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Primary Epithelioid Angiomyolipoma of Adrenal Gland: Case Report and Literature Review. 原发性肾上腺上皮样血管平滑肌脂肪瘤1例报告并文献复习。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-01-01 DOI: 10.14712/23362936.2022.19
Muhammet Cicek, Huseyin Ozgur Kazan, Ramazan Gokhan Atis, Asif Yildirim

Angiomyolipomas (AMLs) are mesenchymal tumours derived from perivascular epithelioid cells. Although AMLs are generally known as benign and extremely rare epithelioid variants of AML, they may be potentially aggressive. Here we present an adrenal epithelioid AML and the literature review. A 64-year-old female patient was diagnosed with a left adrenal mass detected incidentally on ultrasonography. Preoperative abdominal CT (computed tomography) showed a 95×68 mm heterogeneous contrast enhancement mass lesion in the left adrenal gland. The lesion was hormone inactive in the endocrinological evaluation, and left laparoscopic adrenalectomy was performed. The patient was discharged on the 2nd postoperative day. Pathology was reported as epithelioid subtype AML. The patient has no local recurrence or metastasis in the 18-month follow-up period and imaging. Adrenal epithelioid AML is an extremely rare and potentially aggressive variant. According to the literature, open or laparoscopic adrenalectomy seems to be suitable option for disease management.

血管平滑肌脂肪瘤(AMLs)是源自血管周围上皮样细胞的间质肿瘤。虽然AML通常被认为是良性的,极其罕见的AML上皮样变异,但它们可能具有潜在的侵袭性。在此,我们报告一例肾上腺上皮样急性髓性白血病并回顾相关文献。一位64岁的女性患者在超声检查中偶然发现左肾上腺肿块。术前腹部CT(计算机断层扫描)显示左侧肾上腺一个95×68毫米的非均匀增强肿块。在内分泌学评估中病变为激素无活性,并行左腹腔镜肾上腺切除术。患者于术后第2天出院。病理报告为上皮样亚型AML。在18个月的随访和影像学检查中,患者未见局部复发或转移。肾上腺上皮样AML是一种极其罕见且具有潜在侵袭性的变种。根据文献,开放或腹腔镜肾上腺切除术似乎是疾病管理的合适选择。
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引用次数: 0
The Manifestations of Covid-19 Infection. Manifestations in Patients with Temporomandibular Joint Disorders. Covid-19感染的表现。颞下颌关节疾病患者的临床表现。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-01-01 DOI: 10.14712/23362936.2022.10
V. Machoň, J. Levorová, Michal Beno, R. Foltán
The authors present a group of patients who were treated for exacerbation of temporomandibular joint disorders (TMD) following Covid-19 infection and who in the past had successfully undergone surgery of the temporomandibular joint (TMJ). The group consisted in total of 21 patients who relapsed after contracting Covid-19. There were 4 men and 17 women, the average age was 45.6 years (28-63). The most common complaint was pain. In all cases, the pain was located in the preauricular area, 4 patients had pain in the lateral side of the neck, 1 patient had pain of the nasal alae. During clinical examination, pain was present on palpation of the masseter muscle (19 patients), temporal muscle (4 patients) and the TMJ area (4 patients). In 4 cases, pain on palpation was present in the area of the nape and sternocleidomastoid muscles. Treatment in all cases was the same: thermotherapy, muscle relaxation massage and non-steroidal anti-inflammatory drugs. Symptoms subsided in all cases within 2 weeks. In light of the Covid-19 pandemic, it is also necessary to expect an increased number of patients with TMD. The authors recommend targeted patient histories regarding Covid-19 infection when examining patients with TMD symptoms - this will certainly facilitate determining the etiology of the pain.
作者介绍了一组因Covid-19感染后颞下颌关节疾病(TMD)加重而接受治疗的患者,这些患者过去曾成功接受过颞下颌关节(TMJ)手术。该组共有21名感染新冠病毒后复发的患者。男性4例,女性17例,平均年龄45.6岁(28 ~ 63岁)。最常见的抱怨是疼痛。所有病例均位于耳前区,4例患者颈部外侧疼痛,1例患者鼻翼疼痛。临床检查时,疼痛表现为咬肌(19例)、颞肌(4例)和颞下颌关节区(4例)。其中4例,触诊疼痛出现在颈背和胸锁乳突肌区域。所有病例的治疗方法都是一样的:热疗、肌肉放松按摩和非甾体抗炎药。所有病例均在2周内症状消退。鉴于2019冠状病毒病大流行,也有必要预计TMD患者人数会增加。作者建议在检查有TMD症状的患者时,有针对性地了解患者的Covid-19感染病史——这肯定有助于确定疼痛的病因。
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引用次数: 3
The Primary Brain Eosinophilic Angiocentric Fibrosis, A Rare Case Report. 原发性脑嗜酸性血管中心性纤维化一例罕见报告。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-01-01 DOI: 10.14712/23362936.2022.12
S. Daneshi, M. Taheri, A. Fattahi, P. Fadavi
Eosinophilic angiocentric fibrosis (EAF) is a rare progressive fibrosing lesion involving the nasal cavity, paranasal sinuses, and the upper respiratory tract. There are few reports that it rarely involves the orbit; however, there is no report of intracranial involvement. Here, we report and share our experience with a rare case of primary intracranial EAF. A 33-year-old woman with a history of a suprasellar mass and unsuccessful surgical and medical treatment referred to us. Physical examination demonstrated right-sided blindness and ptosis, left-sided decreased visual acuity, and visual field defect. The brain imaging revealed an extra-axial intradural well-defined large suprasellar mass with parasellar (more on the right side) and retrosellar extension. Via pterional craniotomy and subfrontal approach, a very firm creamy-brownish well-defined fibrotic mass was encountered. The tumour texture was too firm to be totally resected. The microscope exited the surgical field off, and the tumour was incompletely resected using a rongeur. The histopathology finding favoured EAF. Further histopathology evaluation failed to show histologic features of IgG4-related disease. Although the preoperative diagnosis of EAF is impossible, in the setting of an indolent slow-growing lesion demonstrating hypointensity on the T2 image sequence of MRI (magnetic resonance imaging), EAF should be considered a differential diagnosis. In the setting of this diagnosis, the systemic and other organ involvement for a diagnosis of IgG4-RD should be evaluated. However, more cases are needed to illustrate the relation between these two entities.
嗜酸性血管中心性纤维化(EAF)是一种罕见的进行性纤维化病变,累及鼻腔、鼻窦和上呼吸道。很少有报道说它很少涉及轨道;然而,没有颅内受累的报道。在此,我们报告并分享一例罕见的原发性颅内脑出血的经验。一位33岁的女性,有鞍上肿块病史,手术和药物治疗均不成功。体格检查显示右侧失明和上睑下垂,左侧视力下降,视野缺损。脑成像显示轴外硬膜内明显的大鞍上肿块伴鞍旁(右侧较多)和鞍后延伸。通过翼点开颅和额下入路,发现了一个非常坚固的、界限清晰的奶油棕色纤维化肿块。肿瘤质地太硬,不能完全切除。显微镜使手术视野消失,用咬合钳不完全切除肿瘤。组织病理学结果有利于EAF。进一步的组织病理学评估未能显示igg4相关疾病的组织学特征。虽然EAF的术前诊断是不可能的,但在MRI(磁共振成像)T2图像序列上表现为缓慢生长的惰性病变时,EAF应被视为鉴别诊断。在此诊断的背景下,应评估IgG4-RD诊断的全身和其他器官受累情况。然而,需要更多的案例来说明这两个实体之间的关系。
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引用次数: 2
Disturbance in Serum Levels of IL-17 and TGF-β1 and in Gene Expression of ROR-γt and FOX-P3 Is Associated with Pathogenicity of Systematic Lupus Erythematosus. 血清IL-17、TGF-β1水平及ROR-γt、FOX-P3基因表达紊乱与系统性红斑狼疮致病性相关
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-01-01 DOI: 10.14712/23362936.2022.15
Hanaa N Ali, Ghassaq T Alubaidi, Faiq I Gorial, Ilham A Jasim

To investigate the disturbance in serum levels of interleukin-17 (IL-17) and transforming growth factor-beta1 (TGF-β1) and gene expression of retinoic acid-related orphan receptor-gamma t (ROR-γt) and forkhead box-P3 (FOX-P3) in patients with systemic lupus erythematosus (SLE) and to study their association with disease pathogenicity and activity. Newly diagnosed active patients with SLE (n=88) and healthy volunteers (n=70) were included. Serum IL-17 and TGF-β1 were measured using enzyme-linked immunosorbent assay. Gene-expression profiles of ROR-γt and FOX-P3 were screened using real-time polymerase chain reaction. The IL-17/TGF-β1 and ROR-γt/FOX-P3 levels were also calculated. The mean age of the patients was 30.96±8.25 years; they were 82 women and 6 men. Of the patients, 11.4% manifested mild disease while 88.6% had severe disease. The serum level of TGF-β1 was significantly lower (70.2±34.9 vs. 200.23±124.77 pg/ml), while both IL-17 (614.7±317.5 vs. 279.76±110.65 pg/ml) and IL-17/TGF-β1 (18.5±30.1 vs. 1.66±0.9) levels were significantly higher, in patients than in controls (p<0.0001). The gene-expression level of FOX-P3 (0.6±0.8 vs. 13.68±39.35) was reported to be lower, while ROR-γt (3.9±3.5 vs. 1.99±2.09) and ROR-γt/FOX-P3 (18.6±21.1 vs. 7.63±17.19) levels were significantly higher, in patients than in controls (p<0.0001). Disturbance in serum levels of IL-17 and TGF-β1 in T helper-17 and T-regulatory cells proliferation was highlighted through an imbalance in the gene expression of FOX-P3 and ROR-γt, as both are signature genes for the two cell types, respectively. These findings underscore the critical role of IL-17 and TGF-β1 in SLE development, rendering them potential targets for developing novel immunotherapeutic strategies.

目的探讨系统性红斑狼疮(SLE)患者血清白细胞介素-17 (IL-17)、转化生长因子-β1 (TGF-β1)水平和视黄酸相关孤儿受体γt (ROR-γt)、forkhead box-P3 (FOX-P3)基因表达的变化及其与疾病致病性和活动性的关系。新诊断活动性SLE患者(88例)和健康志愿者(70例)被纳入研究。采用酶联免疫吸附法检测血清IL-17和TGF-β1。实时聚合酶链反应筛选ROR-γt和FOX-P3基因表达谱。同时计算IL-17/TGF-β1和ROR-γt/FOX-P3水平。患者平均年龄30.96±8.25岁;他们是82名女性和6名男性。轻症患者占11.4%,重症患者占88.6%。血清TGF-β1水平显著低于对照组(70.2±34.9∶200.23±124.77 pg/ml), IL-17(614.7±317.5∶279.76±110.65 pg/ml)和IL-17/TGF-β1(18.5±30.1∶1.66±0.9)水平显著高于对照组(p<0.0001)。FOX-P3基因表达水平(0.6±0.8比13.68±39.35)较低,而ROR-γt(3.9±3.5比1.99±2.09)和ROR-γt/FOX-P3(18.6±21.1比7.63±17.19)水平显著高于对照组(p<0.0001)。血清IL-17和TGF-β1水平在T- helper-17和T-调节性细胞增殖中的紊乱是通过FOX-P3和ROR-γt基因表达的不平衡来突出的,这两个基因分别是两种细胞类型的标志基因。这些发现强调了IL-17和TGF-β1在SLE发展中的关键作用,使它们成为开发新的免疫治疗策略的潜在靶点。
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引用次数: 2
Malignancy Rates in Thyroid Nodules Classified as Bethesda III and IV; Correlating Fine Needle Aspiration Cytology with Histopathology. 甲状腺结节Bethesda III型和IV型的恶性率分析细针抽吸细胞学与组织病理学的相关性。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-01-01 DOI: 10.14712/23362936.2022.22
Chirag Pereira

Fine needle aspiration cytology (FNAC) is an integral part in the diagnostic work up of thyroid nodules. FNAC reports are based on Bethesda system for thyroid cytopathology which is one of the most commonly used systems worldwide. The main objective of the present study was to evaluate the malignancy rates in Bethesda category III and IV thyroid nodules over a six-year period. 642 thyroid FNAC were performed over a six-year period. The medical records of all these patients were reviewed using electronic patient records. Cases reported to have Bethesda category III and IV were included in the study. Data for these patients were reviewed to determine the relationship between these categories and thyroid cancer. There were 41 cases of category III of which 19 underwent surgery and the malignancy rates were found to be 26.3%. Category IV consisted of 50 cases of which 45 underwent surgery and the malignancy rates were 26.6%. The results from our study are similar to findings in larger multicentric studies which found that malignancy rates for Bethesda category III and IV were 10-30% and 25-40%, respectively.

细针穿刺细胞学(FNAC)是甲状腺结节诊断工作中不可或缺的一部分。FNAC报告是基于Bethesda系统的甲状腺细胞病理学,这是世界上最常用的系统之一。本研究的主要目的是评估六年内Bethesda III类和IV类甲状腺结节的恶性率。在六年的时间里进行了642例甲状腺FNAC。所有这些患者的医疗记录都使用电子病历进行审查。报告的Bethesda III和IV类病例包括在研究中。我们对这些患者的资料进行了回顾,以确定这些类别与甲状腺癌之间的关系。第三类41例,其中19例行手术治疗,恶性肿瘤发生率为26.3%。IV类50例,其中手术治疗45例,恶性肿瘤发生率为26.6%。我们的研究结果与大型多中心研究的结果相似,后者发现Bethesda III类和IV类的恶性肿瘤发生率分别为10-30%和25-40%。
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引用次数: 2
POEMS Syndrome Diagnosis in a Patient with Mixed Polyneuropathy: Case Report. 混合性多发性神经病的POEMS综合征诊断:1例报告。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-01-01 DOI: 10.14712/23362936.2022.3
M. I. Ocampo-Navia, María Andrea Negret Noreña, Luis Rafael Chaparro Santos, José Ricardo Morera Afanador, R. Farías, J. Sánchez
POEMS syndrome is a rare condition of paraneoplasic origin characterized by the presence of a sensorimotor polyneuropathy associated with the presence of a proliferative disorder of plasmatic monoclonal cells and overproduction of vascular endothelial growth factor. The acronym "POEMS" represents multisystem findings including polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder and skin changes; nevertheless, clinical presentation is heterogeneous. We describe a clinical case, the diagnostic and therapeutic approach in a patient with sensorimotor polyneuropathy in whom POEMS syndrome was diagnosed; to understand this pathology, its clinical and paraclinical manifestations in order to make a diagnosis or to avoid a delayed one and to provide an adequate treatment.
POEMS综合征是一种罕见的副肿瘤起源疾病,其特征是存在感觉运动多神经病变,伴有血浆单克隆细胞增生障碍和血管内皮生长因子的过度产生。首字母缩略词“POEMS”代表多系统发现,包括多神经病变、器官肿大、内分泌病变、单克隆浆细胞疾病和皮肤变化;然而,临床表现是不同的。我们描述了一个临床病例,诊断和治疗方法的感觉运动多神经病变患者的诗综合征诊断;了解这种病理,它的临床和临床表现,以便作出诊断或避免延误,并提供适当的治疗。
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引用次数: 1
Pelvic Floor Muscles Contribution in Surgical Outcome of Children with High-type Anorectal Malformations. 盆底肌肉对儿童高型肛肠畸形手术结果的影响。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2021-01-01 DOI: 10.14712/23362936.2021.16
Stylianos Roupakias, Xenophon Sinopidis

As a consequence of high-type anorectal malformations (ARMs) pathogenesis, the pelvic floor muscles remain severely underdeveloped or hypoplastic, the rectal pouch is located at the level or above the puborectalis sling, and the bowel terminates outside the sphincter muscle complex support. For children with high-type ARMs the ultimate objective of therapy is mainly to grow up having bowel continence function that is compatible with a good quality of life, and the final prognosis depends significantly on the grade of development of pelvic floor muscles and the successful entering of the anorectum fully within the support of the external anal sphincter due to intraoperative conservation of the puborectalis sling. Pelvic magnetic resonance imaging (MRI) has recently become the preferred imaging study for prediction of functional outcomes, since it can define the anatomy and evaluate the development of the sphincteric muscles before and after surgical correction. Based on recent literature and our clinical experience, we will discuss the relevance of pelvic floor muscles MRI to the clinical outcome of children with high type ARMs.

由于高型肛门直肠畸形(ARMs)的发病机制,盆底肌肉严重发育不全或发育不全,直肠袋位于耻骨直肠悬吊的水平或以上,肠在括约肌复合体支撑外终止。对于高型ARMs患儿,治疗的最终目的主要是使其长大后具有与良好生活质量相适应的排便功能,最终预后主要取决于盆底肌肉发育的等级以及术中保留耻骨直肠吊索在肛门外括约肌的支持下能否完全成功进入肛肠。骨盆磁共振成像(MRI)最近成为预测功能预后的首选影像学研究,因为它可以定义括约肌矫正手术前后的解剖结构和评估括约肌的发育。根据最近的文献和我们的临床经验,我们将讨论骨盆底肌肉MRI与高型ARMs儿童临床结果的相关性。
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引用次数: 1
Patella Fracture Identified Using Point-of-care Ultrasound. 使用护理点超声识别髌骨骨折。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2021-01-01 DOI: 10.14712/23362936.2021.29
Mark Richman, Andrew Kieffer, Rachel Moss, Daniel Dexeus

A 49-year-old female fell from standing. Her right knee extended into the air. She had acute right knee pain preventing weight-bearing. Her knee was most comfortable fully-extended. She could not flex it due to pain, nor extend it against resistance. Tenderness and a horizontal defect were noted over the anterior knee. Bedside ultrasound demonstrated a horizontally-fractured patella (confirmed on X-ray) with intact femoral and patellar tendons. She was put in a knee immobilizer and underwent surgery, with return to full function and activities. Ultrasound can identify patella fractures and help with early evaluation, management, and specialty referral, as well as ordering more-focused imaging. In one study, POCUS (point-of-care ultrasound) for patella fracture had 95% sensitivity, 63% specificity, 86% positive predictive value, and 83% negative predictive value. The dynamic nature of ultrasound allows a ruptured patella (87% sensitivity) or quadriceps tendon (100% sensitivity) to be excluded with high certainty.

一名49岁的女性从站立的位置跌落。她的右膝向空中伸展。她有严重的右膝疼痛,无法负重。她的膝盖完全伸直,非常舒服。由于疼痛,她不能弯曲它,也不能在阻力下伸展它。膝关节前侧有压痛和水平缺损。床边超声显示髌骨水平骨折(x线证实),股骨和髌骨肌腱完整。她被植入了膝盖固定器并接受了手术,恢复了全部功能和活动。超声可以识别髌骨骨折,并有助于早期评估、管理和专科转诊,以及订购更集中的成像。在一项研究中,POCUS(点护理超声)对髌骨骨折的敏感性为95%,特异性为63%,阳性预测值为86%,阴性预测值为83%。超声的动态特性使得髌骨断裂(87%的敏感性)或股四头肌肌腱断裂(100%的敏感性)被高度确定地排除在外。
{"title":"Patella Fracture Identified Using Point-of-care Ultrasound.","authors":"Mark Richman,&nbsp;Andrew Kieffer,&nbsp;Rachel Moss,&nbsp;Daniel Dexeus","doi":"10.14712/23362936.2021.29","DOIUrl":"https://doi.org/10.14712/23362936.2021.29","url":null,"abstract":"<p><p>A 49-year-old female fell from standing. Her right knee extended into the air. She had acute right knee pain preventing weight-bearing. Her knee was most comfortable fully-extended. She could not flex it due to pain, nor extend it against resistance. Tenderness and a horizontal defect were noted over the anterior knee. Bedside ultrasound demonstrated a horizontally-fractured patella (confirmed on X-ray) with intact femoral and patellar tendons. She was put in a knee immobilizer and underwent surgery, with return to full function and activities. Ultrasound can identify patella fractures and help with early evaluation, management, and specialty referral, as well as ordering more-focused imaging. In one study, POCUS (point-of-care ultrasound) for patella fracture had 95% sensitivity, 63% specificity, 86% positive predictive value, and 83% negative predictive value. The dynamic nature of ultrasound allows a ruptured patella (87% sensitivity) or quadriceps tendon (100% sensitivity) to be excluded with high certainty.</p>","PeriodicalId":35490,"journal":{"name":"Prague medical report","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39850493","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Supine Percutaneous Nephrolithotomy in a Patient with Solitary Lung: A Case Report and Literature Review. 仰卧位经皮肾镜取石术治疗单发肺1例并文献复习。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2021-01-01 DOI: 10.14712/23362936.2021.27
Yavuz Onur Danacıoğlu, Yusuf Arıkan, Fatih Akkaş, Emre Şam, Deniz Noyan Özlü, Nalan Saygı Emir, Feyzi Arda Atar

Percutaneous nephrolithotomy (PNL) surgeries are performed with different patient positions, anesthesia methods and different-sized access sheaths in order to reduce the complication rates. Supine positioned PNL can be performed safely in the high-risk group patients with comorbidities. Herein, we present a patient who had a past surgical history of right pneumonectomy and underwent a supine PNL procedure under regional anesthesia for a staghorn renal stone in the right kidney.

经皮肾镜取石术(PNL)采用不同的患者体位、麻醉方式和不同尺寸的导管鞘,以减少并发症的发生率。有合并症的高危人群可安全进行仰卧位PNL。在此,我们报告了一位有右侧全肺切除术病史的患者,他在区域麻醉下接受了仰卧PNL手术,治疗右侧肾鹿角状肾结石。
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引用次数: 0
Comparison of the Chemiluminescence Immunoassay LIAISON® with the Radioimmunoassay for Aldosterone and Renin Measurement. 化学发光免疫分析法LIAISON®与放射免疫分析法测定醛固酮和肾素的比较。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2021-01-01 DOI: 10.14712/23362936.2021.9
Jana Uhrová, Hana Benáková, Zdislava Vaníčková, Tomáš Zima

Determination of renin plasma levels is useful in the diagnosis of hypertension and in the therapeutic follow-up of hypertensive patients. Plasmatic concentration of renin decreases in patients with hypertension due to a primary hyperaldosteronism, contrary to renovascular hypertension where concentrations of renin and aldosterone are both elevated. Blood samples (serum, EDTA plasma) were analysed using two different chemiluminiscent methods CLIA LIAISON® and radioimmunoassay for aldosterone (IMMUNOTECH Beckman Coulter) and renin (Cisbio Bioassay) measurements were compared. We used both methods to ascertain the correlation between serum vs. EDTA plasma levels of aldosterone (RIA, CLIA) and renin (IRMA, CLIA) and to compare aldosterone to renin ratios for CLIA and for radioimmunoassay: serum aldosterone to plasma renin and plasma aldosterone to plasma renin. We compared serum aldosterone CLIA vs. RIA (rP=0.933, P<0.001) and plasma renin determined using CLIA vs. IRMA (rP=0.965, P=0.062). Furthermore, we used both methods to establish the correlation between the serum vs. plasma levels of aldosterone: RIA (rP=0.980, P<0.001); CLIA (rP=0.994, P=0.353) and serum vs. plasma levels of renin: IRMA (rP=0.948, P<0.001); CLIA (rP=0.921, P=0.011). Aldosterone (serum, plasma) to plasmatic renin ratios for CLIA (rP=0.999, P=0.286) and for radioimmunoassay (rP=0.992, P=0.025). Our data demonstrate that renin and aldosterone concentrations obtained using CLIA correlate with renin and aldosterone concentrations using radioimmunoassay methods. Correlation coefficients of pair results ranged from 0.921 to 0.994. Aldosterone (serum, EDTA plasma) to plasmatic renin ratios are comparable and any of them can be used with no significant differences found.

肾素血浆水平的测定在高血压的诊断和高血压患者的治疗随访中是有用的。原发性醛固酮增多症导致高血压患者血浆肾素浓度降低,与肾素和醛固酮浓度均升高的肾血管性高血压相反。血液样本(血清、EDTA血浆)分析采用两种不同的化学发光方法CLIA LIAISON®和放射免疫分析法醛固酮(IMMUNOTECH Beckman Coulter)和肾素(Cisbio Bioassay)测量进行比较。我们使用这两种方法来确定血清与EDTA血浆醛固酮(RIA, CLIA)和肾素(IRMA, CLIA)水平之间的相关性,并比较CLIA和放射免疫测定中醛固酮与肾素的比值:血清醛固酮与血浆肾素和血浆醛固酮与血浆肾素的比值。我们比较了CLIA和RIA测定的血清醛固酮(rP=0.933, P<0.001)和CLIA和IRMA测定的血浆肾素(rP=0.965, P=0.062)。此外,我们使用两种方法建立血清和血浆醛固酮水平之间的相关性:RIA (rP=0.980, P<0.001);CLIA (rP=0.994, P=0.353)和血清与血浆肾素水平:IRMA (rP=0.948, P<0.001);CLIA (rP=0.921, P=0.011)。CLIA测定血清、血浆醛固酮与血浆肾素比值(rP=0.999, P=0.286)和放射免疫测定醛固酮与血浆肾素比值(rP=0.992, P=0.025)。我们的数据表明,使用CLIA获得的肾素和醛固酮浓度与使用放射免疫测定方法获得的肾素和醛固酮浓度相关。相关系数为0.921 ~ 0.994。醛固酮(血清、血浆EDTA)与血浆肾素的比值具有可比性,任何一种都可以使用,没有发现显著差异。
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引用次数: 1
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