Nutritional Regulation of Bone
骨骼的营养调节
基本信息
- 批准号:8744648
- 负责人:
- 金额:$ 3.95万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2013
- 资助国家:美国
- 起止时间:2013-12-20 至 2015-12-19
- 项目状态:已结题
- 来源:
- 关键词:AddressAdipose tissueAdultAffectAfrican AmericanAgeAsiansAttenuatedBiological MarkersBody Weight ChangesBody Weight decreasedBone DensityBone ResorptionBone TissueCalciumCaloric RestrictionCaloriesCarbohydratesCaucasiansCaucasoid RaceChronicDataDiabetes MellitusDietDietary CalciumDietary ProteinsEndocrineEstrogensEthnic OriginEthnic groupFat-Restricted DietFatty AcidsFatty acid glycerol estersFractureGeometryGoalsHealthHigh PrevalenceHormonesInsulin-Like Growth Factor IInsulin-Like Growth-Factor-Binding ProteinsIntakeKnowledgeMetabolicMetabolic syndromeMinorityNutritionalObesityOsteoporosisOsteoporosis preventionOutcomeOverweightParathyroid glandPlacebosPopulationPostmenopausePreventionProteinsRecommendationRegulationRiskRisk FactorsSerumSiteSkeletal MuscleSouth AsianStomachTrochantersVariantVisceralVitamin DWeightWeight maintenance regimenWomanblood glucose regulationbonebone geometrybone lossbone massbone qualitybone strengthbone turnovercalcium absorptioncalcium intakecalcium metabolismcytokinedisorder riskhigh riskhigh standardhypercalciuriaimprovedinterestmoderate obesitymuscle formnovelobesity preventionpreventprimary outcomeprotein intakeresponsesoft tissueweight maintenance
项目摘要
In the USA, minority populations are growing rapidly. The expected population increase
from 2010 to 2015 is 37% for Asians and 20% for Black/African Americans (AA) compared
to only 13% for White/Caucasians (C). It is well known that endocrine profiles may vary in
these ethnic groups, and this may be associated with adipose depots that differ from Cs. For
example, AA’s have higher rates of obesity than Cs, and metabolic syndrome is more
prevalent in South Asians (SAs) as compared to other ethnic groups. While bone mineral
density (BMD) in SAs is similar to Cs, fracture risk begins at an earlier age, and it is unclear
if this is related to their lower muscle mass, higher visceral adipose tissue or altered an
endocrine profile. AAs have higher muscle mass, BMD and lower fracture risk, compared
to C. There are a rising number of fragility fractures in all ethnicities, and more recently, it
has been shown that higher BMD in the obese is not protective. Weight loss is
recommended to reduce risks associated with obesity and metabolic syndrome, but there are
also changes in BMD and geometry and increased fracture risk. Previous weight loss studies
have shown that postmenopausal women are particularly vulnerable to BMD loss, yet these
studies reflect the response in C women. Weight loss also differentially attenuates BMD
and skeletal muscle mass at different anatomical sites and these same sites show variation in
fracture risk by ethnicity. Since visceral adiposity is associated with compromised BMD,
this too may affect bone differently across ethnic groups. Moreover, the variations in
hormones and cytokines among ethnic groups may explain a differential bone response to
wt change in these populations. In addition, Ca absorption is compromised during caloric
restriction, and therefore it is important to determine if it is a risk factor for weight loss
induced bone loss across ethnicities. The central hypothesis is that there will be BMD loss
in all ethnic groups due to wt loss that will be partially explained by a reduction in Ca
absorption, whereas site specific BMD loss will differ between ethnic groups and be related
to the regional changes in muscle mass. In the proposed studies, we will study 3 ethnic
groups (SA, AA and C) of postmenopausal overweight/obese women before and after
weight loss to: 1) determine the effect on BMD, bone geometry and strength; 2) determine
how BMD changes relate to changes in total and regional muscle mass and fat depots; and
3) examine if Ca absorption contributes to BMD changes with weight loss. Understanding
ethnic-specific responses of bone and soft tissue to weight loss is novel and important due
the unique metabolic profiles and disease risks in these ethnic groups. The ultimate goal is
to develop and encourage healthy weight control strategies that are tailored to address ethnic
diversity in the prevention of obesity and osteoporosis.
在美国,少数民族人口正在迅速增长。预期人口增长。
从 2010 年到 2015 年,亚洲人的这一比例为 37%,黑人/非裔美国人 (AA) 的比例为 20%
白人/白种人的这一比例仅为 13% (C) 众所周知,内分泌特征可能有所不同。
这些种族群体,这可能与不同于 Cs 的脂肪库有关。
例如,AA 人群的肥胖率高于 C 人群,代谢综合征的发病率更高
与其他种族相比,南亚人(SA)普遍存在骨矿物质。
SAs 中的密度 (BMD) 与 Cs 相似,骨折风险开始于较早年龄,目前尚不清楚
如果这与他们较低的肌肉质量、较高的内脏脂肪组织或改变的
相比之下,AA 具有更高的肌肉质量、BMD 和更低的骨折风险。
到 C. 所有种族中脆性骨折的数量都在增加,最近,
已经表明,肥胖者较高的骨密度并不能起到保护作用。
建议降低与肥胖和代谢综合征相关的风险,但也有
先前的减肥研究还显示 BMD 和几何形状的变化以及骨折风险的增加。
研究表明,绝经后妇女特别容易遭受 BMD 损失,但这些
研究反映了 C 类女性的反应,体重减轻也会不同程度地减弱 BMD。
不同解剖部位的骨骼肌质量,这些相同部位表现出差异
由于内脏肥胖与 BMD 受损有关,
这也可能对不同种族的骨骼产生不同的影响。
不同种族之间的激素和细胞因子可能解释骨骼反应的差异
此外,这些人群的体重变化在热量摄入期间会受到影响。
限制,因此确定它是否是减肥的风险因素很重要
导致跨种族骨质流失的核心假设是骨密度会下降。
在所有种族中,由于重量损失,部分原因是 Ca 减少
吸收,而特定部位的 BMD 损失在种族之间会有所不同,并且相关
在拟议的研究中,我们将研究 3 个种族。
绝经后超重/肥胖妇女前后组(SA、AA 和 C)
体重减轻:1) 确定对 BMD、骨骼几何形状和强度的影响;2) 确定
BMD 变化与总和局部肌肉质量和脂肪库的变化有何关系;以及
3) 检查钙吸收是否会导致体重减轻时的 BMD 变化。
骨骼和软组织对减肥的种族特异性反应是新颖且重要的,因为
这些种族群体独特的代谢特征和疾病风险的最终目标是。
制定并鼓励针对种族问题量身定制的健康体重控制策略
预防肥胖和骨质疏松症的多样性。
项目成果
期刊论文数量(19)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Is bone loss after gastric bypass surgery associated with the extent of weight loss?
胃绕道手术后骨质流失与体重减轻程度有关吗?
- DOI:
- 发表时间:2009-02
- 期刊:
- 影响因子:0
- 作者:Shapses; Sue A
- 通讯作者:Sue A
Vitamin D and prevention of cardiovascular disease and diabetes: why the evidence falls short.
维生素 D 与心血管疾病和糖尿病的预防:证据不足的原因。
- DOI:
- 发表时间:2011-06-22
- 期刊:
- 影响因子:0
- 作者:Shapses, Sue A;Manson, JoAnn E
- 通讯作者:Manson, JoAnn E
Three Doses of Vitamin D and Cognitive Outcomes in Older Women: A Double-Blind Randomized Controlled Trial.
三种剂量的维生素 D 与老年女性的认知结果:双盲随机对照试验。
- DOI:
- 发表时间:2020-04-17
- 期刊:
- 影响因子:0
- 作者:Castle, Monica;Fiedler, Nancy;Pop, Lilliana Claudia;Schneider, Stephen J;Schlussel, Yvette;Sukumar, Deeptha;Hao, Lihong;Shapses, Sue A
- 通讯作者:Shapses, Sue A
Vitamin D supplementation during short-term caloric restriction in healthy overweight/obese older women: Effect on glycemic indices and serum osteocalcin levels.
健康超重/肥胖老年女性短期热量限制期间补充维生素 D:对血糖指数和血清骨钙素水平的影响。
- DOI:
- 发表时间:2015-07-15
- 期刊:
- 影响因子:4.1
- 作者:Sukumar, D;Shapses, S A;Schneider, S H
- 通讯作者:Schneider, S H
Do We Need to Be Concerned about Bone Mineral Density in Vegetarians and Vegans?
我们需要关注素食者和严格素食者的骨矿物质密度吗?
- DOI:
- 发表时间:2020-05-01
- 期刊:
- 影响因子:0
- 作者:Shapses; Sue A
- 通讯作者:Sue A
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Sue Amy Shapses其他文献
Sue Amy Shapses的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Sue Amy Shapses', 18)}}的其他基金
相似国自然基金
脂肪组织新型内分泌因子的鉴定及功能研究
- 批准号:82330023
- 批准年份:2023
- 资助金额:220 万元
- 项目类别:重点项目
基于“脂肪-肝脏对话”探讨脂肪组织代谢重编程相关活性代谢因子AMRM2调控RNF8/RXRα/PPARα轴在肝脏脂质代谢稳态维持中的作用与机制
- 批准号:82300971
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
巨噬细胞GP73-CXCL5调节脂肪组织适应性产热的机制研究
- 批准号:32300573
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
脂肪干细胞外泌体miRNA-299a-3p调控巨噬细胞Thbs1缓解脂肪组织衰老的机制研究
- 批准号:82301753
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
棕色脂肪组织源外泌体circ-JARID2调控线粒体功能在延缓卵巢衰老中的作用及机制研究
- 批准号:82301848
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
相似海外基金
Regulation of neuronal function by mitochondrial uncoupling
通过线粒体解偶联调节神经元功能
- 批准号:
10664198 - 财政年份:2023
- 资助金额:
$ 3.95万 - 项目类别:
Identifying Proteomic Markers of Exercise Training in Heart Failure
识别心力衰竭运动训练的蛋白质组标记
- 批准号:
10663612 - 财政年份:2023
- 资助金额:
$ 3.95万 - 项目类别:
Regulation of neuronal function by mitochondrial uncoupling
通过线粒体解偶联调节神经元功能
- 批准号:
10664198 - 财政年份:2023
- 资助金额:
$ 3.95万 - 项目类别:
Glyoxalase 1 and its Role in Metabolic Syndrome
乙二醛酶 1 及其在代谢综合征中的作用
- 批准号:
10656054 - 财政年份:2023
- 资助金额:
$ 3.95万 - 项目类别:
PDGFRB Signaling in Progressive Skin Disease
进行性皮肤病中的 PDGFRB 信号传导
- 批准号:
10583948 - 财政年份:2023
- 资助金额:
$ 3.95万 - 项目类别: