PTH

PTH
  • 文章类型: Journal Article
    目的:关于骨小梁评分(TBS)及其相关因素的人群特异性规范信息有限。这里,我们提供了亚裔印度人的TBS规范及其与血清25-羟基维生素D[25(OH)D]和完整甲状旁腺激素(iPTH)的关系。
    方法:TBS,骨矿物质密度(BMD),在923名健康的亚洲印度人(年龄20-60岁)中,使用双能X线骨密度仪评估了椎骨骨折(VFs)。血清25(OH)D,iPTH,T4/TSH,,测量糖化血红蛋白(HbA1c),并使用多变量线性回归评估与TBS的相关性.任何部位BMDZ评分≤-2.0或≥2.0的受试者,VFs,TSH>10.0或<0.05µIU/ml,排除血糖>11.1mmol/L或HbA1c>8.0%的亚裔-印度标准.
    结果:在744名健康的亚裔印度人中产生了TBS规范(M:F,389:385)。为“正常”生成的截止值,\'部分降级\',和“降级的”TBS分别>1.305、1.204-1.305和<1.204。女性的平均TBS低于男性(p<.001)。亚洲-印度和现有规范之间的TBS类别一致性为75%。特异性(97.8vs.77.9%,p<.001)和诊断准确性(97.8%与78.4%,p<.001)的TBS检测骨质疏松症与亚洲-印度规范相比更高。与亚洲-印度规范相比,“部分降解的”TBS诊断骨质减少的敏感性也更高。在多变量回归中,性别,身体质量指数(BMI),BMD-L1-L4,血清PTH,每日膳食热量摄入和钙摄入与TBS相关.尽管25(OH)D与PTH呈负相关,25(OH)D与TBS无关。
    结论:这项研究为亚裔印度人的TBS提供了具有性别差异的规范。年龄的增加和较高的BMI与较低的TBS相关。TBS与循环PTH和/或25(OH)D的关联需要在进一步研究中确认。
    OBJECTIVE: There is limited information on population-specific norms of trabecular-bone-score (TBS) and its associated factors. Here, we provide norms of TBS in Asian-Indians and its relationship with serum 25-hydroxyvitamin D [25(OH)D] and intact-parathyroid hormone (iPTH).
    METHODS: TBS, bone-mineral-density (BMD), and vertebral-fractures (VFs) were assessed using dual-energy X-ray absorptiometry in 923 healthy Asian-Indians (aged 20-60 years). Serum 25(OH)D, iPTH, T4/TSH,, glycosylated-haemoglobin (HbA1c) were measured and associations with TBS assessed using multivariable linear regression. Subjects with BMD Z-score ≤ -2.0 or ≥2.0 at any sites, VFs, TSH > 10.0 or <0.05 µIU/ml, blood-glucose >11.1 mmol/L or HbA1c > 8.0% were excluded for generating Asian-Indian norms.
    RESULTS: TBS norms were generated in 744 healthy Asian-Indians (M:F,389:385). The cut-offs generated for \'normal\', \'partially-degraded\', and \'degraded\' TBS were >1.305, 1.204-1.305 and <1.204, respectively. Mean TBS was lower in females than males (p < .001). There was 75% congruency in TBS categories between Asian-Indian and existing norms. Specificity (97.8 vs. 77.9%, p < .001) and diagnostic-accuracy (97.8% vs. 78.4%, p < .001) of TBS to detect osteoporosis were higher with Asian-Indian norms. The sensitivity of \'partially-degraded\' TBS to diagnose osteopenia was also higher with Asian-Indian norms. In multivariable regression, gender, body-mass-index (BMI), BMD-L1-L4, serum PTH, daily dietary-calorie intake and calcium intake were associated with TBS. Though 25(OH)D inversely correlated with PTH, 25(OH)D was not associated with TBS.
    CONCLUSIONS: This study provides norms for TBS in Asian-Indians with gender-specific differences. Increasing age and higher BMI were associated with lower TBS. Associations of TBS with circulating PTH and/or 25(OH)D need confirmation in further studies.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Case Reports
    棕色肿瘤,严重原发性(PHP)或肾脏(继发性)甲状旁腺功能亢进(RHP)的特殊骨并发症,是由长期存在的,甲状旁腺激素(PTH)诱导的破骨细胞活化,除了局部产生细胞因子和生长因子外,还导致多核巨细胞团和铁血黄素沉积。我们的目标是提供一个成人病例系列,其中包括两名女性,这些女性表现出这种并发症,作为高PTH相关疾病的多学科复杂小组的一部分。这种方法是不同的,因为他们有不同的医学背景,并在现实生活中提出了广泛的挑战,即,一位38岁的女性患有PHP和长期不受控制的高钙血症(有怀孕相关的PHP病史,切除囊性颌骨肿瘤,以及多囊肾病的家庭和个人阳性诊断,可能是PHP-颌骨肿瘤综合征),还有,一名患有先天性单肾和慢性肾病相关RHP的26岁女性,透析控制不佳,出现严重贫血和代谢性酸中毒发作(包括一次需要紧急血液透析并并发惊厥性癫痫发作,随后复苏呼吸停止)。两名受试者均表现出严重的PHP/RHP图片,PTH水平>1000pg/mL和>2000pg/mL,血清骨转换标志物升高。此外,他们在肋骨和骨盆(无症状)和脊柱水平有多个棕色肿瘤,头骨,和骨盆(并发自发性颈椎骨折)。作为一种内分泌方法,通过RHP中的医学干预(使用维生素D类似物),通过PHP中的手术(用于甲状旁腺切除术后饥饿骨综合征)控制了基础甲状旁腺疾病.此外,在这种情况下,由于诊断不清楚,采取了多学科的决定进行活检(事实证明没有定论),切除颅骨肿瘤以确认组织学特征。本系列强调了解决整个多学科合并症小组的重要性,以改善PHP/RHP相关棕色肿瘤患者的预后。然而,在现实生活中的医学中,依从性差和对建议的依从性降低可能会损害整体健康状况.因此,有时,考虑到囊性病变级别的直接方法;这代表狭窄的决策框架,这是一个个性化的决定。正如在这里看到的,棕色肿瘤代表PHP/RHP的隐藏面,主要是复杂和严重的形式,即使在现代,意识也是必不可少的。
    Brown tumors, an exceptional bone complication of severe primary (PHP) or renal (secondary) hyperparathyroidism (RHP), are caused by long-standing, elevated parathormone (PTH)-induced osteoclast activation causing multinucleated giant cell conglomerates with hemosiderin deposits in addition to the local production of cytokines and growth factors. We aim to present an adult case series including two females displaying this complication as part of a multidisciplinary complex panel in high PTH-related ailments. The approach was different since they had distinct medical backgrounds and posed a wide area of challenges amid real-life settings, namely, a 38-year-old lady with PHP and long-term uncontrolled hypercalcemia (with a history of pregnancy-associated PHP, the removal of a cystic jaw tumor, as well as a family and personal positive diagnosis of polycystic kidney disease, probably a PHP-jaw tumor syndrome), as well as, a 26-year-old woman with congenital single kidney and chronic renal disease-associated RHP who was poorly controlled under dialysis and developed severe anemia and episodes of metabolic acidosis (including one presentation that required emergency hemodialysis and was complicated with convulsive seizures, followed by resuscitated respiratory arrest). Both subjects displayed a severe picture of PHP/RHP with PTH levels of >1000 pg/mL and >2000 pg/mL and elevated serum bone turnover markers. Additionally, they had multiple brown tumors at the level of the ribs and pelvis (asymptomatically) and the spine, skull, and pelvis (complicated with a spontaneous cervical fracture). As an endocrine approach, the control of the underlying parathyroid disease was provided via surgery in PHP (for the postparathyroidectomy hungry bone syndrome) via medical intervention (with vitamin D analogs) in RHP. Additionally, in this case, since the diagnosis was not clear, a multidisciplinary decision to perform a biopsy was taken (which proved inconclusive), and the resection of the skull tumor to confirm the histological traits. This series highlights the importance of addressing the entire multidisciplinary panel of co-morbidities for a better outcome in patients with PHP/RHP-related brown tumors. However, in the instance of real-life medicine, poor compliance and reduced adherence to recommendations might impair the overall health status. Thus, sometimes, a direct approach at the level of cystic lesion is taken into consideration; this stands for a narrow frame of decision, and it is a matter of personalized decision. As seen here, brown tumors represent the hidden face of PHP/RHP, primarily the complex and severe forms, and awareness is essential even in the modern era.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    镉(Cd)被认为是对人类健康的重大危害,暴露与包括各种癌症在内的各种不良后果有关,心血管疾病,慢性肾病,和骨质疏松症。居住在受Cd污染的地区无疑是发展上述条件的风险因素。然而,个体之间发生Cd相关疾病的风险并不一致。缺铁,锌,还有钙,伴随着缺铁性贫血,肺功能下降常见于慢性阻塞性肺疾病(COPD),和低循环水平的甲状旁腺激素(PTH),可增强肠道对Cd的吸收。相反,慢性肝病可导致肝细胞的进行性丢失和游离Cd释放到循环中,导致血液中Cd含量升高。此外,比较一个国家不同地区之间或两组个体之间的Cd血液水平的研究,例如,那些有和没有骨质疏松症的人,应该考虑所有可能影响Cd水平的变量。这些包括年龄,性别,酒精消费,血液中的铁含量,钙,还有锌,贫血的存在,COPD,PTH水平,以及肝脏或肾脏疾病的存在。在这次审查中,我们深入研究了所有可能影响Cd血液水平的因素,提供全面的分析。
    Cadmium (Cd) is recognized as a significant hazard to human health, with exposure linked to a variety of adverse outcomes including various cancers, cardiovascular diseases, chronic kidney disease, and osteoporosis. Residing in areas contaminated with Cd is undoubtedly a risk factor for developing the aforementioned conditions. However, the risk of developing Cd-related disorders is not uniform among individuals. Deficiencies in iron, zinc, and calcium, along with iron deficiency anemia, decreased lung function often seen in chronic obstructive pulmonary disease (COPD), and low circulating levels of parathyroid hormone (PTH), may enhance Cd intestinal absorption. Conversely, chronic liver disorders can lead to the progressive loss of hepatocytes and the release of free Cd into the circulation, resulting in elevated Cd blood levels. Moreover, studies comparing Cd blood levels between different regions within a country or between two groups of individuals, for example, those with and without osteoporosis, should consider all variables that may impact Cd levels. These include age, sex, alcohol consumption, blood levels of iron, calcium, and zinc, the presence of anemia, COPD, PTH levels, and the presence of liver or kidney disease. In this review, we delve into all factors that could influence Cd blood levels, providing a comprehensive analysis.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Case Reports
    尽管临床指南建议测量血浆总25-羟基维生素D(25[OH]D)以评估维生素D(VitD)状态,该指数不考虑VitD结合蛋白(VDBP)水平的3倍个体间差异。我们提供了3名总血浆25(OH)D水平为10.8至12.3ng/mL(27-30.7nmol/L)的个体。由于内分泌学会指南将VitD缺乏症定义为25(OH)D≤20ng/mL(50nmol/L),所有3个将被判断为VitD缺乏。补充VitD3可将25(OH)D增加到31.7至33.8ng/mL(79.1-84.4nmol/L)。患者#1表现出继发性甲状旁腺功能亢进;VitD3补充使甲状旁腺激素(PTH)降低34%,而在其他2个个体中PTH水平无临床显著变化。因此,25(OH)D水平无法区分1例继发性甲状旁腺功能亢进患者和2例未发生继发性甲状旁腺功能亢进患者。因此,我们询问VitD代谢物比率(不依赖VDBP)是否可以在这3个个体中进行区分。在所有评估的比率中,1,25(OH)2D/24,25(OH)2D比率是信息最丰富的,在继发性甲状旁腺功能亢进的个体中,该值为102pg/ng,但在其他2个个体中,该值较低(41和20pg/ng)。这些病例说明了1,25(OH)2D/24,25(OH)2D比率的值,以提供关于VitD状态的临床相关信息。
    Although clinical guidelines recommend measuring total plasma 25-hydroxyvitamin D (25[OH]D) to assess vitamin D (VitD) status, this index does not account for 3-fold inter-individual variation in VitD binding protein (VDBP) level. We present 3 individuals with total plasma 25(OH)D levels of 10.8 to 12.3 ng/mL (27-30.7 nmol/L). Because Endocrine Society guidelines define VitD deficiency as 25(OH)D ≤ 20 ng/mL (50 nmol/L), all 3 would be judged to be VitD deficient. VitD3 supplementation increased 25(OH)D to the range of 31.7 to 33.8 ng/mL (79.1-84.4 nmol/L). Patient #1 exhibited secondary hyperparathyroidism; VitD3 supplementation decreased parathyroid hormone (PTH) by 34% without a clinically significant change in PTH levels in the other 2 individuals. Thus, 25(OH)D level did not distinguish between the 1 patient who had secondary hyperparathyroidism and the 2 who did not. We therefore inquired whether VitD metabolite ratios (which are VDBP-independent) might distinguish among these 3 individuals. Of all the assessed ratios, the 1,25(OH)2D/24,25(OH)2D ratio was the most informative, which had a value of 102 pg/ng in the individual with secondary hyperparathyroidism but lower values (41 and 20 pg/ng) in the other 2 individuals. These cases illustrate the value of the 1,25(OH)2D/24,25(OH)2D ratio to provide clinically relevant information about VitD status.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    目的:妊娠期原发性甲状旁腺功能亢进(PHPT)的治疗可以是手术治疗,也可以是保守治疗。这项研究比较了手术和非手术治疗的不良结果。此外,这项研究调查了血清钙值与并发症发生率之间的相关性。
    方法:回顾性研究的系统综述,案例系列,和病例报告。生化参数,干预措施,并记录每次妊娠的结局.研究人群包括两组:非手术组和手术组。不良结局被归类为孕产妇,产科,或新生儿。
    结果:手术组和非手术组分别为163和185例患者,分别。孕妇平均孕钙值与母婴并发症呈正相关。在所有母体钙值中保守治疗的患者中,新生儿并发症更为普遍(p<0.001)。研究组之间的产妇结局和总体产科结局没有显着差异,尽管手术组的平均血清钙值(12.3mg/dL)高于非手术组(11.1mg/dL)。
    结论:鉴于非手术组新生儿不良结局明显低于手术组,除了手术组的非劣质孕产妇和产科结果,本研究的总体数据表明,即使在轻度高钙血症的情况下,甲状旁腺切除术也有利于非手术治疗.
    OBJECTIVE: The management of primary hyperparathyroidism (PHPT) during pregnancy may be surgical or conservative. This study compared adverse outcomes between surgical and non-surgical treatments. Additionally, the study investigated the correlation between serum calcium values and complication rates.
    METHODS: A systematic review of retrospective studies, case series, and case reports. Biochemical parameters, interventions, and outcomes of each pregnancy were recorded. The study population comprised two groups: the non-surgical and surgical groups. Adverse outcomes were categorized as maternal, obstetric, or neonatal.
    RESULTS: The surgical and non-surgical groups consisted of 163 and 185 patients, respectively. A positive correlation was observed between the mean maternal gestational calcium value and both maternal and obstetric complication. Neonatal complications were more prevalent in patients treated conservatively across all maternal calcium values (p < 0.001). No significant differences were observed in maternal outcomes and overall obstetric outcomes between the study groups, albeit a higher mean serum calcium value in the surgical group (12.3 mg/dL) compared with the non-surgical group (11.1 mg/dL).
    CONCLUSIONS: Given the significantly lower neonatal adverse outcomes in the non-surgical group compared to the surgical group, along with non-inferior maternal and obstetric outcomes in the surgical group, the overall data of this study suggest that parathyroidectomy is favorable to non-surgical management even in cases of mild hypercalcemia.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    背景/目标:在考虑种植牙的长期和短期生存时,种植患者的一般状况至关重要。该研究的目的是评估新的皮质化指数(CI)与患者病情之间的相关性,以及它对导致植入物失败的边缘骨丢失(MBL)的影响,仅使用像素级别的射线照相(RTG)图像。方法:检查牙种植体颈部附近的骨,并对纹理特征进行了分析。统计分析包括计算相关系数(CC)和R2的简单回归分析。当p<0.05时,检测到的关系被认为是统计学上显著的。StatgraphicsCenturion版本18.1.12(统计点技术,Warrenton,VA,美国)用于进行统计分析。结果:3个月后MBL与BMI有相关性,PTH,TSH,血清中的Ca2+水平,血清中的磷酸盐,和维生素D。还观察到CI和PTH之间的相关性,血清中的Ca2+水平,维生素D,LDL,HDL,手术当天的甘油三酯.经过3个月的观察期,CI与PTH相关,TSH,血清中的Ca2+水平,和甘油三酯。结论:研究结果证实,患者的一般状况与CI和MBL相对应。患者的一般状况对种植牙周围的骨代谢有影响。如果患者的一般状况不稳定,应考虑植入植入物。然而,CI尚未得到充分调查。需要进一步的研究来检查和分类皮质化对牙科植入物附近边缘骨丢失的影响。
    Background/Objectives: The general condition of implantology patients is crucial when considering the long- and short-term survival of dental implants. The aim of the research was to evaluate the correlation between the new corticalization index (CI) and patients\' condition, and its impact on marginal bone loss (MBL) leading to implant failure, using only radiographic (RTG) images on a pixel level. Method: Bone near the dental implant neck was examined, and texture features were analyzed. Statistical analysis includes analysis of simple regression where the correlation coefficient (CC) and R2 were calculated. Detected relationships were assumed to be statistically significant when p < 0.05. Statgraphics Centurion version 18.1.12 (Stat Point Technologies, Warrenton, VA, USA) was used to conduct the statistical analyses. Results: The research revealed a correlation between MBL after 3 months and BMI, PTH, TSH, Ca2+ level in blood serum, phosphates in blood serum, and vitamin D. A correlation was also observed between CI and PTH, Ca2+ level in blood serum, vitamin D, LDL, HDL, and triglycerides on the day of surgery. After 3 months of the observation period, CI was correlated with PTH, TSH, Ca2+ level in blood serum, and triglycerides. Conclusion: The results of the research confirm that the general condition of patients corresponds with CI and MBL. A patient\'s general condition has an impact on bone metabolism around dental implants. Implant insertion should be considered if the general condition of the patient is not stable. However, CI has not yet been fully investigated. Further studies are necessary to check and categorize the impact of corticalization on marginal bone loss near dental implants.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Case Reports
    背景:甲状腺切除术是一种常用于治疗甲状腺疾病的外科手术。并发症包括,但不限于,术后低钙血症。为了有效管理甲状腺切除术后的低钙血症,全面的方法至关重要。
    方法:我们介绍了一个有趣的病例,该患者在甲状腺全切除术后出现了严重的短暂性低钙血症,对常规治疗干预有抵抗力。
    结论:甲状腺全切除术后低钙血症是一种公认的并发症,可导致破坏性后果。一些促成因素包括术前优化失败,自身免疫性疾病,恶性肿瘤,延长手术时间。在管理与低钙血症相关的危险因素方面,确定因素的综合方法至关重要。
    结论:本病例强调了对甲状腺切除术后低钙血症风险患者的术前升高和管理以及密切监测和个体化治疗计划的重要性。该患者严重低钙血症的成功治疗涉及多学科团队方法和替代治疗方案的考虑。
    BACKGROUND: Thyroidectomy is a surgical procedure commonly employed in the management of thyroid disorders. Complications include, but not limited to, postoperative hypocalcemia. In order to effectively manage hypocalcemia following thyroidectomy, a comprehensive approach is essential.
    METHODS: We present an intriguing case of a patient who developed severe transient hypocalcemia that was resistant to conventional therapeutic interventions following a total thyroidectomy.
    CONCLUSIONS: Hypocalcemia post total thyroidectomy is a well-established complication which can lead to devastating consequences. Some of the contributing factors include failure of pre-operative optimization, autoimmune disease, malignancy, and prolonged surgical time. A comprehensive approach to identify the contributors is essential in managing the risk factors associated with hypocalcemia.
    CONCLUSIONS: This case highlights the importance of pre-operative elevation and management as well as the close monitoring and individualized treatment plans for patients at risk for post-thyroidectomy hypocalcemia. The successful management of severe hypocalcemia in this patient involved a multidisciplinary team approach and consideration of alternative treatment options.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    继发性甲状旁腺功能亢进(SHPT)是慢性肾脏疾病(CKD)的常见并发症。它始于甲状旁腺激素水平的适应性增加,以防止钙和磷酸盐紊乱。随着时间的推移,这种情况变得适应不良,并与发病率和死亡率增加有关。目前的治疗包括降低磷酸盐的策略,维生素D类似物,拟钙剂和甲状旁腺切除术。这些方法具有固有的局限性,激发人们对开发SHPT新药的兴趣,以克服这些局限性并提高CKD患者的生存率和生活质量。
    本综述深入探讨了SHPT的主要病理生理机制,以及目前可用和正在积极调查的治疗方案。本文提供的数据来自在PubMed进行的全面搜索,WebofScience,ClinicalTrials.gov和国际临床试验注册平台(ICTRP)从2000年开始。
    SHPT研究药物的进步在提高治疗效果的同时最大限度地减少与常规疗法相关的副作用方面具有重要的前景。尽管一些挑战仍然阻碍它们在临床实践中的采用,正在进行的研究可能会继续扩大可用的治疗方案,完善治疗策略,并根据患者的个人情况定制它们。
    UNASSIGNED: Secondary hyperparathyroidism (SHPT) is a common complication of chronic kidney disease (CKD). It begins as an adaptive increase in parathyroid hormone levels to prevent calcium and phosphate derangements. Over time, this condition becomes maladaptive and is associated with increased morbidity and mortality. Current therapies encompass phosphate-lowering strategies, vitamin D analogues, calcimimetics and parathyroidectomy. These approaches harbor inherent limitations, stimulating interest in the development of new drugs for SHPT to overcome these limitations and improve survival and quality of life among CKD patients.
    UNASSIGNED: This review delves into the main pathophysiological mechanisms involved in SHPT, alongside the treatment options that are currently available and under active investigation. Data presented herein stem from a comprehensive search conducted across PubMed, Web of Science, ClinicalTrials.gov and International Clinical Trials Registry Platform (ICTRP) spanning from 2000 onwards.
    UNASSIGNED: The advancements in investigational drugs for SHPT hold significant promise for enhancing treatment efficacy while minimizing side effects associated with conventional therapies. Although several challenges still hinder their adoption in clinical practice, ongoing research will likely continue to expand the available therapeutic options, refine treatment strategies, and tailor them to individual patient profiles.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    背景:低血清甲状旁腺激素(PTH)是无动力骨疾病的公认标志物,其特征是维持性血液透析(MHD)患者的发病率和死亡率增加。根据已知的PTH和营养不良-炎症综合征之间的横断面关联,我们旨在研究低PTH的MHD患者PTH与营养和炎症参数变化以及临床结局之间的纵向关联.
    方法:这项历史性的前瞻性和纵向研究分析了单个血液透析中心的临床数据库,包含459名MHD患者的医疗记录(平均年龄71.4±12.9岁,171名妇女),在2007-2020年之间进行治疗。骨周转,在0,6,12,18,24,30和36个月时记录营养和炎症标志物水平,然后进行中位额外24个月的临床观察.根据以前使用的维生素D类似物和/或钙敏感受体激动剂,研究参与者被分为治疗相关组和疾病相关组.针对基线人口统计学和临床参数调整线性混合效应模型。
    结果:在459例MHD患者中,81(17.6%)的PTH低于150pg/ml。其中,30例患者与治疗相关,51例患者与疾病相关的低PTH。在基线,与疾病相关组相比,具有治疗相关低PTH的MHD患者的糖尿病发生率更高。在线性混合效应模型中,随着时间的推移,PTH的增加与碱性磷酸酶(ALP)和C反应蛋白(CRP)水平的降低以及血红蛋白和白蛋白的增加有关,但不是3年随访时的老年营养风险指数(GNRI)。两组之间的生存率没有差异,在疾病相关组中,骨折导致的住院风险较高(HR4.04,95%CI1.51-10.8).在多变量模型中加入CRP或ALP后,这种关联的统计学意义消失。
    结论:MHD患者的低血清PTH表现不同,取决于其原因,在疾病相关组中骨折的风险较高。这种关联取决于炎症。我们的结果应该在更大的流行病学研究中得到证实。
    BACKGROUND: Low serum parathyroid hormone (PTH) is an accepted marker for adynamic bone disease which is characterized by increased morbidity and mortality in maintenance hemodialysis (MHD) patients. In light of the known cross-sectional associations between PTH and malnutrition-inflammation syndrome, we aimed to examine the longitudinal associations between PTH with changes in nutritional and inflammatory parameters and clinical outcomes in MHD patients with low PTH.
    METHODS: This historical prospective and longitudinal study analyzed a clinical database at a single hemodialysis center, containing the medical records of 459 MHD patients (mean age of 71.4 ± 12.9 years old, 171 women), treated between the years 2007-2020. Bone turnover, nutritional and inflammatory marker levels were recorded at 0, 6, 12, 18, 24, 30, and 36 months followed by a median of 24 additional months of clinical observations. According to previous use of vitamin D analogs and/or calcium-sensing receptor agonists, the study participants were divided into treatment-related and disease-related groups. A linear mixed effects model was adjusted for baseline demographics and clinical parameters.
    RESULTS: Of 459 MHD patients, 81 (17.6%) had PTH lower than 150pg/mL. Among them, 30 patients had treatment-related and 51 had disease-related low PTH. At baseline, MHD patients with treatment-related low PTH had a higher rate of diabetes compared to the disease-related group. In a linear mixed effects model, increased PTH over time was associated with decreased levels of alkaline phosphatase and C-reactive protein and with increased hemoglobin and albumin, but not the geriatric nutritional risk index at 3-year follow-up. The survival rate did not differ between the groups, with the risk of hospitalizations due to fractures being higher (HR: 4.04 with 95% CI: 1.51-10.8) in the disease-related group. Statistical significance of this association was abolished after adding C-reactive protein or alkaline phosphatase to the multivariate models.
    CONCLUSIONS: Low serum PTH in MHD patients behaves differently depending on its cause, with a higher risk of fractures in the disease-related group. This association is dependent on inflammation. Our results should be verified in larger epidemiological studies.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    自身免疫性疾病的病因是多因素的,包括荷尔蒙因素。治疗伴随的甲状旁腺功能亢进后观察到自身免疫的缓解。此外,自身免疫性疾病患者显示甲状旁腺激素受体(PTH1R)表达增加,B细胞亚群分布改变。因此,这项研究旨在评估PTH刺激对B淋巴细胞的潜在机制和体外作用。
    使用人B细胞系Ramos(RA.1),在有和没有不同浓度的甲状旁腺激素(PTH)刺激的情况下,评估了各种生物学效应。采用流式细胞术评估基于IgD和CD38表达的B淋巴细胞表型,通过膜联蛋白V诱导凋亡和使用CFSE的增殖。IgM产生通过ELISA定量,进行蛋白质印迹分析以评估作为细胞活化指标的syk蛋白磷酸化。
    Ramos细胞(RA.1)在人PTH刺激下证明了表型的统计学显着变化,证明当用高浓度PTH刺激时,生发中心细胞(Bm3-Bm4)的比例增加。
    PTH在B细胞亚群中的体外作用与先前在自身免疫性疾病患者中表达PTH1R的B淋巴细胞表型改变的发现一致,提示这种激素在自身免疫性疾病的病理生理学中的潜在作用。然而,需要进一步的研究来阐明PTH在B淋巴细胞中产生观察到的作用的机制,并确定PTH是否在自身免疫中起作用.
    UNASSIGNED: The etiopathogenesis of autoimmune diseases is multifactorial, including hormonal factors. Remission of autoimmunity has been observed following treatment for concomitant hyperparathyroidism. Additionally, patients with autoimmune diseases have shown increased expression of parathyroid hormone receptor (PTH1R) and altered distribution of B cells subsets. Hence, this study aims to evaluate potential mechanisms and in vitro effects of PTH stimulation on B lymphocytes.
    UNASSIGNED: Using the human B-cell line Ramos (RA.1), various biological effects were evaluated with and without parathyroid hormone (PTH) stimulation at varying concentrations. Flow cytometry was employed to evaluate the phenotype of B lymphocytes based on IgD and CD38 expression, apoptosis induction via Annexin V and proliferation using CFSE. IgM production was quantified through ELISA, and Western blot analysis was performed to assess syk protein phosphorylation as an indicator of cell activation.
    UNASSIGNED: Ramos cells (RA.1) evidenced a statistically significant change in the phenotype under human PTH stimulation, demonstrating an increased proportion of germinal centre cells (Bm3-Bm4) when stimulated with high concentrations of PTH.
    UNASSIGNED: The in vitro effects of PTH in B cells subsets align with previous findings of an altered phenotype in B lymphocytes expressing PTH1R among autoimmune disease patients, suggesting a potential role of this hormone in the pathophysiology of autoimmune diseases. However, further studies are necessary to elucidate the mechanisms by which PTH generates observed effects in B lymphocytes and to determine if PTH plays a role in autoimmunity.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

公众号