Abstract
Introduction
Assessing cognitive function could help to provide appropriate care for nursing home residents. The aim of the study was to identify the factors affecting cognitive function in nursing home residents in Poland and assess how it influenced the mortality rate during a 3-year observational period.
Methods
This study included 202 elderly individuals from a nursing home in 2015. The investigation included examination of cognitive function using the MMSE and bioelectrical impedance analysis. Collected data included sex, age, blood pressure (BP), heart rate, number of comorbidities, years spent in the nursing home, educational level, and cigarette-smoking.
Results
The mean MMSE score was 21.36 ± 6.35, which was negatively correlated with age and diastolic BP (p = 0.001 and p = 0.024, respectively) and positively correlated with body mass, BMI, fat-free mass, fat, muscle mass, and education level (p = 0.004, p = 0.004, p = 002, p = 0.049, p = 0.005, and p ˂ 0.001, respectively). Patients who died during the observational period had lower MMSE scores than those who survived (23.34 ± 5.68 vs. 20.16 ± 6.45; p < 0.001). Smokers had better MMSE results than nonsmokers (23.34 ± 5.98 vs. 20.08 ± 4.94; p < 0.001).
Discussion
Polish nursing home residents had mild cognitive impairment depending on their age, sex, educational level, and nutritional status. Lower MMSE score was a prognostic factor for mortality in the 3-year observational period.
Keywords: Nursing home residents, Cognitive function, Mortality
Introduction
Older people can suffer from a number of different conditions, including comorbidity and dementia, which result in susceptibility to different stimuli that are detrimental to their health.
Dementia encompasses a loss of cognitive function and the ability to perform the activities of daily living. It results from neurodegenerative disorders and includes several subtypes. The symptoms of dementia are progressive and long-lasting [1], and affect 6–8% of individuals ≥60 years of age, and up to 25% of individuals ≥85 years of age [2]. Since old age is a major risk factor for dementia, the dementia rate will rise in the coming years as the population ages [3]. It is estimated that 50 million people globally had dementia in 2018, and that this number will rise to 152 million by 2050 [4].
People suffering from dementia have special care needs resulting from cognitive and functional impairment, difficulty communicating, and other neuropsychiatric symptoms. Diagnosis of dementia can have numerous benefits. It can potentially enable immediate initiation of treatment and adjustment of medications to reduce any side effects that influence cognitive functions. It may also help to ensure adequate support for patients and their families and allow them to make plans for the future [5]. In nursing practice, knowledge about cognitive impairments and rehabilitation techniques is crucial since each type of activity may have a therapeutic effect on the patient. Assessment of the cognitive functions of elderly patients enables customization of the type of care provided according to the severity of the cognitive impairment, potentially including assistance with everyday living, home-based care, institutional daycare, or round-the-clock care in a residential facility.
Residents of nursing homes have a higher burden of dementia that those found in the general population [6]. Despite the benefits of an early diagnosis of cognitive impairment, a missed diagnosis could lead to inappropriate treatment and even increase the incidence of challenging behaviors due to the patient's needs not being met. The Mini-Mental State Examination (MMSE) is used to assess cognitive impairment in the clinical and research settings. It is a short, easy to apply, commonly accepted, and available tool.
The aim of this study was to assess cognitive function in the elderly residents of a nursing home in Poland, by identifying the factors affecting it, and determining its influence on the mortality rate.
Methods
Participants and Procedure
The cross-sectional study was conducted at a nursing home in Warsaw, Poland, in 2015. The investigated group comprised 202 residents. The inclusion criterion was the capacity of the patient to give informed consent. To assess the influence of cognitive function on the mortality rate, an assessment of the number of survivors and those who had died was made after 3 years. During this period, 126 (62.37%) patients died. The study protocol included a cognitive function evaluation using the MMSE, Polish version [7], and bioelectrical impedance analysis using the BioScan 920–2 (Maltron Int. Ltd., Rayleigh, UK). The MMSE consists of 11 items that test 5 areas of cognitive function: orientation registration, attention and calculation, recall, and language. The possible score ranges from 0 to 30, where >24 = normal cognitive function, 19–23 = mild, 9–18 = moderate, and <9 = severe impairment of cognitive function.
Sociodemographic data were obtained from the study-specific questionnaire and medical documentation. Data collected included age, sex, blood pressure (BP), heart rate, comorbidities, years spent in the nursing home, educational level, and cigarette-smoking. In the analysis, comorbidities were generalized to “number of comorbidities.” Due to only a few different diseases being identified, i.e., cardiovascular diseases, diabetes, and respiratory disease, separate analyses were not possible. Smokers were those who smoked on a daily basis. The participants' names were not recorded on the questionnaire, thus rendering the data anonymous. All investigations were completed on one occasion and on site.
Statistical Analysis
Statistical analysis was performed using IBM SPSS v23. Descriptive statistics were generated using standard parameters, including percentage, mean and standard deviation, and median and range. The Kolmogorov-Smirnov test revealed that the MMSE results did not show a normal distribution, so nonparametric tests were used for all calculations.
Between-group differences were analyzed using the Mann-Whitney U test or the Kruskal-Wallis test. The Spearman test was used to analyze correlations between MMSE scores and the investigated parameters. The preliminary selection of variables for logistic regression models was carried out based on the prior statistical tests. The assumed level of significance of potential variables that could be included in the model was p < 0.1. Subsequently, the stepwise selection algorithm with the Akaike information criterion was applied to the variables selected in the above manner. Survivability curves were plotted using the Kaplan-Meier estimator. Results were considered statistically significant when p < 0.05.
Results
The investigated group consisted of 202 participants, including females (n = 157, 77, 72%) and males (n = 45, 22, 78%). The demographic and clinical characterization of the participants stratified by sex is shown in Table 1.
Table 1.
Characteristics of the investigated group, stratified by sex
| Total group (n = 202) |
Males (n = 45) |
Females (n = 157) |
||||
|---|---|---|---|---|---|---|
| mean±SD | median; min–max | mean±SD | median; min–max | mean±SD | median; min–max | |
| Age, years | 82.16±8.58 | 83; 65–99 | 81.67±9.21 | 83; 65–96 | 82.31±8.41 | 83; 65–99 |
| Body mass, kg | 65.53±14.75 | 65; 34–118 | 71.4±14.25 | 73; 39–98 | 63.85±14.50 | 64; 34–118 |
| BMI | 25.11±5.61 | 24.95; 13.2–42.2 | 25.36±4.64 | 25.4; 16.2–33.9 | 25.03±5.87 | 24.8; 13.2–42.2 |
| FFM, kg | 43.37±7.55 | 42.06; 28.05–74.05 | 51.70±8.61 | 52.67; 30.66–74.05 | 40.98±5.18 | 41.04; 28.05–56.83 |
| Fat, kg | 22.16±10.56 | 21.75; 4.36–61.17 | 19.77±8.64 | 18.24; 8.04–40.27 | 22.84±10.98 | 22.07; 4.63–61.17 |
| Muscle mass, kg | 20.40±10.97 | 18.21; 10.77–94.97 | 26.01±9.67 | 25.43; 12.97–83.62 | 18.79±10.81 | 17.31; 10.77–94.97 |
| SBP, mm Hg | 120.07±20.09 | 119; 75–186 | 118.51±25.09 | 111; 86–186 | 120.52±18.48 | 120; 75–167 |
| DBP, mm Hg | 71.29±12.42 | 70; 42–134 | 69.87±13.39 | 66; 42–105 | 71.70±12.12 | 70; 50–134 |
| HR, beats/min | 74.24±12.00 | 74; 51–112 | 72.38±11.69 | 73; 53–105 | 74.77±12.07 | 74; 51–112 |
| Years resident in nursing home | 3.44±4.04 | 2; 1–44 | 3.22±2.98 | 2; 1–14 | 3.49±4.30 | 2; 1–44 |
| Smokers, n (%) | 66 (32.67) | 24 (53.33) | 42 (26.75) | |||
| Alcohol consumption, n (%) | ||||||
| None | 162 (80.2) | 17 (37.78) | 145 (92.36) | |||
| <2 units/week | 16 (7.92) | 10 (22.22) | 6 (3.82) | |||
| >2 units/week | 24 (11.88) | 18 (40) | 6 (3.82) | |||
| Comorbidities, n (%) | ||||||
| 0 | 10 (4.95) | 3 (6.67) | 7 (4.46) | |||
| 1 | 122 (60.4) | 28 (62.22) | 94 (59.87) | |||
| 2 | 65 (32.18) | 11 (24.44) | 54 (34.40) | |||
| 3 | 5 (2.47) | 3 (6.67) | 2 (1.27) | |||
| Education level, n (%) | ||||||
| Elementary school Vocational school High school University |
94 (46.54) 21 (10.4) 71 (35.15) 16 (7.91) |
18 (40) 3 (6.67) 19 (42.22) 5 (11.11) |
76 (48.41) 18 (11.46) 52 (33.12) 11 (7.01) |
|||
| Place of residence, n (%) | ||||||
| Village Town |
30 (14.85) 172 (85.15) |
10 (22.22) 35 (77.78) |
20 (12.74) 137 (87.26) |
|||
BMI, body mass index; FFM, fat-free mass; SBP, systolic blood pressure; DBP, diastolic blood pressure; HR, heart rate.
The mean MMSE score was 21.36 ± 6.35, indicating mild cognitive impairment. The results of MMSE subscales stratified by sex are shown in Table 2. Total MMSE results did not significantly differ between women and men. However, men had significantly better MMSE scores for “orientation to time” (p = 0.03) and “attention and calculation” (p = 0.035).
Table 2.
Mini-Mental State Examination (MMSE) results stratified by sex and differences between females and males
| MMSE scores | Total (n = 202) |
Males (n = 45) |
Females (n = 157) |
p value | |||
|---|---|---|---|---|---|---|---|
| mean±SD | median (range) | mean±SD | median (range) | mean±SD | median (range) | ||
| Total/task | 21.36±6.35 | 22.50 (4–30) | 22.78±5.83 | 25 (8–30) | 20.95±6.43 | 22 (4–30) | 0.081 |
| Orientation to time | 4.21±1.24 | 5 (0–5) | 4.56±0.89 | 5 (2–5) | 4.11±1.31 | 5 (0–5) | 0.030 |
| Orientation to place | 4.31±1.08 | 5 (1–5) | 4.62±0.75 | 5 | 4.22±1.15 | 5 (1–5) | 0.057 |
| Registration | 2.50±1.08 | 3 (0–3) | 2.58±0.97 | 3 (0–3) | 2.48±1.11 | 3 (0–3) | 0.786 |
| Attention and calculation | 2.34±2.09 | 2 (0–5) | 2.91±2.08 | 4 (0–5) | 2.18±2.08 | 1 (0–5) | 0.035 |
| Recall | 0.6±1.02 | 0 (0–3) | 0.53±0.94 | 0 (0–3) | 0.62±1.04 | 0 (0–3) | 0.746 |
| Naming | 1.95±0.32 | 2 (0–2) | 1.93±0.33 | 2 (0–2) | 1.95±0.32 | 2 (0–2) | 0.523 |
| Repetition | 0.84±0.37 | 1 (0–1) | 0.84±0.37 | 1 (0–1) | 0.83±0.37 | 1 (0–1) | 0.873 |
| Comprehension | 2.56±1.05 | 3 (0–3) | 2.62±0.98 | 3 (0–3) | 2.54±1.07 | 3 (0–3) | 0.660 |
| Reading | 0.72±0.45 | 1 (0–1) | 0.73±0.45 | 1 (0–1) | 0.72±0.45 | 1 (0–1) | 0.858 |
| Writing | 0.67±0.47 | 1 (0–1) | 0.71±0.46 | 1 (0–1) | 0.66±0.47 | 1 (0–1) | 0.540 |
| Drawing | 0.64±0.48 | 1 (0–1) | 0.73±0.45 | 1 (0–1) | 0.62±0.49 | 1 (0–1) | 0.155 |
The correlations between MMSE results and selected parameters with stratification by sex is shown in Table 3.
Table 3.
Correlations between Mini-Mental State Examination (MMSE) results and selected parameters, with stratification by sex
| MMSE |
|||
|---|---|---|---|
| whole group (n = 202) |
males (n = 45) |
females (n = 157) |
|
| Age, years | ρ = −0.234 | ρ = −0.308 | ρ = −0.209 |
| p = 0.001 | p = 0.040 | p = 0.009 | |
| Body mass, kg | ρ = 0.201 | ρ = 0.100 | ρ = 0.216 |
| p = 0.004 | p = 0.513 | p = 0.006 | |
| BMI | ρ = 0.201 | ρ = 0.155 | ρ = 0.210 |
| p = 0.004 | p = 0.311 | p = 0.008 | |
| FFM, kg | ρ = 0.213 | ρ = 0.157 | ρ = 0.189 |
| p = 0.002 | p = 0.303 | p = 0.018 | |
| Fat, kg | ρ = 0.138 | ρ = −0.005 | ρ = 0.198 |
| p = 0.049 | p = 0.976 | p = 0.013 | |
| Muscle mass, kg | ρ = 0.197 | ρ = 0.106 | ρ = 0.190 |
| p = 0.005 | p = 0.487 | p = 0.017 | |
| SBP, mm Hg | ρ = −0.082 | ρ = −0.059 | ρ = −0.083 |
| p = 0.244 | p = 0.698 | p = 0.303 | |
| DBP, mm Hg | ρ = −0.158 | ρ = −0.125 | ρ = −0.173 |
| p = 0.024 | p = 0.414 | p = 0.030 | |
| HR, beats/min | ρ = −0.071 | ρ = −0.226 | ρ = −0.024 |
| p = 0.317 | p = 0.135 | p = 0.768 | |
| Level of education | ρ = 0.326 | ρ = 0.079 | ρ = 0.383 |
| p < 0.001 | p = 0.608 | p < 0.001 | |
| Years resident in nursing home | ρ = −0.050 | ρ = −0.009 | ρ = −0.043 |
| p = 0.481 | p = 0.952 | p = 0.592 | |
BMI, body mass index; FFM, fat-free mass; SBP, systolic blood pressure; DBP, diastolic blood pressure; HR, heart rate.
MMSE scores were negatively correlated with age, both in the whole investigated group and men and women separately. In the whole group and among women, but not among men, MMSE results were positively correlated with body mass, body mass index (BMI), fat-free mass (FFM), fat, muscle mass, and education level, and negatively correlated with diastolic BP (DBP).
Smokers had better MMSE scores than nonsmokers (23.34 ± 5.98 vs. 20.08 ± 4.94; p < 0.001). MMSE score was not significantly associated with the number of comorbidities.
Compared to patients who died during the observational period (n = 126), survivors (n = 76) had significantly better MMSE scores (23.34 ± 5.68 vs. 20.16 ± 6.45; p < 0.001). Applying backward stepwise regression, the model explaining the risk of dying during the 3-year observation was obtained (and covers MMSE, age, and DBP). Each point scored on the MMSE scale decreased the risk of the patient's death by 9.19% on average, assuming that the other factors remained unchanged. Each subsequent year lived by the patient increased the risk of death by 6.4% on average, assuming that the other factors remained unchanged. DBP found to be higher by 1 unit (Hg) decreased the risk of death by 3.13% on average, assuming that the other factors remained unchanged.
Survival curves in groups with normal cognitive function, or mild, moderate, or severe impairment of cognitive function, were plotted using the Kaplan-Meier estimator and appear in Figure 1. The log rank test revealed a statistically significant difference between the groups (p = 0.0011).
Fig. 1.
Kaplan-Meyer survival curves for patients with different impairment of cognitive function assessed with the use of the MMSE.
Discussion
The average MMSE score among study participants indicated mild cognitive impairment and was higher than the results obtained by Kowalska et al. [8] who investigated 254 people admitted to a nursing home in Wrocław (Poland) between 2007 and 2010. Similar study of residents in care homes in Spain [9] and the UK [10] also indicated lower scores than in our study. MMSE scores of our participants were similar to the results obtained by Weidung et al. [11], who investigated very elderly people who were not resident in of nursing homes. In our study, BP, heart rate, and BMI were all in the normal range, suggesting that our participants enjoyed good health, in contrast to those in the abovementioned studies. Our participants had, on average, only 1 disease. In general, the median number of chronic conditions in the population of people >65 years of age is 3 [12]. Differences in MMSE scores may be attributable to the different criteria for admission to nursing homes in Poland and other countries, and that Polish nursing home residents are generally in a better cognitive and physical condition than patients admitted to such facilities in other countries.
Our results showed a higher general MMSE score for men than women, although this difference was not significant. Other researchers have also reported better cognitive results in men [13, 14]. We found that men had significantly higher scores in the categories of “orientation to time” and “attention and calculation.” This could be related to the fact that our study included more women than men. However, we cannot exclude the role of confounding factors such as social life, lower education level, or type of work [13, 14].
MMSE score was negatively correlated with age and positively correlated with education level, in line with findings by other authors [15, 16]. The correlation with age was expected since age is the most well-recognized risk factor for dementia [13]. To explain the relationship between low education level and cognitive decline, various mechanisms have been proposed, including a hypothesis involving lower brain reserve and a lack of occupational activities leading to lower intellectual demands, a proposal relating to low cognitive stimulation throughout life [16] and the concept that lower education level is related to reduced access to intellectually stimulating entertainment [15].
MMSE scores were positively correlated with body mass, BMI, FFM, muscle mass, and fat. Higher BMI and fat may contribute to maintaining better cognitive functions during the ageing process [17]. However, the associations of body mass and BMI with the risk of dementia are far from clear. Overweight and obese individuals carry a higher risk of developing diseases that influence cognitive function [18]. However, in later life, the detrimental consequences of being obese or overweight are less apparent, and there may even be protective effects [19]. Importantly, weight loss is a frequent side effect of dementia and might worsen outcomes in elderly patients. Therefore, patients with cognitive dysfunction should be regularly screened for malnutrition to enable early nutritional intervention.
MMSE scores were negatively correlated with DBP, in line with the findings of other studies [20]. Surprisingly, we did not detect an association between systolic BP (SBP) and cognitive function level. The mechanisms underlying the association between arterial hypertension and impaired cognition are not completely understood. High DBP may decrease tissue perfusion. It is possible that a higher SBP is needed to maintain brain perfusion in older individuals [21]. On the other hand, high BP directly or indirectly causes cerebral vascular damage which can lead to dementia [22].
Previous evidence indicates that impaired cognitive function is an independent predictor of mortality in elderly individuals, after accounting for numerous different variables [23, 24]. It has been suggested that the association between cognitive dysfunction and mortality reflects a global deterioration of health status that both affects cognitive functions and directly contributes to mortality [25]. Our data confirm that the patients who died during the 3-year observation period had worse MMSE results than those who survived the entire observation period. Cognitive impairment complicates neurological and cerebrovascular diseases, and other chronic illnesses, which are known risk factors for mortality [26]. However, while higher mortality is reportedly associated with moderate-to-severe cognitive impairment, its correlation with milder cognitive impairments is less obvious [27]. We did not show a correlation between multiple morbidity and the MMSE results, which has been identified in other studies [28]. Such correlations are in line with the dynamic polygon hypothesis, which considers that several pathological processes (e.g., amyloid aggregation or vascular damage), interlinked with the positive or negative consequences of environmental exposure (e.g., exercise or obesity), will potentially influence the size and functioning of the brain [29].
Cigarette-smoking was correlated with a higher MMSE score, which has not been previously reported [30]. The mechanisms by which smoking affects cognitive performance remain unclear [31]. Some evidence suggests that the impact of smoking on adverse cognitive outcomes may be underestimated due to the selection effects resulting from the higher midlife mortality of smokers [32]. Our findings may have been affected by the selection of the sample group. On the other hand, nicotine increases acetylcholine release, elevates the number of nicotinic receptors, and improves attention and information-processing, although these actions may be opposed by the high oxidative stress caused by smoking [31].
The study has some limitations. The inclusion criterion was the capacity to give informed consent for participation, which could have resulted in an underestimation of the prevalence of cognitive impairment in the nursing home residents. We also conducted our study in only 1 nursing home in Warsaw. Our assessment was based only on the MMSE and not on a full cognitive evaluation. The results may partly be explained by the effect of the selective survival of the study participants. Mortality rate is also influenced by other factors and conditions not assessed in this study, e.g., frailty syndrome and metabolic disorders.
Conclusions
Our findings showed that nursing home residents in Poland had higher cognitive function, as indicated by MMSE score, than nursing home residents in other countries. This may be attributable to variable admission criteria and our patients being in a better cognitive and physical condition than the patients admitted to such facilities in other countries. We demonstrated that the MMSE scores were associated with patients' sex, age, education, and nutritional status. The relationship found between MMSE score and cigarette-smoking could be coincidental.
A lower MMSE score was associated with a higher mortality rate during 3-year observational period. We propose using MMSE as a tool for screening cognitive function and determining prognostic factors for the mortality of nursing home residents.
Statement of Ethics
The study protocol was approved by the Bioethics Committee of the Medical University of Warsaw (No. KB/13/2015, dated February 17, 2015). Each participant received instructions from the author explaining the purpose of the study and ensuring confidentiality. Every person enrolled in the study provided written informed consent to participate.
Conflict of Interest Statement
The authors have no conflicts of interest to declare.
Funding Sources
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Author Contributions
D.P.: design of the study, collecting data, interpretation of results, literature collection, writing of manuscript; B.C.-P.: design of the study, interpretation of results, writing of the manuscript.
Acknowledgments
The English version was edited by San Francisco Edit.
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