Analysis of the Prevalence of Mild Cognitive Impairment and its Influencing Factors in the Elderly Population in Huzhou City
Weiliang He, Zheli Chen, Liang Xu, Fei Fang, Xin Zu, Xilong Jin, Jing Chen

TL;DR
This study finds that 10.54% of elderly people in Huzhou City have mild cognitive impairment, with risk factors including age, gender, and depression.
Contribution
The study provides new insights into MCI prevalence and risk factors specific to the elderly population in Huzhou City.
Findings
The prevalence of MCI among the elderly in Huzhou City is 10.54%.
Risk factors for MCI include being female, older age, and higher depression scores.
Early intervention is recommended to improve cognitive function and quality of life.
Abstract
Mild cognitive impairment (MCI) is a critical stage in the development of Alzheimer’s disease, and early intervention in patients during this stage may reverse or delay their disease progression. As one of the regions with severe aging in China, it is necessary to understand the prevalence of MCI in Huzhou and adopt effective intervention measures. The study was aimed to investigate the prevalence rate and influencing factors of MCI in the elderly population in Huzhou city. A cross-sectional study was conducted involving 800 elderly residents of Huzhou city. The Montreal Cognitive Assessment (MoCA) and the activity of daily living (ADL) were used to assess the occurrence of MCI in the elderly. The influencing factors of MCI were investigated by univariate analysis and multi-factor analysis. A total of 800 questionnaires were sent out in this survey, and 778 were effectively collected,…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
| Variable | n | Non-MCI group (n = 668) | MCI group (n = 82) |
| ||
| Gender (n) | 6.295 | 0.012 | ||||
| Male | 354 | 326 | 28 | |||
| Female | 396 | 342 | 54 | |||
| Age (years) | 70.31 | 72.99 | 3.717 | |||
| Marital status (n) | - | 0.136 | ||||
| Married | 656 | 586 | 70 | |||
| Unmarried | 1 | 0 | 1 | |||
| Divorced | 8 | 8 | 0 | |||
| Widowed | 85 | 74 | 11 | |||
| Occupation (n) | - | 0.037 | ||||
| Retired | 520 | 461 | 59 | |||
| Retirement | 8 | 7 | 1 | |||
| Farming | 177 | 155 | 22 | |||
| Employed | 45 | 45 | 0 | |||
| Education level (n) | 11.503 | 0.042 | ||||
| No formal education | 145 | 120 | 25 | |||
| Primary school | 243 | 215 | 28 | |||
| Junior high school | 207 | 186 | 21 | |||
| High school/vocational school | 110 | 104 | 6 | |||
| College/vocational college | 19 | 18 | 1 | |||
| University or higher | 26 | 25 | 1 | |||
| Nature of resident (n) | 0.033 | 0.856 | ||||
| Rural | 304 | 270 | 34 | |||
| Urban | 446 | 398 | 48 | |||
| Living arrangement (n) | - | 0.053 | ||||
| Living alone | 160 | 139 | 21 | |||
| With children | 47 | 45 | 2 | |||
| In elderly care | 116 | 100 | 16 | |||
| With spouse | 426 | 384 | 42 | |||
| With caregiver | 1 | 0 | 1 | |||
| Smoking status (n) | 2.445 | 0.294 | ||||
| Never smoked | 502 | 441 | 61 | |||
| Quit smoking | 96 | 87 | 9 | |||
| Current smoker | 152 | 140 | 12 | |||
| Drinking status (n) | 1.784 | 0.410 | ||||
| Never drank | 541 | 480 | 61 | |||
| Quit drinking | 55 | 47 | 8 | |||
| Current drinker | 154 | 141 | 13 | |||
| CSI-D score (points) | 9 (8, 9) | 8 (7, 9) | 5.358 | |||
| AD8 score (points) | 0 (0, 1) | 3 (2, 5) | 12.092 | |||
| PHQ-9 score (points) | 0 (0, 2) | 2 (1, 5) | 6.519 | |||
| AIS score (points) | 1 (0, 3) | 3 (1, 6) | 4.666 | |||
| Insomnia (n) | 0.033 | 0.856 | ||||
| Yes | 35 | 31 | 4 | |||
| No | 715 | 637 | 78 | |||
| Depression (n) | - | 1.000 | ||||
| Yes | 1 | 1 | 0 | |||
| No | 749 | 667 | 82 | |||
| Hypertension (n) | 0.643 | 0.423 | ||||
| Yes | 505 | 453 | 52 | |||
| No | 245 | 215 | 30 | |||
| Diabetes (n) | 0.020 | 0.887 | ||||
| Yes | 142 | 126 | 16 | |||
| No | 608 | 542 | 66 | |||
| Coronary heart disease (n) | 0.343 | 0.558 | ||||
| Yes | 78 | 71 | 7 | |||
| No | 672 | 597 | 75 | |||
| Cerebral infarction (n) | 1.908 | 0.167 | ||||
| Yes | 47 | 39 | 8 | |||
| No | 703 | 629 | 74 | |||
| Cerebral hemorrhage (n) | 0.407 | 0.523 | ||||
| Yes | 2 | 1 | 1 | |||
| No | 748 | 667 | 81 | |||
| Hyperthyroidism (n) | 0.407 | 0.523 | ||||
| Yes | 2 | 2 | 0 | |||
| No | 748 | 666 | 82 | |||
| Hypothyroidism (n) | 0.104 | 0.747 | ||||
| Yes | 7 | 6 | 1 | |||
| No | 743 | 662 | 81 | |||
| Hearing disorder (n) | 0.474 | 0.491 | ||||
| Yes | 23 | 22 | 1 | |||
| No | 727 | 646 | 81 | |||
| Visual disturbance (n) | 0.000 | 1.000 | ||||
| Yes | 41 | 37 | 4 | |||
| No | 709 | 631 | 78 | |||
| Chronic gastritis (n) | 0.543 | 0.461 | ||||
| Yes | 66 | 57 | 9 | |||
| No | 684 | 611 | 73 | |||
| Enteritis (n) | - | 0.381 | ||||
| Yes | 12 | 12 | 0 | |||
| No | 738 | 656 | 82 | |||
| Hepatobiliary disease (n) | 0.036 | 0.849 | ||||
| Yes | 60 | 53 | 7 | |||
| No | 690 | 615 | 75 | |||
| Cerebral trauma (n) | 0.799 | 0.371 | ||||
| Yes | 7 | 5 | 2 | |||
| No | 743 | 663 | 80 | |||
| Surgical history (n) | 2.078 | 0.149 | ||||
| Yes | 429 | 376 | 53 | |||
| No | 321 | 292 | 29 | |||
| Family history of dementia (n) | - | 0.620 | ||||
| Yes | 11 | 11 | 0 | |||
| No | 739 | 657 | 82 | |||
| Family history of depression (n) | - | 1.000 | ||||
| Yes | 5 | 5 | 0 | |||
| No | 745 | 663 | 82 | |||
| Family history of neurasthenia (n) | - | 1.000 | ||||
| Yes | 1 | 1 | 0 | |||
| No | 749 | 667 | 82 | |||
| Variables | B | Standard error | Wald | Odds ratio | 95% CI | ||
| Lower | Upper | ||||||
| Gender | 0.671 | 0.301 | 4.966 | 0.026 | 1.956 | 1.084 | 3.530 |
| Age | 0.060 | 0.023 | 6.808 | 0.009 | 1.062 | 1.015 | 1.111 |
| Occupation | –0.481 | 0.340 | 2.003 | 0.157 | 0.618 | 0.317 | 1.204 |
| Education level | –0.223 | 0.318 | 0.493 | 0.483 | 0.800 | 0.429 | 1.492 |
| CSI-D | –0.278 | 0.103 | 7.257 | 0.007 | 0.758 | 0.619 | 0.927 |
| AD8 | 0.451 | 0.056 | 64.491 | 1.569 | 1.406 | 1.752 | |
| PHQ-9 | 0.140 | 0.067 | 4.361 | 0.037 | 1.150 | 1.009 | 1.312 |
| AIS | –0.066 | 0.055 | 1.438 | 0.230 | 0.936 | 0.841 | 1.043 |
| Constant | –5.365 | 2.076 | 6.675 | 0.010 | 0.005 | ||
- —Huzhou Science and Technology Plan Project
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Taxonomy
TopicsDementia and Cognitive Impairment Research
Introduction
Senile cognitive dysfunction is a prevalent neurological degeneration, second only to cerebrovascular disease, and is a common neurological disorder [1, 2]. Studies have shown that with the intensification of population aging, the prevalence rate of cognitive dysfunction in people over 60 years old in China has been rising year by year, which has brought a heavy burden to society and families [3, 4]. Mild cognitive impairment (MCI), first characterized by Petersen RC et al. [5] 2014, describes a specific state of cognitive decline and is considered an intermediate stage between normal aging and dementia. Although MCI patients do not meet the diagnostic criteria for dementia and generally maintain basic daily living skills, they often exhibit declines in cognitive functions such as memory, executive function, language, and attention, as well as difficulties with complex daily living activities [6].
Studies have shown that MCI is a key stage in the development of Alzheimer’s disease [7, 8]. Compared to the annual incidence of dementia in the normal population of 1% to 2%, the number of MCI patients developing dementia every year accounts for 10% to 15% [9]. Alzheimer’s disease, especially in its advanced stages, imposes a significant burden on the families of the patient due to the lack of effective treatments and the need for long-term care, making it a major contributor to national healthcare costs. Early intervention during the MCI stage may delay or even prevent progression to dementia [10]. Therefore, early screening and analysis of MCI-related factors are crucial for developing preventive and therapeutic strategies to improve cognitive function and reduce the socioeconomic burden on families and society.
While large-scale epidemiological surveys have been conducted across China, there is a lack of systematic studies in Zhejiang, especially in Huzhou, a region with a high prevalence of aging. Understanding the prevalence and risk factors of MCI in Huzhou is essential for implementing effective interventions. This study aimed to investigate the prevalence and determinants of MCI in the elderly population of Huzhou and provide scientific foundation for prevention, early detection, and intervention. The findings from this research will contribute to enhancing cognitive function, improving quality of life, and promoting healthy aging in the elderly population.
Material and Methods
Study Participants
Eight hundred elderly people aged 60 and above were selected by multi-stage
stratified cluster random sampling method from January 2022 to December 2022. The
sample size was estimated using the formula: n =
(u / )^2^
p (1 – p), with
= 0.05, u = 1.96, and allowable error ( ) of 0.03. Based on an
estimated MCI prevalence rate (p) of 0.212, the required sample size was
calculated to be 713. Accounting for a 10% inefficiency rate, the sample size
was expanded by 10% to 785 cases and rounded to 800 cases. The specific sampling
method is as follows: 2 streets are randomly selected from the 7 streets of
Aishan, Feiying, Yuehe, Chaoyang, Hudong, Longquan and Huanzhu in Wuxing District
of Huzhou, and then 2 communities are randomly selected from these 2 streets, a
total of 4 communities. From each community, 2 residential areas were selected,
resulting in 8 residential areas where 100 individuals were screened, totaling
800 participants. Out of 800 questionnaires distributed, 778 were completed,
yielding an effective response rate of 97.25%.
Inclusion criteria: (1) Age 60 and above; (2) Residence in the community for at least one year; (3) Ability to understand and complete interview. Exclusion criteria: (1) Sensory impairment significantly affecting data collection (e.g., severe deafness, blindness); (2) Presence of mental disorders; (3) Acute phase of major physical illnesses (e.g., stroke).
Procedures
All raters received consistent training. The purpose, process, significance, and estimated study duration were explained to participants, and informed consent was obtained. Participants were instructed to complete the questionnaire independently. For some patients who cannot fill in the questionnaire due to illness or educational level, the investigator will ask them one by one and record them truthfully. All questionnaires were collected and verified on the same day by designated personnel. The questionnaire included the following: (1) General information: marital status, occupation, educational level, nature of residents, way of living, smoking history (smoking 4 cigarettes/week in the past 6 months), alcohol consumption ( 25 g/day for men, 15 g/day for women), medical history (e.g., insomnia, depression, hypertension, diabetes, coronary heart disease, cerebral infarction, cerebral hemorrhage, hyperthyroidism, hypothyroidism, hearing impairment, visual impairment, taste impairment, smell impairment, chronic gastritis, enteritis, hepatobiliary disease, traumatic brain injury), surgical history, family history, family history of dementia, family history of depression, family history of neurasthenia. (2) Cognitive assessments: Scores from the Community Screening Instrument for Dementia (CSI-D) [11] (coefficient alpha = 0.9157 [12]), Dementia Screening Questionnaire (AD8) [13] (coefficient alpha = 0.84 [14]), Patient Health Questionnaire Depression Scale (PHQ-9) [15] (coefficient alpha = 0.894 [16]), and Athens Insomnia Scale (AIS) [17] (coefficient alpha = 0.87 [18]). MCI diagnostic criteria: The patient’s cognitive function was diagnosed according to Petersen’s MCI diagnostic criteria [19]: (1) Memory complaints confirmed by the informant; (2) Memory impairment on the Montreal Cognitive Assessment (MoCA) [20] (coefficient alpha = 0.75 [21]), with 11 points MoCA score 15 points for illiterates, 14 points MoCA score 20 points for primary school literacy students and 16 points MoCA score 23 points for those with junior high school education or above; (3) Normal overall cognitive changes; (4) Normal daily living activities [activity of daily living (ADL) score 22 points [22] (coefficient alpha = 0.827 [23])]; (5) Did not meet the diagnostic criteria for dementia.
Statistical Analysis
Statistical analysis was performed using SPSS v23.0 (IBM SPSS Corp.; Armonk, NY, USA). Categorical variables were analyzed using the Chi-Squared or Fisher exact tests, expressed as frequencies (n). The Shapiro-Wilk normality test assessed the normality of continuous data (age and CSI-D, AD8, PHQ-9, AIS scores). Normally distributed data were presented as mean standard deviation ( s) and analyzed using the independent samples t-test. Non-normally distributed data were expressed as median (min, max) and analyzed using the Mann-Whitney U test. Univariate analysis and multiple logistic regression analysis were performed to identify factors influencing MCI in the elderly population. A p-value 0.05 was considered statistically significant.
Results
Prevalence of MCI
Among the 778 elderly participants in Huzhou City, 668 had normal cognitive function, 82 had MCI, and 28 had dementia, resulting in an MCI prevalence of 10.54% (82/778).
Univariate Analysis of MCI
Participants were categorized into an MCI group (n = 82) and a non-MCI group (n = 668) based on cognitive status. Univariate analysis identified gender, age, occupation, educational level, and scores on the CSI-D, AD8, PHQ-9, and AIS scales as factors associated with MCI in the elderly population of Huzhou City (Table 1).
Multiple Logistic Regression Analysis of MCI
Multiple logistic regression was performed using MCI prevalence as the dependent variable and gender (male = 0, female = 1), age, occupation (retired = 0, employed/farming = 1), education level (primary school and below = 0, junior high school and above = 1), and scores on the CSI-D, AD8, PHQ-9, and AIS scales as independent variables. The analysis identified female (*p *= 0.026), high age (*p *= 0.009), low CSI-D score (*p *= 0.007), high AD8 score (*p * 0.001), and high PHQ-9 score (*p *= 0.037) as significant risk factors for MCI in the elderly urban population of Huzhou City (Table 2).
Discussion
As a transitional state between normal aging and dementia, the prevalence of MCI increases year by year with the intensification of population aging, posing a serious threat to the physical and mental health of the elderly [24]. Studies have shown that early cognitive training, lifestyle modifications, and enhanced social support can effectively stabilize or improve cognitive function in MCI patients, thereby enhancing their quality of life [25, 26]. However, the clinical manifestations of MCI are varied, and some patients may remain stable for a period of time, while others may rapidly progress to dementia. Additionally, the early diagnosis of MCI is challenging due to the lack of specific biomarkers [27]. Therefore, it is of great significance to conduct an in-depth epidemiological investigation of MCI patients.
In this study, 778 elderly people in Huzhou City included 668 people with normal cognitive function, 82 people with MCI and 28 people with dementia. The prevalence rate of MCI was 10.54%. Hu Y et al. [28] conducted MCI screening on 5715 people over 60 years old in China and found that the incidence of MCI in the non-sarcopenia group was 10.1%, which was similar to the results in this paper. Jia L et al. [29] investigated 46,011 people aged 60 or above from 96 sites in China and found that the total prevalence of MCI was 15.5%. Cong L et al. [30] investigated 5068 Chinese residents aged 60 and above, and found that the prevalence rate of MCI was 26.48%. The prevalence rate of MCI in the above studies was significantly higher than that in this survey. Jia L et al. [29] surveyed all residents, and Cong L et al. [30] surveyed rural residents.
Through further analysis, this study determined that female, high age, low CSI-D score, high AD8 score, and high PHQ-9 score were all risk factors for MCI in the elderly population in Huzhou City.
The risk of MCI in elderly female residents in this region is higher than that of male residents, and the reasons may include the following: differences in physiological structure, estrogen regulation of cognitive-related brain neurons and thinking processes, the risk of MCI in elderly women may increase due to the decrease of estrogen with age. In the early period of China, there was a serious traditional social concept of “son preference”. In addition, due to the low social and economic level and limited national educational resources at that time, women’s education level was generally low, which affected women’s cognitive reserve. In addition, the subjects of this survey are aged 60 and above, most of whom were born in the early years of the founding of the People’s Republic of China, when women’s social participation was lower than that of men.
Lee S et al. [31] also proposed that women’s cognitive function was affected by social activities and the number of friends. Chen HF et al. [32] and Li W et al. [33] respectively conducted cross-sectional studies on patients with type 2 diabetes and schizophrenia, and found that women had a higher proportion of cognitive dysfunction and were inferior to men in terms of overall cognitive function and executive function. Son YJ et al. [34] investigated 152 patients in intensive care units in South Korea using a prospective cohort study, and found that the proportion of persistent cognitive impairment in female patients was significantly higher than that in male patients. Yang H et al. [35] pointed out that living with others in men with poor sleep quality is conducive to reducing the risk of MCI, but there is no such protective effect in women, and speculated that this may be another factor leading to the higher prevalence of MCI in women. Okamoto S et al. [36] also came to a conclusion consistent with this study by taking elderly people in Japan as the investigation objects.
Age has been identified as an independent factor influencing MCI in the elderly population of Huzhou city. This correlation is attributed to age-related memory decline, reduced physical function, and decreased social activity. As people age, there is a gradual reduction in cerebral blood flow, oxygen and glucose metabolism, and blood-brain barrier function. Concurrently, brain tissue undergoes organic changes and atrophy, leading to cognitive dysfunction across multiple domains. Additionally, after retirement, the elderly often experience reduced mental engagement, decreased participation in social activities, and diminished exposure to new information, all of which contribute to cognitive decline. The CSI-D and AD8 scales effectively detect early-stage dementia, and their scores correlate directly with MCI, reinforcing their utility in assessing cognitive impairment.
This study also found that a high PHQ-9 score is a significant risk factor for MCI, indicating a strong association between depressive symptoms and MCI in the elderly. Numerous studies have explored the biological mechanisms underlying cognitive decline due to depression [37, 38, 39, 40]. Some suggest that depression disrupts the neuroendocrine axis, increasing corticosteroid secretion and leading to hippocampal neuron death and neural inhibition (endocrine hypothesis). Others propose that depressive symptoms cause glial cell damage, trigger inflammatory factors, and lead to myelin degradation (neuroinflammatory hypothesis). Additional theories include the vascular depression hypothesis, neurotrophic factor hypothesis, and amyloid hypothesis. Hou Z et al. [41] found that the intensification of depressive symptoms was significantly related to the rapid decline of cognitive ability. Shin M [42] investigated elderly people in South Korea and found that depressive symptoms could increase the risk of cognitive dysfunction. Ma W et al. [43] took 7525 Chinese elderly people as investigation objects and found that depression, social relations and cognitive function were significantly correlated. Alexopoulos P et al. [44] also identified a link between cognitive dysfunction and depressive symptoms in patients with rheumatoid arthritis (RA) and systemic sclerosis. These findings highlight the need for early intervention to address depressive symptoms and mitigate their impact on cognitive function in elderly populations.
This study has several limitations: (1) The sample was limited to eight residential communities in two streets of Wuxing District, Huzhou, which may not fully represent the elderly population aged 60 and above in the area; (2) The CSI-D, AD8, PHQ-9, and AIS questionnaires used may be influenced by subjective factors; (3) This is a cross-sectional study, and MCI is a progressive condition, meaning that new cases may continue to emerge; (4) Other studies have linked MCI to factors such as hearing impairment, enteritis, and thyroid function, which were not observed in this study, possibly due to limited sample size. In the follow-up study, we will expand the sample size, survey scope and survey time, and comprehensively consider diet, exercise and other lifestyle factors to confirm the universal significance of the findings.
Conclusion
This study provides valuable insights into the prevalence and influencing factors of MCI among the elderly population in Huzhou City, revealing a prevalence rate of 10.54%. MCI incidence was found to be significantly associated with gender, age, health status, and depressive symptoms. Given these findings, it is necessary to focus on these high-risk groups and implement targeted interventions as early as possible to enhance cognitive function and quality of life among the elderly population.
Availability of Data and Materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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