Case-control studies

病例对照研究
  • 文章类型: Journal Article
    目的:我们旨在评估白细胞介素-6(IL-6)表达水平与卒中的相关性。
    方法:根据设定的搜索策略,我们使用PubMed系统筛选相关研究,并从文献中提取有关IL-6的研究结果进行综合定量分析,以探讨IL-6水平与卒中风险之间的关系.
    结果:这项研究包括15篇出版物,共有1696名参与者,病例组975例,对照组721例。Meta分析结果显示,卒中人群IL-6水平明显高于对照组(标准化平均差=1.22,95%置信区间=0.79~1.64)。亚组分析显示,两组IL-6检测方法的异质性差异无统计学意义(I2=0,P=0.47)。关于地理区域的异质性测试结果差异具有统计学意义(I2=89.7%,P<0.01)。参与者平均年龄的异质性测试结果也具有统计学意义(I2=84.3%,P=0.01)。
    结论:本研究结果显示,IL-6可能与卒中发展显著相关。
    OBJECTIVE: We aimed to evaluate the association of interleukin-6 (IL-6) expression levels with stroke.
    METHODS: According to the set search strategy, we systematically screened relevant studies using PubMed and extracted study results regarding IL-6 from the literature for comprehensive quantitative analysis to explore the relationship between IL-6 level and stroke risk.
    RESULTS: This study included 15 publications with a total of 1696 participants, with 975 cases in the case group and 721 cases in the control group. Meta-analysis showed that IL-6 levels were significantly higher in the stroke population than those in the control group (standardized mean difference = 1.22, 95% confidence interval = 0.79-1.64). Subgroup analysis showed that there was no significant difference in heterogeneity for IL-6 detection methods between the two groups (I2 = 0, P = 0.47). The difference in heterogeneity test results regarding geographic region was statistically significant (I2 = 89.7%, P < 0.01). The results of heterogeneity testing for mean participant age were also statistically significant (I2 = 84.3%, P = 0.01).
    CONCLUSIONS: The present study results showed that IL-6 may be significantly associated with stroke development.
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  • 文章类型: Journal Article
    背景:保留网膜(OP)对局部晚期胃癌(LAGC)的影响仍存在争议。本研究旨在探讨OP与大网膜切除术(OR)对LAGC患者远期预后的影响。
    方法:对包括PubMed、WebofScience,Embase,Cochrane图书馆一直持续到2024年2月。采用Stata12.0软件进行统计学分析。主要结果是评估OP对LAGC患者长期预后的影响,包括总生存期(OS)和无复发生存期(RFS)。
    结果:共纳入6项病例对照研究,包括1897名患者。OP组包括844名患者,而OR组包括1053例患者。研究结果表明,OP组的OS(HR=0.72,95%CI:0.58-0.90,P=0.003)和5年RFS(HR=0.79,95%CI:0.63-0.99,P=0.038)优于OR组。亚组分析表明,在韩国,OP组的5年OS(HR=0.64,P=0.003)和5年RFS(HR=0.69,P=0.005)也优于OR组。然而,对T3-T4期肿瘤进行的亚组分析显示,两组间OS(P=0.083)和5年RFS(P=0.173)无统计学差异.
    结论:与OR相比,OP在LAGC患者中显示出非劣效性,可以被认为是根治性胃切除术的潜在治疗选择。
    BACKGROUND: The effect of omentum preservation (OP) on locally advanced gastric cancer (LAGC) remains controversial. This study aimed to investigate the long-term prognosis of LAGC patients with OP versus omentum resection (OR).
    METHODS: A comprehensive search of databases including PubMed, Web of Science, Embase, and Cochrane Library was conducted up until February 2024. Statistical analysis was performed using Stata 12.0 software. The primary outcome was to assess the impact of OP on the long-term prognosis of patients with LAGC, including overall survival (OS) and recurrence-free survival (RFS).
    RESULTS: A total of six case-control studies were included, encompassing a cohort of 1897 patients. The OP group consisted of 844 patients, while the OR group comprised 1053 patients. The study results showed that the OS (HR = 0.72, 95% CI: 0.58-0.90, P = 0.003) and 5-year RFS (HR = 0.79, 95% CI: 0.63-0.99, P = 0.038) in the OP group were superior to those observed in the OR group. Subgroup analysis indicated that 5-year OS (HR = 0.64, P = 0.003) and 5-year RFS (HR = 0.69, P = 0.005) in the OP group were also better than those in the OR group in Korea. However, the subgroup analysis conducted on stage T3-T4 tumors revealed no statistically significant differences in OS (P = 0.083) and 5-year RFS (P = 0.173) between the two groups.
    CONCLUSIONS: Compared with OR, OP shows non-inferiority in patients with LAGC and can be considered a potential treatment option for radical gastrectomy.
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  • 文章类型: Journal Article
    背景:本综述的目的是评估人类观察研究提供的证据的质量和强度,以证明暴露于射频电磁场(RF-EMF)与大多数研究的肿瘤疾病的风险之间存在因果关系。
    方法:合格标准:我们纳入了与三种类型的RF-EMF暴露有关的肿瘤形成风险的队列和病例对照研究:近场,头部局部化,无线电话使用暴露(SR-A);远场,整个身体,固定站点发射器(SR-B)的环境暴露;在工作场所使用手持式收发器或RF发射设备(SR-C)的近/远场职业暴露。虽然对肿瘤类型没有限制,在当前的论文中,我们专注于对选定的“关键”中枢神经系统肿瘤(脑,脑膜,脑垂体,听神经)和唾液腺肿瘤(SR-A);脑肿瘤和白血病(SR-B,SR-C)。我们专注于与特定暴露源(即E-O对)相关的特定肿瘤的调查,注意,一篇文章可能涉及多个E-O对。
    方法:通过Medline的文献检索确定了符合条件的研究,Embase,和EMF门户。偏倚风险(RoB)评估:我们使用了健康评估和翻译办公室(OHAT)RoB工具的定制版本来评估每个研究的内部有效性。在总结RoB步骤中,根据研究的总体偏见潜力将研究分为三个层次(低,中等和高)。
    结果:我们使用随机效应限制最大似然(REML)模型(二分和分类暴露变量的总体和亚组荟萃分析)综合了研究结果,和加权混合效应模型(终生暴露强度的剂量-反应荟萃分析)。证据评估:使用建议分级评估对证据的信心,评估,开发和评估(等级)方法。
    结果:我们纳入了63篇病因学文章,1994年至2022年出版,来自22个国家的参与者,报告119个不同的E-O对。手机的RF-EMF暴露(曾经或定期使用与没有或不定期使用)与胶质瘤的风险增加无关[相对风险(mRR)的meta估计=1.01,95%CI=0.89-1.13),脑膜瘤(mRR=0.92,95%CI=0.82-1.02),听神经瘤(mRR=1.03,95%CI=0.85-1.24),垂体肿瘤(mRR=0.81,95%CI=0.61-1.06),唾液腺肿瘤(mRR=0.91,95%CI=0.78-1.06),或儿科(儿童,青少年和年轻人)脑肿瘤(mRR=1.06,95%CI=0.74-1.51),具有不同程度的跨研究异质性(I2=0%-62%)。对于研究最多的肿瘤(神经胶质瘤,脑膜瘤,和听神经瘤)随着手机开始(TSS)使用时间的增加,累计通话时间(CCT),或累计通话次数(CNC)。无绳电话使用与脑膜瘤[mRR=1.04,95%CI=0.74-1.46;I2=74%](mRR=0.91,95%CI=0.70-1.18;I2=59%),或听神经瘤(mRR=1.16;95%CI=0.83-1.61;I2=63%)。固定站点发射器(广播天线或基站)的暴露与儿童白血病或小儿脑瘤风险无关,与模拟的射频暴露水平无关。职业性射频暴露后胶质瘤风险没有显著增加(从未与从未),并且在建模的累积暴露水平的增加类别之间没有检测到差异。
    结论:在胶质瘤的敏感性分析中,脑膜瘤,和与手机使用相关的听神经瘤风险(曾经使用过,TSS,CCT,和CNC)提出的结果是稳健的,不受研究聚集变化的影响。在与手机使用相关的神经胶质瘤风险的留一荟萃分析中,我们确定了一项有影响力的研究。在排除本研究后进行的后续荟萃分析中,我们观察到mRR的大幅降低和研究之间的异质性,对于对比剂,从未使用(常规)(mRR=0.96,95%CI=0.87-1.07,I2=47%),在增加TSS类别的分析中(“<5年”:mRR=0.97,95%CI=0.83-1.14,I2=41%;“5-9年”:mRR=0.96,95%CI=0.83-1.11,I2=34%;“10年”:mRR=0.97,95%CI=0.87-1.08,I2=10%)。RoB中优先领域的研究差异有限(选择/减员,暴露和结果信息),研究数量均匀地分为低和中等偏倚风险(49%的一级和51%的二级),没有被归类为高偏倚风险的研究(第3层)。偏差对研究结果(数量和方向)的影响难以预测,而RoB工具本来就无法解释竞争偏见的影响。然而,敏感性荟萃分析按偏倚层分层,表明,在我们的主要荟萃分析中观察到的异质性,在TSS上层的神经胶质瘤和听神经瘤的研究中(I2=77%和76%),由摘要RoB-tier解释。在一级研究亚组中,长期(10年以上)用户的mRRs(95%CI;I2)是胶质瘤的0.95(0.85-1.05;5.5%),听神经瘤为1.00(0.78-1.29;35%)。时间趋势模拟研究,根据外部有效性的三角剖分方法评估为补充证据,这表明在一些病例对照研究中观察到的增加的风险与在几个国家和长期观察到的神经胶质瘤/脑癌的实际发病率不相容。这些模拟研究中的三个一致报道,在10年以上的诱导期,RR估计值>1.5肯定是不可信的,并可用于设置“信誉基准”。在TSS上层类胶质瘤风险的敏感性荟萃分析中,不包括5项报告不合理效应大小的研究,我们观察到mRR[mRR为0.95(95%CI=0.86-1.05)]的显著降低,以及不同研究的异质性程度(I2=3.6%)。
    结论:与已发布的方案一致,我们的最终结论是针对每个暴露-结果组合单独制定的,主要基于最高可信度的证据,考虑到从剂量学研究中推断的按暴露水平对RF源的排名,以及与时间趋势模拟研究结果的外部一致性(仅限于与手机使用有关的神经胶质瘤)。对于从手机使用到头部的近场RF-EMF暴露,有适度的确定性证据表明它可能不会增加神经胶质瘤的风险,脑膜瘤,听神经瘤,垂体肿瘤,成人的唾液腺肿瘤,或小儿脑肿瘤。对于从无绳电话使用到头部的近场RF-EMF暴露,有低确定性的证据表明它可能不会增加神经胶质瘤的风险,脑膜瘤或听神经瘤。对于来自固定站点发射器(广播天线或基站)的全身远场RF-EMF暴露,有中度确定性证据表明它可能不会增加儿童白血病的风险,而低确定性证据表明它可能不会增加儿童脑肿瘤的风险.没有适合纳入研究的研究来自固定站点发射器和成人关键肿瘤的RF-EMF暴露。对于职业性RF-EMF暴露,有低确定性证据表明它可能不会增加脑癌/神经胶质瘤的风险,但没有纳入白血病(SR-C的第二个关键结局)的研究.应谨慎解释儿科脑肿瘤与固定部位发射器环境射频暴露相关的证据评级。由于研究数量少。类似的解释性警告适用于神经胶质瘤/脑癌与职业性射频暴露之间关系的证据评级。由于少数纳入研究的暴露来源和指标存在差异。
    该项目由世界卫生组织(WHO)委托和部分资助。共同供资由新西兰卫生部提供;IstitutoSuperiorediSanità作为世卫组织辐射与健康合作中心;ARPANSA作为世卫组织辐射防护合作中心。
    背景:PROSPEROCRD42021236798。公布的协议:[(Lagorio等人,2021)DOIhttps://doi.org/10.1016/j。envint.2021.106828]。
    BACKGROUND: The objective of this review was to assess the quality and strength of the evidence provided by human observational studies for a causal association between exposure to radiofrequency electromagnetic fields (RF-EMF) and risk of the most investigated neoplastic diseases.
    METHODS: Eligibility criteria: We included cohort and case-control studies of neoplasia risks in relation to three types of exposure to RF-EMF: near-field, head-localized, exposure from wireless phone use (SR-A); far-field, whole body, environmental exposure from fixed-site transmitters (SR-B); near/far-field occupational exposures from use of hand-held transceivers or RF-emitting equipment in the workplace (SR-C). While no restrictions on tumour type were applied, in the current paper we focus on incidence-based studies of selected \"critical\" neoplasms of the central nervous system (brain, meninges, pituitary gland, acoustic nerve) and salivary gland tumours (SR-A); brain tumours and leukaemias (SR-B, SR-C). We focussed on investigations of specific neoplasms in relation to specific exposure sources (i.e. E-O pairs), noting that a single article may address multiple E-O pairs.
    METHODS: Eligible studies were identified by literature searches through Medline, Embase, and EMF-Portal. Risk-of-bias (RoB) assessment: We used a tailored version of the Office of Health Assessment and Translation (OHAT) RoB tool to evaluate each study\'s internal validity. At the summary RoB step, studies were classified into three tiers according to their overall potential for bias (low, moderate and high).
    RESULTS: We synthesized the study results using random effects restricted maximum likelihood (REML) models (overall and subgroup meta-analyses of dichotomous and categorical exposure variables), and weighted mixed effects models (dose-response meta-analyses of lifetime exposure intensity). Evidence assessment: Confidence in evidence was assessed using the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) approach.
    RESULTS: We included 63 aetiological articles, published between 1994 and 2022, with participants from 22 countries, reporting on 119 different E-O pairs. RF-EMF exposure from mobile phones (ever or regular use vs no or non-regular use) was not associated with an increased risk of glioma [meta-estimate of the relative risk (mRR) = 1.01, 95 % CI = 0.89-1.13), meningioma (mRR = 0.92, 95 % CI = 0.82-1.02), acoustic neuroma (mRR = 1.03, 95 % CI = 0.85-1.24), pituitary tumours (mRR = 0.81, 95 % CI = 0.61-1.06), salivary gland tumours (mRR = 0.91, 95 % CI = 0.78-1.06), or paediatric (children, adolescents and young adults) brain tumours (mRR = 1.06, 95 % CI = 0.74-1.51), with variable degree of across-study heterogeneity (I2 = 0 %-62 %). There was no observable increase in mRRs for the most investigated neoplasms (glioma, meningioma, and acoustic neuroma) with increasing time since start (TSS) use of mobile phones, cumulative call time (CCT), or cumulative number of calls (CNC). Cordless phone use was not significantly associated with risks of glioma [mRR = 1.04, 95 % CI = 0.74-1.46; I2 = 74 %) meningioma, (mRR = 0.91, 95 % CI = 0.70-1.18; I2 = 59 %), or acoustic neuroma (mRR = 1.16; 95 % CI = 0.83-1.61; I2 = 63 %). Exposure from fixed-site transmitters (broadcasting antennas or base stations) was not associated with childhood leukaemia or paediatric brain tumour risks, independently of the level of the modelled RF exposure. Glioma risk was not significantly increased following occupational RF exposure (ever vs never), and no differences were detected between increasing categories of modelled cumulative exposure levels.
    CONCLUSIONS: In the sensitivity analyses of glioma, meningioma, and acoustic neuroma risks in relation to mobile phone use (ever use, TSS, CCT, and CNC) the presented results were robust and not affected by changes in study aggregation. In a leave-one-out meta-analyses of glioma risk in relation to mobile phone use we identified one influential study. In subsequent meta-analyses performed after excluding this study, we observed a substantial reduction in the mRR and the heterogeneity between studies, for both the contrast Ever vs Never (regular) use (mRR = 0.96, 95 % CI = 0.87-1.07, I2 = 47 %), and in the analysis by increasing categories of TSS (\"<5 years\": mRR = 0.97, 95 % CI = 0.83-1.14, I2 = 41 %; \"5-9 years \": mRR = 0.96, 95 % CI = 0.83-1.11, I2 = 34 %; \"10+ years\": mRR = 0.97, 95 % CI = 0.87-1.08, I2 = 10 %). There was limited variation across studies in RoB for the priority domains (selection/attrition, exposure and outcome information), with the number of studies evenly classified as at low and moderate risk of bias (49 % tier-1 and 51 % tier-2), and no studies classified as at high risk of bias (tier-3). The impact of the biases on the study results (amount and direction) proved difficult to predict, and the RoB tool was inherently unable to account for the effect of competing biases. However, the sensitivity meta-analyses stratified on bias-tier, showed that the heterogeneity observed in our main meta-analyses across studies of glioma and acoustic neuroma in the upper TSS stratum (I2 = 77 % and 76 %), was explained by the summary RoB-tier. In the tier-1 study subgroup, the mRRs (95 % CI; I2) in long-term (10+ years) users were 0.95 (0.85-1.05; 5.5 %) for glioma, and 1.00 (0.78-1.29; 35 %) for acoustic neuroma. The time-trend simulation studies, evaluated as complementary evidence in line with a triangulation approach for external validity, were consistent in showing that the increased risks observed in some case-control studies were incompatible with the actual incidence rates of glioma/brain cancer observed in several countries and over long periods. Three of these simulation studies consistently reported that RR estimates > 1.5 with a 10+ years induction period were definitely implausible, and could be used to set a \"credibility benchmark\". In the sensitivity meta-analyses of glioma risk in the upper category of TSS excluding five studies reporting implausible effect sizes, we observed strong reductions in both the mRR [mRR of 0.95 (95 % CI = 0.86-1.05)], and the degree of heterogeneity across studies (I2 = 3.6 %).
    CONCLUSIONS: Consistently with the published protocol, our final conclusions were formulated separately for each exposure-outcome combination, and primarily based on the line of evidence with the highest confidence, taking into account the ranking of RF sources by exposure level as inferred from dosimetric studies, and the external coherence with findings from time-trend simulation studies (limited to glioma in relation to mobile phone use). For near field RF-EMF exposure to the head from mobile phone use, there was moderate certainty evidence that it likely does not increase the risk of glioma, meningioma, acoustic neuroma, pituitary tumours, and salivary gland tumours in adults, or of paediatric brain tumours. For near field RF-EMF exposure to the head from cordless phone use, there was low certainty evidence that it may not increase the risk of glioma, meningioma or acoustic neuroma. For whole-body far-field RF-EMF exposure from fixed-site transmitters (broadcasting antennas or base stations), there was moderate certainty evidence that it likely does not increase childhood leukaemia risk and low certainty evidence that it may not increase the risk of paediatric brain tumours. There were no studies eligible for inclusion investigating RF-EMF exposure from fixed-site transmitters and critical tumours in adults. For occupational RF-EMF exposure, there was low certainty evidence that it may not increase the risk of brain cancer/glioma, but there were no included studies of leukemias (the second critical outcome in SR-C). The evidence rating regarding paediatric brain tumours in relation to environmental RF exposure from fixed-site transmitters should be interpreted with caution, due to the small number of studies. Similar interpretative cautions apply to the evidence rating of the relation between glioma/brain cancer and occupational RF exposure, due to differences in exposure sources and metrics across the few included studies.
    UNASSIGNED: This project was commissioned and partially funded by the World Health Organization (WHO). Co-financing was provided by the New Zealand Ministry of Health; the Istituto Superiore di Sanità in its capacity as a WHO Collaborating Centre for Radiation and Health; and ARPANSA as a WHO Collaborating Centre for Radiation Protection.
    BACKGROUND: PROSPERO CRD42021236798. Published protocol: [(Lagorio et al., 2021) DOI https://doi.org/10.1016/j.envint.2021.106828].
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  • 文章类型: Systematic Review
    自闭症谱系障碍(ASD)是一种神经发育障碍,其特征是社交互动和交流能力受损。儿童患病率的惊人增长促使研究人员更好地了解这种疾病的原因。遗传因素被认为是至关重要的,ASD倾向于在家庭中运行。近年来,随着技术的进步,ASD中结构变异(SV)的重要性开始显现。大部分研究,然而,重点是高加索人口。作为一个人口稠密的种族,ASD在中国将是一个重大的健康问题。本系统综述旨在总结中国人群中与ASD相关的SVs的病例对照研究。提供了在所包括的9项研究中鉴定的基因列表。它还表明,需要针对其他遗传背景的类似研究来证明不同种族的疾病病因,并协助发展准确的面向民族的基因诊断。
    Autistic spectrum disorder (ASD) is a neurodevelopmental disability characterised by the impairment of social interaction and communication ability. The alarming increase in its prevalence in children urged researchers to obtain a better understanding of the causes of this disease. Genetic factors are considered to be crucial, as ASD has a tendency to run in families. In recent years, with technological advances, the importance of structural variations (SVs) in ASD began to emerge. Most of these studies, however, focus on the Caucasian population. As a populated ethnicity, ASD shall be a significant health issue in China. This systematic review aims to summarise current case-control studies of SVs associated with ASD in the Chinese population. A list of genes identified in the nine included studies is provided. It also reveals that similar research focusing on other genetic backgrounds is demanded to manifest the disease etiology in different ethnic groups, and assist the development of accurate ethnic-oriented genetic diagnosis.
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  • 文章类型: Systematic Review
    背景:蜂窝织炎是一种倾向于复发的细菌性皮肤感染。先前的研究已经确定了可能导致其发病的几种危险因素。肥胖是一种日益普遍的世界性疾病,其与皮肤和软组织感染有关。
    目的:我们的系统评价和荟萃分析的目的是探讨蜂窝织炎与肥胖的关系。
    方法:OvidMEDLINE,Embase,Cochrane中央控制试验登记册,从每个数据库开始到2021年3月13日,都搜索了和WebofScience数据库的相关研究。病例控制,横截面,纳入了研究蜂窝织炎患者BMI升高几率或风险的队列研究.这项研究是根据PRISMA(系统审查和荟萃分析的首选报告项目)指南进行的。采用纽卡斯尔-渥太华量表(NOS)评价纳入研究的偏倚风险。
    结果:总计,9项病例对照研究纳入我们的定量荟萃分析,共有68,148名研究参与者。发现蜂窝织炎和肥胖之间存在显著关联(合并比值比[OR]2.67,95%CI1.91-3.71)。在蜂窝织炎和超重之间没有观察到显著的相关性(合并OR1.69,95%CI0.99-2.88)。还发现蜂窝织炎患者为男性的几率增加了1.63倍(汇总OR1.63,95%CI1.12-2.38)。
    结论:我们的研究结果表明蜂窝织炎与肥胖显著相关。对于出现蜂窝织炎的患者,可能需要保持健康的BMI。
    BACKGROUND: Cellulitis is a bacterial skin infection that tends to recur. Previous studies have identified several risk factors that may contribute to its pathogenesis. Obesity is an increasingly prevalent worldwide disease that has been associated with skin and soft tissue infections.
    OBJECTIVE: The aim of our systematic review and meta-analysis was to investigate the association of cellulitis with obesity.
    METHODS: The Ovid MEDLINE, Embase, Cochrane Central Register of Controlled Trials, and Web of Science databases were searched for the relevant studies from the inception of each respective database to March 13, 2021. Case-control, cross-sectional, or cohort studies that examined the odds or risk of increased BMI in patients with cellulitis were included. This study was carried out in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. The Newcastle-Ottawa scale (NOS) was used to evaluate the risk of bias in included studies.
    RESULTS: In total, 9 case-control studies were included in our quantitative meta-analysis with a total of 68,148 study participants. A significant association was found between cellulitis and obesity (pooled odds ratio [OR] 2.67, 95% CI 1.91-3.71). No significant association was observed between cellulitis and being overweight (pooled OR 1.69, 95% CI 0.99-2.88). Patients with cellulitis were also found to have 1.63-fold increased odds of being male (pooled OR 1.63, 95% CI 1.12-2.38).
    CONCLUSIONS: Our findings suggest that cellulitis is significantly associated with obesity. Maintaining a healthy BMI may be indicated for patients presenting with cellulitis.
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  • 文章类型: Journal Article
    在近端尿道下裂患者中,尽管进行了广泛的基因检测,但通常没有发现遗传原因。参与性发育的许多基因编码转录因子,基因产物的时间和剂量严格。我们假设,尿道下裂男孩的DNA甲基化可能会反复出现差异,并且这些差异可能在出生时较小的患者与适合胎龄的患者之间有所不同。全基因组甲基化DNA测序(MeD-seq)在RE消化后对来自16名不明原因近端尿道下裂男孩的白细胞中的32bpLpnPI限制性内切酶片段进行了,一位患有不明原因的XX睾丸疾病/性发育差异(DSD)和十二位,健康,性别和年龄匹配的对照。患者和XY对照之间的七个差异甲基化区域(DMRs)中的五个在长基因间非蛋白编码RNA665(LINC00665;CpG24525)中。3例患者显示MAP3K1甲基化过度。最后,在XX男孩和XX对照中,没有发现XX睾丸DSD相关基因的DMRs。总之,我们在16例XY近端尿道下裂的男孩中没有观察到可识别的表观遗传特征,出生时小与适合胎龄的儿童之间没有差异.与先前在尿道下裂患者中的甲基化研究相比,没有显示出一致的发现。可能是由于使用了不同的纳入标准,组织和方法。
    In patients with proximal hypospadias, often no genetic cause is identified despite extensive genetic testing. Many genes involved in sex development encode transcription factors with strict timing and dosing of the gene products. We hypothesised that there might be recurrent differences in DNA methylation in boys with hypospadias and that these might differ between patients born small versus appropriate for gestational age. Genome-wide Methylated DNA sequencing (MeD-seq) was performed on 32bp LpnPI restriction enzyme fragments after RE-digestion in leucocytes from 16 XY boys with unexplained proximal hypospadias, one with an unexplained XX testicular disorder/difference of sex development (DSD) and twelve, healthy, sex- and age-matched controls. Five of seven differentially methylated regions (DMRs) between patients and XY controls were in the Long Intergenic Non-Protein Coding RNA 665 (LINC00665; CpG24525). Three patients showed hypermethylation of MAP3K1. Finally, no DMRs in XX testicular DSD associated genes were identified in the XX boy versus XX controls. In conclusion, we observed no recognizable epigenetic signature in 16 boys with XY proximal hypospadias and no difference between children born small versus appropriate for gestational age. Comparison to previous methylation studies in individuals with hypospadias did not show consistent findings, possibly due to the use of different inclusion criteria, tissues and methods.
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  • 文章类型: Journal Article
    目的:关于癫痫和肥胖之间的关系一直存在争论。因此,这项研究的目的是研究癫痫与肥胖之间的相关性.
    方法:本研究遵循PRISMA系统评价和荟萃分析指南。在Prospero网站上,本研究已成功注册(CRD42023439530),从Cochr-ane图书馆搜索电子数据库,PubMed,WebofSciences和Embase直到2024年2月10日。搜索关键词包括\"癫痫\",“肥胖”,“病例对照研究”,“队列研究”,“随机对照试验”和“横断面研究”。利用PubMed的医学主题词(MeSH)搜索相关主题词和自由词,并制定了全面的搜索策略。两名审稿人进行了文章筛选,严格按照包括和排除研究的预定标准进行数据提取和偏倚风险评估。预定义的纳入标准如下:1)纳入病例对照,队列,随机对照试验,和横断面研究;2)将受试者分为癫痫患者和健康对照;3)肥胖作为结果测量;4)全面数据的可用性;5)英文出版。排除标准如下:1)排除动物实验,reviews,和其他类型的研究;2)缺乏健康对照组;3)数据不完整;4)不可提取或不可转换的数据;5)低质量,医疗保健研究和质量机构(AHRQ)评分为5分或更低,或纽卡斯尔-渥太华量表(NOS)得分小于3。研究对象包括成人和儿童,肥胖的诊断标准在不同年龄使用。在这项研究中,肥胖定义为成人的体重指数(BMI)为25kg/m2或更高,且儿童的BMI高于85百分位.我们使用肥胖作为使用RevMan进行荟萃分析的结果指标,5.3版。
    结果:对总共17项临床研究进行了荟萃分析,其中涉及5329名癫痫患者和480837名健康对照。这些研究是从先前提到的四个电子数据库获得的1497篇文章中选择的。根据所采用的搜索策略,删除了重复的研究。与健康对照组相比,癫痫患者肥胖的结局指标未观察到显着的异质性(p=0.01,I2=49%)。因此,本研究采用固定效应模型。研究结果表明,癫痫患者与健康对照组之间的肥胖患病率存在显着差异(OR=1.28,95CI:1.20-1.38,p<0.01)。
    结论:这项荟萃分析的结果表明,癫痫患者比健康人更容易肥胖,所以临床上需要注意癫痫后肥胖的问题。目前,缺乏大规模的前瞻性研究。有必要进行其他临床研究,以更深入地研究肥胖是否是癫痫的合并症,以及肥胖是否可能引发癫痫。
    OBJECTIVE: There is ongoing debate regarding the association between epilepsy and obesity. Thus, the aim of this study was to examine the correlation between epilepsy and obesity.
    METHODS: This study adhered to the PRISMA guidelines for systematic reviews and meta-analyses. On The Prospero website, this study has been successfully registered (CRD42023439530), searching electronic databases from the Cochr-ane Library, PubMed, Web of Sciences and Embase until February 10, 2024.The search keywords included \"Epilepsy\", \"Obesity\", \"Case-Control Studies\", \"cohort studies\", \"Randomized Controlled Trial\" and \"Cross-Sectional Studies\". The medical subject headings(MeSH) of PubMed was utilized to search for relevant subject words and free words, and a comprehensive search strategy was developed. Two reviewers conducted article screening, data extraction and bias risk assessment in strict accordance with the predefined criteria for including and excluding studies. The predefined inclusion criteria were as follows: 1) Inclusion of case-control, cohort, randomized controlled trial, and cross-sectional studies; 2) Segregation of subjects into epileptic patients and healthy controls; 3)Obesity as the outcome measure; 4) Availability of comprehensive data; 5) Publication in English. The exclusion criteria were as follows: 1) Exclusion of animal experiments, reviews, and other types of studies; 2) Absence of a healthy control group; 3) Incomplete data; 4) Unextractable or unconvertible data; 5) Low quality, indicated by an Agency for Healthcare Research and Quality(AHRQ) score of 5 or lower,or a Newcastle-Ottawa Scale (NOS) score less than 3. The subjects included in the study included adults and children, and the diagnostic criteria for obesity were used at different ages. In this study, obesity was defined as having a body mass index(BMI) of 25 kg/m2 or higher in adults and being above the 85th percentile of BMI for age in children. We used obesity as an outcome measure for meta-analysis using RevMan, version 5.3.
    RESULTS: A meta-analysis was conducted on a total of 17 clinical studies, which involved 5329 patients with epilepsy and 480837 healthy controls. These studies were selected from a pool of 1497 articles obtained from four electronic databases mentioned earlier. Duplicate studies were removed based on the search strategies employed. No significant heterogeneity was observed in the outcome measure of obesity in epileptic patients compared with healthy controls(p = 0.01,I2 = 49%). Therefore, a fixed effects model was utilized in this study. The findings revealed a significant difference in obesity prevalence between patients with epilepsy and healthy controls(OR = 1.28, 95%CI: 1.20-1.38, p<0.01).
    CONCLUSIONS: The results of this meta-analysis indicate that epilepsy patients are more prone to obesity than healthy people, so we need to pay attention to the problem of post-epilepsy obesity clinically. Currently, there is a scarcity of largescale prospective studies. Additional clinical investigations are warranted to delve deeper into whether obesity is a comorbidity of epilepsy and whether obesity can potentially trigger epilepsy.
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  • 文章类型: Journal Article
    腹部手术被认为是发生手术部位感染(SSI)的高风险程序。很少有研究评估手术部位感染危险因素在腹部手术一致性方面的相对重要性。因此,这篇全面的综述文章绘制并总结了旨在确定腹部手术中SSIs的危险因素和发生率的相对重要性的证据。
    使用电子数据库和诸如Scopus之类的搜索引擎进行了文献综述,PubMed,和WebofScience截至2023年3月16日。研究中的论文没有语言限制。使用JoannaBriggs研究所的方法测量和评估风险因素的相对一致性。如果包括所有类型的SSIs,则包括原始同行评审的队列和病例对照研究。进行荟萃分析以确定SSI发病率的汇总估计值。
    在14,237条确定的记录中,107篇文章被纳入审查。SSI的合并发生率为10.6%(95%CI:9.02-12.55%,χ2=12986.44,P<0.001)。手术时间和较高的伤口等级是SSI发生率的显著一致的危险因素。患者的教育状况,营养不良,功能状态,和神经/精神疾病的历史都是一致的危险因素的候选人,证据不足。
    本研究的结果表明,腹部手术中的SSI是一种多因素现象,具有相当大的风险,并且具有不同的相对重要性的危险因素。强烈建议确定危险因素对预防和控制SSI的相对重要性。该手稿已在研究广场上作为预印本发布:(https://doi.org/10.21203/rs.3。rs-3219597/v1)。
    UNASSIGNED: Abdominal surgery is considered a high-risk procedure for the development of surgical site infection (SSI). Few studies have evaluated the relative importance of surgical site infection risk factors in terms of consistency in abdominal surgery. Therefore, this comprehensive review article mapped and summarized the evidence aimed to determine the relative importance of the risk factors and incidence of SSIs in abdominal surgery.
    UNASSIGNED: A literature review was conducted using electronic databases and search engines such as Scopus, PubMed, and Web of Science up to March 16, 2023. There was no language restriction for the papers to be included in the study. The relative consistency of the risk factors was measured and evaluated using the methodology of the Joanna Briggs Institute. Original peer-reviewed cohort and case-control studies were included if all types of SSIs were included. Meta-analysis was performed to determine the pooled estimates of SSI incidences.
    UNASSIGNED: Of 14,237 identified records, 107 articles were included in the review. The pooled incidence of SSI was 10.6% (95% CI: 9.02-12.55%, χ2=12986.44, P<0.001). Operative time and higher wound class were both significant consistent risk factors for SSI incidence. Patients\' educational status, malnutrition, functional status, and history of neurological/psychiatric disorders were all candidates for consistent risk factors, with insufficient evidence.
    UNASSIGNED: The findings of the present study indicated that SSI in abdominal surgery was a multifactorial phenomenon with a considerable risk and had different risk factors with various relative importance. Determining the relative importance of the risk factors for the prevention and control of SSI is strongly recommended.This manuscript has been released as a preprint at the research square: (https://doi.org/10.21203/rs.3.rs-3219597/v1).
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  • 文章类型: Systematic Review
    随着激素替代疗法(HRT)的使用增加,有必要了解其对女性恶性肿瘤发生的影响。本系统评价和荟萃分析旨在评估与HRT相关的卵巢癌风险及其相关危险因素。
    PUBMED,OVID,Embase,科克伦,和WebofScience从1980年到2022年4月进行搜索,以确定有关卵巢癌和激素替代疗法风险的研究。随机效应模型用于估计卵巢癌中HRT的合并风险,在队列研究和病例对照研究中。此外,该分析检查了与不同类型的雌激素+孕激素方案相关的结局.采用Meta回归和敏感性分析评价异质性。
    分析了21项队列研究(涉及15,313例和4,564,785名参与者)和30项病例对照研究(包括18,738例和57,747名对照)。来自队列研究的HRT使用者的卵巢癌合并风险为1.20(95%置信区间[CI]1.01-1.44),来自病例对照研究的1.13(95CI1.04-1.22)。然而,在将研究时间限制在最近几十年之后,在2010年之后进行的队列研究和2006年之后进行的病例对照研究中,表明较高风险的显著结果消失了.此外,持续使用雌激素-孕激素替代治疗(EPRT)的风险与序贯使用的风险相当.亚组分析显示,雌激素替代治疗(ERT)和EPRT均存在较小的风险;随着暴露时间的延长,风险进一步增加。特别是超过10年的持续时间。此外,浆液性卵巢癌似乎比其他病理类型更易感。
    随着时间的推移,与HRT相关的卵巢癌风险一直在降低。然而,ERT可能会增加这种风险,特别是长时间使用时。建议长期用户考虑将连续EPRT作为更安全的替代方案。
    www.crd.约克。AC.英国/普华永道/,标识符CRD42022321279。
    UNASSIGNED: With the increasing use of hormone replacement therapy (HRT), there is a need to understand its impact on the occurrence of female malignant tumors. This systematic review and meta-analysis aimed to assess the risk of ovarian cancer associated with HRT and its related risk factors.
    UNASSIGNED: PUBMED, OVID, Embase, Cochrane, and Web of Science were searched from 1980 to April 2022 to identify studies on the risk of ovarian cancer and hormone replacement therapy. The random-effects model was used to estimate the pooled risk of HRT in ovarian cancer, both in cohort studies and case-control studies. Additionally, the analysis examined the outcomes associated with different types of estrogen plus progesterone regimens. Meta-regression and sensitive analysis were performed to evaluate the heterogeneity.
    UNASSIGNED: 21 cohort studies (involving 15,313 cases and 4,564,785 participants) and 30 case-control studies (including 18,738 cases and 57,747 controls) were analyzed. The pooled risks of ovarian cancer for HRT users were 1.20 (95% confidence interval [CI] 1.01-1.44) from cohort studies and 1.13 (95%CI 1.04-1.22) from case-control studies. However, after restricting the study period to recent decades, the significant results indicating a higher risk disappeared in cohort studies conducted after 2010 and in case-control studies conducted after 2006. Furthermore, the continuous use of estrogen-progesterone replacement therapy (EPRT) was associated with a risk comparable to that of sequential use. Subgroup analysis showed that both estrogen replacement treatment (ERT) and EPRT had minor risks; The risk further increased with prolonged exposure time, particularly for durations exceeding 10 years. Additionally, serous ovarian cancer appeared to be more susceptible than other pathological types.
    UNASSIGNED: The risk of ovarian cancer associated with HRT has been decreasing over time. However, ERT may increase this risk, particularly when used for an extended period. It is recommended that long-time users consider continuous EPRT as a safer alternative.
    UNASSIGNED: www.crd.york.ac.uk/prospero/, identifier CRD42022321279.
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  • 文章类型: Systematic Review
    暴露于环境污染物,如金属,杀虫剂,生命早期的空气污染物,是神经发育障碍(NDD)的危险因素,包括自闭症谱系障碍(ASD)。我们的系统评价旨在选择和总结最近的病例对照研究,这些研究检查了产前和产后早期暴露于环境污染物与NDD之间的关系。我们搜索了五个数据库(WebofScience,PubMed,Embase,Scopus,Ovid),筛选了2,261条记录,纳入24项符合条件的病例对照研究。对至少三项共享结果和暴露的研究的亚组进行了荟萃分析。本文献综述中值得注意的发现是在暴露于某些金属与ASD风险之间存在非线性或非单调的剂量反应关系。荟萃分析显示,生命第一年暴露于特定物质(PM)10与ASD风险之间存在显着关联。总的来说,我们的系统评价中包含的研究表明,在生命的前3年内暴露于多种污染物与NDD的风险显著相关.
    Exposure to environmental pollutants, such as metals, pesticides, and air pollutants during early life, is a risk factor for neurodevelopmental disorders (NDDs), including Autism Spectrum Disorder (ASD). Our systematic review aimed to select and summarize more recent case-control studies that examined the association between prenatal and early postnatal exposure to environmental pollutants and NDDs. We searched five databases (Web of Science, PubMed, Embase, Scopus, Ovid), screened 2261 records, and included 24 eligible case-control studies. Meta-analyses were conducted on subgroups of at least three studies that shared both the outcome and the exposure. A noteworthy discovery from this literature review is the existence of non-linear or non-monotonic dose-response relationships between the exposure to certain metals and the risk of ASD. The meta-analysis revealed a significant association between exposure to particular matter (PM)10 during the first year of life and the risk of ASD. Overall, studies included in our systematic review indicate that exposure to several pollutants within the first three years of life was significantly associated with the risk of NDDs.
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