908。这些文章受到质疑,因为它们似乎在多个不相关的研究中重用了来自共享库的相同或相似的图形元素和图像:徐长鹏,刘鹏,谭杰,胡德芳。长链非编码RNA LINC00052通过上调KLF6抑制胶质瘤细胞的增殖、迁移和侵袭。中华医学杂志,2019;23(11):4822-4827。doi: 10.26355 / eurrev_201906_18068。PMID: 31210314。郑凤霞,王小强,郑文霞,赵军。龙非编码RNA HOXA-AS2作为癌基因通过上调IGF-2促进非小细胞肺癌细胞迁移和侵袭。中华医学杂志,2019;23(11):4793-4799。doi: 10.26355 / eurrev_201906_18064。PMID: 31210310。廖静,谢宁。长非编码RNA DSCAM-AS1靶向BCL11A在非小细胞肺癌中的作用。医药科学进展,2019;23(3):1087-1092。doi: 10.26355 / eurrev_201902_16998。PMID: 30779076。吕军,徐凤青,郭建军,林普乐,胡丽珍,李军,李东,卢晓华,安勇。长链非编码RNA GAS5通过抑制ALK5抑制心房颤动的心脏成纤维细胞增殖。医药科学进展,2019;23(17):7605-7610。doi: 10.26355 / eurrev_201909_18883。PMID: 31539152。石建强,王斌,曹小强,王云云,程霞,贾春林,温涛,罗炳军,刘志东。环状RNA_LARP4通过调节SMAD7的表达抑制非小细胞肺癌的进展。欧洲医学与药物科学,2020年2月;24(4):1863-1869。doi: 10.26355 / eurrev_202002_20364。PMID: 32141555。崔凯,张宏,王广光。MiR-483在乳腺癌中通过靶向SOX3抑制细胞增殖,促进细胞凋亡。医药科学进展,2019;23(5):2069-2074。doi: 10.26355 / eurrev_201903_17248。PMID: 30915751。任磊,翟辉,王晓林,李建中,夏玉华。Hsa_circ_0011946通过诱导EMT过程促进肝癌的迁移和侵袭。医药科学,2020;24(3):1108-1115。doi: 10.26355 / eurrev_202002_20161。PMID: 32096173。引用本文:陈瑞霞,刘海龙,杨丽丽,康红华,辛丽萍,黄立荣,郭启峰,王玉玲。环状RNA circRNA_0000285通过调控FUS促进宫颈癌的发展。医药科学进展,2019;23(20):8771-8778。doi: 10.26355 / eurrev_201910_19271。PMID: 31696463。刘涛,王伟,徐玉春,李志伟,周军。龙非编码RNA NEAT1靶向miR-29a-3p在人喉癌中的致癌作用。中华医学杂志,2019;23(14):6234-6241。doi: 10.26355 / eurrev_201907_18442。PMID: 31364125。长非编码RNA XIST通过海绵介导miR-200b-3p促进肝癌进展。医药科学进展,2019;23(22):9857-9862。doi: 10.26355 / eurrev_201911_19549。PMID: 31799653。翁晓东,严涛,刘春林。环状RNA_LARP4通过靶向FOXO3A抑制前列腺癌细胞迁移和侵袭。中华医学杂志,2020;24(10):5303-5309。doi: 10.26355 / eurrev_202005_21312。PMID: 32495863。何学勇,潘晓明,金敏,杨玉玲,杨志强,闫东,马建新。长链非编码RNA AK027294通过上调胃癌PCNA促进肿瘤生长。中华医学杂志,2019;23(13):5762-5769。doi: 10.26355 / eurrev_201907_18314。PMID: 31298327。王艳华,霍宝玲,李超,马刚,曹伟。 低敲长链非编码RNA SNHG7通过下调BDNF抑制甲状腺癌细胞增殖并促进细胞凋亡。中华医学杂志,2019;23(11):4815-4821。doi: 10.26355 / eurrev_201906_18067。PMID: 31210313。杨振涛,安芳,胡建东,赵文辉。长链非编码RNA AFAP1-AS1通过抑制RBM5的表达加速前列腺癌的增殖和转移。医药科学进展,2019;23(8):3284-3290。doi: 10.26355 / eurrev_201904_17690。PMID: 31081081。引用本文:马丽丽,谢晓文,马丽,庞建林,熊晓明,郑海华,沈晓玲,文志刚,王海燕。下调长链非编码RNA TRPM2-AS通过激活p53- p66shc通路抑制非小细胞肺癌细胞顺铂耐药。中华医学杂志,2017;21(11):2626-2634。PMID: 28678322。以下出版物因在大量文章中显示反复出现的结构模式和视觉内容(如Kaplan-Meier图、相关图等)而受到质疑:Li XF, Aierken AL, Shen L. IPO5通过激活MMP7促进食管癌的恶性进展。中华医学杂志,2020,24(8):446 -4254。doi: 10.26355 / eurrev_202004_21004。PMID: 32373960。高伟,杨刚,王军,何建明,王鹏。CSN6下调TIM
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引用次数: 0
Exploring nutraceutical solutions for prediabetes: a narrative review on the effects of banaba and chromium picolinate. 探索糖尿病前期的营养解决方案:对香蕉和吡啶甲酸铬的影响的叙述综述。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-06-01 DOI: 10.26355/eurrev_202506_37275
G Derosa, P Maffioli, A D'Angelo, V Foscaldi, R Piazza, M Mangrella, F Fogacci, A F G Cicero

Prediabetes is an intermediary metabolic state marked by impaired glucose control, often preceding the development of type 2 diabetes (T2D). Early detection of prediabetes and intervention are critical to prevent the progression to T2D and its associated complications. This review examines the effects of nutraceuticals on regulating metabolism, with a focus on glucose control, specifically chromium picolinate (CrP) and banaba leaf extract. CrP has been extensively studied, and its role in regulating metabolism has been officially recognized. Preclinical research demonstrates its ability to improve glucose control by enhancing insulin sensitivity. These effects explain the reductions in fasting plasma glucose, elevated hemoglobin A1c, and insulin levels observed in clinical studies, particularly in patients with T2D. Banaba (Lagerstroemia speciosa) leaf extract, rich in corosolic acid and ellagitannins, has also shown promising results in improving glycemic control. As observed in preclinical studies, both banaba extract and corosolic acid exert insulin-sensitizing, glucose-lowering, and lipid-lowering properties. Clinical trials have confirmed these effects in individuals with T2D and prediabetes. Based on this evidence, combining CrP and banaba leaf extract may offer synergistic benefits in managing dysglycemia and delaying the onset of T2D in individuals with prediabetes. Only one study has evaluated the effects of the CrP and banaba extract combination, showing positive outcomes in individuals with prediabetes. Further research is needed to corroborate these preliminary findings. In conclusion, nutraceuticals like CrP and banaba leaf extract hold promise as complementary therapies to be used alongside lifestyle modifications for individuals with prediabetes.

Graphical abstract: https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-1-1-scaled.jpg.

前驱糖尿病是一种中间代谢状态,以葡萄糖控制受损为标志,通常在2型糖尿病(T2D)发展之前。糖尿病前期的早期发现和干预对于预防t2dm及其相关并发症的进展至关重要。本文综述了营养保健品在调节代谢方面的作用,重点是葡萄糖控制,特别是吡啶甲酸铬(CrP)和香蕉叶提取物。CrP已被广泛研究,其在调节代谢中的作用已被正式认可。临床前研究表明,它能够通过增强胰岛素敏感性来改善血糖控制。这些影响解释了临床研究中观察到的空腹血糖降低、糖化血红蛋白升高和胰岛素水平降低,特别是在糖尿病患者中。香蕉(Lagerstroemia speciosa)叶提取物富含花椰树酸和鞣花单宁,在改善血糖控制方面也有很好的效果。在临床前研究中观察到,香蕉提取物和科罗索酸都具有胰岛素增敏、降血糖和降脂的特性。临床试验证实了这些作用在T2D和前驱糖尿病患者身上。基于这一证据,将CrP和香蕉叶提取物联合使用可能在糖尿病前期患者控制血糖异常和延迟T2D发作方面提供协同效益。只有一项研究评估了CrP和香蕉提取物组合的效果,显示出对糖尿病前期患者的积极效果。需要进一步的研究来证实这些初步发现。总之,像c蛋白和香蕉叶提取物这样的营养保健品有望作为补充疗法,与改变生活方式一起用于糖尿病前期患者。图形摘要:https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-1-1-scaled.jpg。
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引用次数: 0
Prognostic role of miR-190, miR-221, and miR-381 in breast cancer: a systematic review and meta-analysis. miR-190、miR-221和miR-381在乳腺癌中的预后作用:一项系统综述和荟萃分析
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-06-01 DOI: 10.26355/eurrev_202506_37272
S Matsas, A Ruiz Simões, P Nazareth Aguiar, Y Abdou, H Krontiras, A Del Giglio

OBJECTIVE: Breast cancer is the most frequently diagnosed malignancy in women and a leading cause of cancer-related mortality. Conventional prognostic tools may not fully capture disease outcomes. MicroRNA (miR) expression has emerged as a potential prognostic factor, though findings remain inconsistent. This systematic review and meta-analysis assess the prognostic role of miR-190, miR-221, and miR-381 in predicting overall survival (OS) among breast cancer patients. MATERIALS AND METHODS: A comprehensive literature search in PubMed, Embase, and Scopus identified relevant studies. Pooled hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to assess the relationship between miR expression and OS. Subgroup analyses were conducted to explore potential sources of heterogeneity. RESULTS: Four studies on miR-221, four on miR-190, and three on miR-381 met inclusion criteria. High miR-190 expression was significantly associated with improved OS (HR: 0.63; 95% CI: 0.47-0.84), as was miR-381 (HR: 0.64; 95% CI: 0.52-0.79). No significant association was found between miR-221 expression and OS (HR: 1.12; 95% CI: 0.86-1.46). Subgroup analysis reinforced these findings, and Newcastle-Ottawa scale assessment indicated low publication bias in 10 out of 11. CONCLUSIONS: Elevated miR-190 and miR-381 levels are associated with improved OS in breast cancer, whereas the prognostic role of miR-221 remains unclear. These findings underscore the potential of miR-190 and miR-381 as prognostic biomarkers.

Graphical abstract: https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-18-scaled.jpg.

目的:乳腺癌是女性中最常见的恶性肿瘤,也是癌症相关死亡的主要原因。传统的预后工具可能无法完全捕捉疾病的结果。MicroRNA (miR)表达已成为潜在的预后因素,尽管研究结果仍不一致。本系统综述和荟萃分析评估了miR-190、miR-221和miR-381在预测乳腺癌患者总生存期(OS)中的预后作用。材料和方法:在PubMed, Embase和Scopus中进行综合文献检索,确定相关研究。计算合并风险比(hr)和95%置信区间(ci)来评估miR表达与OS之间的关系。进行亚组分析以探索异质性的潜在来源。结果:4项关于miR-221的研究,4项关于miR-190的研究,3项关于miR-381的研究符合纳入标准。miR-190高表达与OS改善显著相关(HR: 0.63;95% CI: 0.47-0.84), miR-381也是如此(HR: 0.64;95% ci: 0.52-0.79)。miR-221表达与OS无显著相关性(HR: 1.12;95% ci: 0.86-1.46)。亚组分析强化了这些发现,纽卡斯尔-渥太华量表评估显示,11篇文章中有10篇的发表偏倚较低。结论:miR-190和miR-381水平升高与乳腺癌OS改善相关,而miR-221在预后中的作用尚不清楚。这些发现强调了miR-190和miR-381作为预后生物标志物的潜力。图形摘要:https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-18-scaled.jpg。
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引用次数: 0
Brain morphology alterations in adult males with stuttering disorder in Saudi Arabia: a pilot study. 沙特阿拉伯患有口吃障碍的成年男性的脑形态学改变:一项初步研究。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-05-01 DOI: 10.26355/eurrev_202505_37226
M Alqarni, A Abujamea, A Almudhi, S Bashir

OBJECTIVE: The neurophysiological and neuroanatomical alterations underlying brain morphology in adult males who stutter remain insufficiently understood. This study aimed to determine whether individuals who stutter exhibit structural differences in frontal brain regions associated with somatosensory and motor systems critical for speech production. MATERIALS AND METHODS: The study protocol was approved by the Institutional Review Board of King Saud University (KSU). A total of 54 adult male participants [27 stutterers (ST) and 27 non-stutterers (NST)], aged 18-55 years, were enrolled. A certified speech-language pathologist assessed all participants using the validated Stuttering Severity Instrument-4 (SSI-4). High-resolution T1-weighted magnetic resonance imaging (MRI) scans (SAG T1 3D MP-RAGE sequence) were acquired using a Siemens Skyra 3.0T scanner at the Department of Medical Imaging, KSU Medical City, Riyadh. RESULTS: Compared to NST participants, individuals in the ST group showed significant volumetric alterations in the left precentral gyrus, right superior frontal gyrus, and right middle frontal gyrus. Additional significant differences were observed in the left middle frontal gyrus, left inferior frontal gyrus pars opercularis, left inferior frontal gyrus pars triangularis, left inferior frontal gyrus, left precuneus, left pole of the superior temporal white matter, and left insular cortex. These regions demonstrated consistent structural differences between ST and NST participants, suggesting a robust association between stuttering and abnormal morphology in frontal and related cortical areas. CONCLUSIONS: These findings provide evidence of structural abnormalities in frontal brain regions implicated in the regulation of somatosensory and motor processes essential for speech production. This supports the hypothesis that stuttering is associated with disrupted neuroanatomical organization in key speech-related cortical networks.

Graphical abstract: https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-17.jpg.

目的:成年男性口吃患者脑形态的神经生理和神经解剖学改变尚不清楚。这项研究的目的是确定口吃的个体在与体感和运动系统相关的大脑额叶区域是否表现出结构上的差异,这些系统对语言的产生至关重要。材料和方法:研究方案由沙特国王大学(KSU)机构审查委员会批准。共纳入54名成年男性参与者[27名口吃者(ST)和27名非口吃者(NST)],年龄18-55岁。一位经过认证的语言病理学家使用经过验证的口吃严重程度量表-4 (SSI-4)对所有参与者进行评估。高分辨率T1加权磁共振成像(MRI)扫描(SAG T1 3D MP-RAGE序列)使用利雅得KSU医学城医学成像部的西门子Skyra 3.0T扫描仪。结果:与NST参与者相比,ST组的个体在左侧中央前回、右侧额上回和右侧额中回中表现出显著的体积变化。另外,在左侧额中回、左侧额下回小叶部、左侧额下回三角部、左侧额下回、左侧楔前叶、左侧颞上白质极和左侧岛叶皮层也观察到显著差异。这些区域在ST和NST参与者之间显示出一致的结构差异,表明口吃与额叶和相关皮质区域的异常形态之间存在密切联系。结论:这些发现为大脑额叶区域的结构异常提供了证据,这些结构异常与语言产生所必需的体感和运动过程的调节有关。这支持了一种假设,即口吃与关键语言相关皮层网络的神经解剖组织紊乱有关。图形摘要:https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-17.jpg。
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引用次数: 0
Retraction note: Effect of exosome-carried miR-30a on myocardial apoptosis in myocardial ischemia-reperfusion injury rats through regulating autophagy. 缩回注:外泌体携带miR-30a通过调节心肌自噬对心肌缺血再灌注损伤大鼠心肌凋亡的影响。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-05-01 DOI: 10.26355/eurrev_202505_37233
Y-Q Xu, Y Xu, S-H Wang

The article "Effect of exosome-carried miR-30a on myocardial apoptosis in myocardial ischemia-reperfusion injury rats through regulating autophagy" by Y.-Q. Xu, Y. Xu, S.-H. Wang, published in Eur Rev Med Pharmacol Sci 2019; 23 (16): 7066-7072-DOI: 10.26355/eurrev_201908_18748-PMID: 31486507 has been retracted in accordance with the Publisher and the Editor in Chief. Following some concerns raised by a third party regarding possible overlaps and duplication in the Figures, the journal has started an investigation to assess the validity of the concerns, as well as a possible Figure manipulation. The journal's investigation revealed a duplication between panels Model and miR-30a inhibitor of Figure 1. Therefore, the manuscript is retracted due to figure duplication. The journal has contacted the authors to inform them of the ongoing investigation and to request the original data supporting the manuscript; however, the authors have not responded to these communications. This article has been retracted. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/18748.

外泌体携带miR-30a通过调节自噬对心肌缺血再灌注损伤大鼠心肌凋亡的影响徐,y,徐,s - h。Wang,发表于《Eur Rev Med Pharmacol Sci 2019》;23 (16): 7066-7072-DOI: 10.26355/eurrev_201908_18748-PMID: 31486507已根据出版商和主编的要求撤回。由于第三方提出了一些关于图表中可能存在的重叠和重复的担忧,该杂志已经开始调查以评估这些担忧的有效性,以及可能的图表操纵。该杂志的调查揭示了图1中面板模型和miR-30a抑制剂之间的重复。因此,由于数字重复,稿件被撤回。期刊已经联系了作者,告知他们正在进行的调查,并要求他们提供支持论文的原始数据;然而,作者没有对这些来文作出回应。这篇文章已被撤回。对于由此造成的任何不便,出版商深表歉意。https://www.europeanreview.org/article/18748。
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引用次数: 0
Dapagliflozin enhances systolic and diastolic function in concordance with clinical response in patients with left ventricular dysfunction. 达格列净增强左心室功能不全患者的收缩和舒张功能与临床反应一致。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-05-01 DOI: 10.26355/eurrev_202505_37222
A E Abou Warda, J D Duarte, M Nabil Salem, H F Salem, A N Moharram, A S Alanazi, A I Alzarea, T G Alsahli, H Sultan, M A Alrashdi, A F Altebainawi, B Emil Ibrahim, S Ibrahim Alnahrawi, K Kamel Megalaa, B Zarif, R M Sarhan

OBJECTIVE: Sodium-glucose co-transporter-2 (SGLT2) inhibitors have reshaped heart failure (HF) management. However, evidence regarding their effects on cardiac structure, particularly for dapagliflozin, remains inconsistent. This study evaluates dapagliflozin's impact on echocardiographic parameters and its concordance with clinical response. MATERIALS AND METHODS: A prospective, randomized controlled study included HF patients with left ventricular (LV) dysfunction, divided into dapagliflozin-treated and dapagliflozin-naïve groups. Echocardiography and speckle-tracking strain analysis were conducted at baseline and six months. The primary outcome was the change in indexed LV mass. Secondary outcomes included LV function, volumes, dimensions, functional mitral regurgitation, global longitudinal strain (GLS), diastolic function, right ventricular (RV) function, and clinical response assessed using the Kansas City Cardiomyopathy Questionnaire (KCCQ) score. RESULTS: Among 240 participants, 160 received dapagliflozin in addition to guideline-directed medical therapy, while 80 were dapagliflozin-naïve. Adjusted regression analysis showed significant improvements in LV mass index (-43.51 g/m², 95% CI: -59.4 to -27.5, p < 0.0001), end-systolic volume (-29.45 mL, 95% CI: -43.9 to -14.9, p < 0.0001), and end-diastolic volume (-29.44 mL, 95% CI: -47.9 to -10.9, p = 0.0021). Improvements were also observed in LV ejection fraction (5.15%, 95% CI: 2.84 to 7.45, p < 0.0001), GLS (-1.99%, 95% CI: -2.87 to -1.11, p < 0.0001), E/A ratio (-0.56, 95% CI: -1.01 to -0.10, p = 0.016), effective regurgitant orifice area (EROA) (-0.18 cm², 95% CI: -0.28 to -0.081, p = 0.0006), tricuspid annular plane systolic excursion (TAPSE) (0.38 cm, 95% CI: 0.15 to 0.62, p = 0.0024), and composite clinical outcome (HR 0.65, 95% CI: 0.43-0.98, p = 0.043). LVEF, GLS, E/A ratio, TAPSE, inferior vena cava diameter, and left atrial area correlated with clinical response. CONCLUSIONS: Dapagliflozin emerges as a potential therapy for patients with left ventricular dysfunction, enhancing LV systolic function and diastolic performance, alongside a favorable clinical response. Future studies with more extensive assessment of right ventricular function and longer follow-up are warranted.

Graphical abstract: https://www.europeanreview.org/wp/wp-content/uploads/abstract.jpg.

目的:钠-葡萄糖共转运蛋白-2 (SGLT2)抑制剂重塑心力衰竭(HF)的管理。然而,关于它们对心脏结构的影响,特别是对达格列净的影响,证据仍然不一致。本研究评估达格列净对超声心动图参数的影响及其与临床反应的一致性。材料和方法:一项前瞻性、随机对照研究纳入了伴有左心室功能障碍的HF患者,分为达格列净组和dapagliflozin-naïve组。在基线和6个月时进行超声心动图和斑点跟踪应变分析。主要观察指标为左室指数质量的变化。次要结果包括左室功能、体积、尺寸、功能性二尖瓣反流、整体纵向应变(GLS)、舒张功能、右心室(RV)功能,以及使用堪萨斯城心肌病问卷(KCCQ)评分评估的临床反应。结果:在240名参与者中,160名在指南指导的药物治疗之外接受了达格列净,80名dapagliflozin-naïve。校正回归分析显示,左室质量指数(-43.51 g/m²,95% CI: -59.4 ~ -27.5, p < 0.0001)、收缩末期容积(-29.45 mL, 95% CI: -43.9 ~ -14.9, p < 0.0001)和舒张末期容积(-29.44 mL, 95% CI: -47.9 ~ -10.9, p = 0.0021)均有显著改善。改进也观察到在LV射血分数(5.15%,95%置信区间CI: 2.84 - 7.45, p < 0.0001), gl(-1.99%, 95%置信区间CI: -2.87 - -1.11, p < 0.0001), E / A比值(-0.56,95%置信区间CI: -1.01 - -0.10, p = 0.016),有效的二尖瓣口面积(EROA)(-0.18厘米²,95%置信区间CI: -0.28 - -0.081, p = 0.0006),三尖瓣环平面收缩偏差(TAPSE)(0.38厘米,95%置信区间CI: 0.15 - 0.62, p = 0.0024),和复合临床结果(HR 0.65, 95%置信区间CI: 0.43 - -0.98, p = 0.043)。LVEF、GLS、E/A比值、TAPSE、下腔静脉内径、左房面积与临床反应相关。结论:达格列净作为左心室功能不全患者的潜在治疗方法,可增强左室收缩功能和舒张功能,并具有良好的临床疗效。未来的研究需要对右心室功能进行更广泛的评估和更长的随访。图形摘要:https://www.europeanreview.org/wp/wp-content/uploads/abstract.jpg。
{"title":"Dapagliflozin enhances systolic and diastolic function in concordance with clinical response in patients with left ventricular dysfunction.","authors":"A E Abou Warda, J D Duarte, M Nabil Salem, H F Salem, A N Moharram, A S Alanazi, A I Alzarea, T G Alsahli, H Sultan, M A Alrashdi, A F Altebainawi, B Emil Ibrahim, S Ibrahim Alnahrawi, K Kamel Megalaa, B Zarif, R M Sarhan","doi":"10.26355/eurrev_202505_37222","DOIUrl":"10.26355/eurrev_202505_37222","url":null,"abstract":"<p><p>OBJECTIVE: Sodium-glucose co-transporter-2 (SGLT2) inhibitors have reshaped heart failure (HF) management. However, evidence regarding their effects on cardiac structure, particularly for dapagliflozin, remains inconsistent. This study evaluates dapagliflozin's impact on echocardiographic parameters and its concordance with clinical response. MATERIALS AND METHODS: A prospective, randomized controlled study included HF patients with left ventricular (LV) dysfunction, divided into dapagliflozin-treated and dapagliflozin-naïve groups. Echocardiography and speckle-tracking strain analysis were conducted at baseline and six months. The primary outcome was the change in indexed LV mass. Secondary outcomes included LV function, volumes, dimensions, functional mitral regurgitation, global longitudinal strain (GLS), diastolic function, right ventricular (RV) function, and clinical response assessed using the Kansas City Cardiomyopathy Questionnaire (KCCQ) score. RESULTS: Among 240 participants, 160 received dapagliflozin in addition to guideline-directed medical therapy, while 80 were dapagliflozin-naïve. Adjusted regression analysis showed significant improvements in LV mass index (-43.51 g/m², 95% CI: -59.4 to -27.5, p < 0.0001), end-systolic volume (-29.45 mL, 95% CI: -43.9 to -14.9, p < 0.0001), and end-diastolic volume (-29.44 mL, 95% CI: -47.9 to -10.9, p = 0.0021). Improvements were also observed in LV ejection fraction (5.15%, 95% CI: 2.84 to 7.45, p < 0.0001), GLS (-1.99%, 95% CI: -2.87 to -1.11, p < 0.0001), E/A ratio (-0.56, 95% CI: -1.01 to -0.10, p = 0.016), effective regurgitant orifice area (EROA) (-0.18 cm², 95% CI: -0.28 to -0.081, p = 0.0006), tricuspid annular plane systolic excursion (TAPSE) (0.38 cm, 95% CI: 0.15 to 0.62, p = 0.0024), and composite clinical outcome (HR 0.65, 95% CI: 0.43-0.98, p = 0.043). LVEF, GLS, E/A ratio, TAPSE, inferior vena cava diameter, and left atrial area correlated with clinical response. CONCLUSIONS: Dapagliflozin emerges as a potential therapy for patients with left ventricular dysfunction, enhancing LV systolic function and diastolic performance, alongside a favorable clinical response. Future studies with more extensive assessment of right ventricular function and longer follow-up are warranted.</p><p><strong>Graphical abstract: </strong>https://www.europeanreview.org/wp/wp-content/uploads/abstract.jpg.</p>","PeriodicalId":12152,"journal":{"name":"European review for medical and pharmacological sciences","volume":"29 5","pages":"231-247"},"PeriodicalIF":3.3,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144186805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retraction Note: LncRNA EBIC promoted proliferation, metastasis and cisplatin resistance of ovarian cancer cells and predicted poor survival in ovarian cancer patients. 注:LncRNA EBIC促进卵巢癌细胞增殖、转移和顺铂耐药,预示卵巢癌患者生存不良。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-05-01 DOI: 10.26355/eurrev_202505_37229
Q-F Xu, Y-X Tang, X Wang

The article "LncRNA EBIC promoted proliferation, metastasis and cisplatin resistance of ovarian cancer cells and predicted poor survival in ovarian cancer patients" by Q.-F. Xu, Y.-X. Tang, X. Wang published in Eur Rev Med Pharmacol Sci 2018; 22 (14): 4440-4447-DOI: 10.26355/eurrev_201807_15495-PMID: 30058681 has been retracted in accordance with the Publisher and the Editor in Chief. Following some concerns raised on PubPeer (link: https://pubpeer.com/publications/4756B8806339A2FA95E3A77A3FB451), the journal has started an investigation to assess the validity of the results as well as possible figure manipulation. The journal's investigation identified a discrepancy between the data described in the text and the content presented in Figure 1, raising concerns about the originality and accuracy of the data. Additionally, detailed information regarding Ethics Approval was missing. The authors have been notified about the ongoing investigation and were asked to provide the original data, however, they have not responded to these communications. As a result, due to unresolved concerns regarding data integrity, lack of ethical approval documentation, and the authors' failure to respond to repeated requests for clarification, the article has been retracted. This article has been retracted. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/15495.

Q.-F的文章《LncRNA EBIC促进卵巢癌细胞增殖、转移和顺铂耐药,预测卵巢癌患者生存不良》。徐,y。Tang X. Wang发表于《Eur Rev Med Pharmacol science》2018;22 (14): 4440-4447-DOI: 10.26355/eurrev_201807_15495-PMID: 30058681已根据出版商和主编的要求撤回。在PubPeer(链接:https://pubpeer.com/publications/4756B8806339A2FA95E3A77A3FB451)上引起了一些关注之后,该杂志已经开始了一项调查,以评估结果的有效性以及可能的数字操纵。该杂志的调查发现,文本中描述的数据与图1所示内容之间存在差异,这引起了人们对数据原创性和准确性的担忧。此外,缺少关于伦理批准的详细信息。作者已被告知正在进行的调查,并被要求提供原始数据,但他们没有对这些来文作出答复。因此,由于未解决的数据完整性问题,缺乏伦理批准文件,以及作者未能回应多次要求澄清的要求,该文章已被撤回。这篇文章已被撤回。对于由此造成的任何不便,出版商深表歉意。https://www.europeanreview.org/article/15495。
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引用次数: 0
Inadvertent sub-macular triamcinolone during pars plana vitrectomy for epiretinal membrane: A case report. 黄斑下曲安奈德治疗视网膜前膜玻璃体切除术1例。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-05-01 DOI: 10.26355/eurrev_202505_37221
T Erakgün, H H Gobeka

BACKGROUND: The study aims to describe an inadvertent sub-macular triamcinolone acetonide (TA) deposition following a TA-assisted pars plana vitrectomy (PPV) for epiretinal membrane (ERM) peeling. CASE REPORT: In this interventional case report, a 75-year-old female with ERM-induced visual distortion underwent TA-assisted 25-gauge three-port PPV, endolaser photocoagulation, and sulfur hexafluoride (SF6) gas (8%) endo tamponade to treat ERM in the left eye. Significant TA deposition was observed intraoperatively in the submacular region, which remained after ERM and internal limiting membrane (ILM) removal. One month after PPV, the retina appeared flat, with no significant vitreoretinal interface defects or macular ultrastructural abnormalities. Vision improved from 0.40 to 0.2 logMAR, and there was no evidence of any ophthalmoscopic damage. CONCLUSIONS: Inadvertent sub-macular TA deposition following ERM peeling did not cause any significant surgical sequelae.

Graphical abstract: https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-13.jpg.

背景:该研究旨在描述TA辅助玻璃体切割(PPV)视网膜前膜(ERM)剥离后黄斑下曲安奈德(TA)沉积。病例报告:在这一介入性病例报告中,一位75岁的女性因ERM引起的视觉扭曲接受了ta辅助的25号三口PPV,内激光光凝和六氟化硫(SF6)气体(8%)内压填塞治疗左眼ERM。术中在黄斑下区域观察到明显的TA沉积,在ERM和内限制膜(ILM)去除后仍然存在。PPV术后1个月,视网膜变平,无明显玻璃体视网膜界面缺损及黄斑超微结构异常。视力从0.40 logMAR改善到0.2 logMAR,没有任何检眼镜损伤的证据。结论:ERM剥离后黄斑下TA沉积不引起任何明显的手术后遗症。图形摘要:https://www.europeanreview.org/wp/wp-content/uploads/Graphical-Abstract-13.jpg。
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引用次数: 0
Retraction Note: MiR-195 alleviates ulcerative colitis in rats via MAPK signaling pathway. 注:MiR-195通过MAPK信号通路缓解大鼠溃疡性结肠炎。
IF 3.3 4区 医学 Q1 Medicine Pub Date : 2025-05-01 DOI: 10.26355/eurrev_202505_37227
X-S Bai, G Bai, L-D Tang, Y Li, Y Huan, H Wang

The article "MiR-195 alleviates ulcerative colitis in rats via MAPK signaling pathway" by X.-S. Bai, G. Bai, L.-D. Tang, Y. Li, Y. Huan, H. Wang, published in Eur Rev Med Pharmacol Sci 2020; 24 (5): 2640-2646-DOI: 10.26355/eurrev_202003_20533-PMID: 32196614 has been retracted in accordance with the Publisher and the Editor in Chief. Following some concerns raised by a third party regarding possible overlaps and duplication in Figure 2, the Editor in Chief has started an investigation to assess the validity of the concerns, as well as a possible Figure manipulation. The journal's investigation revealed overlaps between panels "Model" and "miR-195 agomir" and between "Control" and "Model" of Figure 2. The authors have been notified about the ongoing investigation and were asked to provide the original data, however, they have not responded to these communications. Therefore, the manuscript is retracted for figure duplication and manipulation. This article has been retracted. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/20533.

文章“MiR-195通过MAPK信号通路缓解大鼠溃疡性结肠炎”由x - s。白,白国,白立德。唐勇,李艳,欢艳,王宏,发表于《欧洲医学与药物科学》2020;24 (5): 2640-2646-DOI: 10.26355/eurrev_202003_20533-PMID: 32196614已根据出版商和主编的要求撤回。在第三方对图2中可能出现的重叠和重复提出一些关注之后,总编辑开始了一项调查,以评估关注的有效性,以及可能的图操作。该杂志的调查发现,图2中的“模型”和“miR-195 agomir”面板之间以及“控制”和“模型”之间存在重叠。作者已被告知正在进行的调查,并被要求提供原始数据,但他们没有对这些来文作出答复。因此,由于图重复和篡改,论文被撤回。这篇文章已被撤回。对于由此造成的任何不便,出版商深表歉意。https://www.europeanreview.org/article/20533。
{"title":"Retraction Note: MiR-195 alleviates ulcerative colitis in rats via MAPK signaling pathway.","authors":"X-S Bai, G Bai, L-D Tang, Y Li, Y Huan, H Wang","doi":"10.26355/eurrev_202505_37227","DOIUrl":"https://doi.org/10.26355/eurrev_202505_37227","url":null,"abstract":"<p><p>The article \"MiR-195 alleviates ulcerative colitis in rats via MAPK signaling pathway\" by X.-S. Bai, G. Bai, L.-D. Tang, Y. Li, Y. Huan, H. Wang, published in Eur Rev Med Pharmacol Sci 2020; 24 (5): 2640-2646-DOI: 10.26355/eurrev_202003_20533-PMID: 32196614 has been retracted in accordance with the Publisher and the Editor in Chief. Following some concerns raised by a third party regarding possible overlaps and duplication in Figure 2, the Editor in Chief has started an investigation to assess the validity of the concerns, as well as a possible Figure manipulation. The journal's investigation revealed overlaps between panels \"Model\" and \"miR-195 agomir\" and between \"Control\" and \"Model\" of Figure 2. The authors have been notified about the ongoing investigation and were asked to provide the original data, however, they have not responded to these communications. Therefore, the manuscript is retracted for figure duplication and manipulation. This article has been retracted. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/20533.</p>","PeriodicalId":12152,"journal":{"name":"European review for medical and pharmacological sciences","volume":"29 5","pages":"221"},"PeriodicalIF":3.3,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144186872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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