scholarly journals The association between loneliness, social isolation and all-cause mortality in a nationally representative sample of older women and men

2021 ◽  
pp. 1-8
Author(s):  
Carin Lennartsson ◽  
Johan Rehnberg ◽  
Lena Dahlberg
2017 ◽  
Vol 73 (9) ◽  
pp. 1272-1279 ◽  
Author(s):  
Beatriz Olaya ◽  
Maria Victoria Moneta ◽  
Joan Doménech-Abella ◽  
Marta Miret ◽  
Ivet Bayes ◽  
...  

Author(s):  
Jacob K Kresovich ◽  
Catherine M Bulka

Abstract α-Klotho (klotho) is a protein involved in suppressing oxidative stress and inflammation. In animal models, it is reported to underlie numerous aging phenotypes and longevity. Among a nationally representative sample of adults aged 40 to 79 in the United States, we investigated whether circulating concentrations of klotho is a marker of mortality risk. Serum klotho was measured by ELISA on 10,069 individuals enrolled in the National Health and Nutrition Examination Survey between 2007-2014. Mortality follow-up data based on the National Death Index were available through December 31, 2015. After a mean follow-up of 58 months (range: 1-108), 616 incident deaths occurred. Using survey-weighted Cox regression models adjusted for age, sex and survey cycle, low serum klotho concentration (< 666 pg/mL) was associated with a 31% higher risk of death (compared to klotho concentration > 985 pg/mL, HR: 1.31, 95% CI: 1.00, 1.71, P= 0.05). Associations were consistent for mortality caused by heart disease or cancer. Associations of klotho with all-cause mortality did not appear to differ by most participant characteristics. However, we observed effect modification by physical activity, such that low levels of serum klotho were more strongly associated with mortality among individuals who did not meet recommendation-based physical activity guidelines. Our findings suggest that, among the general population of American adults, circulating levels of klotho may serve as a marker of mortality risk.


SLEEP ◽  
2021 ◽  
Vol 44 (Supplement_2) ◽  
pp. A66-A67
Author(s):  
Zhuozhi Lin ◽  
Darlynn Rojo-Wissar ◽  
Paul Nestadt ◽  
Jacek Urbanek ◽  
Junrui Di ◽  
...  

Abstract Introduction Chronotype is a potentially modifiable contributor to human well-being and longevity, with eveningness commonly linked to poorer outcomes. We examined the relationship between actigraphy-measured chronotype and all-cause mortality in a nationally representative sample of US adults. We also examined the association between social jetlag, a measure of circadian misalignment, and all-cause mortality. Methods Data were from 2,256 participants ≥50 from the National Health and Nutrition Examination Survey 2003-2006 cohorts. Participants were asked to wear a hip-worn Actigraph 7164 uni-axial activity monitor for 7 days, and to remove the device for sleep. Objectively-measured bedtime (OBT) was computed as the start of the non-wear period with the longest duration within each 24h period. Duration of the in-bed period (OBT-D) was computed as the hours from OBT to the end of the in-bed period. Midpoint of OBT (OBT-M) was computed as the midpoint between OBT and the end of the in-bed period. Chronotype was estimated using the average OBT-M separately for weekdays, weekends (Friday and Saturday nights), and all days combined. A weekend OBT-M corrected for sleep debt for participants with weekend OBT-D>weekday OBT-D was also computed. The following formula was applied to correct for sleep debt: weekend OBT-M minus ((weekend OBT-D minus weekday OBT-D)/2). Consistent with previous research, OBT-Ms were categorized into intermediate (≥3:30am & ≤4:30am), morningness (<3:30am), and eveningness (>4:30am) chronotypes. Social jetlag was defined as the difference between weekend and weekday OBT-Ms and expressed in hours. Survey-weighted Cox proportional hazard models were used to examine the relationship between circadian factors and all-cause mortality. There were 642 deaths, excluding accidental deaths. Results Adjusted for age, sex, race, SES, BMI, smoking and drinking status, comorbidities, and average OBT-D, an eveningness chronotype (i.e., weekend OBT-M corrected for sleep debt) was associated with a greater hazard of death compared to an intermediate chronotype (HR=1.68, 95% CI=1.25, 2.26). There were no other significant associations. Conclusion Evening-oriented chronotype is associated with greater mortality risk in adults aged ≥50. To our knowledge, this is the first study to report the link between chronotype, estimated objectively via actigraphy, and all-cause mortality in a nationally representative sample. Support (if any) NIH grant 5T32MH014592-39.


Circulation ◽  
2021 ◽  
Vol 143 (Suppl_1) ◽  
Author(s):  
Madeline B Zipperer ◽  
James R Churilla ◽  
Michael R Richardson

Introduction: There is limited evidence examining the combined effects of cognitive function and C-reactive protein (CRP) on mortality risk using a large nationally representative sample of U.S. adults. Hypothesis: We assessed the hypothesis that cognitive function and CRP produce a combined effect in predicting all-cause mortality risk. Objective: Examine the combined effects of cognitive function and CRP in predicting all-cause mortality in a large nationally representative sample of U.S. adults. Methods: The study sample (n=2,111) included older adults (≥ 60 years of age) who participated in the 1999-2002 National Health and Nutrition Examination Survey. A four-level variable was created based on CRP concentration and cognitive function (high cognitive function and low to average CRP; high cognitive function and high CRP; low cognitive function and low to average CRP; low cognitive function and high CRP). Results: Compared to a referent group with low to average CRP and high cognitive function, analysis revealed a statistically significant increase in risk of all-cause mortality in adults with high CRP and low cognitive function (Hazards Ratio [HR] 1.97; 95% Confidence Interval [CI], 1.52-2.55, p<0.0001) and in adults with low to average CRP and low cognitive function (HR 1.76; 95% CI, 1.44-2.15, p<0.0001). Similar relationships were not revealed in adults with high cognitive function, regardless of CRP concentration. Conclusions: In a large nationally representative sample of older U.S. adults, low cognitive function was associated with increased all-cause mortality risk independent of CRP concentration.


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