Journals of Gerontology Series A-Biological Sciences and Medical Sciences最新文献

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Development and Validation of an Abridged Physical Frailty Phenotype for Clinical Use: A Cohort Study Among Kidney Transplant Candidates. 用于临床的身体虚弱表型简编的开发与验证:肾移植候选者队列研究。
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2024-01-01 DOI: 10.1093/gerona/glad173
Xiaomeng Chen, Nadia M Chu, Valerie Thompson, Evelien E Quint, Sami Alasfar, Qian-Li Xue, Daniel C Brennan, Silas P Norman, Bonnie E Lonze, Jeremy D Walston, Dorry L Segev, Mara A McAdams-DeMarco
{"title":"Development and Validation of an Abridged Physical Frailty Phenotype for Clinical Use: A Cohort Study Among Kidney Transplant Candidates.","authors":"Xiaomeng Chen, Nadia M Chu, Valerie Thompson, Evelien E Quint, Sami Alasfar, Qian-Li Xue, Daniel C Brennan, Silas P Norman, Bonnie E Lonze, Jeremy D Walston, Dorry L Segev, Mara A McAdams-DeMarco","doi":"10.1093/gerona/glad173","DOIUrl":"10.1093/gerona/glad173","url":null,"abstract":"<p><strong>Background: </strong>Frailty is associated with poor outcomes in surgical patients including kidney transplant (KT) recipients. Transplant centers that measure frailty have better pre- and postoperative outcomes. However, clinical utility of existing tools is low due to time constraints. To address this major barrier to implementation in the preoperative evaluation of patients, we developed an abridged frailty phenotype.</p><p><strong>Methods: </strong>The abridged frailty phenotype was developed by simplifying the 5 physical frailty phenotype (PFP) components in a two-center prospective cohort of 3 220 KT candidates and tested for efficiency (time to completion) in 20 candidates evaluation (January 2009 to March 2020). We examined area under curve (AUC) and Cohen's kappa agreement to compare the abridged assessment with the PFP. We compared waitlist mortality risk (competing risks models) by frailty using the PFP and abridged assessment, respectively. Model discrimination was assessed using Harrell's C-statistic.</p><p><strong>Results: </strong>Of 3 220 candidates, the PFP and abridged assessment identified 23.8% and 27.4% candidates as frail, respectively. The abridged frailty phenotype had substantial agreement (kappa = 0.69, 95% CI: 0.66-0.71) and excellent discrimination (AUC = 0.861). Among 20 patients at evaluation, abridged assessment took 5-7 minutes to complete. The PFP and abridged assessment had similar associations with waitlist mortality (subdistribution hazard ratio [SHR] = 1.62, 95% CI: 1.26-2.08 vs SHR = 1.70, 95% CI: 1.33-2.16) and comparable mortality discrimination (p = .51).</p><p><strong>Conclusions: </strong>The abridged assessment is an efficient and valid way to identify frailty. It predicts waitlist mortality without sacrificing discrimination. Surgical departments should consider utilizing the abridged assessment to evaluate frailty in patients when time is limited.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":""},"PeriodicalIF":4.3,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10733181/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10440338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association of Kidney Function With Dementia and Structural Brain Differences: A Large Population-Based Cohort Study. 肾功能与痴呆症和大脑结构差异的关系:一项基于人口的大型队列研究
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2024-01-01 DOI: 10.1093/gerona/glad192
Shuqi Wang, Jiao Wang, Jie Guo, Abigail Dove, Hong Xu, Xiuying Qi, Weili Xu
{"title":"Association of Kidney Function With Dementia and Structural Brain Differences: A Large Population-Based Cohort Study.","authors":"Shuqi Wang, Jiao Wang, Jie Guo, Abigail Dove, Hong Xu, Xiuying Qi, Weili Xu","doi":"10.1093/gerona/glad192","DOIUrl":"10.1093/gerona/glad192","url":null,"abstract":"<p><strong>Background: </strong>The association between kidney function and dementia risk and the mechanisms underlying this relationship remain unclear.</p><p><strong>Methods: </strong>Within the UK Biobank, 191 970 dementia-free participants aged ≥60 (mean age: 64.1 ± 2.9 years) were followed for 16 years to detect incident dementia. Serum creatinine and Cystatin C were measured at baseline to calculate estimated glomerular filtration rate (eGFR, mL/min/1.73 m2). Kidney function was categorized as normal (eGFR ≥ 90), mildly impaired (60 ≤ eGFR < 90), or moderately to severely impaired (eGFR < 60). Dementia was assessed based on self-reported medical history and medical records. During the follow-up, a subsample of 12 637 participants underwent brain MRI scans. Volumes of total brain, gray matter, white matter, hippocampus, and white matter hyperintensities were assessed.</p><p><strong>Results: </strong>Over the follow-up, 5 327 (2.8%) participants developed dementia. Compared to normal kidney function, there was an increased risk of dementia with moderate to severely impaired kidney function (hazard ratio = 1.53, 95% confidence interval [CI]: 1.32-1.76) but not mildly impaired kidney function. In Laplace regression, dementia onset among people with moderate to severely impaired kidney function occurred 1.53 (95% CI: 0.98-2.08) years earlier than those with normal kidney function. Moderate to severely impaired kidney function was related to significantly lower gray matter volume (β = -0.11, 95% CI: -0.19 to -0.03), but not to other brain magnetic resonance imaging measures.</p><p><strong>Conclusions: </strong>Impaired kidney function is associated with about 50% increased risk of dementia and anticipates dementia onset by more than 1.5 years. Brain neurodegeneration may underlie the kidney function-dementia association.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":""},"PeriodicalIF":4.3,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10733178/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9997293","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Olfactory Dysfunction and Depression Trajectories in Community-Dwelling Older Adults. 居住在社区的老年人嗅觉功能障碍和抑郁轨迹。
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2024-01-01 DOI: 10.1093/gerona/glad139
Vidyulata Kamath, Kening Jiang, Kevin J Manning, R Scott Mackin, Keenan A Walker, Danielle Powell, Frank R Lin, Honglei Chen, Willa D Brenowitz, Kristine Yaffe, Eleanor M Simonsick, Jennifer A Deal
{"title":"Olfactory Dysfunction and Depression Trajectories in Community-Dwelling Older Adults.","authors":"Vidyulata Kamath, Kening Jiang, Kevin J Manning, R Scott Mackin, Keenan A Walker, Danielle Powell, Frank R Lin, Honglei Chen, Willa D Brenowitz, Kristine Yaffe, Eleanor M Simonsick, Jennifer A Deal","doi":"10.1093/gerona/glad139","DOIUrl":"10.1093/gerona/glad139","url":null,"abstract":"<p><strong>Background: </strong>We examined the relationship between baseline olfactory performance and incident significant depressive symptoms and longitudinal depression trajectories in well-functioning older adults. Inflammation and cognitive status were examined as potential mediators.</p><p><strong>Methods: </strong>Older adults (n = 2 125, 71-82 years, 51% female, 37% Black) completed an odor identification task at Year 3 (our study baseline) of the Health, Aging, and Body Composition study. Cognitive assessments, depressive symptoms, and inflammatory markers were ascertained across multiple visits over 8 years. Discrete-time complementary log-log models, group-based trajectory models, and multivariable-adjusted multinomial logistic regression were employed to assess the relationship between baseline olfaction and incident depression and longitudinal depression trajectories. Mediation analysis assessed the influence of cognitive status on these relationships.</p><p><strong>Results: </strong>Individuals with lower olfaction had an increased risk of developing significant depressive symptoms at follow-up (hazard ratio = 1.04, 95% confidence interval [CI]: 1.00, 1.08). Of the 3 patterns of longitudinal depression scores identified (stable low, stable moderate, and stable high), poorer olfaction was associated with a 6% higher risk of membership in the stable moderate (relative risk ratio [RRR] = 1.06, 95% CI: 1.02, 1.10)/stable high (RRR = 1.06, 95% CI: 1.00, 1.12) groups, compared to the stable low group. Poor cognitive status, but not inflammation, partially mediated the relationship between olfactory performance and incident depression symptom severity.</p><p><strong>Conclusions: </strong>Suboptimal olfaction could serve as a prognostic indicator of vulnerability for the development of late-life depression. These findings underscore the need for a greater understanding of olfaction in late-life depression and the demographic, cognitive, and biological factors that influence these relationships over time.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":""},"PeriodicalIF":4.3,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10733184/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10042291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fluoxetine Promotes Longevity via Reactive Oxygen Species in Caenorhabditis elegans. 氟西汀通过活性氧促进秀丽隐杆线虫的寿命
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2024-01-01 DOI: 10.1093/gerona/glad220
Can Zhou, Yiming Zhou, Yu Liang, Lijuan Chen, Li Liu, Fang Wei, Guolin Li
{"title":"Fluoxetine Promotes Longevity via Reactive Oxygen Species in Caenorhabditis elegans.","authors":"Can Zhou, Yiming Zhou, Yu Liang, Lijuan Chen, Li Liu, Fang Wei, Guolin Li","doi":"10.1093/gerona/glad220","DOIUrl":"10.1093/gerona/glad220","url":null,"abstract":"<p><p>Although several antidepressants have been identified as potential geroprotectors, the effect and mechanism of fluoxetine, a representative selective serotonin reuptake inhibitor, on longevity have not been fully elucidated. Here, we found that fluoxetine promoted longevity in Caenorhabditis elegans with a concomitant extension of a healthy life span as indicated by increasing mobility, reducing fertility and lipofuscin accumulation, and enhanced resistance to different abiotic stresses. Fluoxetine increased the level of reactive oxygen species (ROS), and antioxidant N-acetylcysteine abolished ROS elevation and the pro-longevity effect of fluoxetine. Additionally, fluoxetine extended life span through the daf-2-sod-3 pathway in daf-16-dependent and -independent manners, and fluoxetine-induced life-span extension was abolished in C. elegans sod-3, daf-2, and daf-16 mutants. In conclusion, these findings suggest that fluoxetine can promote health and longevity in C. elegans via the interaction of ROS and insulin signaling.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":""},"PeriodicalIF":4.3,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10245509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Associations Between Mid- to Late-Life Body Mass Index and Chronic Disease-Free Survival: A Nationwide Twin Study. 中晚期体重指数与无慢性病生存率之间的关系:一项全国性双胞胎研究。
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2024-01-01 DOI: 10.1093/gerona/glad111
Jie Guo, Abigail Dove, Ying Shang, Anna Marseglia, Kristina Johnell, Debora Rizzuto, Weili Xu
{"title":"Associations Between Mid- to Late-Life Body Mass Index and Chronic Disease-Free Survival: A Nationwide Twin Study.","authors":"Jie Guo, Abigail Dove, Ying Shang, Anna Marseglia, Kristina Johnell, Debora Rizzuto, Weili Xu","doi":"10.1093/gerona/glad111","DOIUrl":"10.1093/gerona/glad111","url":null,"abstract":"<p><strong>Background: </strong>Some studies have linked late-life overweight to a reduced mortality risk compared to normal body mass index (BMI). However, the impact of late-life overweight and its combination with mid-life BMI status on healthy survival remains unclear. We aimed to investigate whether and to what extent mid- and/or late-life overweight are associated with chronic disease-free survival.</p><p><strong>Methods: </strong>Within the Swedish Twin Registry, 11 597 chronic disease-free twins aged 60-79 years at baseline were followed up for 18 years. BMI (kg/m2) was recorded at baseline and 25-35 years before baseline (ie, midlife) and divided as underweight (<20), normal (≥20-25), overweight (≥25-30), and obese (≥30). Incident chronic diseases (cardiovascular diseases, type 2 diabetes, and cancer) and deaths were ascertained via registries. Chronic disease-free survival was defined as years lived until the occurrence of any chronic diseases or death. Data were analyzed using multistate survival analysis.</p><p><strong>Results: </strong>Of all participants, 5 640 (48.6%) were overweight/obese at baseline. During the follow-up, 8 772 (75.6%) participants developed at least 1 chronic disease or died. Compared to normal BMI, late-life overweight and obesity were associated with 1.1 (95% CI, 0.3, 2.0) and 2.6 (1.6, 3.5) years shorter chronic disease-free survival. Compared to normal BMI through mid- to late life, consistent overweight/obesity and overweight/obesity only in mid-life led to 2.2 (1.0, 3.4) and 2.6 (0.7, 4.4) years shorter disease-free survival, respectively.</p><p><strong>Conclusions: </strong>Late-life overweight and obesity may shorten disease-free survival. Further research is needed to determine whether preventing overweight/obesity from mid- to late life might favor longer and healthier survival.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":""},"PeriodicalIF":4.3,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10733179/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9391585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epigenetic Aging and Rheumatoid Arthritis. 表观遗传老化与类风湿关节炎。
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2024-01-01 DOI: 10.1093/gerona/glad213
Nandini Mukherjee, Tracie C Harrison
{"title":"Epigenetic Aging and Rheumatoid Arthritis.","authors":"Nandini Mukherjee, Tracie C Harrison","doi":"10.1093/gerona/glad213","DOIUrl":"10.1093/gerona/glad213","url":null,"abstract":"<p><p>This is the first known comparative assessment of the associations of epigenetic age estimates with the prevalence of rheumatoid arthritis (RA). We used data available in Gene Expression Omnibus (GSE42861) from the Swedish Epidemiological Investigation of Rheumatoid Arthritis study. Information regarding RA diagnosis and 450K DNA methylation (DNAm) of 18- to 70-year-old participants was available. Utilizing Horvath's online DNAm Age Calculator, we determined the DNAm estimate of Telomere length (DNAmTL), Hannum's epigenetic age, Horvath's 2013 and 2018 epigenetic ages, PhenoAge, GrimAge, and the respective age-acceleration measures. The association of RA prevalence with epigenetic age measures was assessed using linear regression, adjusting for sex and smoking status. The p values were corrected for multiple testing using a false discovery rate. We identified statistically significant associations of RA with Horvath 2013 age acceleration (estimate: -1.34; FDR p value: 1.0 × 10-2), Horvath 2018 age acceleration (estimate: -1.32; FDR p value: 4.0 × 10-5), extrinsic age acceleration (estimate: 1.34; FDR p value: 1.0 × 10-2), PhenoAge acceleration (estimate: 2.31; FDR p value: 1.1 × 10-5), GrimAge (estimate: 2.54; FDR p value: 1.0 × 10-2), and GrimAge acceleration (estimate: 3.15; FDR p-value: 1.7 × 10-17). Of note, the raw and age-adjusted GrimAge surrogate DNAm protein components were significantly higher in RA cases than controls. Interestingly, the first-generation measures were associated only with women. No sex-specific effects were identified for PhenoAge or GrimAge accelerations. In this cross-sectional assessment, the second-generation clocks show promise as markers of biological aging, with higher epigenetic age acceleration observed in RA cases compared with healthy controls.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":""},"PeriodicalIF":4.3,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10211203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Air Pollution: A Pressing Threat to Functioning in the Older Adults. 空气污染:对老年人功能的紧迫威胁。
IF 5.1 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2023-12-01 DOI: 10.1093/gerona/glad145
Zilong Zhang, Hualiang Lin
{"title":"Air Pollution: A Pressing Threat to Functioning in the Older Adults.","authors":"Zilong Zhang, Hualiang Lin","doi":"10.1093/gerona/glad145","DOIUrl":"10.1093/gerona/glad145","url":null,"abstract":"","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":"2307-2308"},"PeriodicalIF":5.1,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9934332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Effect of the Human Brainstem Myelination on Gait Speed in Normative Aging. 人脑干髓鞘形成对正常衰老步态速度的影响。
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2023-12-01 DOI: 10.1093/gerona/glad193
Mohammad A B S Akhonda, Mary E Faulkner, Zhaoyuan Gong, John P Laporte, Sarah Church, Jarod D'Agostino, Jan Bergeron, Christopher M Bergeron, Luigi Ferrucci, Mustapha Bouhrara
{"title":"The Effect of the Human Brainstem Myelination on Gait Speed in Normative Aging.","authors":"Mohammad A B S Akhonda, Mary E Faulkner, Zhaoyuan Gong, John P Laporte, Sarah Church, Jarod D'Agostino, Jan Bergeron, Christopher M Bergeron, Luigi Ferrucci, Mustapha Bouhrara","doi":"10.1093/gerona/glad193","DOIUrl":"10.1093/gerona/glad193","url":null,"abstract":"<p><p>The brainstem functions as a relay and integrative brain center and plays an essential role in motor function. Whether brainstem tissue deterioration, including demyelination, affects motor function has not been studied. Understanding the potential relationship between brainstem demyelination and motor function may be useful for the early diagnosis of neurodegenerative diseases and to understand age-related gait impairments that have no apparent cause. In this work, we investigated the associations between rapid or usual gait speeds, as integrative measures of motor function, and cerebral myelin content. In 118 individuals (age 22-94 years) free of neurodegenerative diseases or cognitive impairment, myelin content was assessed as the myelin water fraction, a direct magnetic resonance imaging measure of myelin content, and longitudinal and transverse relaxation rates (R1 and R2), which are sensitive magnetic resonance imaging measures of myelin content. Our results indicate that participants with lower usual or rapid gait speed exhibited lower values of myelin water fraction and R1 in the main brainstem regions, which were more evident and statistically significant in the midbrain. In contrast, we found no significant associations between gait speeds and R2, an expected result because various physiological factors confound R2. These original findings provide evidence that the level of brainstem myelination may affect gait performance among cognitively unimpaired adults who are free from any clinically detectable neurodegenerative diseases. Further studies are needed to understand the longitudinal changes in brainstem myelination with aging and neurodegenerative diseases, including Alzheimer's disease and Parkinson's disease.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":"2214-2221"},"PeriodicalIF":4.3,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491737/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9957937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association Between the Healthy Lifestyle Index and Risk of Multimorbidity in the Women's Health Initiative. 妇女健康倡议中健康生活方式指数与多病风险之间的关系
IF 4.3 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2023-12-01 DOI: 10.1093/gerona/glad170
Rita Peila, Xiaonan Xue, Aladdin H Shadyab, Jean Wactawski-Wende, Mark A Espeland, Linda G Snetselaar, Nazmus Saquib, Farha Ikramuddin, JoAnn E Manson, Robert B Wallace, Thomas E Rohan
{"title":"Association Between the Healthy Lifestyle Index and Risk of Multimorbidity in the Women's Health Initiative.","authors":"Rita Peila, Xiaonan Xue, Aladdin H Shadyab, Jean Wactawski-Wende, Mark A Espeland, Linda G Snetselaar, Nazmus Saquib, Farha Ikramuddin, JoAnn E Manson, Robert B Wallace, Thomas E Rohan","doi":"10.1093/gerona/glad170","DOIUrl":"10.1093/gerona/glad170","url":null,"abstract":"<p><strong>Background: </strong>Multimorbidity, defined as the presence of 2 or more chronic health conditions, is increasingly common among older adults. The combination of lifestyle characteristics such as diet quality, smoking status, alcohol intake, physical activity (PA), sleep duration, and body fat as assessed by body mass index (BMI) or waist circumference, and risk of multimorbidity are not well understood.</p><p><strong>Objectives: </strong>We investigated the association between the healthy lifestyle index (HLI), generated by combining indicators of diet quality, smoking, alcohol, PA, sleep amount, and BMI, and risk of multimorbidity, a composite outcome that included cardiovascular disease (CVD), diabetes, cancer, and fracture.</p><p><strong>Methods: </strong>We studied 62 037 postmenopausal women aged 50-79 years at enrollment in the Women's Health Initiative, with no reported history of CVD, diabetes, cancer, or fracture at baseline. Lifestyle characteristics measured at baseline were categorized and a score (0-4) was assigned to each category. The combined HLI (0-24) was grouped into quintiles, with higher quintiles indicating a healthier lifestyle. Multivariable adjusted estimates of hazard ratios (HRs) and 95% confidence intervals (95% CIs) for the risk of developing multimorbidity were obtained using Cox proportional hazard models.</p><p><strong>Results: </strong>Over an average follow-up period of 16.3 years, 5 656 women developed multimorbidity. There was an inverse association between the HLI levels and risk of multimorbidity (compared to the HLI_1st quintile: HR_2nd quintile = 0.81 95% CI 0.74-0.83, HR_3rd quintile = 0.77 95% CI 0.71-0.83, HR_4th quintile = 0.70 95% CI 0.64-0.76, and HR_5th quintile = 0.60 95% CI 0.54-0.66; p trend < .001). Similar associations were observed after stratification by age or BMI categories.</p><p><strong>Conclusions: </strong>Among postmenopausal women, higher levels of the HLI were associated with a reduced risk of developing multimorbidity.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":"2282-2293"},"PeriodicalIF":4.3,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491747/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9831699","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unclean Cooking Fuel Use and Slow Gait Speed Among Older Adults From 6 Countries. 来自6个国家的老年人不清洁的烹饪燃料使用和缓慢的步态速度。
IF 5.1 2区 医学
Journals of Gerontology Series A-Biological Sciences and Medical Sciences Pub Date : 2023-12-01 DOI: 10.1093/gerona/glad109
Lee Smith, Guillermo F López Sánchez, Damiano Pizzol, Masoud Rahmati, Dong Keon Yon, Andrew Morrison, Jasmine Samvelyan, Nicola Veronese, Pinar Soysal, Mark A Tully, Laurie Butler, Yvonne Barnett, Jae Il Shin, Ai Koyanagi
{"title":"Unclean Cooking Fuel Use and Slow Gait Speed Among Older Adults From 6 Countries.","authors":"Lee Smith, Guillermo F López Sánchez, Damiano Pizzol, Masoud Rahmati, Dong Keon Yon, Andrew Morrison, Jasmine Samvelyan, Nicola Veronese, Pinar Soysal, Mark A Tully, Laurie Butler, Yvonne Barnett, Jae Il Shin, Ai Koyanagi","doi":"10.1093/gerona/glad109","DOIUrl":"10.1093/gerona/glad109","url":null,"abstract":"<p><strong>Background: </strong>Outdoor air pollution has been reported to be associated with frailty (including slow gait speed) in older adults. However, to date, no literature exists on the association between indoor air pollution (eg, unclean cooking fuel use) and gait speed. Therefore, we aimed to examine the cross-sectional association between unclean cooking fuel use and gait speed in a sample of older adults from 6 low- and middle-income countries (China, Ghana, India, Mexico, Russia, and South Africa).</p><p><strong>Methods: </strong>Cross-sectional, nationally representative data from the World Health Organization Study on global AGEing and adult health were analyzed. Unclean cooking fuel use referred to the use of kerosene/paraffin, coal/charcoal, wood, agriculture/crop, animal dung, and shrubs/grass based on self-report. Slow gait speed referred to the slowest quintile based on height, age, and sex-stratified values. Multivariable logistic regression and meta-analysis were done to assess associations.</p><p><strong>Results: </strong>Data on 14 585 individuals aged ≥65 years were analyzed (mean [standard deviation] age 72.6 [11.4] years; 45.0% males). Unclean cooking fuel use (vs clean cooking fuel use) was significantly associated with higher odds for slow gait speed (odds ratio = 1.45; 95% confidence interval: 1.14-1.85) based on a meta-analysis using country-wise estimates. The level of between-country heterogeneity was very low (I2 = 0%).</p><p><strong>Conclusions: </strong>Unclean cooking fuel use was associated with slower gait speed among older adults. Future studies of longitudinal design are warranted to provide insight into the underlying mechanisms and possible causality.</p>","PeriodicalId":49953,"journal":{"name":"Journals of Gerontology Series A-Biological Sciences and Medical Sciences","volume":" ","pages":"2318-2324"},"PeriodicalIF":5.1,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692420/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9759171","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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