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Glycemic Control and Bone Turnover in Older Mexican Americans with Type 2 Diabetes. 老年墨西哥裔美国人2型糖尿病患者的血糖控制和骨转换
IF 1.9 Q3 Medicine Pub Date : 2018-05-13 eCollection Date: 2018-01-01 DOI: 10.1155/2018/7153021
Nahid J Rianon, Scott M Smith, MinJae Lee, Hannah Pervin, Paul Musgrave, Gordon P Watt, Shahla Nader, Sundeep Khosla, Catherine G Ambrose, Joseph B McCormick, Susan P Fisher-Hoch

Altered bone quality, caused by underlying metabolic changes of type 2 diabetes (T2D), has been hypothesized to cause altered bone strength and turnover leading to increased fracture risk in T2D patients. Current understanding about changes in bone turnover markers in T2D patients is mainly based on studies focused on Caucasian men and women. However, Hispanic populations have the highest prevalence of both T2D and osteoporosis in the US. We investigated associations of glycemic control (in terms of glycated hemoglobin [HbA1c]) and bone turnover rate in 69 older (≥50 years) Mexican American Cameron County Hispanic Cohort (CCHC) participants with T2D. Multivariable analyses were conducted to assess the associations between HbA1c (%), serum osteocalcin (OC), and serum sclerostin. In agreement with published reports from other racial/ethnic populations, our study found that lower bone turnover (indicated by lower serum OC) occurred in Mexican American men with T2D who had poorer glycemic control. For the women in our study, we found no significant association between glycemic control and OC. In contrast, HbA1c was positively associated with sclerostin for women, with near significance (p = 0.07), while no association was found in men. We recommend screening Mexican American individuals with T2D, specifically those with poor glycemic control, for bone loss and fracture risk.

由2型糖尿病(T2D)的潜在代谢变化引起的骨质量改变被认为会导致T2D患者骨强度和骨转换的改变,从而增加骨折风险。目前对T2D患者骨转换标志物变化的了解主要基于对白人男性和女性的研究。然而,西班牙裔人群在美国T2D和骨质疏松症的患病率最高。我们研究了69名老年(≥50岁)墨西哥裔美国人Cameron县西班牙裔队列(CCHC) T2D患者的血糖控制(根据糖化血红蛋白[HbA1c])和骨周转率的关系。进行多变量分析以评估HbA1c(%)、血清骨钙素(OC)和血清硬化蛋白之间的关系。与其他种族/民族人群发表的报告一致,我们的研究发现,较低的骨转换(由较低的血清OC表示)发生在血糖控制较差的墨西哥裔美国男性T2D患者中。在我们的研究中,我们发现血糖控制和OC之间没有明显的联系。相比之下,HbA1c与女性的硬化蛋白呈正相关,接近显著性(p = 0.07),而在男性中没有发现相关。我们建议筛查墨西哥裔美国人T2D患者,特别是那些血糖控制不良的患者,以了解其骨质流失和骨折风险。
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引用次数: 10
Corrigendum to "Potential Extensions of the US FRAX Algorithm". “美国FRAX算法的潜在扩展”的勘误。
IF 1.9 Q3 Medicine Pub Date : 2018-04-02 eCollection Date: 2018-01-01 DOI: 10.1155/2018/3021801
Journal Of Osteoporosis

[This corrects the article DOI: 10.1155/2012/528790.].

[这更正了文章DOI: 10.1155/2012/528790。]
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引用次数: 0
The Impact of Multifaceted Osteoporosis Group Education on Patients' Decision-Making regarding Treatment Options and Lifestyle Changes. 骨质疏松症群体教育对患者治疗选择和生活方式改变决策的影响。
IF 1.9 Q3 Medicine Pub Date : 2018-03-26 eCollection Date: 2018-01-01 DOI: 10.1155/2018/9703602
Annesofie L Jensen, Gitte Wind, Bente Lomholt Langdahl, Kirsten Lomborg

Introduction: Patients with chronic diseases like osteoporosis constantly have to make decisions related to their disease. Multifaceted osteoporosis group education (GE) may support patients' decision-making. This study investigated multifaceted osteoporosis GE focusing on the impact of GE on patients' decision-making related to treatment options and lifestyle.

Material and methods: An interpretive description design using ethnographic methods was utilized with 14 women and three men diagnosed with osteoporosis who attended multifaceted GE. Data consisted of participant observation during GE and individual interviews.

Results: Attending GE had an impact on the patients' decision-making in all educational themes. Patients decided on new ways to manage osteoporosis and made decisions regarding bone health and how to implement a lifestyle ensuring bone health. During GE, teachers and patients shared evidence-based knowledge and personal experiences and preferences, respectively, leading to a two-way exchange of information and deliberation about recommendations. Though teachers and patients explored the implications of the decisions and shared their preferences, teachers stressed that the patients ultimately had to make the decision. Teachers therefore refrained from participating in the final step of the decision-making process.

Conclusion: Attending GE has an impact on the patients' decision-making as it can initiate patient reflection and support decision-making.

患有骨质疏松症等慢性疾病的患者经常需要做出与疾病相关的决定。骨质疏松症群体教育(GE)可以支持患者的决策。本研究调查了骨质疏松症的多方面GE,重点关注GE对患者治疗方案和生活方式决策的影响。材料和方法:采用民族志方法对14名女性和3名男性骨质疏松症患者进行了解释性描述设计。数据包括GE期间的参与者观察和个人访谈。结果:参加GE会影响患者对所有教育主题的决策。患者决定了新的方法来管理骨质疏松症,并做出了有关骨骼健康的决定,以及如何实施确保骨骼健康的生活方式。在GE期间,教师和患者分别分享基于证据的知识、个人经验和偏好,从而导致双向信息交流和对建议的审议。尽管教师和患者探讨了这些决定的含义,并分享了他们的偏好,但教师强调,最终必须由患者做出决定。因此,教师不愿参与决策过程的最后一步。结论:参加GE对患者的决策有影响,可以引发患者的反思,支持患者的决策。
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引用次数: 4
"Omics" Signatures in Peripheral Monocytes from Women with Low BMD Condition. 低骨密度女性外周血单核细胞的组学特征
IF 1.9 Q3 Medicine Pub Date : 2018-03-18 eCollection Date: 2018-01-01 DOI: 10.1155/2018/8726456
Bhavna Daswani, M Ikram Khatkhatay

Postmenopausal osteoporosis (PMO) is a result of increased bone resorption compared to formation. Osteoclasts are responsible for bone resorption, which are derived from circulating monocytes that undertake a journey from the blood to the bone for the process of osteoclastogenesis. In recent times, the use of high throughput technologies to explore monocytes from women with low versus high bone density has led to the identification of candidate molecules that may be deregulated in PMO. This review provides a list of molecules in monocytes relevant to bone density which have been identified by "omics" studies in the last decade or so. The molecules in monocytes that are deregulated in low BMD condition may contribute to processes such as monocyte survival, migration/chemotaxis, adhesion, transendothelial migration, and differentiation into the osteoclast lineage. Each of these processes may be crucial to the overall route of osteoclastogenesis and an increase in any/all of these processes can lead to increased bone resorption and subsequently low bone density. Whether these molecules are indeed the cause or effect is an arena currently unexplored.

绝经后骨质疏松症(PMO)是骨吸收与形成增加的结果。破骨细胞负责骨吸收,骨吸收来自循环单核细胞,这些单核细胞从血液到骨骼进行破骨细胞形成的过程。近年来,利用高通量技术探索低骨密度和高骨密度女性的单核细胞,发现了可能在PMO中失调的候选分子。本文综述了近十年来通过“组学”研究发现的与骨密度相关的单核细胞分子。在低骨密度条件下,单核细胞中的分子失调可能有助于单核细胞存活、迁移/趋化、粘附、跨内皮迁移和向破骨细胞谱系分化等过程。这些过程中的每一个都可能对破骨细胞形成的整体途径至关重要,任何/所有这些过程的增加都可能导致骨吸收增加,随后导致骨密度降低。这些分子是否确实是原因还是结果,目前还没有研究。
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引用次数: 2
The Femoral Neck Mechanoresponse to Hip Extensors Exercise: A Case Study 髋关节伸肌运动的股骨颈机械反应:一个案例研究
IF 1.9 Q3 Medicine Pub Date : 2017-01-11 DOI: 10.1155/2017/5219541
S. Martelli, H. Mokhtarzadeh, P. Pivonka, P. Ebeling
Physical activity is recommended to prevent age-related bone loss. However, the proximal femur mechanoresponse is variable, possibly because of a muscle-dependant mechanoresponse. We compared the proximal femur response with the femoral strain pattern generated by the hip extensor muscles. A healthy participant underwent a six-month unilateral training of the hip extensor muscles using a resistance weight regularly adjusted to the 80% of the one-repetition maximum weight. DXA-based measurements of the areal Bone Mineral Density (aBMD) in the exercise leg were adjusted for changes in the control leg. The biomechanical stimulus for bone adaptation (BS) was calculated using published models of the musculoskeletal system and the average hip extension moment in elderly participants. Volumetric (ΔvBMD) and areal (ΔaBMD) BMD changes were calculated. The measured and calculated BMD changes consistently showed a positive and negative effect of exercise in the femoral neck (ΔaBMD = +0.7%; ΔvBMD = +0.8%) and the trochanter region (ΔaBMD = −4.1%; ΔvBMD = −0.5%), respectively. The 17% of the femoral neck exceeded the 75th percentile of the spatially heterogeneous BS distribution. Hip extensor exercises may be beneficial in the proximal femoral neck but not in the trochanteric region. DXA-based measurements may not capture significant aBMD local changes.
建议进行体育锻炼以防止与年龄相关的骨质流失。然而,股骨近端机械反应是可变的,可能是由于肌肉依赖的机械反应。我们比较了股骨近端反应与髋伸肌产生的股骨应变模式。一名健康的参与者接受了为期六个月的髋伸肌单侧训练,使用阻力重量定期调整到一次重复最大重量的80%。根据对照腿的变化调整运动腿中基于dxa的面积骨矿物质密度(aBMD)测量值。骨适应的生物力学刺激(BS)是使用已发表的肌肉骨骼系统模型和老年参与者的平均髋关节伸展力矩来计算的。计算体积(ΔvBMD)和面积(ΔaBMD)骨密度变化。测量和计算的骨密度变化一致显示运动对股骨颈的正、负影响(ΔaBMD = +0.7%;ΔvBMD = +0.8%)和转子区(ΔaBMD =−4.1%;ΔvBMD =−0.5%)。17%的股骨颈超过了BS空间异质性分布的第75百分位。髋关节伸肌运动可能对股骨颈近端有益,但对股骨粗隆区无效。基于dxa的测量可能无法捕获重要的aBMD局部变化。
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引用次数: 6
A Review on the Relationship between Aspirin and Bone Health 阿司匹林与骨骼健康关系的研究进展
IF 1.9 Q3 Medicine Pub Date : 2017-01-09 DOI: 10.1155/2017/3710959
K. Chin
Aspirin is a cyclooxygenase inhibitor commonly used in primary prevention of cardiovascular diseases and cancers. Its users are elderly population susceptible to osteoporosis. It also inhibits the synthesis of prostaglandin E2 essential in bone remodeling. This prompts the question whether it can influence bone health among users. This review aimed to summarize the current literature on the use of aspirin on bone health. A literature search on experimental and clinical evidence on the effects of aspirin on bone health was performed using major scientific databases. In vitro studies showed that aspirin could enhance the survival of bone marrow mesenchymal stem cells, the progenitors of osteoblasts, and stimulate the differentiation of preosteoblasts. Aspirin also inhibited the nuclear factor kappa-B (NFκB) pathway and decreased the expression of receptor activator of NFκB ligand, thus suppressing the formation of osteoclast. Aspirin could prevent bone loss in animal models of osteoporosis. Despite a positive effect on bone mineral density, the limited human epidemiological studies revealed that aspirin could not reduce fracture risk. A study even suggested that the use of aspirin increased fracture risk. As a conclusion, aspirin may increase bone mineral density but its effect on fracture prevention is inconclusive. More data are needed to determine the effects of aspirin and bone health in human.
阿司匹林是一种环氧化酶抑制剂,常用于心血管疾病和癌症的一级预防。其使用者为易患骨质疏松症的老年人群。它还能抑制骨重塑所必需的前列腺素E2的合成。这引发了一个问题,即它是否会影响使用者的骨骼健康。本文综述了阿司匹林对骨骼健康的影响。利用主要的科学数据库对阿司匹林对骨骼健康影响的实验和临床证据进行文献检索。体外研究表明,阿司匹林能提高成骨细胞的祖细胞骨髓间充质干细胞的存活率,刺激成骨前细胞的分化。阿司匹林还能抑制核因子κ b (NFκB)通路,降低NFκB配体受体激活因子的表达,从而抑制破骨细胞的形成。阿司匹林可预防骨质疏松动物模型骨质流失。尽管阿司匹林对骨密度有积极作用,但有限的人类流行病学研究显示阿司匹林不能降低骨折风险。一项研究甚至表明,服用阿司匹林会增加骨折的风险。因此,阿司匹林可增加骨密度,但对骨折的预防作用尚无定论。还需要更多的数据来确定阿司匹林对人体骨骼健康的影响。
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引用次数: 32
Nutritional Aspects of Bone Health and Fracture Healing. 骨骼健康和骨折愈合的营养方面。
IF 1.9 Q3 Medicine Pub Date : 2017-01-01 Epub Date: 2017-12-31 DOI: 10.1155/2017/4218472
Athanasios Karpouzos, Evangelos Diamantis, Paraskevi Farmaki, Spyridon Savvanis, Theodore Troupis

Introduction: Fractures are quite common, especially among the elderly. However, they can increase in prevalence in younger ages too if the bone health is not good. This may happen as a result of bad nutrition.

Methods: A customized, retrospective review of available literature was performed using the following keywords: bone health, nutrition, and fractures.

Results: Insufficient intake of certain vitamins, particularly A and D, and other nutrients, such as calcium, may affect bone health or even the time and degree of bone healing in case of fracture. The importance of different nutrients, both dietary and found in food supplements, is discussed concerning bone health and fracture healing.

Conclusion: A healthy diet with adequate amounts of both macro- and micronutrients is essential, for both decreasing fracture risk and enhancing the healing process after fracture.

骨折是很常见的,尤其是在老年人中。然而,如果骨骼健康状况不佳,在年轻人中患病率也会增加。这可能是营养不良的结果。方法:采用以下关键词:骨骼健康、营养和骨折,对现有文献进行个性化的回顾性回顾。结果:某些维生素,特别是A和D,以及其他营养物质,如钙摄入不足,可能会影响骨骼健康,甚至在骨折时影响骨愈合的时间和程度。不同的营养,无论是膳食和食物补充剂的重要性,讨论了骨骼健康和骨折愈合。结论:健康的饮食中含有足量的宏量和微量元素对于降低骨折风险和促进骨折后愈合至关重要。
{"title":"Nutritional Aspects of Bone Health and Fracture Healing.","authors":"Athanasios Karpouzos,&nbsp;Evangelos Diamantis,&nbsp;Paraskevi Farmaki,&nbsp;Spyridon Savvanis,&nbsp;Theodore Troupis","doi":"10.1155/2017/4218472","DOIUrl":"https://doi.org/10.1155/2017/4218472","url":null,"abstract":"<p><strong>Introduction: </strong>Fractures are quite common, especially among the elderly. However, they can increase in prevalence in younger ages too if the bone health is not good. This may happen as a result of bad nutrition.</p><p><strong>Methods: </strong>A customized, retrospective review of available literature was performed using the following keywords: bone health, nutrition, and fractures.</p><p><strong>Results: </strong>Insufficient intake of certain vitamins, particularly A and D, and other nutrients, such as calcium, may affect bone health or even the time and degree of bone healing in case of fracture. The importance of different nutrients, both dietary and found in food supplements, is discussed concerning bone health and fracture healing.</p><p><strong>Conclusion: </strong>A healthy diet with adequate amounts of both macro- and micronutrients is essential, for both decreasing fracture risk and enhancing the healing process after fracture.</p>","PeriodicalId":45384,"journal":{"name":"Journal of Osteoporosis","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2017/4218472","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35848866","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 57
Corrigendum to "Predictors of Fracture Risk and Bone Mineral Density in Men with Prostate Cancer on Androgen Deprivation Therapy". 对“雄激素剥夺治疗前列腺癌患者骨折风险和骨密度的预测因素”的更正。
IF 1.9 Q3 Medicine Pub Date : 2017-01-01 Epub Date: 2017-07-12 DOI: 10.1155/2017/4982312
Katherine Neubecker, Beverley Adams-Huet, Irfan M Farukhi, Rosinda Castanon, Ugis Gruntmanis

[This corrects the article DOI: 10.4061/2011/924595.].

[这更正了文章DOI: 10.4061/2011/924595。]
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引用次数: 0
Corrigendum to "Mikkeli Osteoporosis Index Identifies Fracture Risk Factors and Osteoporosis and Intervention Thresholds Parallel with FRAX". “Mikkeli骨质疏松指数识别骨折危险因素和骨质疏松症和干预阈值与FRAX平行”的勘误表。
IF 1.9 Q3 Medicine Pub Date : 2017-01-01 Epub Date: 2017-08-20 DOI: 10.1155/2017/3074151
Ville Juhana Waris, Joonas P Sirola, Vesa V Kiviniemi, Marjo T Tuppurainen, V Pekka Waris

[This corrects the article DOI: 10.4061/2011/732560.].

[这更正了文章DOI: 10.4061/2011/732560]。
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引用次数: 1
Monitoring of Cellular Changes in the Bone Marrow following PTH(1-34) Treatment of OVX Rats Using a Portable Stray-Field NMR Scanner. 使用便携式杂散场核磁共振扫描仪监测OVX大鼠PTH(1-34)治疗后骨髓细胞变化。
IF 1.9 Q3 Medicine Pub Date : 2017-01-01 Epub Date: 2017-05-30 DOI: 10.1155/2017/7910432
Inbar Hillel, Itzhak Binderman, Yifat Sarda, Uri Nevo

Osteoporosis is characterized by reduction in trabecular bone in conjunction with increased marrow cell adiposity. While these changes occur within weeks, monitoring of treatment efficacy as performed by DEXA is sensitive only to long-term changes. MRI is sensitive to bone marrow changes but is less affordable. In a recent study, we have shown that a stray-field NMR can monitor bone marrow cellular changes that are related to osteoporosis. Objectives. To demonstrate sensitivity of a low-field tabletop NMR scanner to bone marrow dynamics following hormonal treatment in rats. Methods. Two-month-old female rats (n = 36) were ovariectomized (OVX) and dosed for the ensuing 3 or 5 weeks with 20 mg/kg of PTH(1-34). Hind limbs femurs and tibiae were isolated and underwent ex vivo microradiography and histology and NMR relaxometry at 6 weeks (preventive experiment) and 11 weeks (therapeutic treatment experiment) after OVX. Results. OVX rats developed osteoporotic changes including adipogenic marrow compared to Sham and PTH treated rats. T2 and ADC NMR relaxation coefficients were found to correlate with marrow composition. Conclusions. This study suggests that stray-field NMR, an affordable method that is sensitive to the rapid cellular changes in bone marrow, may have a clinical value in monitoring hormonal treatment for osteoporosis.

骨质疏松症的特点是小梁骨减少,同时骨髓细胞肥胖增加。虽然这些变化发生在几周内,但DEXA监测治疗效果仅对长期变化敏感。核磁共振成像对骨髓变化很敏感,但价格较低。在最近的一项研究中,我们已经证明了一种杂散场核磁共振可以监测与骨质疏松症相关的骨髓细胞变化。目标。演示低场台式核磁共振扫描仪对大鼠激素治疗后骨髓动力学的敏感性。方法。两个月大的雌性大鼠(n = 36)切除卵巢(OVX),在随后的3或5周内给予20 mg/kg的甲状旁腺激素(1-34)。OVX术后6周(预防性实验)和11周(治疗性治疗实验),分别分离后肢股骨和胫骨,进行离体放射线照相、组织学和核磁共振弛豫测量。结果。与Sham和PTH治疗的大鼠相比,OVX大鼠出现骨质疏松性改变,包括脂肪生成骨髓。T2和ADC核磁共振弛豫系数与骨髓成分相关。结论。这项研究表明,杂散场核磁共振是一种负担得起的方法,对骨髓细胞的快速变化敏感,可能在监测骨质疏松症的激素治疗方面具有临床价值。
{"title":"Monitoring of Cellular Changes in the Bone Marrow following PTH(1-34) Treatment of OVX Rats Using a Portable Stray-Field NMR Scanner.","authors":"Inbar Hillel,&nbsp;Itzhak Binderman,&nbsp;Yifat Sarda,&nbsp;Uri Nevo","doi":"10.1155/2017/7910432","DOIUrl":"https://doi.org/10.1155/2017/7910432","url":null,"abstract":"<p><p>Osteoporosis is characterized by reduction in trabecular bone in conjunction with increased marrow cell adiposity. While these changes occur within weeks, monitoring of treatment efficacy as performed by DEXA is sensitive only to long-term changes. MRI is sensitive to bone marrow changes but is less affordable. In a recent study, we have shown that a stray-field NMR can monitor bone marrow cellular changes that are related to osteoporosis. <i>Objectives.</i> To demonstrate sensitivity of a low-field tabletop NMR scanner to bone marrow dynamics following hormonal treatment in rats. <i>Methods.</i> Two-month-old female rats (<i>n</i> = 36) were ovariectomized (OVX) and dosed for the ensuing 3 or 5 weeks with 20 mg/kg of PTH(1-34). Hind limbs femurs and tibiae were isolated and underwent ex vivo microradiography and histology and NMR relaxometry at 6 weeks (preventive experiment) and 11 weeks (therapeutic treatment experiment) after OVX. <i>Results.</i> OVX rats developed osteoporotic changes including adipogenic marrow compared to Sham and PTH treated rats. <i>T</i><sub>2</sub> and ADC NMR relaxation coefficients were found to correlate with marrow composition. <i>Conclusions</i>. This study suggests that stray-field NMR, an affordable method that is sensitive to the rapid cellular changes in bone marrow, may have a clinical value in monitoring hormonal treatment for osteoporosis.</p>","PeriodicalId":45384,"journal":{"name":"Journal of Osteoporosis","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2017/7910432","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35109323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Journal of Osteoporosis
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