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Association between chronic periodontitis and the risk of Alzheimer’s disease: a retrospective, population-based, matched-cohort study

Alzheimer's Research & Therapy20179:56

https://doi.org/10.1186/s13195-017-0282-6

©  The Author(s). 2017

  • Received: 24 April 2017
  • Accepted: 27 June 2017
  • Published:

Abstract

Background

Although recent short-term cross-sectional studies have revealed that chronic periodontitis (CP) may be a risk factor for increased cognitive impairment in patients with Alzheimer’s disease (AD), systematic reviews and long-term longitudinal studies have provided less clear evidence regarding the relationship between CP and AD. Therefore, we conducted a retrospective cohort study using the National Health Insurance Research Database (NHIRD) of Taiwan to determine whether patients with CP are at increased risk of developing AD.

Methods

We conducted a retrospective matched-cohort study using the NHIRD of Taiwan. We identified 9291 patients newly diagnosed with CP between 1997 and 2004. A total of 18,672 patients without CP were matched to the patient cohort according to sex, age, index year, co-morbidity and urbanisation level. Cox proportional hazards regression analyses were performed to evaluate the subsequent risk of AD.

Results

Patients with CP had a higher prevalence of hyperlipidaemia, depression, traumatic brain injury and co-morbidities, as well as higher urbanisation levels, than those in the unexposed cohort (all p < 0.01). At the final follow-up, totals of 115 (1.24%) and 208 (1.11%) individuals in the CP exposed and unexposed groups, respectively, had developed AD. Patients with 10 years of CP exposure exhibited a higher risk of developing AD than unexposed groups (adjusted HR 1.707, 95% CI 1.152–2.528, p = 0.0077).

Conclusions

Our findings demonstrate that 10-year CP exposure was associated with a 1.707-fold increase in the risk of developing AD. These findings highlight the need to prevent progression of periodontal disease and promote healthcare service at the national level.

Keywords

  • Alzheimer’s disease
  • Periodontitis
  • Risk factors
  • Nationwide population
  • Cohort study

Background

Alzheimer’s disease (AD) is a neurodegenerative disease characterised by progressive cognitive decline and memory loss, inevitably leading to complete loss of mental faculties and death [1]. AD is the most common cause of dementia in older adults [2–5]. Furthermore, due to increasing life expectancy and lifestyle changes, recent projections have indicated that 1 in 85 individuals will be diagnosed with AD by 2050 [6].

Recent evidence indicates that peripheral infections, blood vessel damage and oxidative stress may aggravate inflammation in the brain and play an important role in the pathogenesis of dementia and AD [7, 8]. Indeed, previous reports have revealed that diabetes mellitus [9], hypertension [10], hyperlipidaemia [11], chronic kidney disease [12], depression [13], stroke [14], traumatic brain injury [15] and periodontal problems [16, 17] are associated with cognitive impairment. Chronic periodontitis (CP) is a peripheral infectious/inflammatory condition that is among the leading risk factors for tooth loss [18]. CP has been associated with increases in serum levels of C-reactive protein (CRP) [19] and pro-inflammatory cytokines (e.g., tumour necrosis factor-α), as well as decreases in anti-inflammatory markers (e.g., interleukin-10) [20]. Studies have further revealed that CP is linked to numerous inflammatory diseases, including cardiovascular disease [21] and diabetes mellitus [22], as well as to other neurodegenerative disorders, such as Parkinson’s disease [23]. Researchers have speculated that this association is due to the increases in systemic inflammation that accompany the growth of periodontal pathogenic microorganisms. In other mechanism by which CP contributes to AD, systemic inflammation caused by periodontal pathogens may also play a role in vascular disease and endothelial dysfunction. With accumulating studies supporting vascular factors in the development of AD, vascular factors could be a mediator in the development of AD [24–26].

Although recent short-term cross-sectional studies have revealed that CP may be a risk factor for increased cognitive impairment in patients with AD [5, 27], systematic reviews and long-term longitudinal studies have provided less clear evidence regarding the relationship between CP and AD [1, 26, 28]. Therefore, we conducted a retrospective cohort study using the National Health Insurance Research Database (NHIRD) of Taiwan to determine whether patients with CP are at increased risk of developing AD.

Methods

Data sources

Developed in 1995, the National Health Insurance Program provides universal and comprehensive healthcare for approximately 99% of residents in Taiwan [29]. In the present study, we used 1996–2013 data from the NHIRD in Taiwan. One million individuals included in the NHIRD were selected at random, representing about 4.5% of all enrolees [30]. There was no significant difference in age or sex between participants included in the study sample and all NHIRD enrolees. We extracted data regarding demographic characteristics, including encrypted identification numbers, sex, dates of birth and death, and diagnostic information. The diagnostic data included the dates of dental procedures, as well as International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM), diagnostic and procedure codes [31]. Approval for the present study was obtained from the institutional review board (IRB) of Chung Shan Medical University (CS2-15071). The requirement for informed consent was waived by the IRB because all NHIRD data had been de-identified.

Study design and sampled participants

The present retrospective, matched-cohort study included patients aged ≥50 years who had been newly diagnosed with CP (between 1 January 1997 and 31 December 2004) on the basis of ICD-9-CM diagnostic criteria: code 523.4 (CP) [32]. In addition, each enrolled patient had been diagnosed with CP following at least two outpatient clinic visits during the 1-year study period [33]. Exclusion criteria were as follows: (1) unknown age and/or sex, (2) diagnosis of CP prior to 1997 and (3) diagnosis of AD (ICD-9-CM code 331.0) prior to 1997 or prior to the first visit for CP [33]. To ensure the accuracy of our findings, we also excluded patients with unknown vital status and those who had not used health services in the past 12 months, because the NHIRD does not include death records. The sample included a total of 9291 patients with CP and 18,672 patients without CP matched according to sex, age and index years (1:2 ratio).

Both cohorts were followed from the index date until the diagnosis of AD, death or 31 December 2013 (Fig. 1). The covariates included sex and age group (50–59, 60–69 and ≥70 years). According to the definition of urbanisation issued by the National Institutes of Health in Taiwan, all 365 townships in Taiwan are divided into 7 clusters according to the following variables: population density (people per square kilometre), proportion of the population with a college-level education or higher, proportion of individuals over 65 years old, number of agricultural workers, and number of physicians per 100,000 people. In the present study, townships of one or two clusters, three or four clusters, and five to seven clusters were categorised as levels 1, 2 and 3, respectively [34].
Fig. 1
Fig. 1

Flowchart of cohort selection of patients from the National Health Insurance Research Database in Taiwan

We also analysed AD-related co-morbidities, including hypertension (ICD-9-CM codes 401.1, 401.9, 402.10, 402.90, 404.10, 404.90, 405.1 and 405.9) [10], hyperlipidaemia (ICD-9-CM codes 272.0–272.9) [11], chronic kidney disease (ICD-9-CM codes 580, 581–589, 753, 403, 404, 250.4, 274.1, 440.1, 442.1, 447.3, 572.4, 642.1 and 646.2) [12], depression (ICD-9-CM code 311) [13], stroke (ICD-9-CM codes 433, 434 and 436) [14], diabetes mellitus (ICD-9-CM codes 250–250.3, 250.7) [22] and traumatic brain injury (ICD-9-CM codes 800–804, 850–854, 905.0, 950.1, 950.3, 907.0, 959.01, 959.9, 310.2 and V15.52) [15]. The Charlson comorbidity index (CCI), which contains 17 weighted co-morbidities, was also calculated for each participant [35].

Statistical analysis

We used t tests and chi-square tests to compare the demographic and clinical characteristics of patients with CP with those of patients without CP. Univariate and multivariate stratified Cox regression models were then used to calculate HRs and 95% CIs. Multivariable models were adjusted for AD-related co-morbidities, CCI score, and urbanisation level. The Kaplan-Meier method was used to assess the AD survival probability between the exposed and unexposed cohorts. The log-rank test was used to compare differences between these two cohorts.

Sensitivity analysis was performed to identify patients diagnosed with CP ≥1 year following the diagnosis of AD, as well as the incidence of AD occurring ≥10 years following the diagnosis of CP [4]. To ensure the stability and accuracy of the statistical model, we excluded from the sensitivity analysis patients diagnosed with AD <1 and <10 years after the diagnosis of CP [36]. We used a mediation model to identify and explain the other pathways or processes underlying an observed relationship between CP (independent variable) and AD (dependent variable) via the hypothetical mediator of cerebrovascular disease (ICD-9 codes 430–438) [26]. All statistical analyses were performed using SAS version 9.3 (SAS Institute, Cary, NC, USA) and IBM SPSS Statistics version 22 (IBM, Armonk, NY, USA) software. The level of statistical significance was set at p < 0.05.

Results

The baseline characteristics of the study sample are presented in Table 1. Patients with CP had a higher prevalence of hyperlipidaemia, depression and traumatic brain injury, as well as a CCI score and urbanisation level, than the unexposed cohort (all p < 0.01). The mean ages and follow-up times for the exposed and unexposed cohorts were 54.1 ± 10.5 vs. 54.2 ± 10.5 years and 11.9 ± 2.6 vs.12.2 ± 2.6 years, respectively.
Table 1

Demographic characteristics of the study cohort at baseline

Variable

Total

Chronic periodontitis

p value

   

With

Without

 
 

n

%

n

%

n

%

 

Total

27,963

100

9291

100

18,672

100

 

Sex

 Female

13,119

46.92

4351

46.83

8768

46.96

0.8402

 Male

14,844

53.08

4940

53.17

9904

53.04

 

Age, years

 50–59

13,947

49.88

4638

49.92

9309

49.86

0.9705

 60–69

8853

31.66

2945

31.70

5908

31.64

 

 ≥70

5163

18.46

1708

18.38

3455

18.50

 

Hypertension

 No

6654

23.80

2251

24.23

4403

23.58

0.2314

 Yes

21,309

76.20

7040

75.77

14,269

76.42

 

Hyperlipidaemia

 No

21,651

77.43

6935

74.64

14,716

78.81

<0.0001

 Yes

6312

22.57

2356

25.36

3956

21.19

 

Chronic kidney disease

 No

17,243

61.66

5697

61.32

11,546

61.84

0.4009

 Yes

10,720

38.34

3594

38.68

7126

38.16

 

Depression

 No

23,283

83.26

7619

82.00

15,664

83.89

<0.0001

 Yes

4680

16.74

1672

18.00

3008

16.11

 

Stroke

 No

21,316

76.23

7081

76.21

14,235

76.24

0.9652

 Yes

6647

23.77

2210

23.79

4437

23.76

 

Diabetes mellitus

 No

14,545

52.02

4627

49.8

9918

53.12

<0.0001

 Yes

13,418

47.98

4664

50.2

8754

46.88

 

Traumatic brain injury

 No

22,517

80.52

7562

81.39

14,955

80.09

0.0099

 Yes

5446

19.48

1729

18.61

3717

19.91

 

CCI score

 0

17,032

60.91

6423

69.13

10,609

56.82

<0.0001

 1

7826

27.99

2206

23.74

5620

30.10

 

 2

3105

11.10

662

7.13

2443

13.08

 

 ≥3

1685

6.03

499

5.37

1186

6.35

 

Urbanisation level

 1

2896

10.36

890

9.58

2006

10.74

<0.0001

 2

3675

13.14

1219

13.12

2456

13.15

 

 3

19,707

70.48

6683

71.93

13,024

69.75

 

CCI Charlson comorbidity index

Totals of 115 (1.24%) and 208 (1.11%) patients were diagnosed with AD in the exposed and unexposed cohorts, respectively (Fig. 1). Table 2 shows the Cox regression analysis of risk factors associated with the development of AD. Although patients with CP exhibited higher crude HRs (1.301, 95% CI 1.012–1.673, p = 0.0404) for the development of AD than those without CP, the adjusted HR was 1.297, indicating a lack of statistical significance (95% CI 0.995–1.692, p = 0.0547) (Table 2). Patients with depression, stroke and traumatic brain injury tended to have a higher risk for the development of AD (all p < 0.05). Moreover, the risk of AD was lower in patients with urbanisation level 2 and level 3 (both p < 0.05). Figure 2 depicts the Kaplan-Meier curve for the cumulative risk of AD in the exposed and unexposed groups. A significant difference was observed between the two groups once 10 years of CP exposure had been reached (p = 0.0264 by log-rank test).
Table 2

Covariates associated with Alzheimer’s disease at end of follow-up with univariate, multivariable and sensitivity analysis of Cox regression analysis

Variable

Univariate analysis

Multivariable analysis

 

Crude HR

95% CI

p value

Adjusted HR

95% CI

p value

1-year exclusion in a diagnosis of AD

      

 Chronic periodontitis

      

  Without

Reference

  

Reference

  

  With

1.301

1.012–1.673

0.0404

1.297

0.995–1.692

0.0547

10-year exclusion in a diagnosis of AD

      

 Chronic periodontitis

      

  Without

Reference

  

Reference

  

  With

1.364

1.079–1.725

0.0095

1.707

1.152–2.528

0.0077

AD Alzheimer’s disease

The multivariable analyses were adjusted for hypertension, hyperlipidaemia, chronic kidney disease, depression, stroke, traumatic brain injury, diabetes mellitus, Charlson comorbidity index score, urbanisation level

Fig. 2
Fig. 2

Kaplan-Meier model based on the Cox-regression analysis with the log-rank test for the cumulative risk of Alzheimer’s disease among the exposed and unexposed cohorts

The results of the sensitivity analysis are presented in Table 2. We performed sensitivity analysis after excluding patients diagnosed with AD <1 year and <10 years after the diagnosis of CP. The association between CP and AD was significant after 10 years of CP exposure (adjusted HR 1.707, p = 0.0077). In statistics, a mediation model explains and underlies an observed relationship between an independent variable (IV) and dependent variable (DV) via the inclusion of a mediator (M). They have significance of a mediation model (IV → M, p < 0.001, 95% CI 3.292–3.763; M → DV, p = 0.0118, 95% CI 1.121–2.506; and IV → D, p = 0.0077, 95% CI 1.152–2.528). This result shows that cerebrovascular disease is a partial mediator between CP and AD. CP can also cause AD directly.

Discussion

The present study is the first nationwide population-based matched-cohort study to demonstrate that patients with 10-year CP exposure exhibit an increased risk of developing AD (adjusted HR 1.707), regardless of co-morbidities, CCI score or urbanisation level. The prevalence of AD significantly increases with age, although AD in general is more common in women than in men [3]. AD is characterised by salient inflammatory features, microglial activation and increased levels of pro-inflammatory cytokines, which contribute to the inflammatory status of the central nervous system [37]. As a low-grade systemic disease, CP may involve the slow release of pro-inflammatory cytokines and CRP into the systemic circulation. This low-grade inflammation is thought to impact general systemic health and exacerbate other systemic disorders [38]. Therefore, CP may be a significant source of covert peripheral inflammation within the general population. Periodontitis has a tendency to infiltrate the systemic circulation with inflammatory mediators, thereby resulting in systemic disease. Researchers have proposed that periodontitis can lead to progression of AD by further increasing levels of pro-inflammatory cytokines and can lead to the invasion of micro-organisms from the dental plaque biofilm into the brain [28]. Moreover, these pro-inflammatory cytokines may penetrate the blood-brain barrier and induce neurodegenerative changes that ultimately influence the development of AD [26]. In the present study, we observed a significant correlation between CP and AD only after the 10-year follow-up for the initial diagnosis of CP. This finding supports the notion that pro-inflammatory factors due to CP may slowly and progressively induce neurodegenerative changes that lead to the development of AD. However, further study is required to verify this hypothesis.

In previous small and/or short-term cross-sectional studies, the authors examined only the associations between periodontal inflammation and AD [5, 27], without investigating the potential cause-and-effect relationship between the two. However, in a previous study, researchers reported that periodontitis is associated with an increased risk of developing dementia [33]. Moreover, a 10-year clinical observational study conducted by Tzeng et al. revealed that patients with at least 8 years of periodontal problems exhibited a significantly higher risk of developing dementia and neurodegenerative diseases than healthy unexposed groups [4]. Despite these crucial findings, neither of the aforementioned studies identified the role of periodontitis in AD development. The present population-based study is the first to demonstrate a significantly increased risk of AD after 10-year CP exposure. Our findings support the notion that infectious diseases associated with low-grade inflammation, such as CP, may play a substantial role in the pathogenesis of AD [39]. In mediation analysis, the role of cerebrovascular disease is as a partial mediator, and CP can also cause AD directly. Systemic inflammation caused by periodontal pathogens, such as Porphyromonas gingivalis and Streptococcus sanguinis, may be a factor in endothelial dysfunction and vascular disease [26]. The mediator model facilitates a better understanding of the relationship between CP and AD. However, it needs more relevant and further investigation to confirm and clarify the pathway.

Co-morbidities including depression, stroke and traumatic brain injury were directly associated with the risk of developing AD in the present study, in accordance with the findings of previous studies. Burke et al. reported that depression was associated with AD in a group of participants who were initially cognitively asymptomatic [13], whereas additional studies have revealed a significant association between stroke/brain damage and dementia [14, 15]. Our findings also indicate that urbanisation level 1 was a significant risk factor for AD. This finding may be explained by differences between urban and rural lifestyles, availability of medical resources and convenience of medical access [3, 40]. Patients with AD also exhibit impairments in chewing function due to progressive neurodegeneration, increasing the risk of periodontal problems [41, 42]. Hence, proper dental care and oral rehabilitation are necessary to improve masticatory function in this patient population.

The present study possesses several advantages over previous work. Firstly, we used a nationwide database, which allowed us to examine a large sample of patients over a 16-year follow-up period. Secondly, because the Taiwanese NHIRD provides continued coverage for the whole population of Taiwan and randomises recruits, in the present study, we were able to minimise the influence of bias associated with data collection, region and institution. Thirdly, the use of the NHIRD eliminated the need to minimise patients in the cohort who were lost to follow-up and enabled us to obtain large, geographically dispersed samples of patients with varying socio-demographic characteristics [34]. Lastly, we defined AD using strict criteria (ICD-9-CM code 331.0) to ensure the accuracy of our statistical analysis.

However, the present study also possesses some limitations of note. Firstly, we could not clarify the medical records of all missing recruited CP and AD subjects, because all the medical records from the NHIRD were de-identified due to ethical considerations. It is possible that the incidence of CP or AD was underestimated in our study because patients who had not received medical records during the study period were excluded. Although this would result in fewer patients with less severe forms of CP or AD in our sample, the exposed-unexposed matched design would also diminish this bias. Secondly, the nationwide database used in the present study did not allow us to obtain data regarding the severity of AD. Furthermore, AD and dementia may overlap in this study because we were not able to clarify the medical records of all defined AD, owing to all the medical records from the NHIRD being de-identified due to ethical considerations. Thirdly, the broad age categories are important variable indexes. However, because of this limitation, there may be residual confounding by age [4]. Finally, in detailed demography concerning smoking habits, the NHIRD did not provide personal information regarding certain and definite variables relevant to our research [43]. Moreover, although education is an important variable index of AD, the education level of individuals in the NHIRD is not available. Further research is needed to explain the complex relationship between urbanisation and education.

Conclusions

Our findings demonstrate that 10-year CP exposure was associated with a 1.707-fold increase in the risk of developing AD. These findings highlight the need to prevent progression of periodontal disease and promote healthcare services at the national level.

Abbreviations

AD: 

Alzheimer’s disease

CCI: 

Charlson co-morbidity index

CP: 

Chronic periodontitis

CRP: 

C-reactive protein

ICD-9-CM: 

International Classification of Diseases, Ninth Revision, Clinical Modification

IRB: 

Institutional review board

NHIRD: 

National Health Insurance Research Database

Declarations

Acknowledgements

The authors thank Dr. Jing-Yang Huang, who participated in the design of the research and data interpretation, and they appreciate Yun-Ju Tsai, Li-Heng Chen and Li-Xin Chen for their help in paper collection.

Funding

Not applicable.

Availability of data and materials

Not applicable.

Authors’ contributions

CKC and YCC conceived of and designed the study. CKC provided administrative support. CKC, YTW and YCC collected and organised data. CKC and YTW analysed and interpreted the data. All authors wrote the manuscript, and all authors read and approved the final manuscript.

Ethics approval and consent to participate

Approval for the present study was obtained from the institutional review board (IRB) of Chung Shan Medical University (CS2-15071). The requirement for informed consent was waived by the IRB because all NHIRD data had been de-identified.

Consent for publication

All authors approved the manuscript for submission.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
School of Dentistry, Chung Shan Medical University, No. 110, Section 1, Jianguo N. Road, Taichung City, 40201, Taiwan
(2)
Section of Dentistry, Zuoying Branch of Kaohsiung Armed Forces General Hospital, Kaohsiung, Taiwan
(3)
Department of Physical Medicine and Rehabilitation, Tri-Service General Hospital, School of Medicine, National Defence Medical Centre, Taipei, Taiwan
(4)
Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan

References

  1. Gaur S, Agnihotri R. Alzheimer’s disease and chronic periodontitis: is there an association? Geriatr Gerontol Int. 2015;15:391–404.View ArticlePubMedGoogle Scholar
  2. Lin RT, Lai CL, Tai CT, Liu CK, Yen YY, Howng SL. Prevalence and subtypes of dementia in southern Taiwan: impact of age, sex, education, and urbanization. J Neurol Sci. 1998;160:67–75.View ArticlePubMedGoogle Scholar
  3. Peng D, Shi Z, Xu J, Shen L, Xiao S, Zhang N, et al. Demographic and clinical characteristics related to cognitive decline in Alzheimer disease in China: a multicenter survey from 2011 to 2014. Medicine (Baltimore). 2016;95:e3727.Google Scholar
  4. Tzeng NS, Chung CH, Yeh CB, Huang RY, Yuh DY, Huang SY, et al. Are chronic periodontitis and gingivitis associated with dementia? A nationwide, retrospective, matched-cohort study in Taiwan. Neuroepidemiology. 2016;47:82–93.View ArticlePubMedGoogle Scholar
  5. Martande SS, Pradeep AR, Singh SP, Kumari M, Suke DK, Raju AP, et al. Periodontal health condition in patients with Alzheimer’s disease. Am J Alzheimers Dis Other Demen. 2014;29:498–502.View ArticlePubMedGoogle Scholar
  6. Brookmeyer R, Johnson E, Ziegler-Graham K, Arrighi HM. Forecasting the global burden of Alzheimer’s disease. Alzheimers Dement. 2007;3:186–91.View ArticlePubMedGoogle Scholar
  7. Marchesi VT. Alzheimer’s dementia begins as a disease of small blood vessels, damaged by oxidative-induced inflammation and dysregulated amyloid metabolism: implications for early detection and therapy. FASEB J. 2011;25:5–13.View ArticlePubMedGoogle Scholar
  8. Tonsekar PP, Jiang SS, Yue G. Periodontal disease, tooth loss and dementia: is there a link? A systematic review. Gerodontology. 2017;34:151–63.View ArticlePubMedGoogle Scholar
  9. Huang CC, Chung CM, Leu HB, Lin LY, Chiu CC, Hsu CY, et al. Diabetes mellitus and the risk of Alzheimer’s disease: a nationwide population-based study. PLoS One. 2014;9, e87095.View ArticlePubMedPubMed CentralGoogle Scholar
  10. Moreno Cervantes C, Mimenza Alvarado A, Aguilar Navarro S, Alvarado Ávila P, Gutiérrez Gutiérrez L, Juárez Arellano S, et al. Factors associated with mixed dementia vs Alzheimer disease in elderly Mexican adults. Neurologia. 2017;32:309–15.View ArticlePubMedGoogle Scholar
  11. Vanhanen M, Koivisto K, Moilanen L, Helkala EL, Hanninen T, Soininen H, et al. Association of metabolic syndrome with Alzheimer disease: a population-based study. Neurology. 2006;67:843–7.View ArticlePubMedGoogle Scholar
  12. Helmer C, Stengel B, Metzger M, Froissart M, Massy ZA, Tzourio C, et al. Chronic kidney disease, cognitive decline, and incident dementia: the 3C Study. Neurology. 2011;77:2043–51.View ArticlePubMedGoogle Scholar
  13. Burke SL, Maramaldi P, Cadet T, Kukull W. Associations between depression, sleep disturbance, and apolipoprotein E in the development of Alzheimer’s disease: dementia. Int Psychogeriatr. 2016;28:1409–24.View ArticlePubMedGoogle Scholar
  14. Huang CY, Li YC, Wang HK, Sung PS, Wang LC, Sun YT, et al. Stroke suggests increased risk of dementia. Curr Alzheimer Res. 2015;12:287–95.View ArticlePubMedGoogle Scholar
  15. Wang HK, Lin SH, Sung PS, Wu MH, Hung KW, Wang LC, et al. Population based study on patients with traumatic brain injury suggests increased risk of dementia. J Neurol Neurosurg Psychiatry. 2012;83:1080–5.View ArticlePubMedGoogle Scholar
  16. Kamer AR, Craig RG, Dasanayake AP, Brys M, Glodzik-Sobanska L, de Leon MJ. Inflammation and Alzheimer’s disease: possible role of periodontal diseases. Alzheimers Dement. 2008;4:242–50.View ArticlePubMedGoogle Scholar
  17. Watts A, Crimmins EM, Gatz M. Inflammation as a potential mediator for the association between periodontal disease and Alzheimer’s disease. Neuropsychiatr Dis Treat. 2008;4:865–76.View ArticlePubMedPubMed CentralGoogle Scholar
  18. Al-Shammari KF, Al-Khabbaz AK, Al-Ansari JM, Neiva R, Wang HL. Risk indicators for tooth loss due to periodontal disease. J Periodontol. 2005;76:1910–8.View ArticlePubMedGoogle Scholar
  19. Paraskevas S, Huizinga JD, Loos BG. A systematic review and meta-analyses on C-reactive protein in relation to periodontitis. J Clin Periodontol. 2008;35:277–90.View ArticlePubMedGoogle Scholar
  20. Passoja A, Puijola I, Knuuttila M, Niemelä O, Karttunen R, Raunio T, et al. Serum levels of interleukin-10 and tumour necrosis factor-α in chronic periodontitis. J Clin Periodontol. 2010;37:881–7.View ArticlePubMedGoogle Scholar
  21. Teles R, Wang CY. Mechanisms involved in the association between periodontal diseases and cardiovascular disease. Oral Dis. 2011;17:450–61.View ArticlePubMedPubMed CentralGoogle Scholar
  22. Lakschevitz F, Aboodi G, Tenenbaum H, Glogauer M. Diabetes and periodontal diseases: interplay and links. Curr Diabetes Rev. 2011;7:433–9.View ArticlePubMedGoogle Scholar
  23. Liu TC, Sheu JJ, Lin HC, Jensen DA. Increased risk of parkinsonism following chronic periodontitis: a retrospective cohort study. Mov Disord. 2013;28:1307–8.View ArticlePubMedGoogle Scholar
  24. Roher AE, Esh C, Kokjohn TA, Kalback W, Luehrs DC, Seward JD, et al. Circle of Willis atherosclerosis is a risk factor for sporadic Alzheimer’s disease. Arterioscler Thromb Vasc Biol. 2003;23:2055–62.View ArticlePubMedGoogle Scholar
  25. Honig LS, Kukull W, Mayeux R. Atherosclerosis and AD: analysis of data from the US National Alzheimer’s Coordinating Center. Neurology. 2005;64:494–500.View ArticlePubMedGoogle Scholar
  26. Uppoor AS, Lohi HS, Nayak D. Periodontitis and Alzheimer’s disease: oral systemic link still on the rise? Gerodontology. 2013;30:239–42.View ArticlePubMedGoogle Scholar
  27. Ide M, Harris M, Stevens A, Sussams R, Hopkins V, Culliford D, et al. Periodontitis and cognitive decline in Alzheimer’s disease. PLoS One. 2016;11, e0151081.View ArticlePubMedPubMed CentralGoogle Scholar
  28. Abbayya K, Puthanakar NY, Naduwinmani S, Chidambar YS. Association between periodontitis and Alzheimer’s disease. N Am J Med Sci. 2015;7:241–6.View ArticlePubMedPubMed CentralGoogle Scholar
  29. Ho Chan WS. Taiwan’s healthcare report 2010. EPMA J. 2010;1:563–85.View ArticlePubMedPubMed CentralGoogle Scholar
  30. Hsu CC, Wahlqvist ML, Lee MS, Tsai HN. Incidence of dementia is increased in type 2 diabetes and reduced by the use of sulfonylureas and metformin. J Alzheimers Dis. 2011;24:485–93.PubMedGoogle Scholar
  31. Romano PS, Roos LL, Jollis JG. Adapting a clinical comorbidity index for use with ICD-9-CM administrative data: differing perspectives. J Clin Epidemiol. 1993;46:1075–9. discussion 1081–90.View ArticlePubMedGoogle Scholar
  32. Gil-Montoya JA, Sanchez-Lara I, Carnero-Pardo C, Fornieles F, Montes J, Vilchez R, et al. Is periodontitis a risk factor for cognitive impairment and dementia? A case-control study. J Periodontol. 2015;86:244–53.View ArticlePubMedGoogle Scholar
  33. Lee YT, Lee HC, Hu CJ, Huang LK, Chao SP, Lin CP, et al. Periodontitis as a modifiable risk factor for dementia: a nationwide population-based cohort study. J Am Geriatr Soc. 2017;65:301–5.View ArticlePubMedGoogle Scholar
  34. Liu CY, Hung YT, Chuang YL, Chen YJ, Weng WS, Liu JS, et al. Incorporating development stratification of Taiwan townships into sampling design of large scale health interview survey. J Health Manag (China). 2006;4:1–22.Google Scholar
  35. Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40:373–83.View ArticlePubMedGoogle Scholar
  36. Wong CS, Lin YC, Hong LY, Chen TT, Ma HP, Hsu YH, et al. Increased long-term risk of dementia in patients with carbon monoxide poisoning: a population-based study. Medicine (Baltimore). 2016;95:e2549.Google Scholar
  37. McGeer PL, McGeer EG. Inflammation, autotoxicity and Alzheimer disease. Neurobiol Aging. 2001;22:799–809.View ArticlePubMedGoogle Scholar
  38. D’Aiuto F, Graziani F, Tete S, Gabriele M, Tonetti MS. Periodontitis: from local infection to systemic diseases. Int J Immunopathol Pharmacol. 2005;18(3 Suppl):1–11.PubMedGoogle Scholar
  39. Yan Q, Zhang J, Liu H, Babu-Khan S, Vassar R, Biere AL, et al. Anti-inflammatory drug therapy alters β-amyloid processing and deposition in an animal model of Alzheimer’s disease. J Neurosci. 2003;23:7504–9.PubMedGoogle Scholar
  40. Llibre Rodriguez JJ, Ferri CP, Acosta D, Guerra M, Huang Y, Jacob KS, et al. Prevalence of dementia in Latin America, India, and China: a population-based cross-sectional survey. Lancet. 2008;372:464–74.View ArticlePubMedGoogle Scholar
  41. Campos CH, Ribeiro GR, Costa JL, Rodrigues Garcia RC. Correlation of cognitive and masticatory function in Alzheimer’s disease. Clin Oral Investig. 2017;21:573–8.View ArticlePubMedGoogle Scholar
  42. Campos CH, Ribeiro GR, Stella F, Rodrigues Garcia RC. Mandibular movements and bite force in Alzheimer’s disease before and after new denture insertion. J Oral Rehabil. 2017;44:178–86.View ArticlePubMedGoogle Scholar
  43. Wen BW, Tsai CS, Lin CL, Chang YJ, Lee CF, Hsu CH, et al. Cancer risk among gingivitis and periodontitis patients: a nationwide cohort study. QJM. 2014;107:283–90.View ArticlePubMedGoogle Scholar

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Alzheimer's Research & Therapy

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