Skip to main content
Aging (Albany NY) logoLink to Aging (Albany NY)
. 2020 Sep 9;12(17):17257–17270. doi: 10.18632/aging.103674

Inactive bowel movement and stroke are associated with increased risks of mild cognitive impairment among community-living Singapore elderly

Kai-Yong Huang 1,*, Xian-Yan Tang 2,*, Li Yang 1,*, Zhi-Yong Zhang 1,3, Kaisy Xinhong Ye 4, Qing-Feng Shen 5, Xiu Wang 6, Xiang-Hua Zhu 5, Xiao-Wei Huang 7, Guo-Dong Lu 7,8,, Lei Feng 4,9,
PMCID: PMC7521501  PMID: 32903214

Abstract

Mild cognitive impairment (MCI), as a preclinical phase of dementia, provides an invaluable time window for intervention. Besides several proposed modifiable risk factors, the associations of MCI with dietary habits and bowel movement are not well clarified. We thus conducted a cross-sectional study of community-living Singapore elderly and focused on the relationship of clinically diagnosed MCI with dietary habits and bowel movement frequencies. The multiple logistic regression results showed that frequent (≥4 days per week) fruit consumption (P = 0.004), active (≥4 days per week) bowel movement within 10 minutes (P = 0.027), and years of schooling were negatively associated with MCI occurrence. In contrast, medical comorbidities including hypertension, stroke, and cataract/glaucoma were found to be risk factors. Furthermore, a Bayesian network model of causal inference detected five hypothesized causal-association paths leading to MCI, namely bowel movement, stroke, years of schooling via fruit consumption, hypertension via stroke and hypertension via cataract/glaucoma. The combination of the two direct factors (inactive bowel movement and stroke) reached a maximum conditional probability of 60.00% for MCI occurrence. Taken together, this study was the first to link bowel movement with MCI occurrence. In addition, it suggested five modifiable hypothesized causal-association paths to MCI.

Keywords: mild cognitive impairment, bowel movement, fruit consumption, dietary habits, stroke

INTRODUCTION

Dementia, which occurs mainly in people older than 65 years, is one of the greatest global challenges for health and social care in the 21st century [1]. Fifty million people worldwide lived with dementia in 2018, and the total number may triple to 152 million by 2050 [2]. The annual global cost of dementia treatment and care has reached one trillion US dollars and will double by 2030 [2]. Unfortunately, there is no effective disease-modifying pharmaceutical treatment available to cure or prevent dementia. Mild cognitive impairment (MCI) is a transitional state between the cognitive changes of normal aging and dementia [3], with a prevalence varying from 4% to 19% among people aged 60 and above [1]. MCI is also regarded as a preclinical phase of dementia, because around 22% of MCI-affected people would progress to dementia within 3 to 10 years upon diagnosis of MCI, while only 3% of non-MCI people develop dementia [4]. This pre-disease state of MCI opens an invaluable therapeutic time window to intervene or prevent further deterioration into dementia.

It was estimated that around one third of dementia burdens could be prevented theoretically by controlling modifiable risk factors [1]. Preventive countermeasures are composed of two major categories: management of medical comorbidities and modifications of lifestyles. First, high-risk medical comorbidities (e.g. midlife hypertension, obesity and hearing loss; late-life depression and diabetes) account for 17% of risks to develop dementia. Active treatments of these medical comorbidities were recommended to control MCI and prevent deterioration into dementia. Second, adopting healthy lifestyles (e.g. active engagements of social and physical activities, cognitive stimulation activities and smoking cessation) may control another 10% risks. Unfortunately, dietary factors were not included in the model, and their contributions are not calculated [1], although adherence to a Mediterranean diet was suggested to be beneficial for controlling vascular and metabolic risk factors. Previous studies have reported that adequate or excess intakes of fruit and/or vegetables were associated with a reduced risk of cognitive impairments [5]. Numerous preclinical studies have found that polyphenolic antioxidants found in fruits and vegetables could effectively decrease and even block neuronal death and thereby reduce the occurrence of dementia, especially in cell studies and in animal models [6].

Another close but neglected connection is bowel movement, which is affected by individuals’ dietary habits and the stool contents. Inactive bowel movement and constipation are common gastrointestinal symptoms (e.g., stool hardness, a prolonged and difficult passage of stool, or a feeling of unfinished evacuation) [7]. It has been proposed that gut-brain axis dysfunction may play a role in neurological diseases, strengthening the importance of gut flora in a biochemical signaling cascade between the gut and central nervous system. Constipation could precede clinical motor symptoms, particularly Parkinson’s disease (PD), by many years [8]. Based on a large-scale prospective cohort study (the Honolulu-Asia Aging Study) with 12 years’ follow-up, Abbott and colleagues made a landmark finding that infrequent bowel movement was correlated with an increased risk of PD [9]. A case-control study by Savica et al. using medical records documentation in the Rochester Epidemiology Project later reiterated the positive association between constipation (which was recorded 20 years or even more before the onset of motor impairments) and an increased risk of PD development. However, it is still unclear whether constipation may affect cognitive functions apart from motor neuron diseases. A few studies [10] have pointed out that patients affected by dementia with Lewy bodies had a higher prevalence of constipation. The authors suggested including examinations of constipation together with other non-cognitive symptoms, e.g., hyposmia and sleep behavior disorders, for the prodromal diagnosis of dementia.

In the present study, we aimed to dissect the associations of bowel movement frequencies and dietary habits with clinical-diagnosed MCI in a population-based cross-sectional study [the Diet and Healthy Aging (DaHA) study] in Singapore. For this observational study, we applied multiple logistic regression analyses to determine the adjusted odds ratios (AOR) of bowel movement on MCI occurrence. A Bayesian network approach that integrates causal diagram model and probabilistic model was then applied to infer the causal relationships between exposure variables (bowel movement frequencies and other possible influencers) and outcome variable (MCI occurrence). Qualitatively, the conceptual framework of causal association and the hypothesized causal-association paths among exposure variables were detected via a direct acyclic graph (DAG). Quantitatively, the magnitudes of causal association were inferred via the conditional probability table of the outcome variable under the combinations of direct factors. Moreover, the predictive reasoning forwarded from exposure variables and the importance scores of exposure variables were determined with a Bayesian network. This methodology has been conducted successfully in the field of neurological diseases. Kuipers and colleagues inferred the causal links between psychotic and neurotic symptoms in the British general population with directed acyclic graphs in a dynamic Bayesian network approach [11]. Rembach et al. employed the same approach to reveal the complex biological interactions specific to Alzheimer’s disease (AD) and assessed the biological connections among AD-associated serum protein biomarkers [12].

RESULTS

Socio-demographic characteristics and medical comorbidities of the study population

Among the enrolled participants (N=751), 119 elders (15.9%) were clinically diagnosed with MCI as described in the Methods section, while the rest were defined as non-MCI elders (or cognitive-healthy ageing control). MCI elders (aged 68.9±6.9 years) were 1.5 years older on average than the non-MCI participants (67.4±5.3, P=0.007, Table 1), but had markedly less education (4.8±4.5 vs. 6.8±4.1 years of schooling, P=0.003). There were no differences between these two groups in gender, marital status, or smoking and drinking habits. On the other hand, MCI patients differed from the non-MCI elders in some medical comorbidities, including hypertension (63.9% vs. 46.0%, P<0.001), hyperlipidemia (63.0% vs. 50.8%, P=0.014), diabetes mellitus (25.2% vs. 16.1%, P=0.017), stroke (8.4% vs. 2.5%, P=0.001), and cataract/glaucoma (48.7% vs. 32.3%, P=0.001).

Table 1. Socio-demographic characteristics and medical comorbidities comparisons between MCI elders and non-MCI elders.

Variables non-MCI n (%) MCI n (%) F or χ2 P-value
Age (Mean ± SD) 67.4 ± 5.3 68.9 ± 6.9 7.426 0.007
Years of schooling (Mean ± SD) 6.8±4.1 4.8±4.5 8.646 0.003
Gender* 0.924 0.336
Male 197 (31.3) 32 (26.9)
Female 432 (68.7) 87 (73.1)
Marital status* 2.253 0.133
Married 455 (72.3) 78 (65.5)
Divorced, widowed or single 174 (27.7) 41 (34.5)
Smoking 0.088 0.767
< 1 per week 594 (94.0) 111 (93.3)
≥1 per week 38 (6.0) 8 (6.7)
Drinking 0.342 0.559
< 1 per week 598 (94.6) 111 (93.3)
≥1 per week 34 (5.4) 8 (6.7)
Hypertension 12.729 < 0.001
Yes 291 (46.0) 76 (63.9)
No 341 (54.0) 43 (36.1)
Hyperlipidemia 6.013 0.014
Yes 321 (50.8) 75 (63.0)
No 311 (49.2) 44 (37.0)
Diabetes mellitus 5.688 0.017
Yes 102 (16.1) 30 (25.2)
No 530 (83.9) 89 (74.8)
Stroke 10.331 0.001
Yes 16 (2.5) 10 (8.4)
No 616 (97.5) 109 (81.6)
Heart attack 1.556 0.212
Yes 22 (3.5) 7 (5.9)
No 610 (96.5) 112 (94.1)
Irregular heart beat 0.601 0.438
Yes 27 (4.3) 7 (5.9)
No 605 (95.7) 112 (94.1)
Heart failure 0.046 0.831
Yes 9 (1.4) 2 (1.7)
No 623 (98.6) 117 (98.3)
Cataracts/glaucoma 11.946 0.001
Yes 204 (32.3) 58 (48.7)
No 428 (67.7) 61 (51.3)
Gastrointestinal problems 0.921 0.337
Yes 52 (8.2) 13 (10.9)
No 580 (91.8) 106 (89.1)
Anxiety disorder 3.627 0.057
Yes 5 (0.8) 4 (3.4)
No 627 (91.2) 115 (96.6)

Note: Continuous variables are expressed by mean±SD. * Due to the missing values in some variables, the total numbers may not equal to 632 or 119. Abbreviations: MCI, mild cognitive impairment; SD, standard deviation.

Comparisons of bowel movement frequencies and dietary habits between MCI elders and non-MCI elders

In order to determine the association of bowel movement frequencies and dietary habits with MCI occurrence, we collected the self-reported frequencies of these factors (e.g., “How often per week do you have a bowel movement within 10 minutes?”) in the studied population. We compared the proportions of bowel movement frequencies and different dietary habits between MCI patients and non-MCI elders. As shown in Table 2, a higher proportion of MCI elders complained infrequent (≤3 days per week) bowel movement than the non-MCI elders (26.7% vs. 17.2%, P = 0.013).

Table 2. Bowel movement and dietary habits variables comparisons between MCI elders and non-MCI elders.

Variables non-MCI n (%) MCI n (%) χ2 P-value
Have a bowel movement within 10 minutes 6.107 0.013
≤3 per week 109 (17.2) 32 (26.7)
≥4 per week 523 (82.8) 87 (73.3)
How often consume meat and meat product 6.074 0.014
≤3 per week 326 (51.6) 76 (63.9)
≥4 per week 306 (48.4) 43 (36.1)
How often consume milk and dairy product 0.001 0.972
≤3 per week 341 (54.0) 64 (53.8)
≥4 per week 291 (46.0) 55 (46.2)
How often consume green vegetables 1.040 0.308
≤3 per week 65 (10.3) 16 (13.4)
≥4 per week 567 (89.7) 103 (86.6)
How often consume fruits 15.740 < 0.001
≤3 per week 120 (19.0) 42 (35.3)
≥4 per week 512 (81.0) 77 (64.7)
How often consume legumes 3.371 0.066
≤3 per week 539 (85.3) 109 (91.6)
≥4 per week 93 (4.7) 10 (8.4)
How often consume eggs 4.238 0.040
≤3 per week 520 (82.3) 107 (90.0)
≥4 per week 112 (17.7) 12 (10.0)
How often consume sea fish* 0.021 0.884
≤3 per week 327 (52.0) 61 (51.3)
≥4 per week 302 (48.0) 58 (48.7)
How often consume seaweed # 0.497
≤3 per week 616 (97.5) 118 (99.2)
≥4 per week 16 (2.5) 1 (0.8)
How often consume tofu * 2.549 0.110
≤3 per week 537 (85.2) 108 (90.8)
≥4 per week 93 (14.8) 11 (9.2)
How often consume carrot* 0.657 0.417
≤3 per week 476 (75.6) 85 (72.0)
≥4 per week 154 (24.4) 33 (28.0)
How often consume celery* 1.011 0.315
≤3 per week 590 (93.8) 115 (96.6)
≥4 per week 39 (6.2) 4 (3.4)
How often consume walnut 1.745 0.187
≤3 per week 587 (92.9) 115 (96.6)
≥4 per week 45 (7.1) 4 (3.4)
How often consume coffee 3.352 0.067
≤3 per week 202 (32.0) 28 (23.5)
≥4 per week 430 (68.0) 91 (76.5)

Note: * Due to the missing values in some variables, the total numbers may not equal to 632 or 119. # Analyzed by Fisher's Exact Test. Abbreviations: MCI, mild cognitive impairment.

Dietary habits were also associated with MCI occurrences. The univariate analyses found that a higher proportion of MCI elders ate fruits infrequently (≤3 days per week) than their cognitive healthy peers (35.3% vs. 19.0%, P<0.001). Similar trends were observed for meat (63.9% vs. 51.6%, P = 0.014) and egg consumption (90.0% vs. 82.3%, P = 0.040). In contrast, there were no statistical differences in their consumptions of milk and dairy products, vegetables (including green vegetables, celery, and carrots), tofu, sea products (including sea fish and seaweed), or walnut between subgroups with or without MCI. The infrequent legume consumption (91.6% vs. 85.3%, P = 0.066) and coffee consumption (23.5% vs. 32.0%, P = 0.067) were slightly different between the two groups but failed to reach the threshold of statistical difference.

Because individuals’ dietary habits may affect stool contents and bowel movements, we then determined whether there were any correlations between bowel movement frequencies and dietary habits. The results (Supplementary Table 1) showed that only fruit consumption but not the other dietary habits were associated with bowel movement. The elders who had active bowel movement consumed fruit in a higher frequency (≥4 days per week, 79.8%) than those who had inactive bowel movement (71.6%, P = 0.033).

Multiple logistic regression analyses confirmed the independent associations of bowel movements and fruit consumption with MCI

To further determine the independent associations of bowel movements and dietary habits with MCI occurrence and adjust for the influences of other factors (e.g., age, education, medical comorbidities), we performed multiple logistic regression analyses. Those factors with statistical differences P < 0.1 in the univariate chi-square or analysis of variance (ANOVA) tests (Tables 1 and 2) were included in a multiple logistic regression model (Table 3). It is worth noting that active bowel movement (≥ 4 days per week) was associated with decreased risk of MCI occurrence [adjusted odds ratios (AOR) = 0.582, 95% confidence interval (CI) = 0.360-0.941, P = 0.027]. Similarly, years of schooling (AOR = 0.906, 95%CI = 0.861-0.954, P < 0.001) and active fruit consumption (AOR = 0.516, 95% CI = 0.330-0.808, P = 0.004) were found to be associated with decreased risk of MCI occurrence. In contrast, medical comorbidities including hypertension (AOR = 1.770, 95%CI = 1.159-2.705, P = 0.008), stroke (AOR = 2.514, 95%CI = 1.065-5.936, P = 0.035), and cataracts/glaucoma (AOR = 1.803, 95%CI = 1.190-2.731, P = 0.005) were statistically associated with increased risks of MCI.

Table 3. Multiple logistic regression analysis for MCI.

Variables β Wald P-value AOR 95% CI
Years of schooling -0.099 14.191 < 0.001 0.906 0.861-0.954
Hypertension 0.571 6.981 0.008 1.770 1.159-2.705
Stroke 0.922 4.423 0.035 2.514 1.065-5.936
Cataracts/glaucoma 0.589 7.740 0.005 1.803 1.190-2.731
Have a bowel movement within 10 minutes (≥4 days per week) -0.541 4.886 0.027 0.582 0.360-0.941
Consume fruits (≥4 times per week) -0.662 8.374 0.004 0.516 0.330-0.808

Note: Model was adjusted for gender, age, marital status, smoking, drinking. Abbreviations: AOR, adjusted odds ratio; CI, confidence interval.

Bayesian network model of the influencing factors of MCI

The hypothesized causal-association paths between MCI occurrence and significant influencers found in the multiple logistic regression analyses were explored by the Bayesian network model of causal inference. As shown in Figure 1, the results indicate five hypothesized causal-association paths leading to MCI occurrence. Among these, both bowel movement and stroke were directly associated with MCI occurrence. Years of schooling might be indirectly associated with MCI through fruit consumption. In addition, hypertension could be indirectly associated with MCI through either stroke or cataracts/glaucoma.

Figure 1.

Figure 1

Causal inference of MCI by Bayesian network analysis. Bayesian network approach detected the hypothesized causal-association diagram between MCI and exposure variables, and the importance of exposure variables. The magnitude of values presented at each node denote the importance of exposure variables. In other words, the higher magnitude the value is, more important the variable. Meanwhile, the importance of variables was visualized via the gradual changes of color of nodes.

Other information obtained from the Bayesian network model of causal inference was the importance of factors. Years of schooling was the most important factor, with an importance score of 0.26, followed by fruit consumption (0.25), stroke (0.16), hypertension (0.13), bowel movement (0.12) and cataract/glaucoma (0.09).

Finally, the inference probabilities of Bayesian network forwarding from the two direct factors (inactive bowel movement and stroke) to MCI were analyzed. Specifically, the combination of inactive bowel movement (≤ 3 days per week) and stroke had a maximum conditional probability of 60.00% (Table 4). But inactive bowel movement alone and stroke alone had lower probabilities of 44.51% and 29.54%, respectively. Furthermore, the combination of active bowel movement and no-stroke medical history had the least probabilities of 12.92%.

Table 4. Probability inference of Bayesian network for the direct factors of MCI.

Paternal nodes MCI
Have a bowel movement within 10 minutes Stroke Yes (%)
≤3 days per week Yes 60.00
≤3 days per week No 44.51
≥4 days per week Yes 29.54
≥4 days per week No 12.92

Abbreviations: MCI, mild cognitive impairment.

DISCUSSION

To the best of our knowledge, the present study was the first to examine the association between bowel movement and MCI. We found that active bowel movement, fruit consumption, and years of schooling were associated with decreased risk of MCI, while medical comorbidities including hypertension, stroke, and cataracts/glaucoma were unfavorable risk factors. The Bayesian network model further revealed that five hypothesized casual-association paths were important for MCI occurrence. Among them, inactive bowel movement and stroke were directly connected with MCI occurrence.

Gut-brain axis dysfunction has been hypothesized to be an essential factor in neurological diseases. Alterations of gut microbiota may mechanically promote neurological inflammation, insulin resistance [7, 13], and consequent neurological pathogenesis [14]. As a common digestive symptom, constipation (or inactive bowel movement) was well documented to increase the risk of motor neurological diseases. In addition to some case-control studies, the prospective Honolulu-Asia Aging Study [9] convincingly demonstrated that people with inactive bowel movement had increased risk for developing PD. However, there is a scarcity of solid epidemiological evidence associating bowel movement (or constipation) with cognitive impairments. Some observational studies have suggested a possible role of bowel movement in MCI or even dementia. On one hand, a few postmortem reports observed higher occurrences of dementia-related pathological changes (e.g., the presence of Lewy bodies and a decrease of substantia nigra neurons) in the brains of those who had been affected by constipation [15, 16]. On the other hand, some studies also reported that about 20% of dementia patients had constipation symptoms [17], which is consistent with findings of the present study that 26.7% MCI-affected elders had inactive bowel movement (Table 2). MCI-affected patients also observed gut microbiota alterations [18]. More importantly, these constipation symptoms can precede the onset of memory impairment by years.

The current study might support the gut-brain axis hypothesis by demonstrating that bowel movement was independently associated with MCI occurrence after adjusting for other influencing factors (Table 3). Furthermore, both bowel movement and stroke were directly associated with MCI in the causal diagram model of Bayesian network. The combination of inactive bowel movement and stroke increased the conditional probability to 60.00%, which was higher than inactive bowel movement alone or stroke alone (Table 4). Very recently, GV-971 (a sodium oligomannate) was found to be effective in relieving neuroinflammation and preventing cognitive impairments in a mouse AD model [19]. The authors concluded that the inhibitory actions of GV-971 on gut dysbiosis were responsible for the observed neuroprotective effects. Some promising results of a phase-III randomized clinical trial using GV-971 to treat mild dementia patients were presented in a conference, but the full results have not been published. It is worth noting that GV-971 was given conditional approval to treat patients with dementia by the China Food and Drug Administration in November 2019. Whether this drug could prove long-term efficacy in multi-regional randomized clinical trials and whether the proposed gut-brain axis dysfunction theory is valid warrant further studies.

The Bayesian network model indicated that education and fruit consumption were two important upstream factors influencing MCI, and they have the highest importance scores at 0.26 and 0.25 respectively (Figure 1). These two factors formed one hypothesized causal path directing from education to fruit consumption and then to MCI. This result is in line with a previous study observing that elderly with high education levels had higher fruit intake [20]. It is well established that childhood education enables individuals to increase cognitive reserve and even maintain cognitive function when they grow old. Education beyond primary school is regarded as the second important modifiable beneficial factor for dementia [1]. In the present study, around 42% of resident elders had no more than 5 years of education. Our results consistently showed that education (years of schooling) was negatively associated with MCI occurrence (Table 3). On the other hand, frequent consumption of fruit (≥4 days per week) was also negatively associated with MCI occurrence (AOR = 0.516, 95% = CI 0.330-0.808, P = 0.004) in our study (Table 3). Because education and fruit consumption belong to the same hypothesized causal path, the combination of poor education (≤ 5 years of schooling) and infrequent fruit consumption (≤3 times per week) reached a conditional probability at 32.86% (Supplementary Table 2), which is far less than the combination of the two direct factors (inactive bowel movement and stroke) with a conditional probability at 60.0% (Table 4).

Besides bowel movement and education via fruit consumption, the other three hypothesized causal-association paths directing to MCI were stroke, hypertension via stroke, and hypertension via cataracts/glaucoma, according to the Bayesian network model of causal inference (Figure 1). These medical comorbidities were statistically associated with MCI occurrence in the multiple logistic regression analyses (Table 3). Stroke and hypertension are well-known risk factors for MCI and dementia [1, 21, 22]. Active treatment of hypertension, however, significantly reduced the risk of stroke and MCI [23]. In addition, hypertension increases the risk of cataracts and/or glaucoma in population studies and rat experimental models [24]. Cataracts and glaucoma caused visual impairment, which usually affected health-related lifestyles (such as participations in social, physical, and cognitive-stimulating activities). However, these health-related lifestyles were well-recognized beneficial factors of MCI [1, 14]. A cross-sectional study in Japan showed that the elderly with mild visual impairments had more than 2 times higher risk of developing dementia [25]. In contrast, cataract surgery may help visual-impaired patients recover eyesight and lower significantly risks of MCI [25].

Based on the Bayesian network model of causal inference (Figure 1), there are three upstream influencers of bowel movement, namely fruit consumption, hypertension, and cataract/glaucoma. Because these three factors converge on the same node of bowel movement, no direct causal path could be inferred. Commonly consumed fruits could promote a healthy microbiota ecosystem by the actions of their fiber and polyphenolics. This conclusion was supported by a recent randomized controlled trial that consumption of fresh mango (a common tropical fruit in Singapore) significantly improved constipation status (frequency of bowel movements, stool consistency and shape, and duration of constipation) in chronically constipated adults [26]. Although bowel movement was associated with fruit consumption (Supplementary Table 1 and Figure 1), the multivariate logistic regression study confirmed their independent associations to MCI occurrence (Table 3). Here we did not find an association of green vegetable consumption with MCI occurrence, probably because the Southeast Asian residents maintain a good dietary habit of consuming green vegetables regularly. In our study, up to 89.2% of the elders ate green vegetables regularly no less than 4 days per week. Thus, it may be advisable for elders to consume fruits more frequently or daily to promote bowel movement and further prevent cognitive impairments.

We found that the elders with inactive bowel movement (≤3 days per week) had a higher proportion (57.4%) of hypertension comorbidity, compared to the peers with active bowel movement (46.9%, P=0.024, Supplementary Table 1). Whether there is a biological causal association directing from hypertension to bowel movement is yet unclear. However, recent studies suggested that the first-line antihypertensive drugs (e.g. diuretics, beta blockers, calcium channel blockers, and angiotensin-converting enzyme/angiotensin receptor blockers) were associated with an increased likelihood of constipation [27, 28].

Finally, a hypothesized connection between cataracts/glaucoma and inactive bowel movement was also suggested by the Bayesian network model of causal inference (Figure 1). The biological connection between these two factors has not been reported in the literature. We speculate that the hypothesized connection might be attributable to behavior or dietary changes among those elders affected by cataracts/glaucoma. Due to compromised vision, the affected elders may experience physical inactivity, which could lead to slower bowel movement. In addition, they may choose to prepare simple dish or have fast food with insufficient fiber consumption, another cause of inactive bowel movement. But these behavior/dietary connections warrant further examination in future cohort studies.

Limitations

Our study has several limitations. First, it was a cross-sectional study, and the causal relationship of bowel movement with MCI could not be determined with certainty. Therefore, future follow-up studies or longitudinal cohort studies should be conducted to validate the causal relationship. Second, the data (such as lifestyle, dietary habits, and bowel movement) were collected based on self-reporting methods, which might lead to recall bias. To minimize this bias, we excluded all dementia patients in the study. Finally, the present study lacked objective measurements of bowel movement and laboratory examination of stool microbiota. Future studies with constipation clinical diagnoses and the relevant measurements/surveys are needed to improve our results.

CONCLUSION

In summary, this study demonstrated that active bowel movement and fruit consumption were significantly associated with decreased risks of MCI in the elderly; while medical comorbidities including stroke, hypertension and cataract/glaucoma were positively associated with MCI. The Bayesian network model of causal inference further revealed five hypothesized causal-association paths leading to MCI, namely stroke, bowel movement, years of schooling via fruit consumption, hypertension via stroke and hypertension via cataracts/glaucoma. Particularly, the combination of stroke and inactive bowel movement reached a maximum conditional probability of 60.00%. Therefore, it would be advisable to decrease risks of MCI by adopting a healthy fruit consumption habit, improving bowel movement and by well management of stroke and hypertension.

MATERIALS AND METHODS

Ethics

The study was approved by the National University of Singapore Institutional Review Board (No. NUS-IRB-Ref 10-517), and we received informed consent from all individuals who agreed to participate in the study.

Participants and procedures

This population-based cross-sectional study was conducted from Jul 2011 to Dec 2016. The study population came from the Diet and Healthy Aging Study (DaHA), a community-based longitudinal cohort study that recruited elderly participants (aged ≥60) from a western district of Singapore [2931]. Well-trained nurses recruited participants via door-to-door census in the district. A demographic questionnaire, the Singapore Modified version of Mini-Mental State Examination (MMSE), the Montreal Cognitive Assessment (MoCA), and a battery of neuropsychological tests were completed by trained research staffs [29, 31]. The inclusive criteria for this study were: 1) Singaporean or permanent residents who live in the West Region of Singapore and 2) aged ≥60. Those who are unable to conduct meaningful face-to-face interviews were excluded. For the current analysis, we further excluded all individuals with a diagnosis of dementia. Finally, a total of 751 respondents were included in the study, of whom 119 were diagnosed with MCI and the remaining 632 individuals without MCI were defined as the cognitive-healthy group.

Variables

We collected socio-demographic variables (age, gender, education, and marital status), lifestyle and habits (drinking and smoking status), chronic disease status (hypertension, diabetes mellitus, hyperlipidemia, stroke, cataracts/glaucoma, and gastrointestinal problems), psychosocial variables (anxiety disorder), dietary habits (consumption of meat, milk, green vegetables, fruits, legumes, eggs, tofu, seaweed, sea fish, nuts, curry, walnut, tea, and coffee), and bowel movement status (assessed by asking “How often per week do you have a bowel movement within 10 minutes?”) using structured questionnaires at the participants’ homes. During analysis, the responses of bowel movement status were condensed into the two categories of “≤3 per week” and “≥4 per week.” based on the “Rome III Diagnostic Criteria for Functional Constipation”.

Neurocognitive assessment and diagnosis

The MMSE and MoCA were used to assess cognitive impairment of participants. The summed scores of MMSE ranged from 0 to 30, with higher scores indicating better cognitive performance [31, 32]. Participants with MMSE total scores below the education-specific cut-off values (≤25 for subjects without formal education, ≤27 for primary school education level, and ≤29 for secondary school and above) might have been suffering cognitive impairment and thus needed further assessment [31]. In addition, MoCA is scored on a 30-point scale, where higher scores correspond to better cognitive status [31, 32]. MCI was defined according to Petersen’s criteria [3, 33]. The diagnosis of MCI was made via consensus of a team consisting of a psychiatric epidemiologist, two senior consultant psychiatrists, and other clinical evaluation specialists [34]. As in our previous studies, cognitive impairment was evaluated by locally normed neuropsychological tests, including the Block Design, Digit Span, Rey Auditory Verbal Learning Test, Semantic Fluency, and Color Trails Test, and all MCI patients also met the criteria of mild neurocognitive disorder in the Diagnostic and Statistical Manual of Mental Disorders (DSM) version 5 [34].

Statistical analyses

Frequencies and percentages were used for categorical variables, while means and standard deviations (SD) were used to describe continuous variables. The comparisons of categorical variables between MCI and non-MCI group were performed using chi-square tests, while continuous variables (age, years of schooling) were compared with ANOVA using Statistic Package for Social Science (SPSS) 22.0. A two-sided P-value <0.05 was considered statistically significant. The factors with significant or moderate differences under the chi-square test and ANOVA (P<0.1) were then included in a multivariate logistic regression model.

After identifying the significant factors underlying the status of MCI, a Bayesian network model, structural equation model (SEM), and directed acyclic graph (DAG) approach were integrated to reveal the structure of hypothesized causal associations between significant factors and MCI Meanwhile, the probability inferences of the Bayesian network for the influencing factors of MCI were calculated, and the importance of each significant factor was quantitatively measured based on the Tree Augmented Naïve (TAN) Bayesian network learning. In general terms, the Bayesian network model was fitted with the bnlearn package via R software 3.5, the structure of the Bayesian network was defined using the hill climbing algorithm, and the BIC indicator was used to optimize and evaluate the fitted model. Moreover, the Bayesian-network-based causal relationships between exposure variables and MCI were visualized using the R package “dagitty.” In addition, the metrics of importance for exposure variables were calculated using SPSS Modeler 18.0.

Supplementary Material

Supplementary Tables
aging-12-103674-s001..pdf (373.9KB, pdf)

ACKNOWLEDGMENTS

We thank the DaHA study investigators and coordinators, who collected data and/or samples for this study, as well as all participants and their families, who made this work possible.

Abbreviations

MCI

mild cognitive impairment

PD

Parkinson’s disease

DaHA

Diet and Healthy Aging

AOR

adjusted odds ratios

AD

Alzheimer’s disease

ANOVA

analysis of variance

CI

confidence interval

MMSE

Mini-Mental State Examination

MoCA

Montreal Cognitive Assessment

DSM

Diagnostic and Statistical Manual of Mental Disorders

SD

standard deviation

SPSS

Statistic Package for Social Science

SEM

structural equation model

DAG

directed acyclic graph

TAN

Tree Augmented Naïve

Footnotes

AUTHOR CONTRIBUTIONS: LGD and FL made the main contributions to the conception and design of this study, critical revision of the article, and final approval of the article. HKY, TXY, and YL contributed equally to the analysis of the data, drafting of the manuscript, and revision of the article. The remaining authors participated in data compilation, data analysis and revision of the article. All authors read and approved the final manuscript.

CONFLICTS OF INTEREST: The authors declare that they have no conflicts of interest.

FUNDING: This study was supported by the National Medical Research Council of Singapore (NMRC/TA/0053/2016) and the National Innovation Challenge on Active and Confident Ageing Programme, Ministry of Health of Singapore (MOH/NIC/COG06/2017) awarded to Lei Feng; the Guangxi Hundred-Talent Program (2016) and the Guangxi Medical University Training Program for Distinguished Young Scholars (2017) awarded to Guo-Dong Lu; the Innovation Project of Guangxi Graduate Education (YCBZ2019034) and the International Communication of Guangxi Medical University Graduate Education (2019) awarded to Kai-Yong Huang; the National Science Foundation of China (Grant No. 81560523, 81760577, and 8196120388) to Zhi-Yong Zhang.

REFERENCES

  • 1.Livingston G, Sommerlad A, Orgeta V, Costafreda SG, Huntley J, Ames D, Ballard C, Banerjee S, Burns A, Cohen-Mansfield J, Cooper C, Fox N, Gitlin LN, et al. Dementia prevention, intervention, and care. Lancet. 2017; 390:2673–734. 10.1016/S0140-6736(17)31363-6 [DOI] [PubMed] [Google Scholar]
  • 2.Patterson C. World Alzheimer report 2018-The state of the art of dementia research: New frontiers. London: Alzheimer’s Disease International, 2018. [Google Scholar]
  • 3.Petersen RC, Doody R, Kurz A, Mohs RC, Morris JC, Rabins PV, Ritchie K, Rossor M, Thal L, Winblad B. Current concepts in mild cognitive impairment. Arch Neurol. 2001; 58:1985–92. 10.1001/archneur.58.12.1985 [DOI] [PubMed] [Google Scholar]
  • 4.Mitchell AJ, Shiri-Feshki M. Rate of progression of mild cognitive impairment to dementia—meta-analysis of 41 robust inception cohort studies. Acta Psychiatr Scand. 2009; 119:252–65. 10.1111/j.1600-0447.2008.01326.x [DOI] [PubMed] [Google Scholar]
  • 5.Ashby-Mitchell K, Peeters A, Anstey KJ. Role of dietary pattern analysis in determining cognitive status in elderly Australian adults. Nutrients. 2015; 7:1052–67. 10.3390/nu7021052 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Patel AK, Rogers JT, Huang X. Flavanols, mild cognitive impairment, and Alzheimer’s dementia. Int J Clin Exp Med. 2008; 1:181–91. [PMC free article] [PubMed] [Google Scholar]
  • 7.Zhang T, Han Y, Wang J, Hou D, Deng H, Deng YL, Song Z. Comparative epidemiological investigation of Alzheimer’s disease and colorectal cancer: the possible role of gastrointestinal conditions in the pathogenesis of AD. Front Aging Neurosci. 2018; 10:176. 10.3389/fnagi.2018.00176 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Winge K, Rasmussen D, Werdelin LM. Constipation in neurological diseases. J Neurol Neurosurg Psychiatry. 2003; 74:13–19. 10.1136/jnnp.74.1.13 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Abbott RD, Petrovitch H, White LR, Masaki KH, Tanner CM, Curb JD, Grandinetti A, Blanchette PL, Popper JS, Ross GW. Frequency of bowel movements and the future risk of Parkinson’s disease. Neurology. 2001; 57:456–62. 10.1212/wnl.57.3.456 [DOI] [PubMed] [Google Scholar]
  • 10.Petrovitch H, Abbott RD, Ross GW, Nelson J, Masaki KH, Tanner CM, Launer LJ, White LR. Bowel movement frequency in late-life and substantia nigra neuron density at death. Mov Disord. 2009; 24:371–76. 10.1002/mds.22360 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Kuipers J, Moffa G, Kuipers E, Freeman D, Bebbington P. Links between psychotic and neurotic symptoms in the general population: an analysis of longitudinal british national survey data using directed acyclic graphs. Psychol Med. 2019; 49:388–95. 10.1017/S0033291718000879 [DOI] [PubMed] [Google Scholar]
  • 12.Rembach A, Stingo FC, Peterson C, Vannucci M, Do KA, Wilson WJ, Macaulay SL, Ryan TM, Martins RN, Ames D, Masters CL, Doecke JD; AIBL Research Group. Bayesian graphical network analyses reveal complex biological interactions specific to Alzheimer's disease. J Alzheimers Dis. 2015; 44:917–25. 10.3233/JAD-141497 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Daulatzai MA. Chronic functional bowel syndrome enhances gut-brain axis dysfunction, neuroinflammation, cognitive impairment, and vulnerability to dementia. Neurochem Res. 2014; 39:624–44. 10.1007/s11064-014-1266-6 [DOI] [PubMed] [Google Scholar]
  • 14.Cattaneo A, Cattane N, Galluzzi S, Provasi S, Lopizzo N, Festari C, Ferrari C, Guerra UP, Paghera B, Muscio C, Bianchetti A, Volta GD, Turla M, et al. , and INDIA-FBP Group. Association of brain amyloidosis with pro-inflammatory gut bacterial taxa and peripheral inflammation markers in cognitively impaired elderly. Neurobiol Aging. 2017; 49:60–68. 10.1016/j.neurobiolaging.2016.08.019 [DOI] [PubMed] [Google Scholar]
  • 15.Schulz-Schaeffer WJ. The synaptic pathology of alpha-synuclein aggregation in dementia with lewy bodies, Parkinson’s disease and Parkinson’s disease Dementia. Acta Neuropathol. 2010; 120:131–43. 10.1007/s00401-010-0711-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Hanson JC, Lippa CF. Lewy body dementia. Int Rev Neurobiol. 2009; 84:215–28. 10.1016/S0074-7742(09)00411-5 [DOI] [PubMed] [Google Scholar]
  • 17.Donaghy PC, McKeith IG. The clinical characteristics of dementia with lewy bodies and a consideration of prodromal diagnosis. Alzheimers Res Ther. 2014; 6:46. 10.1186/alzrt274 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Li B, He Y, Ma J, Huang P, Du J, Cao L, Wang Y, Xiao Q, Tang H, Chen S. Mild cognitive impairment has similar alterations as Alzheimer’s disease in gut microbiota. Alzheimers Dement. 2019; 15:1357–66. 10.1016/j.jalz.2019.07.002 [DOI] [PubMed] [Google Scholar]
  • 19.Wang X, Sun G, Feng T, Zhang J, Huang X, Wang T, Xie Z, Chu X, Yang J, Wang H, Chang S, Gong Y, Ruan L, et al. Sodium oligomannate therapeutically remodels gut microbiota and suppresses gut bacterial amino acids-shaped neuroinflammation to inhibit Alzheimer’s disease progression. Cell Res. 2019; 29:787–803. 10.1038/s41422-019-0216-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Dijkstra SC, Neter JE, Brouwer IA, Huisman M, Visser M, van Lenthe FJ, Kamphuis CB. Socio-economic differences in the change of fruit and vegetable intakes among dutch adults between 2004 and 2011: the GLOBE study. Public Health Nutr. 2018; 21:1704–16. 10.1017/S1368980017004219 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Faraco G, Iadecola C. Hypertension: a harbinger of stroke and dementia. Hypertension. 2013; 62:810–17. 10.1161/HYPERTENSIONAHA.113.01063 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Ivan CS, Seshadri S, Beiser A, Au R, Kase CS, Kelly-Hayes M, Wolf PA. Dementia after stroke: the framingham study. Stroke. 2004; 35:1264–68. 10.1161/01.STR.0000127810.92616.78 [DOI] [PubMed] [Google Scholar]
  • 23.Williamson JD, Pajewski NM, Auchus AP, Bryan RN, Chelune G, Cheung AK, Cleveland ML, Coker LH, Crowe MG, Cushman WC, Cutler JA, Davatzikos C, Desiderio L, et al. , and SPRINT MIND Investigators for the SPRINT Research Group. Effect of intensive vs standard blood pressure control on probable dementia: a randomized clinical trial. JAMA. 2019; 321:553–61. 10.1001/jama.2018.21442 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.De Moraes CG, Cioffi GA, Weinreb RN, Liebmann JM. New recommendations for the treatment of systemic hypertension and their potential implications for glaucoma management. J Glaucoma. 2018; 27:567–71. 10.1097/IJG.0000000000000981 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Miyata K, Yoshikawa T, Morikawa M, Mine M, Okamoto N, Kurumatani N, Ogata N. Effect of cataract surgery on cognitive function in elderly: results of fujiwara-kyo eye study. PLoS One. 2018; 13:e0192677. 10.1371/journal.pone.0192677 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Venancio VP, Kim H, Sirven MA, Tekwe CD, Honvoh G, Talcott ST, Mertens-Talcott SU. Polyphenol-rich mango (mangifera indica L.) ameliorate functional constipation symptoms in humans beyond equivalent amount of fiber. Mol Nutr Food Res. 2018; 62:e1701034. 10.1002/mnfr.201701034 [DOI] [PubMed] [Google Scholar]
  • 27.Cubeddu LX, Aranda J, Singh B, Klein M, Brachfeld J, Freis E, Roman J, Eades T. A comparison of verapamil and propranolol for the initial treatment of hypertension. Racial differences in response. JAMA. 1986; 256:2214–21. [PubMed] [Google Scholar]
  • 28.White WB, Johnson MF, Anders RJ, Elliott WJ, Black HR. Safety of controlled-onset extended-release verapamil in middle-aged and older patients with hypertension and coronary artery disease. Am Heart J. 2001; 142:1010–15. 10.1067/mhj.2001.119127 [DOI] [PubMed] [Google Scholar]
  • 29.Feng L, Cheah IK, Ng MM, Li J, Chan SM, Lim SL, Mahendran R, Kua EH, Halliwell B. The association between mushroom consumption and mild cognitive impairment: a community-based cross-sectional study in Singapore. J Alzheimers Dis. 2019; 68:197–203. 10.3233/JAD-180959 [DOI] [PubMed] [Google Scholar]
  • 30.Deng JH, Huang KY, Hu XX, Huang XW, Tang XY, Wei X, Feng L, Lu GD. Midlife long-hour working and later-life social engagement are associated with reduced risks of mild cognitive impairment among community-living Singapore elderly. J Alzheimers Dis. 2019; 67:1067–77. 10.3233/JAD-180605 [DOI] [PubMed] [Google Scholar]
  • 31.Liew TM, Yu J, Mahendran R, Ng TP, Kua EH, Feng L. Neuropsychiatric and cognitive subtypes among community-dwelling older persons and the association with DSM-5 mild neurocognitive disorder: latent class analysis. J Alzheimers Dis. 2018; 62:675–86. 10.3233/JAD-170947 [DOI] [PubMed] [Google Scholar]
  • 32.Feng L, Chong MS, Lim WS, Ng TP. The modified mini-mental state examination test: normative data for Singapore Chinese older adults and its performance in detecting early cognitive impairment. Singapore Med J. 2012; 53:458–62. [PubMed] [Google Scholar]
  • 33.Petersen RC. Mild cognitive impairment as a diagnostic entity. J Intern Med. 2004; 256:183–94. 10.1111/j.1365-2796.2004.01388.x [DOI] [PubMed] [Google Scholar]
  • 34.Yu J, Mahendran R, Rawtaer I, Kua EH, Feng L. Poor sleep quality is observed in mild cognitive impairment and is largely unrelated to depression and anxiety. Aging Ment Health. 2017; 21:823–28. 10.1080/13607863.2016.1161007 [DOI] [PubMed] [Google Scholar]

Associated Data

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

Supplementary Materials

Supplementary Tables
aging-12-103674-s001..pdf (373.9KB, pdf)

Articles from Aging (Albany NY) are provided here courtesy of Impact Journals, LLC

RESOURCES