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Neurology Research International
Volume 2014, Article ID 423602, 4 pages
http://dx.doi.org/10.1155/2014/423602
Research Article

Past Cigarette Smoking Is More Common among Those with Cholinergic Than Noncholinergic Dementias

1Pitzer College, Claremont, CA 91711, USA
2Neurology Division, Los Angeles Biomedical Research Institute, Torrance, CA 90502, USA
3Neurology Department, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-6975, USA
4Neurology Department, Harbor-UCLA Medical Center, Building N-25, 1000 West Carson Street, Torrance, CA 90509, USA
5Neurology Department, Straub Hospital and Clinics, Honolulu, HI 96813, USA
6Neurology Division, Department of Medicine, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA

Received 19 September 2014; Revised 24 November 2014; Accepted 25 November 2014; Published 10 December 2014

Academic Editor: Herbert Brok

Copyright © 2014 Kyle Dalrymple et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background. Patients with progressive dementing disorders associated with cortical cholinergic dysfunction gradually develop cholinergic deficits many years before symptom onset and may begin to smoke cigarettes during midlife as a form of self-medication. The aim of this study was to compare self-reported past smoking rates between those with and without cholinergic dementias, to determine if those who developed cholinergic dementias were more likely to smoke during midlife than those who did not. Methods. Retrospective cross-sectional study of past smoking status among patients treated at an outpatient clinic during a three-year period. Results. A total of 440 patients were evaluated during the study period, including 224 with cholinergic dementias and 216 with noncholinergic dementias and controls. Past smoking rates were greater among those with cholinergic dementias compared to those without cholinergic dementias (43.92% versus 26.96%, ). Additionally, smokers with cholinergic dementias reported significantly greater mean pack-years of smoking (). Conclusions. Greater midlife smoking rates and greater pack-years of smoking were associated with cholinergic dementias. These results suggest midlife smoking may be an early indicator for those developing brain cholinergic deficits related to progressive dementing disorders and support initiating treatment prior to symptom onset in cholinergic dementias.

1. Introduction

Cholinergic dementias, those associated with progressive degeneration of cortical cholinergic neurons such as Alzheimer’s disease (AD), dementia in Parkinson’s disease (PDD) vascular dementia, and Lewy body dementia (LBD), show symptoms of cognitive decline related to gradually decreasing levels of brain acetylcholine (ACh) [1, 2]. The cortical cholinergic deficit is especially notable in LBD, which may display the largest relative deficit of cortical cholinergic function out of these disorders [3, 4]. In LBD and other cholinergic dementias, there is an inverse relationship between cortical cholinergic function and disease symptoms, with reduced cortical cholinergic function correlating with worsening cognitive deficits and other symptoms [5]. As cortical ACh levels decrease, there is downregulation of postsynaptic AchRs, resulting in further reduction of cortical ACh levels through decreased reuptake and consequently further worsening of cholinergic system functioning [6, 7].

Cholinesterase inhibitor therapy has long been used in patients with cholinergic dementias as a means of providing symptomatic relief. However, treatment with cholinesterase inhibitors does not prevent neuronal loss and has not demonstrated any disease modifying effect. It is possible that in order for treatment of these disorders to be effective and change the course of the disease it must be started much earlier, before symptomatic onset and before substantial neuronal degeneration has occurred. However, while there have been recent advances with brain amyloid neuroimaging and other potential biomarkers for dementias, there is currently no consensus regarding how to identify potentially at-risk individuals while still young and healthy or the ages at which cortical cholinergic deficits typically begin to occur in these disorders. Consequently, the optimal ages to begin interventions for these disorders are not yet known.

Nicotine has been shown to bind and exert its action at nicotinic AChRs (nAChR) in the brain and is considered a nonselective AChR agonist. Studies have correlated nAChR dysfunction with the neurodegeneration and cognitive deficits of Alzheimer’s disease [8]. Functional neuroimaging studies have shown that cigarette smoking results in occupancy and upregulation of nAChR in the human brain [9, 10]. Chronic nicotine treatment has shown protection from nAChR synaptic impairments believed to be induced by A oligomers in rat models of Alzheimer’s disease and prevention of impaired learning and short-term memory [11]. Consequently, nicotine obtained from cigarette smoking may be regarded as a form of unknowingly attempted self-medication when used by those developing cholinergic dementias.

Our study was designed to investigate the potential relationship between a history of past cigarette smoking and clinical dementia diagnosis. We hypothesized that those with cholinergic dementias would report greater past smoking rates compared to those with noncholinergic dementias and normal controls. A greater frequency of past cigarette smoking among those with cholinergic dementias compared to those with noncholinergic dementias would add support to the contention that the cortical cholinergic deficit in cholinergic dementias begins many years earlier in life and also add support for earlier intervention before symptom onset.

2. Materials and Methods

2.1. Participants

This study was determined to be exempt by the local institutional review board since it consisted of a retrospective review of deidentified clinical data. Participants were all adults, over the age of 18 years, who presented sequentially to a community based outpatient neurology subspecialty clinic during a three-year period from January 1, 2010, to December 31, 2013, for evaluation and treatment of cognitive problems, dementia, or Parkinson’s disease. All participants underwent a history and physical examination by a board certified neurologist and dementia diagnoses were determined through retrospective analysis of chart notes according to standard clinical diagnostic criteria.

2.2. Determination of Cholinergic and Noncholinergic Dementias

For the purposes of this study participants were divided into two groups based on their clinical diagnosis, one for cholinergic dementia present and one for cholinergic dementia absent. The group of participants with cholinergic dementia present included those with diagnoses in which a deficit of brain acetylcholine levels has previously been established as part of the underlying neurochemistry of the disorder, such as Alzheimer’s disease, dementia in Parkinson’s disease, vascular dementia, and Lewy body dementia [1, 2, 4, 12, 13]. The group with cholinergic dementia absent included diagnoses in which brain cholinergic deficits are not considered a prominent feature of the neurochemistry, such as frontotemporal dementia, Parkinson’s disease without dementia, and cognitively normal controls [12].

2.3. Determination of Past Smoking Status

A positive history of past cigarette smoking was determined by retrospective chart review of physician outpatient clinic notes. A positive past cigarette smoking status was determined to be present if the patient, caregiver, or family reported the patient smoked cigarettes on a regular basis earlier in life. Pack-year quantifications of past cigarette smoking were recorded when documented in the chart notes.

2.4. Statistical Analysis

Participants were divided into two groups for statistical analysis: (1) those with cholinergic dementias and (2) those without cholinergic dementias including those with noncholinergic dementias and cognitively normal controls. Mean values for continuous demographic factors and other continuous variables, including pack-years of smoking, were compared between groups using two-tailed -tests. Nonparametric data, including positive or negative past smoking status, were compared between groups using the chi-square test. All statistical calculations were performed using SPSS version 22.

3. Results

A total of 440 patients were evaluated during the study period. One hundred and thirty-six of these patients were excluded from the study because a reliable past smoking history, either positive or negative, was not documented in the chart notes. Past smoking histories were able to be obtained on 304 patients, including 140 with Alzheimer’s disease, 16 with dementia with Lewy bodies, 4 with vascular dementia, 21 with frontotemporal dementia, and 29 with dementia in Parkinson’s disease, as well as 75 patients with Parkinson’s disease without dementia and 19 cognitively normal individuals who presented with memory complaints. Additional information quantifying past smoking amount in pack-years was able to be obtained from 50 of the 114 smokers (43.86%), including 45 of the 83 smokers with cholinergic dementias (54.22%) and 5 of the 25 smokers with noncholinergic dementias and controls (20.00%).

Subjects with cholinergic dementias were significantly older and had a greater mean age of onset compared to those without cholinergic dementias (see Table 1). Those with and without cholinergic dementias did not differ significantly for gender distribution (48.15% and 40.00% female, resp.; see Table 1). A positive history of past cigarette smoking was significantly greater among those with cholinergic dementias compared to those without cholinergic dementias (43.92% versus 26.96%, resp.; ; see Table 1). Mean pack-years of cigarette smoking were also significantly greater among those with cholinergic dementias compared to those without cholinergic dementias for those participants who had this data recorded in the chart notes (; see Table 1).

Table 1: Comparison of demographic and past smoking history information between those with and without cholinergic dementias.

4. Discussion

In this study, we identified an association between presence of cholinergic dementias and a positive history of cigarette smoking, as well as significantly greater pack-years of cigarette smoking among smokers with cholinergic dementias compared to smokers with noncholinergic dementias and normal controls. Because cortical cholinergic deficits are theorized to develop very gradually over several decades prior to symptom onset in these disorders, it is possible that the greater frequency and pack-year history of smoking may indicate a form of unknowingly attempted self-medication used by these patients to treat symptoms from gradually developing brain cholinergic deficits. These findings also suggest that elderly individuals with a positive smoking history who start developing cognitive impairment may be at relatively higher risk for developing cholinergic rather than noncholinergic dementias, although further prospective study in elderly individuals would be needed to determine any predictive value associated with this finding.

The relationship between cigarette smoking, AD, and dementia in general is complicated. In some groups, specifically those with the APOE4 allele, it has been found that smokers have an increased risk for developing dementia and AD [14]. Other reports of studies in the general population have also supported cigarette smoking as an important risk factor for both dementia and AD [15]. Among those with early signs of AD, smokers are known to have greater rates of brain atrophy than nonsmokers, for both generalized atrophy and specifically atrophy of areas related to development of AD such as the hippocampus [16]. However, high levels of lifetime smoking (>50 pack-years) are reported to have an inverse relationship with other degenerative dementias and are associated with a reduced risk for development of LBD and PD [17]. With Parkinson’s disease, the inverse relationship is dose dependent and those with the greatest pack-year histories are the least likely to develop these disorders [18].

This study has several limitations. First, the decision to study an outpatient population rather than an inpatient population may have introduced a selection bias, since smoking is a risk factor for nursing home placement [19]. Additionally, because past smoking status and pack-year histories were determined by retrospective chart review of already existing notes, it is possible that smoking histories were actually underreported. Others have shown that smoking histories are frequently underestimated when assessed from patient chart notes, and it is possible that another mechanism for obtaining smoking histories such as an anonymous questionnaire may have provided a more accurate assessment [20]. Also, we were unable to determine the smoking history for many of the patients seen in the clinic because it simply was not documented in the chart notes, raising the possibility of a reporting bias. However, all three of these potential biases would be expected to have affected both groups equally, so we feel that overall the results are relatively reliable. Further study of other community and research center populations using anonymous questionnaires to determine smoking histories would be warranted.

5. Conclusions

The results of this study suggest that patients with cholinergic dementias may have greater past cigarette smoking rates than those with noncholinergic dementias and controls. It is possible that the nicotine in cigarettes may act as a form of self-medication for people who are gradually developing a cortical cholinergic deficit. Additional research focusing on the role of nicotinic AchRs in the development and progression of Alzheimer’s disease and other cholinergic dementias is indicated. Additionally, future research to identify nicotinic AchR mediated treatments may help to reduce the severity of symptoms patients face as cholinergic dementias progress and may even have the potential for disease modifying effects.

Conflict of Interests

The authors declare they have no conflict of interests regarding publication of this paper.

References

  1. J. Corey-Bloom, “The ABC of Alzheimer's disease: cognitive changes and their management in Alzheimer's disease and related dementias,” International Psychogeriatrics, vol. 14, supplement 1, pp. 51–75, 2002. View at Publisher · View at Google Scholar · View at Scopus
  2. E. K. Perry, B. E. Tomlinson, G. Blessed, K. Bergmann, P. H. Gibson, and R. H. Perry, “Correlation of cholinergic abnormalities with senile plaques and mental test scores in senile dementia,” British Medical Journal, vol. 2, no. 6150, pp. 1457–1459, 1978. View at Publisher · View at Google Scholar · View at Scopus
  3. I. McKeith and J. O'Brien, “Dementia with Lewy bodies,” The Australian and New Zealand Journal of Psychiatry, vol. 33, no. 6, pp. 800–808, 1999. View at Publisher · View at Google Scholar · View at Scopus
  4. P. Tiraboschi, L. A. Hansen, M. Alford et al., “Cholinergic dysfunction in diseases with LEWY bodies,” Neurology, vol. 54, no. 2, pp. 407–411, 2000. View at Publisher · View at Google Scholar · View at Scopus
  5. I. G. McKeith, J. B. Grace, Z. Walker, E. J. Byrne, and D. Wilkinson, “Rivastigmine in the treatment of dementia with Lewy bodies: preliminary findings from an open trial,” International Journal of Geriatric Psychiatry, vol. 15, no. 5, pp. 387–392, 2000. View at Google Scholar
  6. D. D. Flynn, G. Ferrari-DiLeo, D. C. Mash, and A. I. Levey, “Differential regulation of molecular subtypes of muscarinic receptors in Alzheimer's disease,” Journal of Neurochemistry, vol. 64, no. 4, pp. 1888–1891, 1995. View at Google Scholar · View at Scopus
  7. Z.-Z. Guan, X. Zhang, R. Ravid, and A. Nordberg, “Decreased protein levels of nicotinic receptor subunits in the hippocampus and temporal cortex of patients with Alzheimer's disease,” Journal of Neurochemistry, vol. 74, no. 1, pp. 237–243, 2000. View at Publisher · View at Google Scholar · View at Scopus
  8. A. L. Brody, M. A. Mandelkern, E. D. London et al., “Cigarette smoking saturates brain α4β2 nicotinic acetylcholine receptors,” Archives of General Psychiatry, vol. 63, no. 8, pp. 907–915, 2006. View at Publisher · View at Google Scholar · View at Scopus
  9. R. Nashmi, M. E. Dickenson, S. McKinney et al., “Assembly of alpha-4beta2 nicotinic acetylcholine receptors assessed with functional fluorescently labeled subunits: effects of localization, trafficking and nicotine-induced upregulation in clonal mammalian cells in cultered midbrain neurons,” The Journal of Neuroscience, vol. 23, no. 37, pp. 11554–11567, 2003. View at Google Scholar
  10. J. K. Staley, S. Krishnan-Sarin, K. P. Cosgrove et al., “Human tobacco smokers in early abstinence have higher levels of β2* nicotinic acetylcholine receptors than nonsmokers,” The Journal of Neuroscience, vol. 26, no. 34, pp. 8707–8714, 2006. View at Publisher · View at Google Scholar · View at Scopus
  11. M. Srivareerat, T. T. Tran, S. Salim, A. M. Aleisa, and K. A. Alkadhi, “Chronic nicotine restores normal Aβ levels and prevents short-term memory and E-LTP impairment in Aβ rat model of Alzheimer's disease,” Neurobiology of Aging, vol. 32, no. 5, pp. 834–844, 2011. View at Publisher · View at Google Scholar · View at Scopus
  12. A. Kadir and A. Nordberg, “Target-specific PET probes for neurodegenerative disorders related to dementia,” Journal of Nuclear Medicine, vol. 51, no. 9, pp. 1418–1430, 2010. View at Publisher · View at Google Scholar · View at Scopus
  13. J. Wang, H. Y. Zhang, and X. C. Tang, “Cholinergic deficiency involved in vascular dementia: possible mechanism and strategy of treatment,” Acta Pharmacologica Sinica, vol. 30, no. 7, pp. 879–888, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. A. Ott, A. J. C. Slooter, A. Hofman et al., “Smoking and risk of dementia and Alzheimer's disease in a population-based cohort study: the Rotterdam Study,” The Lancet, vol. 351, no. 9119, pp. 1840–1843, 1998. View at Publisher · View at Google Scholar · View at Scopus
  15. Y. Ho, X. Yang, S. Yeung et al., “Cigarette smoking accelerated brain aging and induced pre-alzheimer-like neuropathology in rats,” PLoS ONE, vol. 7, no. 5, Article ID e36752, 2012. View at Publisher · View at Google Scholar
  16. T. C. Durazzo, P. S. Insel, and M. W. Weiner, “Greater regional brain atrophy rate in healthy elderly subjects with a history of cigarette smoking,” Alzheimer's & Dementia, vol. 8, no. 6, pp. 513–519, 2012. View at Publisher · View at Google Scholar · View at Scopus
  17. J. M. Gorell, B. A. Rybicki, C. C. Johnson, and E. L. Peterson, “Smoking and Parkinson's disease: a dose-response relationship,” Neurology, vol. 52, no. 1, pp. 116–119, 1999. View at Publisher · View at Google Scholar · View at Scopus
  18. M. A. Hernán, S. M. Zhang, A. M. Rueda-DeCastro, G. A. Colditz, F. E. Speizer, and A. Ascherio, “Cigarette smoking and the incidence of Parkinson's disease in two prospective studies,” Annals of Neurology, vol. 50, no. 6, pp. 780–786, 2001. View at Publisher · View at Google Scholar · View at Scopus
  19. J. J. Wang, P. Mitchell, W. Smith, R. G. Cumming, and S. R. Leeder, “Incidence of nursing home placement in a defined community,” Medical Journal of Australia, vol. 174, no. 6, pp. 271–275, 2001. View at Google Scholar · View at Scopus
  20. A. Havard, L. R. Jorm, and S. Lujic, “Risk adjustment for smoking identified through tobacco use diagnoses in hospital data: a validation study,” PLoS ONE, vol. 9, no. 4, Article ID e95029, 2014. View at Publisher · View at Google Scholar · View at Scopus