Abstract
Background
Social distancing and similar measures in response to the coronavirus disease 2019 pandemic have greatly increased loneliness and social isolation among older adults. Understanding the association between loneliness and mortality is therefore critically important. We examined whether combinations of loneliness and social isolation, using a metric named social asymmetry, was associated with increased mortality risk.
Methods
The sample was derived from participants in The Irish Longitudinal Study on Ageing, a nationally representative sample of community-dwelling older adults aged ≥50. Survey data were linked to official death registration records. Cox proportional hazards regressions and competing risk survival analyses were used to examine the association between social asymmetry and all-cause and cause-specific mortality.
Results
Of four social asymmetry groups, concordant low lonely (low loneliness, low isolation) included 35.5% of participants; 26.4% were concordant high lonely (high loneliness, high isolation); 19.2% were discordant robust (low loneliness, high isolation) and 18.9% discordant susceptible (high loneliness, low isolation). The concordant high lonely (hazard ratio [HR] = 1.43, 95% confidence interval [CI]: 1.09–1.87) and discordant robust (HR = 1.37, 95% CI: 1.04–1.81) groups had an increased mortality risk compared to those in the concordant low lonely group. The concordant high lonely group had an increased risk of mortality due to diseases of the circulatory system (sub-distribution hazard ratio = 1.52, 95% CI: 1.03–2.25).
Conclusion
We found that social asymmetry predicted mortality over a 7-year follow-up period. Our results confirm that a mismatch between subjective loneliness and objective social isolation, as well as the combination of loneliness and social isolation, were associated with an increased all-cause mortality risk.
Keywords: mortality, loneliness, social isolation, social asymmetry, ageing, older people
Key points
Social asymmetry captures the degree of overlap between subjective loneliness and objective social isolation.
Combinations of loneliness and social isolation are associated with premature mortality.
Loneliness and social isolation are distinct constructs that are independently associated with premature mortality.
Policies in response to the COVID-19 pandemic have greatly increased loneliness and social isolation among older adults.
Introduction
The absence of strong social ties in the form of loneliness and social isolation have been shown to be harmful to both physical and psychological well-being [1–5]. A recent meta-analysis by Holt-Lunstad et al. found that the risk of mortality associated with both actual and perceived social isolation was comparable to that of established risk factors, including smoking [6]. Findings such as these have led to loneliness being of critical concern to public health practitioners. This concern has been heightened by health policy responses to the coronavirus disease 2019 (COVID-19) pandemic which have greatly curtailed opportunities for social interactions. Social distancing and similar measures in response to the COVID-19 pandemic have greatly increased loneliness and social isolation among older adults [7–9]. The negative impacts of these measures on the physical and psychological well-being of older adults are not yet understood but are likely to be dramatic and long lasting.
Loneliness is the subjective assessment of an individual’s satisfaction with the quality of their social relationships and is typically considered the psychological embodiment of social isolation [10]. Social isolation on the other hand, is an objective measure or count of an individual’s social contacts [11]. Studies have previously reported on the association between loneliness and social isolation and mortality risk, with mixed results. Julsing et al. [12] found no association between loneliness and all-cause, cardiovascular and non-cardiovascular deaths among Dutch men, whereas research from the US Health and Retirement Study [13] and elsewhere [14] found that loneliness did predict early mortality. On the other hand, research from the English Longitudinal Study of Ageing found that although both loneliness and social isolation were associated with premature mortality, social isolation was the more important factor [10].
The correlation between loneliness and social isolation tends to be weak [2,3,10,15] and the level of agreement or discordance between the two may be important, particularly as loneliness and social isolation relate differently to health outcomes, including mortality [6,10,12,14]. There may also be important discordance between loneliness and social isolation whereby individuals may report high levels of loneliness despite being objectively socially integrated and vice versa [15]. Despite this, few studies have examined the two constructs concurrently which has potentially limited our understanding of their intersection [6,16]. Furthermore, it has been suggested that the adverse effects of loneliness may be overestimated when an objective measure of social isolation is not accounted for in analyses [10,17].
Among the competing theories that aim to explain loneliness in later life, cognitive discrepancy theory states that loneliness stems from a mismatch between desired and actual frequency and quality of social interactions [1,18]. To accurately capture this concept requires that we derive a measure that takes account of both an individual’s subjective feelings of loneliness and an objective measure of their social integration or isolation. To achieve this, we used a measure of ‘social asymmetry’. This construct was first proposed by McHugh et al. (2017) who found that a mismatch between loneliness and isolation was associated with cognitive performance, and suggested that this metric may be useful to distinguish the effects of loneliness and social isolation on other health-related outcomes. Since previous studies on the mortality risk associated with loneliness and/or social isolation have not explicitly captured combinations of the two constructs, our aim was to examine whether the concordance and discordance between the two was associated with increased mortality risk.
Methodology
Data were from The Irish Longitudinal Study on Ageing (TILDA), a prospective nationally representative study of community-dwelling adults aged ≥50 years resident in the Republic of Ireland. Details of the methodology employed by TILDA are described elsewhere [19–22]. In summary, TILDA participants were selected using multi-stage stratified random sampling whereby 640 geographical areas, stratified by socioeconomic characteristics, were initially selected. Forty households were then randomly selected within each of these areas. The Irish GeoDirectory listing of all residential addresses provided the sampling frame. The first wave of data collection was conducted between 2009 and 2011, with subsequent waves collected at 2-year intervals. At Wave 1, 8,175 CAPI interviews were completed with a response rate of 62%, and 85% (n = 6,915) of these respondents returned Self-Completion Questionnaires (SCQs). Details of the sample maintenance strategies used by TILDA are also reported elsewhere [19]. A full description of all the variables used in our analyses is provided in Appendix A and summarised here.
Dependent variable
Cause of death was identified from official death registration data and linked to individual level survey data from TILDA. Linked survey-death registration data were available for 550 decedents [23].
Independent variables
Baseline loneliness was measured using a modified version of the University of California Los Angeles Loneliness scale [24]. The size of social networks was measured using the Berkman-Syme Social Network Index [11]. To capture the level of overlap and discordance between loneliness and social isolation, we constructed a measure of social asymmetry according to the method proposed by McHugh et al. (2017). The four groups arrived at were: Concordant high lonely (high loneliness, high isolation); Concordant low lonely (low loneliness, low isolation); Discordant susceptible (high loneliness, low isolation); and Discordant robust (low loneliness, high isolation).
Statistical approach
We used Cox proportional hazards regression models to estimate the hazard ratios for the association between social asymmetry and all-cause mortality. Respondents lost to follow-up were right-censored at the end of the follow-up-period (March 2017). We chose the concordant low lonely group (low loneliness and low social isolation) as the reference category as based on previous literature, we hypothesised that this would be the group with the lowest risk of premature mortality. To estimate the association between social asymmetry and cause-specific mortality for deaths due to neoplasms and diseases of the circulatory system, we conducted a competing risk survival analysis [25]. This approach takes account of the fact that there are competing risks to survival when examining cause-specific mortality. Participants can survive, die from the specific cause of interest, or die from another, competing cause. Interpretation of the resulting sub-distribution hazard ratios (SHR) is similar to that of the Cox hazard ratio (HR) [26]. Survey weights were applied to adjust our estimates for clustering and stratification due to the complex multi-stage sampling design. These weights also accounted for systematic differences in participation among different sub-groups to ensure that any estimates derived from the sample are representative of the wider population of community-dwelling adults aged 50+. All analyses were conducted using Stata/MP 14.2 [27].
Results
Figure 1 shows the distribution of social isolation and loneliness scores. Overall, 7.5% (95% CI: 6.8–8.2) of the sample were in the most isolated group which included those with one or fewer regular social contacts, whereas 23.1% (95% CI: 22.1–24.1) were in the most integrated group. In terms of loneliness, 34.3% (95% CI: 33.1–35.5) had the lowest loneliness score.
Figure 1 .

Distribution of social isolation and loneliness scores.
The percentage of participants in each social asymmetry category is shown in Figure 2. The concordant low lonely group was largest and included 35.5% (95% CI: 34.2–36.9) of participants. The next largest category was concordant high lonely (26.4%, 95% CI: 25.2–27.6). These were followed by discordant robust (19.2%, 95% CI: 18.1–20.4) and discordant susceptible (18.9%, 95% CI: 17.8–20.0). The characteristics of the total sample and within each social asymmetry group are reported in Appendix B.
Figure 2 .

Percentage (and 95% error bars) of participants in each of the four social asymmetry categories.
The results of the unadjusted Cox proportional hazards regression model for all-cause mortality and competing risk survival analyses for neoplasms and diseases of the circulatory system are presented in Table 1. Concordant low lonely (low loneliness and low social isolation) was the reference social asymmetry category. Participants in the concordant high lonely (HR = 1.55, 95% CI: 1.22–1.98), discordant susceptible (HR = 1.43, 95% CI: 1.10–1.87), and discordant robust (HR = 1.54, 95% CI: 1.18–2.00) categories, had an increased mortality risk. An increased risk of mortality from diseases of the circulatory system was observed among the concordant high lonely group (SHR = 1.75, 95% CI: 1.20–2.54) and the discordant susceptible group (SHR = 1.66, 95% CI: 1.05–2.61).
Table 1.
Unadjusted association between social asymmetry and all-cause and cause-specific mortality. The reference category is concordant low lonely
| Concordant high lonely | Discordant susceptible | Discordant robust | |||||||
|---|---|---|---|---|---|---|---|---|---|
| (S)HR | 95% CI | P value | (S)HR | 95% CI | P value | (S)HR | 95% CI | P value | |
| All-causea (n = 550) | 1.55 | 1.22–1.98 | <0.001 | 1.43 | 1.10–1.87 | 0.008 | 1.54 | 1.18–2.00 | <0.001 |
| Neoplasms (n = 215) | 1.19 | 0.86–1.67 | 0.297 | 0.96 | 0.65–1.43 | 0.845 | 1.07 | 0.72–1.58 | 0.749 |
| Circulatory system (n = 183) | 1.75 | 1.20–2.54 | 0.003 | 1.66 | 1.05–2.61 | 0.029 | 1.45 | 0.93–2.24 | 0.101 |
aCoefficients for all-cause mortality are reported as hazard ratios estimated using standard Cox proportional hazards regression. Coefficients for cause-specific mortality are sub-distribution hazard ratios [25]. Median follow-up time = 3.8 years.
Next, we adjusted the three risk models by sociodemographic and health-related covariates. These adjusted estimates are presented in Table 2. We found that the pattern of risk among the social asymmetry categories was unchanged by the inclusion of covariates. Participants in the concordant high lonely (HR = 1.43, 95% CI: 1.09–1.87) and discordant robust (HR = 1.37, 95% CI: 1.04–1.81) categories, each had an increased mortality risk compared to those in the concordant low lonely group. Furthermore, participants in the concordant high lonely group had an increased risk of mortality due to diseases of the circulatory system (SHR = 1.52, 95% CI: 1.03–2.25).
Table 2.
Association between social asymmetry and all-cause and cause-specific mortality, adjusted for covariates. Estimates of the risk associated with each covariate are also shown
| All-causea (550 deaths) | Neoplasms (215 deaths) | Circulatory system (183 deaths) | |||||||
|---|---|---|---|---|---|---|---|---|---|
| HR | 95% CI | P value | SHR | 95% CI | P value | SHR | 95% CI | P value | |
| Concordant low lonely | Reference category | Reference category | Reference category | ||||||
| Concordant high lonely | 1.43 | 1.09–1.87 | 0.009 | 1.18 | 0.82–1.69 | 0.375 | 1.52 | 1.03–2.25 | 0.036 |
| Discordant susceptible | 1.26 | 0.94–1.68 | 0.118 | 1.02 | 0.68–1.53 | 0.923 | 1.28 | 0.77–2.12 | 0.345 |
| Discordant robust | 1.37 | 1.04–1.81 | 0.027 | 0.99 | 0.65–1.49 | 0.946 | 1.19 | 0.75–1.88 | 0.469 |
| Female (versus male) | 0.58 | 0.48–0.71 | <0.001 | 0.73 | 0.55–0.97 | 0.030 | 0.57 | 0.41–0.78 | <0.001 |
| Urban (versus rural) | 0.94 | 0.77–1.16 | 0.576 | 1.06 | 0.80–1.40 | 0.711 | 1.04 | 0.77–1.41 | 0.793 |
| Primary education | Reference category | Reference category | Reference category | ||||||
| Secondary | 0.90 | 0.72–1.12 | 0.350 | 1.15 | 0.84–1.58 | 0.394 | 0.74 | 0.52–1.05 | 0.090 |
| Third/higher | 0.93 | 0.71–1.21 | 0.562 | 1.13 | 0.79–1.62 | 0.504 | 0.56 | 0.35–0.88 | 0.012 |
| Never smoked | Reference category | Reference category | Reference category | ||||||
| Past | 1.05 | 0.84–1.30 | 0.680 | 0.98 | 0.70–1.36 | 0.883 | 1.15 | 0.80–1.64 | 0.445 |
| Current | 2.12 | 1.62–2.78 | <0.001 | 2.06 | 1.38–3.09 | <0.001 | 2.00 | 1.30–3.06 | 0.002 |
| Walk minutes | 1.00 | 1.00–1.00 | 0.167 | 1.00 | 1.00–1.00 | 0.527 | 1.00 | 1.00–1.00 | 0.235 |
| Problem alcohol | 1.03 | 0.71–1.50 | 0.864 | 1.29 | 0.81–2.04 | 0.283 | 1.18 | 0.68–2.06 | 0.564 |
| Obese | 1.03 | 0.82–1.30 | 0.776 | 0.91 | 0.66–1.27 | 0.589 | 0.99 | 0.69–1.41 | 0.940 |
| Any CVD | 0.83 | 0.66–1.05 | 0.128 | 0.80 | 0.58–1.09 | 0.153 | 1.16 | 0.78–1.72 | 0.458 |
| Any chronic condition | 1.25 | 0.90–1.75 | 0.183 | 1.61 | 0.99–2.60 | 0.054 | 0.98 | 0.58–1.64 | 0.923 |
| Depressive symptoms | 1.02 | 1.00–1.04 | 0.044 | 1.01 | 0.99–1.04 | 0.307 | 1.01 | 0.99–1.04 | 0.254 |
| Polypharmacy | 1.25 | 1.01–1.55 | 0.044 | 0.89 | 0.64–1.24 | 0.476 | 1.24 | 0.89–1.73 | 0.202 |
aCoefficients for all-cause mortality are reported as hazard ratios estimated using standard Cox proportional hazards regression. Coefficients for cause-specific mortality are sub-distribution hazard ratios [25]. Median follow-up time = 3.8 years.
Women were less likely than men to have died during the study follow-up period and were also less likely than men to have died due to cancers or diseases of the circulatory system. Given these differences and established gender differences in mortality, we estimated gender specific hazard models according to the same specifications as above. These results are presented in Figure 3. Women in the discordant susceptible (HR = 1.67, 95% CI: 1.09–2.56) and discordant robust group (HR = 1.66, 95% CI: 1.08–2.54) had an increased risk of all-cause mortality, whereas men in these groups did not.
Figure 3 .

Association between social asymmetry and all-cause and cause-specific mortality, adjusted for covariates and stratified by gender.
Discussion
We found that social asymmetry did predict mortality over a 7-year follow-up period. Our results therefore suggest that a mismatch between subjective loneliness and objective social isolation/integration, as well as the combination of high loneliness and social isolation, were associated with an increased all-cause mortality risk. We also showed that the nature of this association was different for men and women and differed according to the specific underlying cause of death. The increased risk of mortality among the discordant groups was due to the increased risk among women. This is despite the fact that women have a lower mortality risk overall. This suggests that discordance between isolation and loneliness may be more keenly felt by women. An analysis of the association between these asymmetry groups among men and women, and other health-related outcomes would enable us to test this contention.
In comparison with the concordant low lonely category, both the concordant high lonely group and the discordant robust group had a greater risk of all-cause mortality. The concordant high lonely group had an increased risk of death from diseases of the circulatory system among men in particular, whereas women in this group had an increased risk of death due to cancers. Although many of the differences in risk estimates were small, they do suggest some potential important patterns.
Some previous studies have compared the effect of both loneliness and social isolation on health outcomes, including frailty [4,5], and mortality [10], and the authors of the social asymmetry metric found that the combination of low loneliness and high social isolation was predictive of cognitive performance cross-sectionally [15]. Our analysis is the first to demonstrate that while the combination of high loneliness and social isolation is the most damaging, a discrepancy between the two is also associated with premature all-cause mortality. Importantly, by combining the two constructs we have also avoided the risk of over estimating the association between loneliness and death noted previously [10,17].
Although loneliness is associated with depressive symptomology, the inclusion of depression in our adjusted survival analyses did not explain the association between social asymmetry and all-cause or cause-specific mortality. Therefore, there are other potential pathways that might explain these associations, such as health-related behaviours, healthcare access and utilisation, and physiological mechanisms. Although the difference in the estimated risk was small (1.37 versus 1.26) the fact that the discordant robust group had a higher risk than the discordant susceptible group suggests that social isolation may be more strongly associated with premature mortality than loneliness. Although this contention is in line with previous findings reported by others, including Steptoe et al. [10], our ability to establish more firmly if this is the case is limited by a lack of precision due to the small number of deaths our estimates are based on. As such, our findings generally support the contention that although loneliness is often seen as the psychological expression of objective social isolation, it does not in fact explain the association between social isolation and mortality.
Research on loneliness and social isolation is characterised by a multitude of definitions of both concepts and disagreement over how they relate to each other. For example, loneliness is sometimes considered akin to a personality trait [28], whereas elsewhere it is understood to be a psychological process [1,29]. In practice, this has resulted in a situation whereby loneliness and social isolation are typically examined separately [6,16], or treated as independent constructs in analyses [10].
An important strength of this research is our use of data from a nationally representative cohort of older adults, and importantly, our inclusion of linked official death registration data. These data allowed us to examine cause specific as well as all-cause mortality and our results highlight the important differences that can only be elucidated using this more finely grained death certificate information.
As our findings are based on an observational study, we cannot wholly discount the possibility that loneliness and social isolation are simply a feature of the end-of-life phase and therefore the observed association between loneliness and mortality is an artefact of multimorbidity. However, we controlled for many health conditions, including multimorbidity, in our analyses and in sensitivity analysis (Appendix C) we re-estimated our models excluding deaths that occurred within 1 year of baseline interview. As these results were similar to those when all deaths were included, it is unlikely that loneliness or social isolation are simply an inevitable feature of older age.
Finally, our findings demonstrate the importance of stratifying analyses of mortality by gender as failing to do so may mask important differences. Furthermore, where data are available to do so, it is important that researchers examine cause-specific mortality as limiting analyses to heterogeneous all-cause mortality data may mask important difference in the association between hypothesised risk factors and death. This in turn may mask insights into potential mechanisms to account for, in this case, the association between loneliness and social isolation and mortality.
Conclusion
Our findings show an association between loneliness, social isolation and premature mortality among older adults. Our results suggest that social isolation in particular may be an important risk factor, independent of other health-related variables, including comorbidities. As such, loneliness and social isolation may be complicit in some of the excess mortality associated with the COVID-19 pandemic. It is important that we consider this in our response to the residual effects of the COVID-19 pandemic.
We have also demonstrated the potential utility of a method by which both loneliness and social isolation can be considered in conjunction with each other so that we can account for both overlap and discrepancies between the two concepts. These combinations may be important as they suggest that a one-size-fits-all approach to local or national policy interventions may not work. As others have noted previously [2,6], we believe that efforts to address this growing public health concern must consider both loneliness and social isolation, as improving either one is unlikely to necessarily enhance the other. These findings take on an increased importance in the wake of responses to the COVID-19 pandemic including social distancing and cocooning. Loneliness and social isolation will have been impacted dramatically during the pandemic and this will have negative consequences for the physical and mental health of older adults. It is therefore critical that we understand the interplay between loneliness and social isolation so that impactful responses can be developed [7,9]. As part of this, our findings support the need for healthcare professionals to consider loneliness during clinical assessments of their patients. These interventions may benefit from the application of social prescribing, whereby clinical staff refers their patients to non-clinical community groups and services. This provides a practical example of how the social, as well as physical, needs of older adults may be met.
Contributor Information
Mark Ward, The Irish Longitudinal Study on Ageing (TILDA), Trinity College Dublin, Ireland.
Peter May, Centre for Health Policy and Management, Trinity College Dublin, Ireland.
Charles Normand, Centre for Health Policy and Management, Trinity College Dublin, Ireland.
Rose Anne Kenny, The Irish Longitudinal Study on Ageing (TILDA), Trinity College Dublin, Ireland; Department of Medical Gerontology, Trinity College Dublin, Ireland.
Anne Nolan, The Irish Longitudinal Study on Ageing (TILDA), Trinity College Dublin, Ireland; The Economic and Social Research Institute (ESRI), Whitaker Square Sir John Rogerson’s Quay, Dublin, Ireland.
Declaration of Sources of Funding
This work was supported by the Health Research Board Investigator led projects scheme (ILP-PHR-2017-022). TILDA is co-funded by the Government of Ireland through the Department of Health, by Atlantic Philanthropies, and by Irish Life PLC.
The funders played no role in designing or conducting the study or in the collection, management, analysis or interpretation of the data, nor did they have any input into preparation, review or approval of this manuscript.
Declaration of Conflicts of Interest
None.
References
- 1. Burholt V, Scharf T. Poor health and loneliness in later life: the role of depressive symptoms, social resources, and rural environments. J Gerontol - Ser B Psychol Sci Soc Sci 2014;69:311–24. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. Coyle CE, Dugan E. Social isolation, loneliness and health among older adults. J Aging Health 2012;24:1346–63. [DOI] [PubMed] [Google Scholar]
- 3. Mund M, Freuding MM, Möbius K, Horn N, Neyer FJ. The stability and change of loneliness across the life span: a meta-analysis of longitudinal studies. Pers Soc Psychol Rev 2020;24:24–52. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Gale CR, Westbury L, Cooper C. Social isolation and loneliness as risk factors for the progression of frailty: the English longitudinal study of ageing. Age Ageing 2018;47:392–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Jarach CM, Tettamanti M, Nobili A, D’avanzo B. Social isolation and loneliness as related to progression and reversion of frailty in the survey of health aging retirement in Europe (SHARE). Age Ageing 2021;50:258–62. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Holt-Lunstad J, Smith TB, Baker M, Harris T, Stephenson D. Loneliness and social isolation as risk factors for mortality: a meta-analytic review. Perspect Psychol Sci 2015;10:227–37. [DOI] [PubMed] [Google Scholar]
- 7. Hwang TJ, Rabheru K, Peisah C, Reichman W, Ikeda M. Loneliness and social isolation during the COVID-19 pandemic. Int Psychogeriatr 2020;32:1217–20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Ward M, McGarrigle C, Hever A et al. Loneliness and social isolation in the COVID-19 Pandemic among the over 70s: Data from The Irish Longitudinal Study on Ageing (TILDA) and ALONE. Dublin: The Irish Longitudinal Study on Ageing, 2020. Available from: https://tilda.tcd.ie/publications/reports/Covid19SocialIsolation/ [Google Scholar]
- 9. Wu B. Social isolation and loneliness among older adults in the context of COVID-19: a global challenge. Global Health Res Pol; 2020;5:154–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Steptoe A, Shankar A, Demakakos P, Wardle J. Social isolation, loneliness, and all-cause mortality in older men and women. Proc Natl Acad Sci U S A 2013;110:5797–801. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23530191%0Ahttp://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC3625264 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. Berkman LF, Syme S. Social networks, host resistance, and mortality: a nine-year follow-up study of Alameda County residents. Am J Epidemiol 1979;109:186–204. [DOI] [PubMed] [Google Scholar]
- 12. Julsing JE, Kromhout D, Geleijnse JM, Giltay EJ. Loneliness and all-cause, cardiovascular, and noncardiovascular mortality in older men: the Zutphen elderly study. Am J Geriatr psychiatry. Elsevier Inc.; 2016;24:475–84. [DOI] [PubMed] [Google Scholar]
- 13. Luo Y, Hawkley LC, Waite LJ, Cacioppo JT. Loneliness, health, and mortality in old age: a national longitudinal study. Soc Sci Med Elsevier Ltd; 2012;74:907–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Tilvis RS, Laitala V, Routasalo PE, Pitkälä KH. Suffering from loneliness indicates significant mortality risk of older people. J Aging Res 2011; 2011: 1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. McHugh JE, Kenny RA, Lawlor BA, Steptoe A, Kee F. The discrepancy between social isolation and loneliness as a clinically meaningful metric: findings from the Irish and English longitudinal studies of ageing (TILDA and ELSA). Int J Geriatr Psychiatry 2017;32:664–74. [DOI] [PubMed] [Google Scholar]
- 16. Cornwell E, Waite L. Measuring social isolation among older adults using multiple indicators from the NSHAP study. J Gerontol B Psychol Sci Soc Sci 2009;64:i38–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Perissinotto CM, Stijacic Cenzer I, Covinsky KE. Loneliness in older persons: a predictor of functional decline and death. Arch Intern Med 2012;172:1078–83. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Perlman D, Peplau LA. Toward a social psychology of loneliness. In: Duck SW, Gilmour R, eds. Personal relationships in disorder. London: Academic Press, 1981; 31–56. [Google Scholar]
- 19. Donoghue O, McGarrigle CA, Foley M, Fagan A, Meaney J, Kenny RA. Cohort profile update: the Irish longitudinal study on ageing (TILDA). Int J Epidemiol 2018;47:1398–1398l. [DOI] [PubMed] [Google Scholar]
- 20. Kearney PM, Cronin H, O’Regan C et al. Cohort profile: the Irish longitudinal study on ageing. Int J Epidemiol 2011;40:877–84. [DOI] [PubMed] [Google Scholar]
- 21. Kenny RA, Whelan B, Cronin H et al. The Design of the Irish Longitudinal Study on Ageing. Dublin: The Irish Longitudinal Study on Ageing, 2010. [Google Scholar]
- 22. Whelan BJ, Savva GM. Design and methodology of the Irish longitudinal study on ageing. J Am Geriatr Soc 2013;61:265–8. [DOI] [PubMed] [Google Scholar]
- 23. Ward M, May P, Briggs R et al. Linking death registration and survey data : procedures and cohort profile for the Irish longitudinal study on ageing. HRB Open Res 2020;3:1–12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Russell D. UCLA loneliness scale (version 3): reliability, validity, and factor structure. J Pers Assess 1996;66:20–40. [DOI] [PubMed] [Google Scholar]
- 25. Fine JP, Gray RJ. A proportional hazards model for the subdistribution of a competing risk stable. J Am Stat Assoc 1999;94:496–509. [Google Scholar]
- 26. Dignam J, Zhang Q, Kocherginsky M. The use and interpretation of competing risks regression models. Clin Cancer Res 2013;18:2301–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. StataCorp . Stata Statistical Software: Release 14. College Station, TX: StataCorp LP, 2015. [Google Scholar]
- 28. Boomsma DI, Willemsen G, Dolan C V., Hawkley LC, Cacioppo JT. Genetic and environmental contributions to loneliness in adults: the Netherlands twin register study. Behav Genet 2005;35:745–52. [DOI] [PubMed] [Google Scholar]
- 29. Ernst JM, Cacioppo JT. Lonely hearts: psychological perspectives on loneliness. Appl Prev Psychol 1999;8:1–22. [Google Scholar]
