Racial and Socioeconomic Differences in Chronic Low Back Pain
慢性腰痛的种族和社会经济差异
基本信息
- 批准号:10656046
- 负责人:
- 金额:$ 70.87万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-07-10 至 2027-12-31
- 项目状态:未结题
- 来源:
- 关键词:AcuteAddressAdultAdverse effectsAnxietyAttitudeBiologicalBlack PopulationsBlack raceBlood PressureC-reactive proteinCOVID-19COVID-19 pandemicCardiovascular systemCessation of lifeChronicChronic low back painClinicalDataDiscriminationDiseaseDisparityDisparity populationDistressEquationEventExposure toFollow-Up StudiesFriendsFundingGlycosylated hemoglobin AGoalsGroup AffiliationHealthHydrocortisoneImmuneIndividualLifeLiteratureLonelinessLow Back PainMeasuresMetabolicMinority GroupsModelingNeurosecretory SystemsNot Hispanic or LatinoPainPain managementPathologyPatternPersistent painPersonsPhysiologicalPrevalencePrimary Care PhysicianPsychosocial FactorRaceReportingResearchRestRisk FactorsSensorySeveritiesSocial isolationSocial supportSocializationSocioeconomic StatusSpiritualityStigmatizationStressStressful EventSymptomsTestingTimeTissuesVertebral columnViolenceVisitWorkadverse childhood eventsallostatic loadchronic painclinical painclinical predictorsdepressive symptomsdisabilityexperiencefollow-uphealth care availabilityimprovedloved oneslow socioeconomic statusminority stressoptimismpain inhibitionpain sensitivitypain symptompeerperceived stresspromote resilienceprospectivepsychologicpsychological distresspsychosocialracial determinantracial differenceracial discriminationracial disparityracial identityracial populationracismresilience factorsocial determinantssocial influencesocial stresssocial stressorsocioeconomicstheories
项目摘要
Project Summary/Abstract
Low back pain is one of the most common disabling conditions in the world. The worldwide point prevalence of
activity-limiting (acute and chronic) low back pain is approximately 12%, which equates to approximately 933
million people globally suffering with low back pain at any given time. Chronic low back pain (cLBP) refers to
pain lasting at least twelve weeks or longer, and it is consistently among the top five most common reasons for
primary care physician visits. Although some individuals with cLBP have clear pathoanatomic causes of pain,
the vast majority of cLBP is “non-specific” and is not accompanied by readily identifiable pathology of the spine
or related tissues. Without a clear target for treatment of cLBP, effective pain management can be difficult to
achieve. Because objective measures of disease activity have not consistently been strong predictors of clinical
symptoms, cLBP provides an excellent model for investigating the influence of social determinants such as racial
background and social stress on the progression of pain and disability over time. During our previous funding
cycle, we found evidence that non-Hispanic Black (NHB) individuals with cLBP reported significantly greater pain
severity and disability than their non-Hispanic White (NHW) counterparts. In addition, we observed racial
differences in pain-related psychosocial and biological measures, which were significantly associated with racial
group disparities in cLBP severity. Furthermore, racial disparities in cLBP were exacerbated by low
socioeconomic status (SES), such that NHBs with low SES demonstrated the absolute greatest burden of cLBP.
While our findings demonstrate clear racial differences in cLBP severity and disability between NHBs and NHWs,
the findings are largely indirect and cross-sectional. Differences in how cLBP progresses over time between
NHBs and NHWs, as well as factors that contribute to cLBP progression, remain poorly understood. Among the
multiple factors that inevitably contribute to racial group differences in cLBP, social stress represents a potentially
important social determinant of greater cLBP severity and disability in NHBs. For this proposed follow-up study,
we will elucidate the contribution of social stress and its biological consequences (i.e., allostatic load) to racial
group disparities in cLBP by prospectively assessing the two-year progression of clinical pain and disability, as
well as pain-relevant psychosocial functioning among NHBs and NHWs with cLBP. We will use minority stress
theory to guide the study aims related to the progression of racial group disparities in cLBP; however, we will
also use a recently developed resilience framework to guide inclusion of psychosocial resilience factors that may
mitigate the effects of social stress on cLBP in NHBs and/or NHWs.
项目摘要/摘要
腰痛是世界上最常见的残疾条件之一。全球的流行率
活动限制(急性和慢性)下背痛约为12%,约为933
在任何给定的时间慢性下腰痛(CLBP)是指
疼痛至少持续十二周或更长时间,并且始终是前五名的最常见原因
初级保健身体访问。尽管有些患有CLBP的人有明显的疗法疼痛原因,但
绝大多数CLBP是“非特异性”,并且不容易识别脊柱病理
或相关的组织。没有明确治疗CLBP的目标,有效的疼痛管理可能很难
达到。因为疾病活性的客观测量并不是临床的强大预测指标
症状,CLBP为研究社会决定者(例如种族)的影响提供了一个绝佳的模型
随着时间的流逝,背景和社会压力对疼痛和残疾的发展。在我们以前的资金中
循环,我们发现有证据表明,非西班牙裔黑人(NHB)患有CLBP的个体报告明显更大的疼痛
与非西班牙裔白人(NHW)相比,严重性和残疾。此外,我们观察到种族
与疼痛相关的社会心理和生物学措施的差异,与种族显着相关
CLBP严重程度的组分布。此外,CLBP中的种族分布因低而加剧
社会经济地位(SES),使得SES低的NHB表现出绝对最大的CLBP燃烧。
尽管我们的发现表明NHB和NHW之间的CLBP严重性和残疾的种族差异,但
这些发现在很大程度上是间接的和横截面。 CLBP随着时间的推移如何随着时间的推移而差异
NHB和NHWS以及导致CLBP进展的因素仍然知之甚少。在
社会压力不可避免地导致种族群体差异的多种因素,社会压力代表了潜在的
NHB中CLBP严重程度更大和残疾的重要社会决定者。对于这项提出的后续研究,
我们将阐明社会压力及其生物学后果(即同性恋负荷)对种族的贡献
通过前瞻性评估临床疼痛和残疾的两年进展,CLBP的群体差异
以及与CLBP的NHB和NHW中的疼痛相关的社会心理功能。我们将使用少数派压力
指导研究的理论与CLBP中种族群体分布的发展有关;但是,我们会的
还使用最近开发的弹性框架来指导可能包含可能
减轻社会压力对NHB和/或NHW中CLBP的影响。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
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 }}
Burel R. Goodin其他文献
The pace of biological aging significantly mediates the relationship between internalized stigma of chronic pain and chronic low back pain severity among non-hispanic black but not non-hispanic white adults
- DOI:
10.1016/j.ynpai.2024.100170 - 发表时间:
2024-07-01 - 期刊:
- 影响因子:
- 作者:
Khalid W. Freij;Fiona B.A.T. Agbor;Kiari R. Kinnie;Vinodh Srinivasasainagendra;Tammie L. Quinn;Hemant K. Tiwari;Robert E. Sorge;Burel R. Goodin;Edwin N. Aroke - 通讯作者:
Edwin N. Aroke
Burel R. Goodin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('Burel R. Goodin', 18)}}的其他基金
Diet Interventions, by Race, Evaluated as Complementary Treatments for Pain (DIRECTPain)
按种族划分的饮食干预措施被评估为疼痛的补充治疗方法 (DIRECTPain)
- 批准号:
10708175 - 财政年份:2022
- 资助金额:
$ 70.87万 - 项目类别:
Sex, Hormones and Identity affect Nociceptive Expression (SHINE)
性别、激素和身份影响伤害感受表达 (SHINE)
- 批准号:
10531740 - 财政年份:2022
- 资助金额:
$ 70.87万 - 项目类别:
Diet Interventions, by Race, Evaluated as Complementary Treatments for Pain (DIRECTPain)
按种族划分的饮食干预措施被评估为疼痛的补充治疗方法 (DIRECTPain)
- 批准号:
10512647 - 财政年份:2022
- 资助金额:
$ 70.87万 - 项目类别:
Sex, Hormones and Identity affect Nociceptive Expression (SHINE)
性别、激素和身份影响伤害感受表达 (SHINE)
- 批准号:
10708822 - 财政年份:2022
- 资助金额:
$ 70.87万 - 项目类别:
The Impact of Insomnia on Pain, Physical Function, and Inflammation in HIV
失眠对 HIV 患者疼痛、身体功能和炎症的影响
- 批准号:
10453431 - 财政年份:2019
- 资助金额:
$ 70.87万 - 项目类别:
The Impact of Insomnia on Pain, Physical Function, and Inflammation in HIV
失眠对 HIV 患者疼痛、身体功能和炎症的影响
- 批准号:
10225460 - 财政年份:2019
- 资助金额:
$ 70.87万 - 项目类别:
Impact of insomnia on substance use in people living with HIV
失眠对艾滋病毒感染者药物使用的影响
- 批准号:
10059153 - 财政年份:2019
- 资助金额:
$ 70.87万 - 项目类别:
The Impact of Insomnia on Pain, Physical Function, and Inflammation in HIV
失眠对 HIV 患者疼痛、身体功能和炎症的影响
- 批准号:
10451208 - 财政年份:2019
- 资助金额:
$ 70.87万 - 项目类别:
The Impact of Insomnia on Pain, Physical Function, and Inflammation in HIV
失眠对 HIV 患者疼痛、身体功能和炎症的影响
- 批准号:
9768852 - 财政年份:2019
- 资助金额:
$ 70.87万 - 项目类别:
Racial and Socioeconomic Differences in Chronic Low Back Pain
慢性腰痛的种族和社会经济差异
- 批准号:
9235624 - 财政年份:2017
- 资助金额:
$ 70.87万 - 项目类别:
相似国自然基金
时空序列驱动的神经形态视觉目标识别算法研究
- 批准号:61906126
- 批准年份:2019
- 资助金额:24.0 万元
- 项目类别:青年科学基金项目
本体驱动的地址数据空间语义建模与地址匹配方法
- 批准号:41901325
- 批准年份:2019
- 资助金额:22.0 万元
- 项目类别:青年科学基金项目
大容量固态硬盘地址映射表优化设计与访存优化研究
- 批准号:61802133
- 批准年份:2018
- 资助金额:23.0 万元
- 项目类别:青年科学基金项目
IP地址驱动的多径路由及流量传输控制研究
- 批准号:61872252
- 批准年份:2018
- 资助金额:64.0 万元
- 项目类别:面上项目
针对内存攻击对象的内存安全防御技术研究
- 批准号:61802432
- 批准年份:2018
- 资助金额:25.0 万元
- 项目类别:青年科学基金项目
相似海外基金
Climate Change Effects on Pregnancy via a Traditional Food
气候变化通过传统食物对怀孕的影响
- 批准号:
10822202 - 财政年份:2024
- 资助金额:
$ 70.87万 - 项目类别:
Developing Real-world Understanding of Medical Music therapy using the Electronic Health Record (DRUMMER)
使用电子健康记录 (DRUMMER) 培养对医学音乐治疗的真实理解
- 批准号:
10748859 - 财政年份:2024
- 资助金额:
$ 70.87万 - 项目类别:
Targeting Alcohol-Opioid Co-Use Among Young Adults Using a Novel MHealth Intervention
使用新型 MHealth 干预措施针对年轻人中酒精与阿片类药物的同时使用
- 批准号:
10456380 - 财政年份:2023
- 资助金额:
$ 70.87万 - 项目类别:
Immunomodulatory ligand B7-1 targets p75 neurotrophin receptor in neurodegeneration
免疫调节配体 B7-1 在神经变性中靶向 p75 神经营养蛋白受体
- 批准号:
10660332 - 财政年份:2023
- 资助金额:
$ 70.87万 - 项目类别:
Mixed methods examination of warning signs within 24 hours of suicide attempt in hospitalized adults
住院成人自杀未遂 24 小时内警告信号的混合方法检查
- 批准号:
10710712 - 财政年份:2023
- 资助金额:
$ 70.87万 - 项目类别: