Idiopathic

特发性
  • 文章类型: Journal Article
    目的:评估新诊断的早发性特发性不宁腿综合征(RLS)患者开始加巴喷丁或多巴胺激动剂(DAs)治疗后自杀意念和行为的发生率,并检查自杀行为风险。比较那些接受加巴喷丁和DA的人。
    方法:使用2012年至2019年的MarketScan索赔数据进行了一项新的用户回顾性队列研究。暴露是在新的RLS诊断后60天内开始的单药加巴喷丁或DA。检查了三种不同的自杀结局指标,并计算了每种指标的发生率。加巴喷丁类药物结果的估计相对风险(RR)的对数二项回归模型。针对基线协变量调整的倾向得分权重,包括年龄,物质使用障碍,高脂血症,抗精神病药的使用,催眠/镇静使用,和情绪稳定剂的使用,在加权之前最不平衡。
    结果:该队列包括6672名患者,4986(74.7%)启动DA,1686(25.3%)启动加巴喷丁。加巴喷丁组所有结局指标的发生率均较高(自杀率:21.6vs.每1000人年10.7;自杀自残:23.0vs.11.1/1000人年;与过量和自杀相关的事件:30.0vs.15.5人年)。相关自杀风险(调整后的RR,1.27[95%CI,0.86-1.88]);自杀与自我伤害(调整后的RR,1.30[95%CI,0.89-1.90]);或过度自杀和自杀相关事件(调整后RR,1.30[95%CI,0.93-1.80])与加巴喷丁类药物无关。
    结论:加巴喷丁类药物组的自杀意念和行为发生率较高,虽然调整后未发现风险增加.鉴于数据的局限性和结果的稀有性,不能排除可能的信号。
    OBJECTIVE: To estimate incidence rates of suicidal ideation and behavior following treatment initiation with gabapentinoids or dopamine agonists (DAs) in patients with newly diagnosed early-onset idiopathic restless legs syndrome (RLS) and to examine suicidal behavior risk, comparing between those receiving gabapentinoids and DAs.
    METHODS: A new user retrospective cohort study using MarketScan claims data from 2012 to 2019 was conducted. Exposures were monotherapy gabapentinoids or DAs initiated within 60 days of new RLS diagnosis. Three varying outcome measures of suicidality were examined and incidence rates were calculated for each. A log-binomial regression model the estimated relative risk (RR) of the outcomes with gabapentinoids. Propensity score weighting adjusted for baseline covariates, including age, substance use disorders, hyperlipidemia, antipsychotic use, hypnotic/sedative use, and mood stabilizer use, which were most imbalanced before weighting.
    RESULTS: The cohort included 6672 patients, with 4986 (74.7%) initiating a DA and 1686 (25.3%) initiating a gabapentinoid. Incidence rates for all outcome measures were higher in the gabapentinoid group (suicidality: 21.6 vs. 10.7 per 1000 person-years; suicidality with self-harm: 23.0 vs. 11.1 per 1000 person-years; overdose- and suicide-related events: 30.0 vs. 15.5 person-years). Associated risk of suicidality (adjusted RR, 1.27 [95% CI, 0.86-1.88]); suicidality with self-harm (adjusted RR, 1.30 [95% CI, 0.89-1.90]); or overdose- and suicide-related events (adjusted RR, 1.30 [95% CI, 0.93-1.80]) was not significant with gabapentinoids.
    CONCLUSIONS: Incidence rates for suicidal ideation and behavior were higher among the gabapentinoid group, although increased risk was not detected after adjustment. A possible signal cannot be ruled out given limitations of the data and rarity of the outcome.
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  • 文章类型: Journal Article
    背景和目标:尽管随着时间的推移提出了不同的假设,缺乏能够预测特发性突发性感音神经性听力损失(ISSNHL)治疗反应和听力恢复的因素的信息.这项研究的目的是在我们的三级学术听力学中心接受ISSNHL治疗的患者的回顾性临床环境中应用单变量和多变量统计模型,以调查临床体征的预后价值。症状,以及与听力恢复有关的合并症。材料和方法:纳入标准为:在Padova或Modena三级学术听力学中心诊断和治疗的ISSNHL病史;年龄≥18岁;临床和听力学结果数据的可用性。排除标准为:听觉神经鞘瘤的听力损失,内淋巴积液,脑膜炎,创伤(头部创伤,颞骨骨折,声学创伤),气压伤,淋巴瘘;在工作环境中暴露于≥80dB的噪声水平;ISSNHL诊断前任何单侧或双侧听力损失(老年性耳聋除外);任何影响外耳或中耳的疾病;任何先前的耳手术;拒绝提供医疗数据用于研究目的。86名连续患者(38名女性,48名男性;平均年龄:58岁;四分位距:47.00-69.00岁)。对所有患者进行全身性类固醇治疗,口服泼尼松或静脉注射甲基泼尼松龙。二线治疗包括鼓室类固醇注射和/或高压氧治疗。结果:采用多因素logistic回归模型,包括非多重共线临床和听力学变量,在单变量分析中显示p值<0.10(即诊断时的年龄,诊断时间到了,口服类固醇剂量,和受影响一侧的PTA)。仅患侧PTA保留其统计学意义(OR:1.0615,95%CI:1.0185-1.1063,p=0.005)。结论:对我们数据的分析表明,治疗前的听力阈值与ISSNHL的恢复之间存在关联。需要对更大的队列(尤其是在前瞻性环境中)进行进一步的研究,以进一步阐明临床参数在ISSNHL患者中的预后作用。在正确的咨询环境中,关于患者对无法恢复听力的担忧,重要的是提供适当的听力康复方法的观点。
    Background and Objectives: Although different hypotheses have been proposed over time, there is a dearth of information on factors able to predict the response to treatment for idiopathic sudden sensorineural hearing loss (ISSNHL) and hearing recovery. The aim of this study was to apply univariate and multivariate statistical models in a retrospective clinical setting of patients given therapy for ISSNHL at our tertiary academic audiological centers to investigate the prognostic value of clinical signs, symptoms, and comorbidities in relation to hearing recovery. Materials and Methods: The inclusion criteria were: history of ISSNHL diagnosed and treated at the Padova or Modena tertiary academic audiological centers; age ≥ 18 years; availability of clinical and audiological outcome data. The exclusion criteria were: hearing loss in acoustic schwannoma, endolymphatic hydrops, meningitis, trauma (head trauma, temporal bone fracture, acoustic trauma), barotrauma, perilymphatic fistula; exposure to noise levels ≥ 80 dB in the work environment; any unilateral or bilateral hearing loss (except for presbycusis) prior to ISSNHL diagnosis; any disorders affecting the external or middle ear; any previous ear surgery; refusal to make medical data available for research purposes. Eighty-six consecutive patients (38 females, 48 males; median age: 58 years; interquartile range: 47.00-69.00 years) were included. A systemic steroid therapy was administered to all patients, either orally with prednisone or intravenously with methylprednisolone. Second-line therapy included intratympanic steroid injections and/or hyperbaric oxygen therapy. Results: A multivariate logistic regression model was used, including the non-multicollinear clinical and audiological variables, which showed a p-value < 0.10 at the univariate analyses (namely age at diagnosis, time to diagnosis, oral steroid dose, and PTA on the affected side). Only PTA on the affected side retained its statistical significance (OR: 1.0615, 95% CI: 1.0185-1.1063, p = 0.005). Conclusions: The analysis of our data showed an association between the hearing threshold before treatment and the recovery from ISSNHL. Further studies on larger cohorts (especially in a prospective setting) are needed to shed more light on the prognostic role of clinical parameters in patients with ISSNHL. In a correct counseling setting, with regard to the patient\'s concern about not being able to recover hearing, it is important to offer perspectives of appropriate hearing rehabilitation approaches.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    扩张型心肌病(DCM)对心力衰竭的患病率有重要贡献,然而,支持流行病学数据很少。这项研究试图估计DCM的患病率和特发性DCM在美国的比例,多样化的电子健康记录(EHR)数据库。
    这次回顾展,观察性研究包括2017年至2019年在OptumEHR中进行访视的56,812,806例患者。使用ICD-10编码鉴定疑似DCM病例。从1000例随机选择的病例中进行鉴定的临床注释,以手动审查以确定DCM的诊断并估计特发性DCM的比例。估计了DCM和特发性DCM的时期患病率和临床负担。
    手动临床审查表明,我们的定义对DCM的阳性预测值为92.5%,特发性DCM比例估计为46.3%。2017年至2019年期间DCM的估计患病率为每100,000人中118.33人。≥65岁的成年人患病率增加,男性,和非洲裔美国人。对2019年美国人口的推断导致约388350名患者的总体负担。调整特发性DCM病例的比例,特发性DCM患病率为每100,000人中59.23人,负担194,385人。在这个人群中进行临床基因检测的证据很少,少于0.43%的DCM病例报告测试代码。
    本研究确立了DCM和特发性DCM的保守期患病率,并证明了DCM的低分子基因检测。这些发现表明,遗传性DCM的临床负担可能被低估了。
    UNASSIGNED: Dilated cardiomyopathy (DCM) contributes significantly to heart failure prevalence, yet supporting epidemiologic data is sparse. This study sought to estimate the period prevalence of DCM and the proportion of idiopathic DCM in the United States using a large, diverse electronic health records (EHR) database.
    UNASSIGNED: This retrospective, observational study included 56,812,806 deidentified patients in Optum EHR with visits between 2017 and 2019. Suspected DCM cases were identified using ICD-10 coding. Deidentified clinical notes from 1000 randomly selected cases were manually reviewed to determine the diagnosis of DCM and estimate the proportion of idiopathic DCM. The period prevalence and clinical burden of DCM and idiopathic DCM were estimated.
    UNASSIGNED: Manual clinical review demonstrated that our definition had a positive predictive value of 92.5% for DCM, with 46.3% estimated as the idiopathic DCM proportion. The estimated period prevalence of DCM between 2017 and 2019 was 118.33 per 100,000. Prevalence increased for adults ≥65 years of age, males, and African Americans. Extrapolation to the 2019 US population led to an overall estimated burden of roughly 388,350 patients. Adjusting for the proportion of cases with idiopathic DCM yielded an idiopathic DCM prevalence of 59.23 per 100,000 and a burden of 194,385 patients. Evidence of clinical genetic testing in this population was scarce, with less than 0.43% of DCM cases reporting a testing code.
    UNASSIGNED: This study establishes a conservative period prevalence for DCM and idiopathic DCM and demonstrates very low molecular genetic testing for DCM. These findings suggest that the clinical burden of genetic DCM may be underestimated.
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  • 文章类型: Case Reports
    背景:特发性胸膜实质纤维弹性增生症(IPPFE)是一种非常罕见且缓慢明显进展的慢性肺部疾病。通常累及肺的上叶。这种不寻常的疾病,2013年首次被认为是罕见的特发性间质性肺炎,其特征是内脏胸膜和下肺实质的致密纤维化,并伴有主要在胸膜下肺泡壁的弹性变性。为了提高我们对这种罕见疾病的认识,我们报告一例由病理结果确定的IPPFE。病例报告:一名73岁的男性患者,吸烟者,有慢性阻塞性肺疾病病史,自2022年1月以来,劳累时呼吸困难逐渐恶化,并伴有体重减轻。胸部X线检查发现胸部扩张。胸部高分辨率计算机断层扫描显示双尖胸膜下实质凝结,右上叶有牵张性支气管扩张和胸膜回缩以及弥漫性双侧中央小叶气肿。扫描引导的跨顶叶肺活检显示肺实质纹身有炭疽病沉积,大部分被纤维组织重塑,在偏振光中与许多波浪状和屈光性畸形结构混合在一起。orcein染色证实了这些病变中存在过量的弹性纤维。所有病因调查均为阴性。他的肺功能研究显示可逆性阻塞性通气障碍。经过多学科的讨论,IPPFE的诊断是根据胸部计算机断层扫描在上肺的分布并结合病理类型来确定的。结论:该病例强调了IPPFE的非典型误导性放射学表现以及病理结果在建立诊断中的关键作用。因此,需要进一步的研究来提高我们对这种罕见疾病的认识,并建立明确的IPPFE诊断和治疗指南.
    Background: Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a very rare and a slowly conspicuous progressing chronic lung disease, which usually involves the upper lobes of the lung. This unusual disease, first recognized as a rare idiopathic interstitial pneumonia in 2013, is characterized by dense fibrosis of the visceral pleura and the subjacent lung parenchyma accompanied by elastosis predominating in the subpleural alveolar walls. In the interest of improving our understanding of this uncommon disease, we report a case of IPPFE established by pathology results. Case report: A 73-year-old male patient, smoker, with a medical history of chronic obstructive pulmonary disease, presented since January 2022 with a gradual worsening of dyspnea on exertion and productive cough with weight loss. The chest X-ray detected a thoracic distention. The chest high resolution computed tomography revealed biapical subpleural parenchymatous condensations with tractive bronchiectasis and pleural retraction in the right upper lobe and diffuse bilateral cento-lobular emphysema. A scan-guided trans-parietal lung biopsy showed lung parenchyma tattooed with anthracosic deposits, largely remodeled by fibrous tissue, intermingled with numerous wavy and refractive dyselastotic structures in polarized light. The orcein staining confirmed the presence of excess elastosic fibers within these lesions. All etiological investigations were negative. His lung function studies revealed a reversible obstructive ventilatory disorder. Following a multidisciplinary discussion, the diagnosis of IPPFE was confirmed on the basis of the distribution in the upper lungs on chest computed tomography combined with pathology pattern. Conclusions: This case emphasizes the atypical misleading radiological presentation of IPPFE and the key role of pathological results in establishing the diagnosis. Hence, further studies are needed to improve our understanding of this uncommon disease and to establish clear-cut guidelines for IPPFE diagnosis and management.
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  • 文章类型: Journal Article
    背景:尽管经支气管肺冷冻活检(TBLC)广泛用于各种间质性肺病(ILD)的诊断算法中,其在ILD患者治疗决策策略中的实际效用仍不清楚,特别是,当判断开始抗纤维化药物的时间。
    方法:我们分析了40例接受TBLC的特发性或纤维化过敏性肺炎患者的医疗记录。基于TBLC的常规间质性肺炎(UIP)评分用于评估三个形态学描述:斑片状纤维化,成纤维细胞灶,蜂蜜梳理。
    结果:在我们的40例ILD患者中,UIP最常见的放射学特征是不确定的(45.0%)。最终诊断为特发性肺纤维化(22.5%),纤维化非特异性间质性肺炎(5.0%),纤维化过敏性肺炎(35.0%),和不可分类的ILD(37.5%)。线性混合效应分析表明,基于TBLC的UIP“评分≥2”的患者的%FVC和%DLCO斜率的下降明显高于“评分≤1”的患者。“在评分≥2(n=24)的患者的随访期间,其中一半以上(n=17)接受了抗纤维化药物,大多数患者(n=13)在TBLC手术后6个月内接受了抗纤维化药物的早期给药。
    结论:基于TBLC的UIP评分≥2表明进行性纤维化病程的可能性增加,这可能有助于预测进行性肺纤维化/进行性纤维化ILD,即使疾病由于抗炎药暂时稳定。通过治疗临床医生,患者可能会从早期引入抗纤维化药物中受益。
    BACKGROUND: Although transbronchial lung cryobiopsy (TBLC) is widely used in diagnostic algorithms for various interstitial lung diseases (ILDs), its real-world utility in the therapeutic decision-making strategy for ILD patients remains unclear, in particular, when judging the time to start antifibrotic agents.
    METHODS: We analyzed medical records of 40 consecutive patients with idiopathic or fibrotic hypersensitivity pneumonitis who underwent TBLC. A TBLC-based usual interstitial pneumonia (UIP) score was used to assess three morphologic descriptors: patchy fibrosis, fibroblastic foci, and honeycombing.
    RESULTS: In our 40 patients with ILD, the most frequent radiological feature was indeterminate for UIP (45.0%). Final diagnosis included idiopathic pulmonary fibrosis (22.5%), fibrotic nonspecific interstitial pneumonia (5.0%), fibrotic hypersensitivity pneumonitis (35.0%), and unclassifiable ILD (37.5%). Linear mixed-effects analysis showed that declines in the slopes of %FVC and %DLCO in patients with TBLC-based UIP \"Score ≥ 2\" were significantly steeper than those of patients with \"Score ≤ 1.\" During follow-up of patients with Score ≥ 2 (n = 24), more than half of them (n = 17) received an antifibrotic agent, with most patients (n = 13) receiving early administration of the antifibrotic agent within 6 months after the TBLC procedure.
    CONCLUSIONS: TBLC-based UIP Score ≥ 2 indicated the increased possibility of a progressive fibrosis course that may prove helpful in predicting progressive pulmonary fibrosis/progressive fibrosing ILD even if disease is temporarily stabilized due to anti-inflammatory agents. Patients may benefit from early introduction of antifibrotic agents by treating clinicians.
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  • 文章类型: Case Reports
    我们想分享一个5岁儿童的案例研究,他抱怨脖子前部有疼痛的肿块,发烧98°F有时,甲状腺脓肿可能由于其稀有性而被忽略,并且在我们的鉴别诊断列表中处于较低水平。颈部超声检查证实了我们的发现。对文献的全面分析表明,几乎所有脓肿都需要因果细菌。然而,在我们的例子中,吸出的液体培养物没有生长,表明脓肿是无菌的。当患者出现严重的颈部肿胀时,本病例报告强调了将甲状腺脓肿作为鉴别诊断之一的重要性,因为早期发现对于降低并发症的风险至关重要.
    We would like to share a case study of a five-year-old child who complained of a painful mass on the front of his neck, with a fever of 98°F. Sometimes thyroid abscesses may be overlooked due to their rarity and are lower down on our list of differential diagnoses. Neck ultrasonography confirmed our findings. A thorough analysis of the literature showed that causal bacteria are required for almost all abscesses. However, in our instance, the aspirated fluid culture revealed no growth, indicating that the abscess was sterile. When patients present with severe neck swelling, this case report emphasizes the significance of considering thyroid abscess as one of the differential diagnoses since early detection is critical to minimize the risk of complications.
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  • 文章类型: Journal Article
    背景:先前的研究表明,T1倾斜与术后肩部平衡(SB)呈正相关。这项研究的目的是探讨术中T1倾斜的作用,作为预测青少年特发性脊柱侧凸(AIS)患者术后SB的潜在参数。
    方法:从一个三级中心对具有结构性胸曲线的AIS患者进行了至少2年随访。术前站立,第1架设,1年和2年的随访;以及术中最终易发的X光片以及临床数据进行了审查。将患者分为2组:A组-最终术中T1倾斜≤5°,B组-最终术中T1倾斜>5°。对于基线右肩或左肩高以及UIV为T2或T3/T4的患者,将这些组的术后SB整体和单独进行比较。就多个SB变量而言,将2年时最佳SB(X线摄影肩高(RSH)<2cm)的患者与次优SB(RSH≥2cm)进行比较。
    结果:55名患者(平均年龄15.1岁,43F,包括平均BMI22,平均胸廓Cobb-49.8°)。根据伦克曲线类型,有13名1A型患者,10例患者为1B,12例1C,7名2A患者,2B型患者4例,3C型患者9例。T1倾斜与RSH显著相关,锁骨角度差(CAD),第一肋角片(FRA),UIV在最初直立时倾斜,1年,和术后2年的X光片(全部p<0.05)。比较群体时,A和B,A组患者的2年SB参数恢复明显更好;RSH(6.8vs11.8mm,p=0.01),CAD(3.9vs9.1p<0.001)和T1倾斜(4.7vs7.8°p=0.01)。对于基线右肩高的患者发现了类似的结果;RSH(p=0.04),CAD(p<0.001)和T1倾斜(p<0.001)以及UIV是否为T2或T3/T4。尽管MTCobb校正无差异,但与47例最佳SB患者相比,8例次最佳SB患者的术中T1倾斜较差(p=0.03)(83.1vs79.8%,p=0.57)。
    结论:术后T1倾斜与首次直立侧肩参数相关,1年,和2年X光片.因此,T1倾斜可以潜在地用作预测术后SB的替代。无论UIV是T2还是T3/T4,术中T1倾斜≤5°的水平都与术后2年的肩部平衡参数有关。尽管所有患者的主胸曲线校正百分比相似,但2年时SB次优的患者最终术中T1倾斜较差。
    BACKGROUND: Previous studies have shown that T1 tilt is positively correlated with post-operative shoulder balance (SB). The aim of this study was to explore the role of intra-operative T1 tilt, among other shoulder parameters as a potential parameter to predict post-operative SB in adolescent idiopathic scoliosis (AIS) patients.
    METHODS: A retrospective review of AIS patients with structural thoracic curves with minimum 2 year follow up was conducted from a single tertiary center. Standing pre-operative, 1st erect, 1 year and 2-year follow-up; and intra-operative final prone radiographs were reviewed along with clinical data. Patients were stratified into 2 cohorts: Group A-Final intra-operative T1 tilt ≤5° and Group B-Final intra-operative T1 tilt >5°. These groups were compared for post-operative SB as a whole and separately for patients with baseline right or left shoulder high and if UIV was T2 or T3/T4. Patients with optimal SB (Radiographic shoulder height (RSH) <2 cm) at 2 years were compared to sub-optimal SB (RSH ≥ 2 cm) with respect to multiple SB variables.
    RESULTS: 55 patients (mean age 15.1 years-old, 43 F, mean BMI 22, mean thoracic Cobb-49.8°) were included. Based on Lenke curve types, there were 13 patients with type 1A, 10 patients with 1B, 12 patients with 1C, 7 patients with 2A, 4 patients with 2B and 9 patients with type 3C. T1 tilt was significantly correlated with RSH, Clavicle angle difference (CAD), First Rib Angle (FRA), and UIV tilt at first erect, 1-year, and 2-year post-op radiographs (p < 0.05 for all). When comparing groups, A and B, Group A patients showed significantly better restoration of their 2-year SB parameters; RSH (6.8 vs 11.8 mm, p = 0.01), CAD (3.9 vs 9.1 p < 0.001) and T1 tilt (4.7 vs 7.8° p = 0.01). Similar results were found for patients with baseline right shoulder high; RSH (p = 0.04), CAD (p < 0.001) and T1 tilt (p < 0.001) and whether UIV was T2 or T3/T4. Eight patients with sub-optimal SB had worse intra-operative T1 tilt (p = 0.03) compared to 47 patients with optimal SB despite no difference in MT Cobb correction (83.1 vs 79.8%, p = 0.57).
    CONCLUSIONS: Post-operative T1 tilt correlates with lateral shoulder parameters at first erect, 1 year, and 2-year radiographs. Therefore, T1 tilt can potentially be used as a surrogate to predict post-operative SB. Leveling intra-operative T1 tilt ≤5° is associated with better 2-year post-operative shoulder balance parameters irrespective of whether the UIV was T2 or T3/T4. Patients with sub-optimal SB at 2 years had worse final intra-operative T1 tilt despite similar percent correction of main thoracic curve for all patients.
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  • 文章类型: Journal Article
    背景:全球,不育影响约15%的育龄夫妇。在许多情况下,不孕症无法治疗,然而,在最近的临床试验中,新的有价值的治疗方案已经涉及.这项临床试验的目的是评估在来曲唑中添加辅酶Q10(CoQ10)对诊断为特发性少弱精子症(iOAT)综合征的男性精子图和性激素测试结果的影响。这是一种病因不明的男性精子发生缺陷。方法:随机,开放标签,平行的双臂介入研究包括67名年龄在18-60岁的成年男性患者,这些患者被确诊为iOAT综合征,这些患者来自Nahrain大学不孕诊断和辅助生殖技术高级研究所。将患者随机分为两组,A组包括29例患者,每周两次口服来曲唑2.5mg片剂,B组包括38例患者,每周两次口服来曲唑2.5mg片剂,每天400mg辅酶Q10。两组均治疗3个月。精液样本,血清卵泡刺激素(FSH),雌二醇(E2),和睾酮(T)在第一天进行分析,在第一个月底,两个和三个。结果:两组精子浓度,形态正常,精子总数和活力,血清睾酮和FSH水平,T/E2比值显著增加,而雌二醇水平在治疗三个月后显著下降。仅A组精液体积变化明显。在两组比较中,所有测量参数,除了精子活力和FSH水平,治疗三个月后表现出显著差异,而精子体积在治疗仅两个月后就达到了显著值。结论:CoQ10作为来曲唑的辅助治疗有效地改善了iOAT伊拉克男性的大多数测试精子参数。注册:ClinicalTrials.gov(NCT05847257,2023年5月6日)。
    Background: Worldwide, infertility affects about 15% of reproductive-age couples. In many cases, infertility can\'t be treated, however new treatment options with promising value have been involved in recent clinical trials. The aim of this clinical trial was to evaluate the impacts of adding coenzyme Q10 (CoQ10) to letrozole on the results of spermiogram and sex hormone tests in men diagnosed with idiopathic oligoasthenoteratozoospermia (iOAT) syndrome, which is a type of male defective spermatogenesis of unknown etiology. Methods: This randomized, open-label, parallel two-arm interventional study included 67 adult male patients aged 18-60 years with a confirmed diagnosis of iOAT syndrome recruited from The High Institute for Infertility Diagnosis & Assisted Reproduction Technologies/Nahrain University. Patients were randomly separated into two groups, Group A included 29 patients treated with letrozole 2.5 mg tablet orally twice a week, Group B included 38 patients treated with a combination of letrozole 2.5 mg tablet orally twice a week plus CoQ10 400 mg per day. Both groups completed treatment for three months. Semen samples, serum follicle-stimulating hormone (FSH), estradiol (E 2), and testosterone (T) were analyzed at day one, and at the end of month one, two and three. Results: Both groups showed that sperm concentration, normal morphology, total sperm count and motility, serum testosterone and FSH levels, and T/E 2 ratio were significantly increased, while estradiol levels significantly decreased after three months of treatment. Seminal fluid volume changed significantly in group A only. In comparing between the two groups, all measured parameters, apart from sperm motility and FSH level, demonstrated a significant difference after three months of treatment, while sperm volume reached significant value after only two months of therapy. Conclusions: CoQ10 as adjuvant treatment to letrozole effectively improved most of the tested sperm parameters in Iraqi men with iOAT. Registration: ClinicalTrials.gov ( NCT05847257, May 6, 2023).
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  • 文章类型: Journal Article
    这项病例对照研究旨在评估猫自然发生的高钙血症中的降钙素反应,评估降钙素与离子钙(iCa)之间的关系,并检查降钙素之间的关系。iCa和骨转换。
    通过医学数据库搜索回顾性鉴定了高钙血猫(iCa浓度持续增加[>1.40mmol/l]);前瞻性招募了其他高钙血猫和正常钙血猫。有关常规生化和尿液检测的数据,获得了诊断成像和额外的血液检测.血清碱性磷酸酶(ALP)活性用作骨转换的标志物。使用先前验证的免疫放射测定法分析血清降钙素浓度。具有增加的降钙素浓度(>0.9ng/L)的高钙血猫被称为反应者。使用连续变量的Mann-Whitney检验和分类变量的χ2检验进行组比较。用Spearman相关系数检验降钙素与降钙素、iCa和ALP。
    招募了26只高血钙猫和25只正常血钙猫。只有5/26(19.2%)的高钙血猫被确定为反应者,所有患者均被诊断为特发性高钙血症。降钙素和iCa的浓度之间没有显着相关性(p=0.929),高钙血猫的降钙素和ALP(p=0.917)或iCa和ALP(p=0.678),然而,当同时分析降钙素浓度升高的正常血钙和高血钙猫时,观察到降钙素和ALP之间存在显著负相关(p=0.037).
    仅在一小部分高钙血猫中存在降钙素浓度的预期增加;在iCa和降钙素浓度之间没有发现相关性。降钙素浓度升高的猫中降钙素和ALP之间的反比关系表明,降钙素纠正高钙血症的能力可能与骨转换程度有关。
    UNASSIGNED: This case-control study aimed to evaluate calcitonin response in naturally occurring hypercalcemia in cats and assess the relationships between calcitonin and ionized calcium (iCa) and examine relationships between calcitonin, iCa and bone turnover.
    UNASSIGNED: Hypercalcemic cats (persistently increased iCa concentration [>1.40 mmol/l]) were identified retrospectively via a medical database search; additional hypercalcemic and normocalcemic cats were recruited prospectively. Data regarding routine biochemical and urine testing, diagnostic imaging and additional blood testing were obtained. Serum alkaline phosphatase (ALP) activity was used as a marker of bone turnover. Serum calcitonin concentration was analyzed using a previously validated immunoradiometric assay. Hypercalcemic cats with an increased calcitonin concentration (>0.9 ng/L) were termed responders. Group comparisons were performed using a Mann-Whitney test for continuous variables and a χ2 test for categorical variables. Spearman\'s correlation coefficient was used to examine the relationships between calcitonin, iCa and ALP.
    UNASSIGNED: Twenty-six hypercalcemic and 25 normocalcemic cats were recruited. Only 5/26 (19.2%) of the hypercalcemic cats were identified as responders, and all were diagnosed with idiopathic hypercalcemia. There was no significant correlation between the concentrations of calcitonin and iCa (p = 0.929), calcitonin and ALP (p = 0.917) or iCa and ALP (p = 0.678) in hypercalcemic cats, however, a significant negative correlation was observed between calcitonin and ALP (p = 0.037) when normocalcemic and hypercalcemic cats with an elevated calcitonin concentration were analyzed together.
    UNASSIGNED: The expected increase in calcitonin concentration was present in only a small subset of hypercalcemic cats; no correlation was found between iCa and calcitonin concentration. The inverse relationship between calcitonin and ALP in cats with increased calcitonin concentrations suggests that the ability of calcitonin to correct hypercalcemia may be related to the degree of bone turnover.
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