Skip to main content
PLOS ONE logoLink to PLOS ONE
. 2022 Jun 14;17(6):e0269795. doi: 10.1371/journal.pone.0269795

The prevalence of mild cognitive impairment by aspects of social isolation

Kyle Masato Ishikawa 1,#, James Davis 1,, John J Chen 1,, Eunjung Lim 1,*,#
Editor: Sophie Pilleron2
PMCID: PMC9197049  PMID: 35700220

Abstract

Objectives

This study describes the prevalence of mild cognitive impairment (MCI) across different aspects of social isolation among adults 65 years or older.

Methods

In this cross-sectional study, we utilized the Wave 3 data from the National Social Life, Health, and Aging Project (NSHAP). MCI was defined as a Montreal Cognitive Assessment (MoCA) score less than 23. Prevalence of MCI was calculated for above and below average social disconnectedness (SD), perceived isolation (PI), and demographic variables age, gender, race/ethnicity, education, and household income.

Results

The overall prevalence [and 95% confidence interval] of MCI was 27.5% [25.5–29.6]. The high prevalence of MCI was found in those who had above average SD (32.0% [29.1–34.9]), above average PI (33.3% [29.7–36.8]), were older in age (43.1% [38.9–47.3]), male (28.7% [25.9–31.5]), Black (61.1% [52.5–69.6]), had less than a high school education (66.3% [58.9–73.8]), or were in the lowest income group (46.2% [39.7–52.7]). Those with above average SD or PI had a higher prevalence of MCI in almost all demographics, compared to those with below average SD or PI. Those who were Black or African American or had less than a high school education did not have a greater prevalence of MCI when SD was above average.

Discussion

This current study adds to the body of literature that links SD and PI to MCI and sheds light on the possible existing socio-demographic disparities. Groups with greater than average SD or PI tend to have a higher prevalence of MCI. Further studies are needed to establish a causal association of SD and PI with MCI.

Introduction

Mild cognitive impairment (MCI) is the transitional stage between normal cognitive functions and early dementia where a person develops memory loss or other cognitive impairment that is not serious enough to interfere with daily activities [1]. The reported prevalence rates of MCI among older adults vary widely in studies across the world from around 3% to 42% [2]. Those with MCI tend to have a lower quality-of-life and greater symptoms of depression and avoid social engagement as a coping mechanism [3]. Sometimes patients with MCI can revert to normal cognitive function, but many times MCI progresses to more serious forms of dementia such as Alzheimer’s disease [4]. The American Academy of Neurology reports that the two year incidence of dementia is 14.9% among patients with MCI aged 65 years or older [5]. Although over 100 drugs have been investigated to slow the progression of dementia or alleviate its symptoms, very few have been authorized for use since 1998 [6]. The Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability (FINGER) was the first study to involve a multi-domain approach to preventing cognitive decline [7]. The study found that older adults who were at-risk of dementia generally improved or maintained their cognitive ability with healthy diet, exercise, cognitive training, and social stimulation.

Social function plays an important role in the mental and physical health of older adults. Cornwell and Waite distinguished two terms, social disconnectedness (SD) and perceived isolation (PI) and described them as the following:

Social disconnectedness can be characterized by a lack of contact with others and indicated by situational factors, such as a small social network, infrequent interaction, and a lack of participation in social activities and groups. Perceived isolation, on the other hand, can be characterized by the subjective experience of a shortfall in one’s social resources such as companionship and support (p. 39) [8].”

Many studies have explored the relationship of PI and/or SD with mental and physical health among older adults. For example, using the National Social Life, Health, and Aging Project (NSHAP) data, Cornwell and Waite found that both SD and PI are independently associated with poorer self-rated physical health but PI has a stronger relationship with mental health than SD [9]. In another study, the influence of SD onto PI is observed with specific mental health illnesses such as depression where PI plays a direct role [10]. A New Zealand study explored the directionality of PI and mental health and found that PI was a better year-to-year predictor of mental health than mental health was to SD [11].

Studies considering both SD and PI often found that both have a significant negative association with cognitive function [1215]. However, this is not always the case. In a study using data from the China Health and Retirement Longitudinal Study, Yu et al. found that SD, and not PI, was significantly associated with poorer cognitive functions measured at follow-up [16]. Conversely, a study of 2,173 community-living older adults in Amsterdam found that the odds of developing dementia within three years was significantly associated with PI but not SD [17].

To our knowledge, there is a dearth of studies that investigate the association between both SD and PI with MCI among older adults in the United States (US). A study utilizing the NSHAP found that participants with MCI or dementia generally had smaller-sized social networks, less social strain, and less community involvement among US older adults [18]. Although these attributes are part of Cornwell and Waite’s SD measure, the study did not include the aspect of PI. A study conducted in low- and middle-income countries such as China, Ghana, India, Mexico, Russia and South Africa found that PI is significantly associated with MCI in individuals who are 65 years or older but not for those who are younger [19]. This study indicates a significant association between PI and MCI.

In this cross-sectional study, we used the most recent data from the NSHAP (Wave 3) to present the prevalence of MCI among different demographics of an older population and also among those with below and above average SD or PI. Whereas Cornwell and Waite examined two aspects of isolation on self-rated mental health [9], this study is unique because it utilizes a performance-based screening test to assess MCI. As the FINGER study concluded [7], exploring the association between social factors and cognitive decline can improve the psychosocial interventions in the future.

Methods

Data source

The NSHAP is a longitudinal population-based study of health and social factors of older Americans with the aim to understand the well-being of older American adults including their physical health, medication use, cognitive function, emotional health, sensory function, health behaviors, social connectedness, sexuality, and relationship quality [20]. So far, the NSHAP has collected three waves of data. In Wave 1 (2005–2006), the NSHAP conducted in-person interviews with 3,005 community-dwelling individuals aged 57–85 years who were born between 1920 and 1947. In Wave 2 (2010–2011), 3,377 interviews were completed with Wave 1 respondents as well as their spouses/partners and those who declined to participate in Wave 1. In Wave 3 (2015–2016), all living participants from Wave 2 and a new cohort of individuals born between 1948 and 1965 were added along with their spouses/partners, totaling 4,777 responses. Detailed information about the survey design and sampling method can be found on the NSHAP website (https://www.norc.org/Research/Projects/Pages/national-social-life-health-and-aging-project.aspx) and the de-identified data is publicly available from the Inter-university Consortium for Political and Social Research (ICPSR) repository (https://www.icpsr.umich.edu/web/NACDA/studies/36873). This study was deemed exempt from review by University of Hawaiʻi Institutional Review Board (IRB #2021–00780).

Measures

The Montreal Cognitive Assessment (MoCA) is a validated 30-point screening tool for MCI [21]. This assessment covers eight domains of cognition including short-term memory, visuospatial abilities, executive function, attention, concentration, working memory, language, and orientation to space and time. An individual’s MoCA score was the total points earned from answering the assessment questions correctly. The reliability of this measure was acceptable in this study (Cronbach’s alpha = 0.75). In this study, any participant who scored below a cutoff threshold of 23 were considered at higher risk of MCI [2224].

Each participant’s SD score was calculated using Cornwell and Waite’s method [8]. SD incorporates social network size and range, frequency of interaction with network members, proportion of network members in the home, number of friends, attendance at group meetings, socializing with friends and family, and volunteering. Each variable was recoded such that greater points indicated connectedness. Next, the responses for each question were standardized before the responses for each participant were averaged and reversed to create the SD scores. If a participant could answer at least one question regarding SD, their respective SD score could be calculated. The SD scores ranged from -1.19 to 1.93 and a SD score above zero indicated greater than the average SD. We computed a Cronbach’s alpha of 0.66 for SD in this study and determined the reliability was acceptable according to Hulin et al. [25].

The score of PI was also calculated using Cornwell and Waite’s method [8]. PI is comprised of emotional and instrumental support from family members, friends, and spouse or partner; lack of companionship; feeling left out; and feeling isolated. The latter three items are questions from the University of California at Los Angeles three-item loneliness scale [26]. Each response was recoded such that greater points indicated loneliness. Next, the responses for each question were standardized before the responses for each participant were averaged to create the PI scores. These scores ranged from -1.06 to 3.34 and a PI score above zero indicated greater than average PI. The reliability of PI in this study was acceptable (Cronbach’s alpha = 0.68).

The following socio-demographic variables were considered as covariates–age, sex, education, race/ethnicity, and income. These variables were known to be associated with MCI among older adults [12, 27]. Education was categorized into four groups: less than high school, high school or equivalent, some college including vocational certificate and associate, and bachelors or more. Race was categorized as White, Black, and Other which included Asian, Pacific Islander, American Indian or Alaskan Native. Lastly, household income was categorized as $0-$24,999; $25,000-$49,999; $50,000-$99,999; and $100k or higher.

Study sample

This study is cross-sectional and only used Wave 3 of the NSHAP because it had the largest amount of MoCA scores available. The inclusion criteria for this study were adults 65 years of age or older with MoCA, SD, and PI scores. Fig 1 depicts the flowchart of our study sample. The final data include 1,985 older adults.

Fig 1. Study flow chart.

Fig 1

Statistical analysis

Descriptive statistics were reported using unweighted frequencies and weighted proportions for SD, PI, and socio-demographic variables. SD, PI, and age were dichotomized to report frequencies, but were analyzed in continuous forms as well. Lastly, weighted percentages of MCI for above and below average SD and PI were calculated for each demographic. All analyses were implemented in R version 4.0.3 and the survey package was used to adjust for the complex sampling design of the NSHAP.

Results

A total of 1,985 participants aged 65 to 95 years with complete scores for MoCA, SD, and PI scores were included in the final analysis. Of these participants, 655 (27.5% weighted) were considered at higher risk for MCI (Table 1). Greater weighted proportions of MCI were seen in those who had above average SD or PI; were older in age, male, less educated, or Black; or had lower household income. Table 2 presents weighted mean and standard error for continuous variables. The weighted mean for SD, PI, and age of those with MCI tended to be higher than those without MCI. Participants who were 65 years or older and excluded from the study due to missing MoCA or PI scores (S1 Table) had a greater proportion of above average SD, were female, older, Black or the Other race, or had the lowest educational attainment or household income. No one older than 65 years had missing SD scores.

Table 1. Prevalence of mild cognitive impairment by socio-demographics.

Variable Unweighted N Weighted % [95% CI] Unweighted N with MCI Weighted % [95% CI] with MCI
Total 1,985 100 655 27.5 [25.5–29.6]
Social Disconnectedness
    Average or below 1,072 54.1 [51.2–57.0] 291 23.7 [20.7–26.8]
    Above average 913 45.9 [43.0–48.8] 364 32.0 [29.1–34.9]
Perceived Isolation
    Average or below 1,139 58.7 [56.2–61.2] 332 23.5 [20.5–26.4]
    Above average 846 41.3 [38.8–43.8] 323 33.3 [29.7–36.8]
Gender
    Female 1,045 52.3 [49.8–54.8] 320 26.4 [23.3–29.6]
    Male 940 47.7 [45.2–50.2] 335 28.7 [25.9–31.5]
Age
    65–74 years old 1,190 68.7 [66.3–71.0] 296 20.4 [18.0–22.8]
    75 years and older 795 31.3 [29.0–33.7] 359 43.1 [38.9–47.3]
Education
    < High school 200 8.6 [6.9–10.2] 147 66.3 [58.9–73.8]
    High school or equivalent 481 24.5 [21.6–27.4] 176 30.4 [25.2–35.6]
    Vocational certificate, some college, or associate 646 34.4 [31.5–37.3] 226 29.3 [25–33.5]
    Bachelors or more 618 32.6 [28.7–36.4] 106 13.2 [10.4–16.1]
Race
    White/Caucasian 1,649 87.9 [85.8–90.0] 446 24.1 [21.9–26.3]
    Black/African American 217 7.3 [5.6–9.0] 137 61.1 [52.5–69.6]
    Other (Asian, Pacific Islander, American Indian or Alaskan Native) 116 4.8 [3.4–6.3] 51 39.0 [27.8–50.3]
Income
    $0-$24,999 311 20.2 [16.9–23.4] 167 46.2 [39.7–52.7]
    $25,000-$49,999 453 26.5 [23.1–29.7] 155 29.0 [24.9–33.1]
    $50,000-$99,999 565 35.6 [32.5–38.6] 128 18.1 [14.4–21.9]
    $100,000 or higher 269 17.8 [14.8–20.9] 42 12.6 [8.2–17.0]

MCI = Mild Cognitive Impairment. CI = Confidence Interval.

Table 2. Weighted mean of continuous variables by mild cognitive impairment status.

Variable Mean (SE) without MCI Mean (SE) with MCI
Social Disconnectedness -0.052 (0.014) 0.060 (0.022)
Perceived Isolation -0.075 (0.019) 0.103 (0.030)
Age (years) 72.0 (0.2) 76.0 (0.3)

SE = Standard Error. MCI = Mild Cognitive Impairment.

Lastly, when comparing those with average SD or PI to those with below average SD or PI (Table 3), the above average group almost always tended to have a higher proportion of MCI. The exceptions to that pattern were those with less than a high school education or Blacks or African Americans. These groups had slightly smaller proportions of MCI when their SD was above average.

Table 3. Weighted proportion [and 95% confidence interval] of mild cognitive impairment by social disconnectedness and perceived isolation.

Social Disconnectedness Perceived Isolation
Variable Average or Below Above Average Average or Below Above Average
Gender
    Female 21.7 [18.0–25.5] 32.8 [28.1–37.6] 22.3 [18.3–26.3] 33.3 [28.3–38.3]
    Male 26.3 [21.5–31.0] 31.2 [26.2–36.2] 24.9 [20.7–29.1] 33.3 [27.8–38.7]
Age
    65–74 years old 18.5 [15.1–21.9] 22.8 [19.0–26.6] 16.3 [13.2–19.3] 26.6 [21.9–31.4]
    75 years and older 36.5 [29.8–43.3] 49.7 [43.9–55.4] 40.6 [34.3–46.8] 46.3 [41.2–51.4]
Education
    < High school 67.0 [51.6–82.5] 65.9 [54.3–77.5] 60.7 [48.6–72.7] 71.1 [60.0–82.2]
    High school or equivalent 25.9 [19.5–32.4] 35.1 [28.4–41.8] 27.3 [19.9–34.8] 34.4 [27.1–41.8]
    Vocational certificate, some college, or associate 26.3 [21.1–31.5] 32.8 [26.3–39.3] 25.9 [19.5–32.3] 34.6 [28.0–41.2]
    Bachelors or more 12.5 [7.5–17.5] 14.3 [10.3–18.3] 10.8 [7.9–13.6] 17.1 [10.6–23.5]
Race
    White/Caucasian 20.3 [17.2–23.3] 28.8 [25.5–32.1] 20.9 [17.9–23.9] 28.8 [25.1–32.6]
    Black/African American 62.8 [50.3–75.2] 59.2 [48.2–70.2] 54.9 [43.7–66.1] 67.9 [54.7–81.0]
    Other (Asian, Pacific Islander,     American Indian or Alaskan Native) 33.4 [14.5–52.4] 43.3 [26.9–59.7] 29.4 [13.6–45.2] 49.0 [32.3–65.6]
Income
    $0-$24,999 44.4 [35.0–53.9] 47.7 [39.6–55.7] 43.8 [36.0–51.7] 48.9 [39.6–58.3]
    $25,000-$49,999 25.6 [19.2–31.9] 32.4 [26.0–38.8] 26.7 [21.0–32.3] 32.0 [25.3–38.7]
    $50,000-$99,999 16.2 [10.9–21.4] 21.1 [15.4–26.9] 13.8 [9.7–17.9] 26.3 [18.5–34.1]
    $100,000 or higher 10.9 [5.5–16.3] 15.2 [7.3–23.1] 8.9 [4.6–13.2] 18.6 [9.1–28.1]

Discussion

Using the nationally representative NSHAP data, we estimated the prevalence of MCI among socioeconomic demographics of older adults in US. We found that the prevalence of MCI among the older population was 27.5%. The prevalence rate of MCI in our study is comparable to existing research. For example, in a systematic review of 35 studies, Ward et al. reported a median prevalence of 26.4% but noted that the range of prevalence was broad within and across different classifications of MCI [2]. Our study adds to the body of literature that discusses the prevalence within older demographic groups and between different levels of social isolation.

Loneliness has numerous dimensions including intimate, relational, and collective loneliness [28]. Intimate loneliness is the feeling of lacking a social network based on emotional support; relational loneliness is based on perceived connections with others; and collective loneliness is based on an individual’s social network and identities that offer low-cost, impersonal support. The PI score used in this study represents intimate loneliness, while SD represents relational and collective loneliness.

Social isolation and MCI are health risk factors which need to be addressed. Using technology to maintain intimacy can work in the case of text messaging with emoticons [29], but there is limited evidence that video calling reduces SD and PI [30]. Teaching older adults how to use video calling may not address a deeper underlying cause of PI, such as lack of family commitment [31]. According to a meta-analysis of interventions to reduce PI, the most successful intervention is treating maladaptive social cognition [32]. People who are aware of their own cognitive decline may avoid social activities as a coping mechanism [3], making it hard to alleviate loneliness. This observation supports a regulatory model that includes PI, insecurity, hypervigilance, negative social expectation, defensive emotions, and distancing; each cascading to one another and perpetuating the loop [33]. Older adults are more likely to enter the loop because, in addition to their declining cognition, they are more likely to experience one or more events that worsen loneliness such as the loss of a loved one, chronic health problems, sensory impairment, and income instability [34]. In another study which used the MoCA to determine MCI status, those with MCI had a significantly lower quality of life and negative affective reactivity, which is the response to cognitive difficulty [35]. In a study of 823 old adults without dementia in Chicago, loneliness was associated with lower cognition at baseline and quicker cognitive decline during follow-up [36]. A meta-analysis also found that loneliness was significantly associated with increased risk for dementia, although it did not have enough evidence to support the association between loneliness and MCI [37]. Therefore, it is important to identify feelings such as PI, insecurity, hypervigilance, and negative social expectation that are associated with loneliness and then determine their longitudinal relationship with cognitive impairment.

Higher prevalence of MCI was observed in participants who were 75 years or older, were Black or of the Other race group, had less education, or had less household income. Studies have shown that MoCA performance varies significantly by age and educational attainment [3840]. Age has a negative correlation with MoCA score while higher levels of education have a positive correlation. Accordingly, older age and less education are associated with higher frequencies of MCI [41]. In our results, we can see a steady decrease in proportions of MCI as education or income increases. Blacks in particular had lower MoCA scores which is consistent with past studies [42, 43]. This could not be explained by educational attainment or household income stratified by race because the Other race group had the highest proportion of individuals who had less than a high school education or made less than $25,000 per year. Further investigation is needed to explain the disparity of MCI among the Black population.

Our results should be interpreted considering the following limitations. First, although the NSHAP is a longitudinal study, we used only Wave 3 data due to the completeness of responses to MoCA questions. Thus, we did not explore the temporal change of MCI or causation of SD or PI on MCI. Investigating which factors are associated with the conversion from normal cognition to MCI is crucial because healthcare providers can gain insight for the development of an early intervention that can prevent or delay the onset of MCI or dementia. This issue may be studied when the Wave 4 data is released. Second, we used the cutoff point of 23 to identify MCI. As mentioned above, some studies suggest using different cutoffs stratified by race/ethnicity and education to ensure detecting MCI from non-MCI from dementia. Using a different cutoff point could lead to different results. However, further research is needed to investigate and validate MoCA cutoff points. Third, the exclusion of participants with incomplete responses to the MoCA could lead to bias because those who did not answer all assessment questions could have gotten lower MoCA scores than those included in the study. As such, those who were excluded from the study had the same characteristics as those with the highest prevalence of MCI.

Despite these limitations, this study has several strengths. First, the NSHAP selected participants using a national frame from either the Health and Retirement Study (participants from Wave 1) or National Opinion Research Center (NORC)’s national frame (additional participants added in Wave 3) [20]. This study incorporates the sampling design to produce weighted results which are likely generalizable to the US older adult population. Second, unlike other studies that used self-rated mental health, this study utilized a performance-based test, the MoCA.

In conclusion, using a nationally representative large sample, we found that across almost all demographics, those with greater than average SD or PI have greater proportions of MCI than those with average or below average SD or PI, respectively. This current study adds to the body of literature that describes the prevalence of MCI among different aspects of social isolation.

Supporting information

S1 Table. Characteristics of those excluded from the study.

(DOCX)

Acknowledgments

The authors thank Ms. Munirih Taafaki for reviewing and editing the manuscript.

Data Availability

The data are available in the Inter-university Consortium for Political and Social Research’s (ICPSR) repository (https://www.icpsr.umich.edu/web/NACDA/studies/36873). The ICPSR’s mission is to provide open and equitable access to all users. There are no restrictions to use the public-use files in the website. We have no affiliation with ICPSR and co-authorship is not required to gain access to the data. The ISPSR complies with the U.S. Government's Section 508 standars for web-based intranet and internet information and applications, and with the Web Content Accessibility Guidelines 2.0, level AA. Therefore, the data will remain available as long as the repository and the university exist. The data we utilized for this study are freely downloaded from the website. Contact information for ICPSR: ICPSR University of Michigan Institute for Social Research P.O. Box 1248 Ann Arbor, MI 48106-1248 Director's Office Email: mshukait@umich.edu Phone: 734-615-8400.

Funding Statement

This research was partially supported by the U54MD007601 (Ola HAWAII) grant from the National Institutes of Health (NIH). The content is solely the responsibility of the authors and does not necessarily represent the official views of NIH.

References

  • 1.Petersen RC, Smith GE, Waring SC, Ivnik RJ, Tangalos EG, Kokmen E. Mild cognitive impairment: clinical characterization and outcome. Arch Neurol. 1999;56(3):303–8. Epub 1999/04/06. doi: 10.1001/archneur.56.3.303 . [DOI] [PubMed] [Google Scholar]
  • 2.Ward A, Arrighi HM, Michels S, Cedarbaum JM. Mild cognitive impairment: Disparity of incidence and prevalence estimates. Alzheimer’s & Dementia. 2012;8(1):14–21. doi: 10.1016/j.jalz.2011.01.002 [DOI] [PubMed] [Google Scholar]
  • 3.Anderson ND. State of the science on mild cognitive impairment (MCI). CNS spectrums. 2019;24(1):78–87. doi: 10.1017/S1092852918001347 [DOI] [PubMed] [Google Scholar]
  • 4.Roberts RO, Knopman DS, Mielke MM, Cha RH, Pankratz VS, Christianson TJ, et al. Higher risk of progression to dementia in mild cognitive impairment cases who revert to normal. Neurology. 2014;82(4):317–25. Epub 2013/12/20. doi: 10.1212/WNL.0000000000000055 ; PubMed Central PMCID: PMC3929198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Petersen RC, Lopez O, Armstrong MJ, Getchius TS, Ganguli M, Gloss D, et al. Practice guideline update summary: Mild cognitive impairment: Report of the guideline development, dissemination, and implementation subcommittee of the American Academy of Neurology. Neurology. 2018;90(3):126–35. doi: 10.1212/WNL.0000000000004826 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Patterson C. World alzheimer report 2018. 2018. [Google Scholar]
  • 7.Ngandu T, Lehtisalo J, Solomon A, Levälahti E, Ahtiluoto S, Antikainen R, et al. A 2 year multidomain intervention of diet, exercise, cognitive training, and vascular risk monitoring versus control to prevent cognitive decline in at-risk elderly people (FINGER): a randomised controlled trial. The Lancet. 2015;385(9984):2255–63. [DOI] [PubMed] [Google Scholar]
  • 8.Cornwell EY, Waite LJ. Measuring Social Isolation Among Older Adults Using Multiple Indicators From the NSHAP Study. The Journals of Gerontology Series B: Psychological Sciences and Social Sciences. 2009;64B(Supplement 1):i38–i46. doi: 10.1093/geronb/gbp037 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Cornwell EY, Waite LJ. Social disconnectedness, perceived isolation, and health among older adults. Journal of health and social behavior. 2009;50(1):31–48. doi: 10.1177/002214650905000103 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Domenech-Abella J, Lara E, Rubio-Valera M, Olaya B, Moneta MV, Rico-Uribe LA, et al. Loneliness and depression in the elderly: the role of social network. Soc Psychiatry Psychiatr Epidemiol. 2017;52(4):381–90. Epub 2017/02/06. doi: 10.1007/s00127-017-1339-3 . [DOI] [PubMed] [Google Scholar]
  • 11.Saeri AK, Cruwys T, Barlow FK, Stronge S, Sibley CG. Social connectedness improves public mental health: Investigating bidirectional relationships in the New Zealand attitudes and values survey. Australian & New Zealand Journal of Psychiatry. 2018;52(4):365–74. doi: 10.1177/0004867417723990 [DOI] [PubMed] [Google Scholar]
  • 12.Griffin SC, Mezuk B, Williams AB, Perrin PB, Rybarczyk BD. Isolation, not loneliness or cynical hostility, predicts cognitive decline in older Americans. Journal of aging and health. 2020;32(1–2):52–60. [DOI] [PubMed] [Google Scholar]
  • 13.Lara E, Caballero FF, Rico‐Uribe LA, Olaya B, Haro JM, Ayuso‐Mateos JL, et al. Are loneliness and social isolation associated with cognitive decline? International journal of geriatric psychiatry. 2019;34(11):1613–22. doi: 10.1002/gps.5174 [DOI] [PubMed] [Google Scholar]
  • 14.Poey JL, Burr JA, Roberts JS. Social Connectedness, Perceived Isolation, and Dementia: Does the Social Environment Moderate the Relationship Between Genetic Risk and Cognitive Well-Being? The Gerontologist. 2017;57(6):1031–40. doi: 10.1093/geront/gnw154 [DOI] [PubMed] [Google Scholar]
  • 15.Shankar A, Hamer M, McMunn A, Steptoe A. Social Isolation and Loneliness: Relationships With Cognitive Function During 4 Years of Follow-up in the English Longitudinal Study of Ageing. Psychosomatic Medicine. 2013;75(2):161–70. doi: 10.1097/PSY.0b013e31827f09cd [DOI] [PubMed] [Google Scholar]
  • 16.Yu B, Steptoe A, Chen Y, Jia X. Social isolation, rather than loneliness, is associated with cognitive decline in older adults: the China Health and Retirement Longitudinal Study. Psychological Medicine. 2020:1–8. doi: 10.1017/S0033291720001014 [DOI] [PubMed] [Google Scholar]
  • 17.Holwerda TJ, Deeg DJ, Beekman AT, van Tilburg TG, Stek ML, Jonker C, et al. Feelings of loneliness, but not social isolation, predict dementia onset: results from the Amsterdam Study of the Elderly (AMSTEL). Journal of Neurology, Neurosurgery & Psychiatry. 2014;85(2):135–42. [DOI] [PubMed] [Google Scholar]
  • 18.Kotwal AA, Kim J, Waite L, Dale W. Social function and cognitive status: Results from a US nationally representative survey of older adults. Journal of General Internal Medicine. 2016;31(8):854–62. doi: 10.1007/s11606-016-3696-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Smith L, Bloska J, Jacob L, Barnett Y, Butler L, Trott M, et al. Is loneliness associated with mild cognitive impairment in low‐and middle‐income countries? International Journal of Geriatric Psychiatry. 2021. doi: 10.1002/gps.5524 [DOI] [PubMed] [Google Scholar]
  • 20.Waite L, Cagney K, Dale W, Hawkley L, Huang E, Lauderdale D, et al. National Social Life, Health and Aging Project (NSHAP): Round 3, [United States], 2015–2016. Inter-university Consortium for Political and Social Research [distributor]; 2019. [Google Scholar]
  • 21.Nasreddine ZS, Phillips NA, Bédirian V, Charbonneau S, Whitehead V, Collin I, et al. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005;53(4):695–9. Epub 2005/04/09. doi: 10.1111/j.1532-5415.2005.53221.x . [DOI] [PubMed] [Google Scholar]
  • 22.Carson N, Leach L, Murphy KJ. A re‐examination of Montreal Cognitive Assessment (MoCA) cutoff scores. International journal of geriatric psychiatry. 2018;33(2):379–88. doi: 10.1002/gps.4756 [DOI] [PubMed] [Google Scholar]
  • 23.Luis CA, Keegan AP, Mullan M. Cross validation of the Montreal Cognitive Assessment in community dwelling older adults residing in the Southeastern US. International Journal of Geriatric Psychiatry. 2009;24(2):197–201. doi: 10.1002/gps.2101 [DOI] [PubMed] [Google Scholar]
  • 24.Saczynski JS, Inouye SK, Guess J, Jones RN, Fong TG, Nemeth E, et al. The Montreal Cognitive Assessment: Creating a Crosswalk with the Mini-Mental State Examination. J Am Geriatr Soc. 2015;63(11):2370–4. Epub 2015/10/28. doi: 10.1111/jgs.13710 ; PubMed Central PMCID: PMC4704083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Hulin C, Netemeyer R, Cudeck R. Can a Reliability Coefficient Be Too High? Journal of Consumer Psychology. 2001;10(1/2):55–8. [Google Scholar]
  • 26.Russell D, Peplau LA, Cutrona CE. The revised UCLA Loneliness Scale: concurrent and discriminant validity evidence. J Pers Soc Psychol. 1980;39(3):472–80. Epub 1980/09/01. doi: 10.1037//0022-3514.39.3.472 . [DOI] [PubMed] [Google Scholar]
  • 27.Qin HY, Zhao XD, Zhu BG, Hu CP. Demographic Factors and Cognitive Function Assessments Associated with Mild Cognitive Impairment Progression for the Elderly. Biomed Res Int. 2020;2020:3054373. Epub 2020/02/25. doi: 10.1155/2020/3054373 ; PubMed Central PMCID: PMC7031731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Cacioppo S, Grippo AJ, London S, Goossens L, Cacioppo JT. Loneliness: Clinical Import and Interventions. Perspectives on Psychological Science. 2015;10(2):238–49. doi: 10.1177/1745691615570616 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Janssen JH, Ijsselsteijn WA, Westerink JH. How affective technologies can influence intimate interactions and improve social connectedness. International Journal of Human-Computer Studies. 2014;72(1):33–43. [Google Scholar]
  • 30.Noone C, McSharry J, Smalle M, Burns A, Dwan K, Devane D, et al. Video calls for reducing social isolation and loneliness in older people: a rapid review. Cochrane Database Syst Rev. 2020;5:CD013632. Epub 2020/05/23. doi: 10.1002/14651858.CD013632 ; PubMed Central PMCID: PMC7387868. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Zamir S, Hennessy CH, Taylor AH, Jones RB. Video-calls to reduce loneliness and social isolation within care environments for older people: an implementation study using collaborative action research. BMC Geriatr. 2018;18(1):62. Epub 2018/03/04. doi: 10.1186/s12877-018-0746-y ; PubMed Central PMCID: PMC5833092. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Masi CM, Chen HY, Hawkley LC, Cacioppo JT. A meta-analysis of interventions to reduce loneliness. Pers Soc Psychol Rev. 2011;15(3):219–66. Epub 2010/08/19. doi: 10.1177/1088868310377394 ; PubMed Central PMCID: PMC3865701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Hawkley LC, Cacioppo JT. Loneliness matters: a theoretical and empirical review of consequences and mechanisms. Ann Behav Med. 2010;40(2):218–27. Epub 2010/07/24. doi: 10.1007/s12160-010-9210-8 ; PubMed Central PMCID: PMC3874845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Social Isolation and Loneliness in Older Adults: Opportunities for the Health Care System. Washington (DC)2020. [PubMed]
  • 35.Ren P, Heffner KL, Jacobs A, Lin F. Acute Affective Reactivity and Quality of Life in Older Adults with Amnestic Mild Cognitive Impairment: A Functional MRI Study. Am J Geriatr Psychiatry. 2017;25(11):1225–33. Epub 2017/08/02. doi: 10.1016/j.jagp.2017.06.019 ; PubMed Central PMCID: PMC5654660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Wilson RS, Krueger KR, Arnold SE, Schneider JA, Kelly JF, Barnes LL, et al. Loneliness and risk of Alzheimer disease. Archives of general psychiatry. 2007;64(2):234–40. doi: 10.1001/archpsyc.64.2.234 [DOI] [PubMed] [Google Scholar]
  • 37.Lara E, Martín-María N, De la Torre-Luque A, Koyanagi A, Vancampfort D, Izquierdo A, et al. Does loneliness contribute to mild cognitive impairment and dementia? A systematic review and meta-analysis of longitudinal studies. Ageing Research Reviews. 2019;52:7–16. doi: 10.1016/j.arr.2019.03.002 [DOI] [PubMed] [Google Scholar]
  • 38.Freitas S, Simões MR, Alves L, Santana I. Montreal Cognitive Assessment (MoCA): normative study for the Portuguese population. Journal of clinical and experimental neuropsychology. 2011;33(9):989–96. doi: 10.1080/13803395.2011.589374 [DOI] [PubMed] [Google Scholar]
  • 39.Malek-Ahmadi M, Powell JJ, Belden CM, O’Connor K, Evans L, Coon DW, et al. Age-and education-adjusted normative data for the Montreal Cognitive Assessment (MoCA) in older adults age 70–99. Aging, Neuropsychology, and Cognition. 2015;22(6):755–61. doi: 10.1080/13825585.2015.1041449 [DOI] [PubMed] [Google Scholar]
  • 40.Santangelo G, Siciliano M, Pedone R, Vitale C, Falco F, Bisogno R, et al. Normative data for the Montreal Cognitive Assessment in an Italian population sample. Neurological Sciences. 2015;36(4):585–91. doi: 10.1007/s10072-014-1995-y [DOI] [PubMed] [Google Scholar]
  • 41.Manly JJ, Bell-McGinty S, Tang M-X, Schupf N, Stern Y, Mayeux R. Implementing diagnostic criteria and estimating frequency of mild cognitive impairment in an urban community. Archives of neurology. 2005;62(11):1739–46. doi: 10.1001/archneur.62.11.1739 [DOI] [PubMed] [Google Scholar]
  • 42.Goldstein FC, Ashley AV, Miller E, Alexeeva O, Zanders L, King V. Validity of the montreal cognitive assessment as a screen for mild cognitive impairment and dementia in African Americans. Journal of geriatric psychiatry and neurology. 2014;27(3):199–203. doi: 10.1177/0891988714524630 [DOI] [PubMed] [Google Scholar]
  • 43.Rossetti HC, Lacritz LH, Hynan LS, Cullum CM, Van Wright A, Weiner MF. Montreal Cognitive Assessment Performance among Community-Dwelling African Americans. Archives of Clinical Neuropsychology. 2016:acn;acw095v1. doi: 10.1093/arclin/acw095 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

S1 Table. Characteristics of those excluded from the study.

(DOCX)

Data Availability Statement

The data are available in the Inter-university Consortium for Political and Social Research’s (ICPSR) repository (https://www.icpsr.umich.edu/web/NACDA/studies/36873). The ICPSR’s mission is to provide open and equitable access to all users. There are no restrictions to use the public-use files in the website. We have no affiliation with ICPSR and co-authorship is not required to gain access to the data. The ISPSR complies with the U.S. Government's Section 508 standars for web-based intranet and internet information and applications, and with the Web Content Accessibility Guidelines 2.0, level AA. Therefore, the data will remain available as long as the repository and the university exist. The data we utilized for this study are freely downloaded from the website. Contact information for ICPSR: ICPSR University of Michigan Institute for Social Research P.O. Box 1248 Ann Arbor, MI 48106-1248 Director's Office Email: mshukait@umich.edu Phone: 734-615-8400.


Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES