prevalence

患病率
  • 文章类型: Journal Article
    这项横断面研究评估了COVID-19疫苗接种与有症状的儿童哮喘之间的关系。
    This cross-sectional study evaluates the association between COVID-19 vaccination and symptomatic child asthma.
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  • 文章类型: Journal Article
    这项研究的目的是调查不同年龄和性别的人脉络膜组织中性激素受体的存在,旨在更好地了解中心性浆液性脉络膜视网膜病变(CSC)发生的明显性别差异。
    14名绝经前妇女的石蜡包埋摘除眼睛,15名绝经后妇女,10名年轻男子(<45岁),使用了10名年龄较大的男性(>60岁)。进行临床认证的免疫染色以检测雄激素受体(AR)的存在,孕激素受体(PR;亚型A和B),和雌激素受体(ERα)。对于相同脉络膜区域的连续切片中的阳性内皮细胞和基质细胞,以盲法方式对染色的载玻片进行评分。
    我们的分析揭示了AR的存在,PR,和血管内皮细胞和脉络膜组织基质细胞中的ERα。年轻男性AR阳性内皮细胞的平均比例(46%±0.15)高于老年女性(29%±0.12;P<0.05,95%置信区间[CI])。绝经前妇女的ERα(5%±0.02)和PR阳性内皮细胞(2%±0.01)的平均比例明显低于绝经后妇女(15%±0.07和19%±0.13;P<0.05,95%CI),年轻男性(13%±0.04和21%±0.10;两者P<0.05,95%CI),和老年男性(18%±0.09和27%±0.14;P<0.05,95%CI)。与其他组相比,绝经前妇女的平均PR阳性基质细胞也较少(12%±0.07)。
    脉络膜组织中的性类固醇受体的数量在不同年龄的男性和女性之间有所不同,这与男性和绝经后女性的CSC流行模式一致。
    UNASSIGNED: The purpose of this study was to investigate the presence of sex-steroid receptors in human choroidal tissue across different ages and sex, aiming to better understand the pronounced sex difference in central serous chorioretinopathy (CSC) occurrence.
    UNASSIGNED: Paraffin-embedded enucleated eyes of 14 premenopausal women, 15 postmenopausal women, 10 young men (<45 years), and 10 older men (>60 years) were used. A clinically certified immunostaining was performed to detect the presence of the androgen receptor (AR), progesterone receptor (PR; isoform A and B), and estrogen receptor (ERα). The stained slides were scored in a blinded manner for positive endothelial cells and stromal cells in consecutive sections of the same choroidal region.
    UNASSIGNED: Our analysis revealed the presence of AR, PR, and ERα in endothelial cells and stromal cells of choroidal tissue. The mean proportion of AR-positive endothelial cells was higher in young men (46% ± 0.15) compared to aged-matched women (29% ± 0.12; P < 0.05, 95% confidence interval [CI]). Premenopausal women showed markedly lower mean proportion of ERα (5% ± 0.02) and PR-positive endothelial cells (2% ± 0.01) compared to postmenopausal women (15% ± 0.07 and 19% ± 0.13; both P < 0.05, 95% CI), young men (13% ± 0.04 and 21% ± 0.10; both P < 0.05, 95% CI), and older men (18% ± 0.09 and 27% ± 0.14; both P < 0.05, 95% CI). Mean PR-positive stromal cells were also less present in premenopausal women (12% ± 0.07) than in other groups.
    UNASSIGNED: The number of sex-steroid receptors in the choroidal tissue differs between men and women across different ages, which aligns with the prevalence patterns of CSC in men and postmenopausal women.
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  • 文章类型: Journal Article
    背景:髋关节骨关节炎(OA)在成人脊柱畸形(ASD)患者中很常见。关于ASD患者髋关节OA患病率的数据有限,或其对基线和术后对齐和患者报告结局指标(PROMs)的影响。因此,本文将评估髋关节OA的患病率和对排列和PROM的影响。
    方法:纳入接受L1-骨盆或更长融合的ASD患者。两名独立的审阅者将髋关节OA与Kellgren-Lawrence(KL)分类进行分级,并按严重程度将其分为非严重(KL等级1或2)和严重(KL等级3或4)。在3个患者组中比较了放射学参数和PROM:髋关节(双侧3或4级髋关节),单侧(UL)-髋部(单侧髋部KL3或4级),或脊柱(双侧髋关节KL1或2级)。
    结果:520名符合OA患病率分析纳入标准的ASD患者中,34%(520中的177例)患有严重的双侧髋关节OA,并且在8.7%(520中的45例)中进行了单侧或双侧髋关节置换术。165例患者的子集具有所有数据成分,并接受了检查:68例髋关节,32UL-Hip,65脊柱髋关节患者年龄较大(67.9±9.5岁,脊柱为59.6±10.1年,UL-Hip为65.8±7.5年;p<0.001),并且具有更高的虚弱指数(UL-Hip为4.3±2.6,而脊柱为2.9±2.0;p<0.001)。在1年,两组有相似的腰椎前凸,然而,髋关节患者的矢状椎体轴(SVA)测量较差(45.9±45.5mm,UL-Hip为25.1±37.1mm,脊柱为19.0±39.3mm;p=0.001)。髋关节患者在基线时的退伍军人RAND-12身体成分汇总评分也较差(UL-Hip为25.7±9.3,与28.7±9.8相比,脊柱为31.3±10.5;p=0.005)和术后1年(UL-Hip为34.5±11.4,与40.3±10.4相比,脊柱为40.1±10.9;p=0.006)。
    结论:这项手术治疗的ASD研究显示,1/3的患者双侧有严重的髋关节OA。这些患有严重双侧髋关节OA的患者在ASD手术后持续1年的基线SVA和PROM较差。尽管矫正了脊柱前凸.
    方法:预后III级。有关证据级别的完整描述,请参阅作者说明。
    BACKGROUND: Hip osteoarthritis (OA) is common in patients with adult spinal deformity (ASD). Limited data exist on the prevalence of hip OA in patients with ASD, or on its impact on baseline and postoperative alignment and patient-reported outcome measures (PROMs). Therefore, this paper will assess the prevalence and impact of hip OA on alignment and PROMs.
    METHODS: Patients with ASD who underwent L1-pelvis or longer fusions were included. Two independent reviewers graded hip OA with the Kellgren-Lawrence (KL) classification and stratified it by severity into non-severe (KL grade 1 or 2) and severe (KL grade 3 or 4). Radiographic parameters and PROMs were compared among 3 patient groups: Hip-Spine (hip KL grade 3 or 4 bilaterally), Unilateral (UL)-Hip (hip KL grade 3 or 4 unilaterally), or Spine (hip KL grade 1 or 2 bilaterally).
    RESULTS: Of 520 patients with ASD who met inclusion criteria for an OA prevalence analysis, 34% (177 of 520) had severe bilateral hip OA and unilateral or bilateral hip arthroplasty had been performed in 8.7% (45 of 520). A subset of 165 patients had all data components and were examined: 68 Hip-Spine, 32 UL-Hip, and 65 Spine. Hip-Spine patients were older (67.9 ± 9.5 years, versus 59.6 ± 10.1 years for Spine and 65.8 ± 7.5 years for UL-Hip; p < 0.001) and had a higher frailty index (4.3 ± 2.6, versus 2.7 ± 2.0 for UL-Hip and 2.9 ± 2.0 for Spine; p < 0.001). At 1 year, the groups had similar lumbar lordosis, yet the Hip-Spine patients had a worse sagittal vertebral axis (SVA) measurement (45.9 ± 45.5 mm, versus 25.1 ± 37.1 mm for UL-Hip and 19.0 ± 39.3 mm for Spine; p = 0.001). Hip-Spine patients also had worse Veterans RAND-12 Physical Component Summary scores at baseline (25.7 ± 9.3, versus 28.7 ± 9.8 for UL-Hip and 31.3 ± 10.5 for Spine; p = 0.005) and 1 year postoperatively (34.5 ± 11.4, versus 40.3 ± 10.4 for UL-Hip and 40.1 ± 10.9 for Spine; p = 0.006).
    CONCLUSIONS: This study of operatively treated ASD revealed that 1 in 3 patients had severe hip OA bilaterally. Such patients with severe bilateral hip OA had worse baseline SVA and PROMs that persisted 1 year following ASD surgery, despite correction of lordosis.
    METHODS: Prognostic Level III. See Instructions for Authors for a complete description of levels of evidence.
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  • 文章类型: Journal Article
    In patients with end-stage kidney disease, kidney transplantation is the kidney replacement therapy option that provides the most successful survival. However, immunosuppression agents administered after kidney transplantation can increase the risk of opportunistic infections. Microsporidia are obligate intracellular pathogens that can be fatal in immunosuppressed patients. The present study aimed to determine the prevalence of microsporidia in kidney transplantation recipients and the molecular characterization of the detected species.
    To evaluate the prevalence of renal microsporidiosis in kidney transplant recipients, the urine samples from a total of 325 patients were analyzed by real-time and nested polymerase chain reaction for Encephalitozoon spp. and Enterocytozoon bieneusi.
    Only one (0.4%) sample from the adult patient was positive for the Encephalitozoon species, while no positivity was found in pediatric patients. It was determined as Encephalitozoon intestinalis by ITS rRNA gene region sequence analysis. A microsporidia species obtained from humans in Türkiye has been characterized for the first time and registered in GenBank.
    Our epidemiological results show that the prevalence of renal microsporidiosis in kidney transplant recipients is very low. In addition, as a result of the phylogenetic analysis of the detected isolate, it was observed that it was 100% identical to the isolates reported from dogs in Kayseri, Türkiye. This situation provided essential data regarding the zoonotic transmission dynamics of microsporidia.
    Böbrek nakli, son dönem böbrek yetmezliği olan hastalarda en başarılı sağkalım sağlayan renal replasman tedavi seçeneğidir. Ancak böbrek nakli sonrasında uygulanan immün baskılayıcı ajanlar fırsatçı enfeksiyon riskini artırmaktadır. Microsporidialar, immün sistemi baskılanmış hastalarda ölümcül olabilen zorunlu hücre içi patojenlerdir. Bu çalışmada böbrek nakil hastalarında microsporidia prevalansının belirlenmesi ve tespit edilen türlerin moleküler karakterizasyonunun yapılması amaçlandı.
    Böbrek nakli hastalarında renal microsporidiosis prevalansını değerlendirmek için toplam 325 hastadan alınan idrar örnekleri Encephalitozoon spp. ve Enterocytozoon bieneusi açısından gerçek zamanlı ve nested polimeraz zincir reaksiyonu ile analiz edildi.
    Erişkin hastalardan sadece biri (%0,4) Encephalitozoon türleri yönünden pozitif belirlendi, çocuk hastalarda ise pozitiflik saptanmadı. ITS rRNA gen bölgesi sekans analizi sonucunda tespit edilen türün Encephalitozoon intestinalis olduğu görüldü. Bu çalışma ile Türkiye’de ilk kez insanlardan izole edilen bir microsporidia türü karakterize edilerek GenBank’a kaydedildi.
    Elde edilen epidemiyolojik sonuçlar, renal transplant hastalarında renal microsiporidiosis prevalansının çok düşük olduğunu göstermektedir. Ayrıca tespit edilen izolatın filogenetik analizi sonucunda Kayseri’de köpeklerden bildirilen izolatlarla %100 benzer olduğu görüldü. Bu çalışma microsporidiaların zoonotik bulaşma dinamikleri açısından önemli bir veri sağlamaktadır.
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  • 文章类型: Journal Article
    UNASSIGNED: Recent studies determined that the amoeboid form of Blastocystis acts as a factor in stimulating the host\'s immune responses and ultimately results in urticaria and other skin disorders. The present study was conducted in order to determine the prevalence of Blastocystis in people referred to Bushehr city health centers and the relationship of this parasite with urticaria.
    UNASSIGNED: Fecal samples were collected from 180 males and females referred to Bushehr health centers and a questionnaire containing demographic information was completed for each person. Samples were examined by preparing direct smear (wet mount) and then formalin-detergent sedimentation techniques. Data were analyzed using SPSS 22.0 software and chi-square test.
    UNASSIGNED: The results showed that 11.1% of cases infected with Blastocystis and 55% of patients with Blastocystis had various gastrointestinal symptoms. Statistical analysis showed that there was no significant relationship between infection with some demographic factors such as sex, age, literacy level and residence, but this was significant with some clinical symptoms such as itching and urticaria.
    UNASSIGNED: Despite the existence of conflicting information and many ambiguities about the Blastocystis, this emerging pathogen is very important in terms of causing allergic and skin disorders in sufferers, therefore, it is necessary that patients with urticaria be evaluated for Blastocystis along with other diagnostic procedures and physicians should request a test before any medical intervention. Thus, diagnosis and treatment of these people can play an important role in improving the health of society.
    UNASSIGNED: Son araştırmalar Blastocystis ameboid formunun konağın bağışıklık yanıtlarını uyaran bir faktör olarak hareket ettiğini ve sonuçta ürtiker ve diğer deri bozukluklarına yol açtığını göstermiştir. Bu çalışma Bushehr şehir sağlık merkezlerine başvuran kişilerde Blastocystis prevalansını ve bu parazitin ürtiker ile ilişkisini belirlemek amacıyla yapılmıştır.
    UNASSIGNED: Bushehr sağlık merkezlerine başvuran 180 erkek ve kadından dışkı örnekleri toplandı ve her kişiye demografik bilgileri içeren bir anket dolduruldu. Örnekler direkt smear (wet mount) hazırlanarak ve ardından formol eter çöktürme teknikleri kullanılarak incelendi. Veriler SPSS 22.0 programı ve ki-kare testi kullanılarak analiz edildi.
    UNASSIGNED: Bulgular olguların %11,1’inin Blastocystis ile enfekte olduğunu ve Blastocystis ile enfekte olan hastaların %55’inde çeşitli gastrointestinal semptomların bulunduğunu gösterdi. İstatistiksel analiz, enfeksiyon ile cinsiyet, yaş, okuryazarlık düzeyi ve yerleşim yeri gibi bazı demografik faktörler arasında anlamlı ilişki olmadığını, ancak enfeksiyon ile kaşıntı ve ürtiker gibi bazı klinik semptomlar arasında anlamlı ilişki olduğunu gösterdi.
    UNASSIGNED: Blastocystis hakkında çelişkili bilgiler ve birçok belirsizlik bulunmasına rağmen bu patojen, alerjik deri bozukluklarına neden olması açısından oldukça önemlidir, bu nedenle ürtikerli hastaların diğer tanı işlemleriyle birlikte Blastocystis açısından da değerlendirilmesi ve hekimlerin herhangi bir tıbbi müdahale öncesinde test istemesi gerekmektedir. Dolayısıyla bu kişilerin tanı ve tedavisi toplum sağlığının iyileştirilmesinde önemli bir rol oynayabilir.
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  • 文章类型: Journal Article
    This article aims to investigate the implications of grief among family members of COVID-19 victims; verify the prevalence of prolonged grief symptoms; and identify family members\' expectations regarding end-of-life care for their loved ones affected by COVID-19. Descriptive, cross-sectional research, with a quantitative-qualitative approach. Data collection was performed using an online questionnaire, guided by the PG-13 instrument. Descriptive and inferential statistics were applied. The results were presented descriptively and with the aid of tables. The study sample included 142 family members, mostly female, who presented emotional, physical, social, and financial implications as a result of grief. A prevalence of prolonged grief symptoms was observed in 11.4% of the mourners with more than six months and 29.6% of those with less than six months. Three thematic categories were identified: transparency in communicating the health situation, access to moments of farewell, and promotion of comfort in care actions. The symptoms of Prolonged Grief Disorder have a significant association with the degree of kinship. In final care, family members\' expectations were classified as: permission for a dignified farewell, effective communication, and promotion of comfort and care.
    O objetivo deste artigo é investigar implicações do luto em familiares de vítimas da COVID-19; verificar a prevalência de sintomas de luto prolongado; identificar expectativas dos familiares acerca do cuidado em fim de vida de seus entes acometidos por COVID-19. Pesquisa descritiva, transversal, com abordagem quanti-qualitativa. Coleta de dados mediante questionário on-line, norteado pelo instrumento PG-13. Aplicou-se estatística descritiva e inferencial. Os resultados foram apresentados de forma descritiva e com auxílio de tabelas. Amostra de 142 familiares, maioria do sexo feminino, que apresentaram implicações emocionais, físicas, sociais e financeiras em decorrência do luto. Houve prevalência de sintomas de luto prolongado em 11,4% dos enlutados com mais de seis meses e 29.6% dos que tinham menos de seis meses. Foram identificadas três categorias temáticas: transparência na comunicação da situação de saúde, acesso a momentos de despedida e promoção de conforto nas ações de cuidado. Os sintomas de Transtorno de Luto Prolongado possuem associação significativa com o grau de parentesco. Nos cuidados finais as expectativas dos familiares foram classificadas em: permissão para despedida digna, comunicação efetiva e promoção de conforto e cuidado.
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  • 文章类型: Journal Article
    诸如由猫免疫缺陷病毒(FIV)和猫白血病病毒(FeLV)引起的疾病代表猫的健康问题。据报道,全国多个城市都有猫利什曼病(FL)。目的是进行FIV的临床流行病学和实验室研究,来自杜拉多斯庇护所的猫中的FeLV和FL,南马托格罗索州,巴西。从75只猫获得结膜和鼻粘膜的血样和拭子,来自四个动物收容所。进行FIV和FeLV的血清学。对于利什曼原虫,对血液进行聚合酶链反应(PCR),结膜和鼻粘膜。在免疫层析血清学测试中,7只猫FIV检测呈阳性,FeLV无一例。在利什曼原虫的PCR中没有样品是阳性的。研究表明,尽管研究地区存在人类和犬类利什曼病,利什曼原虫。在研究的猫中不存在。为了避免避难所的传染增加,它是必不可少的隔离猫与FIV。
    Diseases such as those caused by feline immunodeficiency virus (FIV) and feline leukemia virus (FeLV) represent health problems for cats. Feline leishmaniasis (FL) has been reported in several cities across the country. The objective was to carry out a clinical-epidemiological and laboratory study of FIV, FeLV and FL in cats from shelters in Dourados, Mato Grosso do Sul, Brazil. Blood samples and swabs from the conjunctival and nasal mucosa were obtained from 75 cats, from four animal shelters. Serology for FIV and FeLV was performed. For Leishmania, polymerase chain reaction (PCR) was performed on blood, conjunctiva and nasal mucosa. In the immunochromatographic serological test, seven cats tested positive for FIV and none for FeLV. No samples was positive in PCR for Leishmania. The study showed that despite the presence of human and canine leishmaniasis in the studied region, Leishmania spp. were absent in the cats studied. To avoid an increase in contagion in shelters, it is essential isolate cats with FIV.
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  • 文章类型: Journal Article
    背景:尽管隐睾是男性新生儿常见的生殖器异常,全球患病率差异显著,在中国,这种情况的流行病学数据明显缺乏。
    目的:本研究的目的是利用全国范围的监测数据,描述过去15年中国人群隐睾病的流行模式。
    方法:分析了中国国家人口出生缺陷监测系统(2007-2021)的数据,以计算隐睾的患病率,按出生年份分层,产妇年龄,产妇住宅,和地理区域。调整后的患病率比率使用泊松回归计算,而患病率和平均年变化百分比(AAPC)的趋势使用连接点回归模型进行评估.
    结果:在研究期间,在2,565,964例男性足月分娩中,共发现1,833例隐睾病例,导致总体患病率为每10,000名新生儿7.14、5.60和1.54,孤立的,和相关的隐睾,分别。总体患病率从每10,000名新生儿3.86增加到11.20名,AAPC为7.9%(95%置信区间:5.5-11.0)。观察到不同母亲年龄的显著差异(<20岁,7.62/万;20-24年,6.14/10000;25-29年,6.96/10000;30-34年,7.48/10,000;≥35岁,9.22/10,000),产妇住宅(城市与农村,10.99/10,000vs.2.86/10,000),和地理区域(东部,12.38/10,000;中央,2.36/10,000;西部,2.63/10000)。大约三分之一的隐睾病例是双侧的,而三分之二是单方面的。常见的相关异常包括先天性睾丸鞘膜积液,以及生殖器官的异常,循环系统,和肌肉骨骼系统.
    结论:尽管与其他国家相比利率较低,隐睾患病率的增加趋势需要进一步的调查和干预.
    BACKGROUND: Despite cryptorchidism being a common genital abnormality in male newborns with significant prevalence variations globally, there is a notable scarcity of epidemiological data on this condition in China.
    OBJECTIVE: This study aimed to delineate the prevalence pattern of cryptorchidism in Chinese population over the past 15 years using nationwide surveillance data.
    METHODS: Data from the China National Population-based Birth Defects Surveillance System (2007-2021) were analyzed to calculate the prevalence rates of cryptorchidism, stratified by birth year, maternal age, maternal residence, and geographic region. Adjusted prevalence rate ratios were computed using Poisson regression, while trends in prevalence and average annual percent change (AAPC) were assessed using the joinpoint regression model.
    RESULTS: During the study period, a total of 1,833 cases of cryptorchidism were identified among 2,565,964 full-term male births, resulting in prevalence rates of 7.14, 5.60, and 1.54 per 10,000 births for overall, isolated, and associated cryptorchidism, respectively. The overall prevalence increased from 3.86 to 11.20 per 10,000 births, with an AAPC of 7.9% (95% confidence interval: 5.5-11.0). Significant variations were observed across maternal age (< 20 years, 7.62/10,000; 20-24 years, 6.14/10,000; 25-29 years, 6.96/10,000; 30-34 years, 7.48/10,000; ≥35 years, 9.22/10,000), maternal residence (urban vs. rural, 10.99/10,000 vs. 2.86/10,000), and geographic region (eastern, 12.38/10,000; central, 2.36/10,000; western, 2.63/10,000). Approximately one-third of cryptorchidism cases were bilaterally, while two-thirds were unilateral. Commonly observed associated abnormalities included congenital hydrocele testis, as well as anomalies in the genital organs, circulatory system, and musculoskeletal system.
    CONCLUSIONS: Despite lower rates compared to other countries, the increasing trend in prevalence of cryptorchidism necessitates further investigation and intervention.
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  • 文章类型: Journal Article
    PANX1(pannexin1),广泛表达的ATP释放膜通道,已经被证明在炎症中起作用,血压调节,和心肌梗塞。然而,尚未研究PANX1在心肌细胞中在心力衰竭进展中的可能作用.
    我们产生了一种在心肌细胞中具有PANX1组成性缺失的新型小鼠品系(Panx1MyHC6)。
    心肌细胞中的PANX1缺失对无压力的心脏功能没有影响,但增加了糖酵解代谢并导致糖酵解ATP的产生,同时减少氧化磷酸化,体内和体外。体外,用异丙肾上腺素治疗H9c2心肌细胞导致PANX1依赖性释放ATP和Yo-Pro-1摄取,通过螺内酯和siRNA介导的PANX1敲低的药物阻断评估。为了研究非缺血性心力衰竭和先前的心脏肥大,我们服用了异丙肾上腺素,我们证明,Panx1MyHC6小鼠受到保护,不会因心肌细胞肥大而导致左心室收缩和舒张体积增加。此外,我们发现,Panx1MyHC6小鼠显示减少异丙肾上腺素诱导的免疫细胞募集(CD45+),特别是中性粒细胞(CD11b+,Ly6g+),心肌。
    一起,这些数据表明,在非缺血性心力衰竭中,PANX1缺乏可增加糖酵解代谢,并至少部分通过减少免疫细胞募集来防止心肌肥大.我们的研究表明,抑制PANX1通道可作为改善心力衰竭患者心功能不全的治疗方法。
    UNASSIGNED: PANX1 (pannexin 1), a ubiquitously expressed ATP release membrane channel, has been shown to play a role in inflammation, blood pressure regulation, and myocardial infarction. However, the possible role of PANX1 in cardiomyocytes in the progression of heart failure has not yet been investigated.
    UNASSIGNED: We generated a novel mouse line with constitutive deletion of PANX1 in cardiomyocytes (Panx1MyHC6).
    UNASSIGNED: PANX1 deletion in cardiomyocytes had no effect on unstressed heart function but increased the glycolytic metabolism and resulting glycolytic ATP production, with a concurrent decrease in oxidative phosphorylation, both in vivo and in vitro. In vitro, treatment of H9c2 cardiomyocytes with isoproterenol led to PANX1-dependent release of ATP and Yo-Pro-1 uptake, as assessed by pharmacological blockade with spironolactone and siRNA-mediated knockdown of PANX1. To investigate nonischemic heart failure and the preceding cardiac hypertrophy, we administered isoproterenol, and we demonstrated that Panx1MyHC6 mice were protected from systolic and diastolic left ventricle volume increases as a result of cardiomyocyte hypertrophy. Moreover, we found that Panx1MyHC6 mice showed decreased isoproterenol-induced recruitment of immune cells (CD45+), particularly neutrophils (CD11b+, Ly6g+), to the myocardium.
    UNASSIGNED: Together, these data demonstrate that PANX1 deficiency in cardiomyocytes increases glycolytic metabolism and protects against cardiac hypertrophy in nonischemic heart failure at least in part by reducing immune cell recruitment. Our study implies PANX1 channel inhibition as a therapeutic approach to ameliorate cardiac dysfunction in patients with heart failure.
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  • 文章类型: Journal Article
    背景:儿童对互联网游戏障碍(IGD)的日益关注强调了理解其决定因素和与心理健康的联系的紧迫性,特别是针对学龄儿童的干预措施。
    目的:本研究旨在评估IGD的患病率和决定因素及其与抑郁症的关系,焦虑,以及在塞勒姆市私立学校就读的8-12岁儿童的行为。
    方法:进行了一项涉及塞勒姆区780名8-12岁儿童的横断面研究。学校是随机抽样的,和数据是通过自我管理问卷收集的。
    方法:数据来自没有遗传的儿童,系统性,或者精神障碍和脑损伤.问卷,改编自AlhamoudMA等人。(2022),包含社会人口统计学特征的部分,游戏行为,和评估IGD的量表,抑郁症,和焦虑。管理发生在上课时间,完成时间为30-35分钟。
    方法:数据分析使用SPSSv23.0,包括描述性统计,方差分析,组间比较的卡方检验,和皮尔逊相关系数来确定关联。
    结果:塞勒姆区IGD患病率为1.2%,在年龄较大的儿童中观察到更高的焦虑和抑郁发生率,尤其是男性。
    结论:IGD之间呈明显正相关,焦虑,和抑郁症。必须采取紧急预防措施,以遏制IGD的上升趋势,如限制屏幕时间和促进户外活动,以提高儿童的整体健康。
    BACKGROUND: The escalating concern over Internet gaming disorder (IGD) among children underscores the urgency of comprehending its determinants and links to mental health, particularly for interventions targeting school-aged children.
    OBJECTIVE: This study aimed to evaluate the prevalence and determinants of IGD and its association with depression, anxiety, and behavior among 8-12-year-old children attending private schools in Salem city.
    METHODS: A cross-sectional study involving 780 children aged 8-12 years from Salem district was conducted. Schools were randomly sampled, and data were collected through a self-administered questionnaire.
    METHODS: Data were gathered from children without genetic, systemic, or mental disorders and brain trauma. The questionnaire, adapted from Alhamoud M A et al. (2022), encompassed sections on sociodemographic characteristics, gaming behavior, and scales for assessing IGD, depression, and anxiety. Administration occurred during school hours with a 30-35 min completion time.
    METHODS: Data analysis utilized SPSS v23.0, including descriptive statistics, ANOVA, Chi-square tests for intergroup comparisons, and Pearson\'s correlation coefficient to determine associations.
    RESULTS: The prevalence of IGD in Salem district was 1.2%, with higher rates of anxiety and depression observed among older children, particularly males.
    CONCLUSIONS: A positive correlation was evident between IGD, anxiety, and depression. Urgent preventive measures have to be warranted to curb the rising trend of IGD, such as limiting screen time and promoting outdoor activities to enhance children\'s overall health.
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