• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Discordant Biological and Chronological Age: Implications for Cognitive Decline and Frailty.生物年龄与实际年龄不相符:对认知能力下降和虚弱的影响。
J Gerontol A Biol Sci Med Sci. 2023 Oct 28;78(11):2152-2161. doi: 10.1093/gerona/glad174.
2
Diabetes, glucose control, and 9-year cognitive decline among older adults without dementia.糖尿病、血糖控制与无痴呆症老年人的9年认知衰退
Arch Neurol. 2012 Sep;69(9):1170-5. doi: 10.1001/archneurol.2012.1117.
3
Relationship between 25-hydroxyvitamin D and cognitive function in older adults: the Health, Aging and Body Composition Study.老年人 25-羟维生素 D 与认知功能的关系:健康、衰老和身体成分研究。
J Am Geriatr Soc. 2014 Apr;62(4):636-41. doi: 10.1111/jgs.12765. Epub 2014 Mar 17.
4
Longitudinal trajectories, correlations and mortality associations of nine biological ages across 20-years follow-up.20 年随访中九种生物年龄的纵向轨迹、相关性和与死亡率的关联。
Elife. 2020 Feb 11;9:e51507. doi: 10.7554/eLife.51507.
5
The Drug Burden Index Is Associated With Measures of Cognitive Function Among Older Adults in the Health, Aging, and Body Composition Study.药物负担指数与健康、衰老和身体成分研究中老年成年人认知功能的衡量标准有关。
J Gerontol A Biol Sci Med Sci. 2024 Jul 1;79(7). doi: 10.1093/gerona/glae097.
6
Comparing Biological Age Estimates Using Domain-Specific Measures From the Canadian Longitudinal Study on Aging.使用加拿大老龄化纵向研究中的特定领域指标比较生物年龄估计。
J Gerontol A Biol Sci Med Sci. 2021 Jan 18;76(2):187-194. doi: 10.1093/gerona/glaa151.
7
Estimating Biological Age in the Singapore Longitudinal Aging Study.估算新加坡纵向老龄化研究中的生物年龄。
J Gerontol A Biol Sci Med Sci. 2020 Sep 25;75(10):1913-1920. doi: 10.1093/gerona/glz146.
8
A Study on the Relationship between Cognitive Performance, Hearing Impairment, and Frailty in Older Adults.老年人认知表现、听力障碍与虚弱关系的研究。
Dement Geriatr Cogn Disord. 2020;49(2):156-162. doi: 10.1159/000507214. Epub 2020 Apr 22.
9
Walking for Cognitive Health: Previous Parity Moderates the Relationship Between Self-Reported Walking and Cognition.步行促进认知健康:先前的一致性调节了自我报告的步行与认知之间的关系。
J Gerontol A Biol Sci Med Sci. 2023 Mar 1;78(3):486-493. doi: 10.1093/gerona/glac123.
10
Role of gait speed and grip strength in predicting 10-year cognitive decline among community-dwelling older people.步速和握力在预测社区居住老年人 10 年内认知能力下降中的作用。
BMC Geriatr. 2019 Jul 5;19(1):186. doi: 10.1186/s12877-019-1199-7.

引用本文的文献

1
Impact of childhood maltreatment on aging: a comprehensive Mendelian randomization analysis of multiple age-related biomarkers.童年期虐待对衰老的影响:多种与年龄相关的生物标志物的综合孟德尔随机分析。
Clin Epigenetics. 2024 Aug 5;16(1):103. doi: 10.1186/s13148-024-01720-z.
2
HOMA-IR is positively correlated with biological age and advanced aging in the US adult population.HOMA-IR 与美国成年人的生物年龄和衰老程度呈正相关。
Eur J Med Res. 2023 Oct 28;28(1):470. doi: 10.1186/s40001-023-01448-1.

本文引用的文献

1
Geroscience for the Next Chapter of Medicine.面向医学新篇章的老年科学。
J Gerontol A Biol Sci Med Sci. 2023 May 11;78(5):791-792. doi: 10.1093/gerona/glad083.
2
Socioeconomic Status, Biological Aging, and Memory in a Diverse National Sample of Older US Men and Women.社会经济地位、生物衰老与美国老年男女多样化样本中的记忆。
Neurology. 2022 Nov 8;99(19):e2114-e2124. doi: 10.1212/WNL.0000000000201032. Epub 2022 Aug 29.
3
Joint Models for Estimating Determinants of Cognitive Decline in the Presence of Survival Bias.联合模型在存在生存偏差的情况下估计认知衰退的决定因素。
Epidemiology. 2022 May 1;33(3):362-371. doi: 10.1097/EDE.0000000000001472.
4
Race, Racism, and Cardiovascular Health: Applying a Social Determinants of Health Framework to Racial/Ethnic Disparities in Cardiovascular Disease.种族、种族主义与心血管健康:应用健康社会决定因素框架分析心血管疾病的种族/民族差异。
Circ Cardiovasc Qual Outcomes. 2022 Jan;15(1):e007917. doi: 10.1161/CIRCOUTCOMES.121.007917. Epub 2022 Jan 18.
5
Testing Black-White Disparities in Biological Aging Among Older Adults in the United States: Analysis of DNA-Methylation and Blood-Chemistry Methods.检测美国老年人生物学衰老的黑-白差异:DNA 甲基化和血液化学方法分析。
Am J Epidemiol. 2022 Mar 24;191(4):613-625. doi: 10.1093/aje/kwab281.
6
Minimal Clinically Important Difference of Executive Function Performance in Older Adults Who Fall: A Secondary Analysis of a Randomized Controlled Trial.老年人跌倒后执行功能表现的最小临床重要差异:一项随机对照试验的二次分析。
Gerontology. 2022;68(7):771-779. doi: 10.1159/000518939. Epub 2021 Oct 15.
7
Asynchronous, contagious and digital aging.异步、传染性和数字老龄化。
Nat Aging. 2021 Jan;1(1):29-35. doi: 10.1038/s43587-020-00015-1. Epub 2021 Jan 14.
8
Reflection on modern methods: shared-parameter models for longitudinal studies with missing data.对现代方法的思考:具有缺失数据的纵向研究的共享参数模型。
Int J Epidemiol. 2021 Aug 30;50(4):1384-1393. doi: 10.1093/ije/dyab086.
9
Quest for a summary measure of biological age: the health and retirement study.寻求生物年龄的综合衡量指标:健康与退休研究。
Geroscience. 2021 Feb;43(1):395-408. doi: 10.1007/s11357-021-00325-1. Epub 2021 Feb 5.
10
Racial Disparities in Incidence and Outcomes Among Patients With COVID-19.COVID-19 患者的发病和结局中的种族差异。
JAMA Netw Open. 2020 Sep 1;3(9):e2021892. doi: 10.1001/jamanetworkopen.2020.21892.

生物年龄与实际年龄不相符:对认知能力下降和虚弱的影响。

Discordant Biological and Chronological Age: Implications for Cognitive Decline and Frailty.

机构信息

Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Neurobiology and Therapeutics of Aging Division, Columbia University College of Physicians and Surgeons, New York State Psychiatric Institute, New York, New York, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2023 Oct 28;78(11):2152-2161. doi: 10.1093/gerona/glad174.

DOI:10.1093/gerona/glad174
PMID:37480573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10613009/
Abstract

BACKGROUND

Older adults with discordant biological and chronological ages (BA and CA) may vary in cognitive and physical function from those with concordant BA and CA.

METHODS

To make our approach clinically accessible, we created easy-to-interpret participant groups in the Health, Aging, and Body Composition Study (N = 2 458, 52% female participants, 65% White participants, age: 73.5 ± 2.8) based on medians of CA, and a previously validated BA index comprised of readily available clinical tests. Joint models estimated associations of BA-CA group with cognition (Modified Mini-Mental State Examination [3MS] and Digit Symbol Substitution Test [DSST]) and frailty over 10 years.

RESULTS

The sample included the following: 32%, Young group (BA and CA < median); 21%, Prematurely Aging group (BA ≥ median, CA < median), 27%, Old group (BA and CA ≥ median), and 20%, Resilient group (BA < median, CA ≥ median). In education-adjusted models of cognition, among those with CA < median, the Prematurely Aging group performed worse than the Young at baseline (3MS and DSST p < .0001), but among those with CA ≥ median, the Resilient group did not outperform the Old group (3MS p = .31; DSST p = .25). For frailty, the Prematurely Aging group performed worse than the Young group at baseline (p = .0001), and the Resilient group outperformed the Old group (p = .003). For all outcomes, groups did not differ on change over time based on the same pairwise comparisons (p ≥ .40).

CONCLUSIONS

Discordant BA and CA identify groups who have greater cognitive and physical functional decline or are more protected than their CA would suggest. This information can be used for risk stratification.

摘要

背景

生物年龄(BA)和实际年龄(CA)不一致的老年人与 BA 和 CA 一致的老年人在认知和身体功能方面可能存在差异。

方法

为了使我们的方法具有临床可操作性,我们根据 CA 的中位数以及之前验证的由易于获得的临床测试组成的 BA 指数,在健康、衰老和身体成分研究(N=2458 名参与者,52%为女性参与者,65%为白人参与者,年龄:73.5±2.8)中创建了易于解释的参与者组。联合模型估计了 BA-CA 组与认知(改良的迷你精神状态检查[3MS]和数字符号替代测试[DSST])和 10 年内衰弱的关联。

结果

该样本包括以下内容:32%,年轻组(BA 和 CA<中位数);21%,过早衰老组(BA≥中位数,CA<中位数),27%,年老组(BA 和 CA≥中位数)和 20%,有弹性组(BA<中位数,CA≥中位数)。在认知的教育调整模型中,在 CA<中位数的人群中,过早衰老组在基线时的表现不如年轻组(3MS 和 DSST p<0.0001),但在 CA≥中位数的人群中,有弹性组与老年组没有差异(3MS p=0.31;DSST p=0.25)。对于虚弱,过早衰老组在基线时的表现不如年轻组(p=0.0001),而有弹性组的表现优于老年组(p=0.003)。对于所有结果,基于相同的两两比较,组间在随时间的变化上没有差异(p≥0.40)。

结论

BA 和 CA 不一致可识别出认知和身体功能下降程度较大或比 CA 所提示的更具保护作用的人群。这些信息可用于风险分层。