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|Year : 2017
: 59 | Issue : 4 | Page
|Early stages of Alzheimer's disease are alarming signs in injury deaths caused by traffic accidents in elderly people (≥60 years of age): A neuropathological study
Printha Wijesinghe1, Catherine Gorrie2, SK Shankar3, Yasha T Chickabasaviah3, Dhammika Amaratunga4, Sanjayah Hulathduwa5, K Sunil Kumara6, Kamani Samarasinghe7, Yoo-Hun Suh8, HW M. Steinbusch9, K Ranil D. De Silva1
1 Department of Anatomy, Faculty of Medical Sciences, Genetic Diagnostic Research Laboratory and Human Brain Bank Tissue Repository, University of Sri Jayewardenepura, Nugegoda, Sri Lanka
2 School of Medical and Molecular Biosciences, University of Technology Sydney, Sydney, Australia
3 Nonclinical Biostatistics, Janssen Research and Development (Retired), Raritan, USA
4 Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India
5 Departments of Forensic Medicine, Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka
6 Department of Judicial Medical Office, Colombo South Teaching Hospital, Colombo, Sri Lanka
7 Department of Pathology, Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka
8 Department of Pharmacology, College of Medicine, Seoul National University, Seoul, South Korea
9 Department of Translational Neuroscience, Faculty Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands
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|Date of Web Publication||18-Jan-2018|
| Abstract|| |
Background: There is little information available in the literature concerning the contribution of dementia in injury deaths in elderly people (≥60 years).
Aim: This study was intended to investigate the extent of dementia-related pathologies in the brains of elderly people who died in traffic accidents or by suicide and to compare our findings with age- and sex-matched natural deaths in an elderly population.
Materials and Methods: Autopsy-derived human brain samples from nine injury death victims (5 suicide and 4 traffic accidents) and nine age- and sex-matched natural death victims were screened for neurodegenerative and cerebrovascular pathologies using histopathological and immunohistochemical techniques. For the analysis, Statistical Package for the Social Sciences (SPSS) version 16.0 was used.
Results: There was a greater likelihood for Alzheimer's disease (AD)-related changes in the elders who succumbed to traffic accidents (1 out of 4) compared to age- and sex-matched suicides (0 out of 5) or natural deaths (0 out of 9) as assessed by the National Institute on Aging – Alzheimer's Association guidelines. Actual burden of both neurofibrillary tangles (NFTs) and (SPs) was comparatively higher in the brains of traffic accidents, and the mean NFT counts were significantly higher in the region of entorhinal cortex (P < 0.05). However, associations obtained for other dementia-related pathologies were not statistically important.
Conclusion: Our findings suggest that early Alzheimer stages may be a contributing factor to injury deaths caused by traffic accidents in elderly people whereas suicidal brain neuropathologies resembled natural deaths.
Keywords: Alzheimer-related pathologies, immunohistochemistry, injury deaths, natural diseases
|How to cite this article:|
Wijesinghe P, Gorrie C, Shankar S K, Chickabasaviah YT, Amaratunga D, Hulathduwa S, Kumara K S, Samarasinghe K, Suh YH, M. Steinbusch H W, D. De Silva K R. Early stages of Alzheimer's disease are alarming signs in injury deaths caused by traffic accidents in elderly people (≥60 years of age): A neuropathological study. Indian J Psychiatry 2017;59:471-7
|How to cite this URL:|
Wijesinghe P, Gorrie C, Shankar S K, Chickabasaviah YT, Amaratunga D, Hulathduwa S, Kumara K S, Samarasinghe K, Suh YH, M. Steinbusch H W, D. De Silva K R. Early stages of Alzheimer's disease are alarming signs in injury deaths caused by traffic accidents in elderly people (≥60 years of age): A neuropathological study. Indian J Psychiatry [serial online] 2017 [cited 2020 May 25];59:471-7. Available from: http://www.indianjpsychiatry.org/text.asp?2017/59/4/471/223469
| Introduction|| |
Unnatural causes of death among elderly people on medicolegally examined autopsies have not been studied extensively. Accidents are the main causes of injury deaths among the elderly followed by suicide, whereas homicide is a rare or uncommon cause of injury death among these people., To date, there have been no studies compared the extent of dementia-related pathologies in the brains of elderly people who died of injuries and natural diseases. There is a small number of studies from Western countries which investigated the extent of dementia-related pathologies in the brains of elderly victims of suicide ,,, and fatal traffic accident brains.,, Autopsy findings, however, were inconclusive. Primary objective of this study was to determine whether there is an over-representation of Alzheimer-related pathologies in the brains of elders (≥60 years) who succumbed to injury deaths caused by traffic accidents and suicide and to compare it with the brains of elders (≥60 years) who died of natural diseases.
| Materials and Methods|| |
Human brain samples were obtained at autopsy from 18 elderly subjects (≥60 years) at the Department of Judicial Medical Office, Colombo South Teaching Hospital, following approval by the Institutional Scientific Ethics Committee to carry out the study and informed consent from kin. Among these samples, nine brains were from injury deaths – five suicide victims and four fatal traffic accident victims (mean age 74.8 years [7.3], mean age [standard deviation]; male:female = 5:4) – and nine brains from natural deaths (mean age 74.8 years [7.6]; male:female = 5:4). Brains of other injury deaths, including falls, drowning, war, adverse outcome of surgery, and homicide, were not obtained during this period. As this study was a retrospective study, an ante-mortem questionnaire was given to kin who were familiar with intellectual and motor functional status of the subjects before death. The purpose of this questionnaire was to obtain information on demographic data, medical history, family history, and health habits of the deceased. This information was held strictly confidential. All the recruited cases had incomplete clinical history, except one case which was clinically diagnosed as Parkinson's disease (PD). Specific neuroanatomical regions were sampled for paraffin embedding and sectioning from both hemispheres: hippocampus along with parahippocampal gyrus, superior frontal gyrus, middle temporal gyrus, superior parietal lobule, midbrain at superior colliculus level and deep white matters from corpus callosum-major inter-hemispheric white matter tract, and the circle of Willis (CW) for the subsequent atherosclerotic study.
Following routine histological evaluation (H and E), formalin-fixed paraffin-embedded brain sections were immunostained by standard immunoperoxidase technique following antigen retrieval by heat and DAB/H2O2 as the chromogen to visualize the immunolabeling (DAKO Envision Detection System). For this screening, three antibodies, namely, (i) β-amyloid (Aβ) – monoclonal antibody (1:200 dilution) from Novacastra™, (ii) ubiquitin – monoclonal antibody (1:150 dilution) from Novacastra™, and (iii) phosphorylated tau – paired helical filament (PHF) −1 monoclonal antibody (1:50 dilution, A gift) were used. Phosphorylated tau- and Aβ-positive pathologies were graded semiquantitatively as given below.
- Semi-quantitative 0–3 scale (0 - none, + - low, ++ - moderate, and +++ - high) for tau-positive neurons (neurons demonstrating tangle and pretangle pathology), neuritic plaques (NPs), and neuropil threads (NTs)
- Semi-quantitative 0–3 scale (0 - none, + - sparse, ++ - moderate, and +++ - frequent) for Aβ-positive senile plaques (SPs – dystrophic neurites and an amyloid core) and diffuse plaques (DPs).
The diagnostic criteria for Alzheimer's disease (AD) neuropathologic change was based on National Institute on Aging − Alzheimer's Association guidelines (NIA-AA) – a practical approach which included:
- Consortium to Establish a Registry for AD (CERAD) protocol for NP scoring 
- Braak and Braak staging scheme for neurofibrillary tangle (NFT) degeneration , which was adapted to four stages that improve inter-rater reliability (stage 0, stage I or II, stage III or IV, and stage V or VI)
- A modified version of Thal phases for Aβ plaque accumulation  which was adapted to four-point scale (phase 0, phase 1 or 2, phase 3, and phase 4 or 5).
AD neuropathologic change was ranked by three parameters: Aβ plaque phase, Braak and Braak NFT stage, and CEARD NP score to obtain ABC scores and then transformed into four levels: not, low, intermediate, or high. Actual burden of AD-related pathologies (NFTs and SPs) were counted in specific brain regions such as hippocampus, parahippocampus, superior frontal gyrus, and midbrain based on the methods described by Purohit et al. For this purpose, a medium high power (×20) objective lens producing a visual field of 0.785 mm2 (field diameter = 2.0 mm) was used. Lesions were counted in medium high (×200, Olympus U-CTR30-2 Trinocular objective tubes and ×10 eye piece) power fields and then converted into average per ×200 as follows: for superior frontal gyrus, areas with high NFTs/SPs were selected and visual counts were carried out in five nonoverlapping fields. For other regions, areas with high NFTs/SPs were identified in each subfield and then visual counts were carried out in nonoverlapping fields (wherever possible five nonoverlapping fields were selected).
Neuropathological criteria for Lewy body diseases (LBDs) including PD and dementia with Lewy bodies (DLBs) were based on NIA-AA  modifications to existing criteria which included Consortium on DLBs 2005 (CDLB05) and Braak PD staging  system. To detect Lewy bodies, α-synuclein immunohistochemistry is recommended as a preferred method; however, in this study, H and E staining and ubiquitin immunohistochemistry which were recommended in CDLB 1996 criteria  were used. Cerebral amyloid angiopathy (CAA) in leptomeningeal and cortical arteries of the specific neuroanatomical regions was graded based on Greenberg and Vonsattel  specifications and the average CAA grade was reported for each case. Intracranial atherosclerosis of the CW (IASCW) was graded into four levels: none, mild, moderate, and severe based on the degree of stenosis of the CW component arteries  and the gross visual inspection (macroscopic grading). Extent of other cerebrovascular pathologies: microscopic infarcts in deep white matters (7 μm thick) stained with Luxol fast blue (LFB) and cresyl violet and white matter hyperintensities (WMHs) in the neocortex and hippocampus regions stained with LFB and eosin were assessed semi-quantitatively as absent (none/rare) and present (above levels). Due to the high variability of morphological findings and multifactorial pathogenesis of vascular cognitive impairment/vascular dementia (VaD),,,, no generally accepted morphologic scheme for quantitating vascular brain injury and no validated neuropathological criteria for VaD have been established to date., On the whole, the basis of VaD diagnosis is simply the presence of brain lesions related to vascular pathology and it highly depends on the neuropathologist's judgment.
Results were analyzed using statistical software SPSS for windows version 16.0, SPSS Inc., Chicago, USA. Mann–Whitney U-test was used to find the differences in AD-related neuropathological scores in different brain regions among injury deaths caused by traffic accidents and suicide and natural deaths.
| Results|| |
This sample consisted of 18 deceased brains aged between 60 and 87 years. The mean age between traffic accidents (78.7 years [3.1]) and natural (78.5 years [3.2]) deaths; suicide (71.6 years [3.4]) and natural deaths (71.8 years [3.2]); and traffic accidents (78.7 years [3.1]) and suicide (71.6 years [3.4]) was not significantly different (P > 0.05, Mann–Whitney U-test). Sample summary on AD, LBD, and CAA neuropathological stages is given in [Table 1]. Among these samples, AD neuropathologic change for intermediate level considered as greater likelihood for dementia or cognitive impairment was found only in one out of four traffic accidents and for low level considered as inadequate evident was found in one out of four traffic accidents, one out of five suicides, and two out of nine natural deaths.
|Table 1: Sample summary on Alzheimer's disease, cerebral amyloid angiopathy, and Lewy body disease neuropathological stages|
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[Figure 1] illustrates the percentage of cases identified with AD-related and cerebrovascular pathologies among injury and natural deaths. AD-related pathologies; Braak NFT stage, Thal Aβ phase, and CERAD NP score were comparatively higher in traffic accidents compared to suicide or natural deaths. CAA and WMHs, which are most frequent coexisting cerebral small vessel diseases in the AD brains, were also identified prominently in the brains of traffic accidents. In contrast, large vessel pathologies; IASCW and white matter microscopic infarcts were identified prominently in natural deaths.
|Figure 1: (a-c) Alzheimer and cerebrovascular neuropathological stages among injury deaths caused by traffic accidents and suicide and natural deaths. NFT – Neurofibrillary tangle; Aβ – β-amyloid; CERAD – Consortium to Establish A Registry for Alzheimer's disease; NP – Neuritic plaque; CAA – Cerebral amyloid angiopathy; WMHs – White matter hyperintensities; IASCW – Intracranial atherosclerosis of the circle of Willis|
Click here to view
Association between cause of death and actual burden of AD-related pathologies is presented in [Table 2]. Mean counts of both NFTs and SPs were comparatively higher in the brains of traffic accidents compared to suicide or natural deaths. In particular, mean NFT counts were significantly higher (P< 0.05) in the region of entorhinal cortex. [Figure 2] illustrates the hallmark lesions of AD including tau-positive NFTs and NPs, and Aβ-positive SPs observed in the brains of injury deaths. One among the 05 suicidal victims who had clinically diagnosed of PD presented brainstem-predominant Lewy bodies (stage 3) at neuropathological diagnosis.
|Figure 2: Hall mark lesions of AD. (a) Tau-positive neurofibrillary tangles in hippocampal CA1 region at ×10 (scale bar 100 μm); (b) tau-positive neuritic plaques in hippocampal subiculum region at × 20 (scale bar 50 μm); (c) Aβ-positive senile plaques in the region of middle temporal cortex at ×20 (scale bar 50 μm)|
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|Table 2: Actual burden of Alzheimer related pathologies among injury deaths caused by traffic accidents and suicide, and natural deaths|
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| Discussion|| |
Our study demonstrates a trend in elderly brain neuropathology where AD-related pathologies are predominant in injury deaths caused by traffic accidents, whereas large vessel pathologies; IASCW and microscopic infarcts are predominant in natural deaths and also in suicide. There is a significant overrepresentation of NFTs identified in the region of entorhinal cortex, the first area of the brain to be affected in AD. Therefore, our results suggest that early AD-related neuropathological changes may contribute sufficiently to elderly injury deaths caused by traffic accidents by affecting their cognitive status. For this screening, we have used the recent NIA-AA guidelines – a practical approach  to assess the neuropathological changes related to AD and LBDs. NIA-AA recommends immunohistochemistry as the most preferred methodology to screen AD-related pathologies and it was followed in this study (β-amyloid for Aβ plaques, phosphorylated tau for Braak and Braak NFT stages, and phosphorylated tau/ubiquitin for CERAD NP score). Further, we have obtained the relative prevalence of comorbid pathologies including CAA, LBDs, IASCW, white matter microscopic infarcts, and WMHs between injury and natural deaths. Thus, apart from AD-related pathologies, other causes of dementia which remain as possible etiological factors in elderly person's injury deaths could be reliably assessed. Moreover, we have employed a vigorous study method to count NFTs and SPs in specific brain regions (hippocampus, entorhinal cortex, superior frontal gyrus, and midbrain); thus, true extent of AD-related pathologies was identified in respect of cause of death.
While this is the first autopsy verification study investigating dementia-related pathologies as etiological factors in injury deaths, we acknowledge that there are limitations such as sample size, incomplete clinical history of the recruited samples lacking objective psychometry and dementia scores, ubiquitin immunohistochemistry for labeling Lewy bodies instead of α-synuclein, semi-quantitative assessments of certain comorbid pathologies lacking exact quantifications, and nonavailability of some brain regions as specified under minimum tissue requirements by the NIA-AA guidelines. In addition to above restrains, our study was based on cases from suicide and fatal traffic accidents, whereas other causes of injury deaths such as falls and drowning which may result from cognitive impairments also need to be included in future concerns.
Suicide in elderly individuals presents unique challenges to clinicians because older people are less likely to report depressive symptoms. While high rates of psychiatric symptoms during the course of illness have been reported, the risk of suicide in people with dementia is generally considered to be low., The contribution of dementia-related pathologies as the cause of suicide in a geriatric population remains questionable. Low risk of suicide in dementia cases has been partly attributed to the higher levels of personal supervision provided in such cases and the difficulties the person with cognitive impairments might have in planning and carrying out suicidal acts. Neuropathological confirmation of AD-related changes in elderly subjects who committed suicide has been limited to few case reports,, a single pilot case–control study, and a large-scale study. Rubio et al. demonstrated that people with moderate-to-severe AD pathology were over-represented among those who committed suicide, suggesting that presence of Alzheimer pathology may increase the risk of suicide. However, a large scale study by Peisah et al. demonstrated that Alzheimer pathology was not over-represented in elderly suicide victims. The above studies were limited by the availability of tissue sections, to hippocampal and neocortical examination. Thus, only prevalence of AD-related changes could be reliably assessed. In the absence of AD-related pathology, other causes of dementia such as LBDs or cerebrovascular diseases remain possible risk factors for the etiology in elderly persons' suicidal behavior.
On the other hand, cognitive decline due to aging has received much attention as a possible risk factor for fatal traffic accidents in elderly populations. As dementia becomes a risk factor in traffic accidents, it is reasonable to expect increased dementia-related neuropathologies in the brains of accident victims. However, neuropathological confirmation of AD-related changes in such cases has also been limited with few numbers of studies. The study of Viitanen et al. in the aged motor vehicle drivers highlighted that incipient AD may contribute to fatal crashes of aged drivers. Therefore, the forensic autopsy of these victims should include neuropathological examination. Another similar study done by Gorrie et al. suggested that increased mild neutritic changes, even sparse NPs in the brains of older drivers may be a factor for their cognitive impairments and needs to be replicated elsewhere to clearly establish the association between early AD pathology and crash involvement. Gorrie et al. also carried out a study in older pedestrians and suggested that AD-related pathologies, especially NFTs, are more frequent in fatally injured elders and suggested that cognitive impairment associated with AD; even the earliest stages of AD may be a risk factor for fatal traffic accidents in older pedestrians. In view of above studies, we found that none of the literature cumulatively reported the contribution of dementia, clinically and/or neuropathologically, to the injury deaths in elderly people. Further, none of the above studies assessed the actual burden/true extent of AD-related pathologies among fatal traffic accidents, suicide, and natural deaths. Therefore, despite small sample size, our study would yield a precise estimate of contribution of AD-related pathologies as an etiological factor in injury deaths caused by traffic accidents in elderly people.
There are limited numbers of studies on pathology of AD from India and other low- and middle-income countries (LMICs),,,,,,,,,,, where the proportion of people affected with dementia is anticipated to rise from 58% in 2010 to 63% in 2030 and 71% in 2050. Within South Asia, Sri Lanka shows the fastest aging; 13% of population was aged over 60 years in 2011 whereas it was ≤8% in rest of the South Asia. Prevalence of dementia in Sri Lanka based on clinical diagnosis is higher by comparing similar studies of other South Asians reported so far; Sri Lanka - 3.98%, India - 2.7%, and Bangladesh - 3.6%. In Sri Lanka, injury deaths are the second major cause of mortality; 233/100,000 populations in 2008, whereas in other South Asian countries, it is comparatively low (Afghanistan -149; Bangladesh - 91; Bhutan - 105; India - 99; Maldives - 53; Nepal - 58; Pakistan - 92/100,000 population in 2008). Among the causes of injury deaths, suicide rate is in peak (34.6 per 100,000 population in 2015) and comparatively higher than in other South Asian populations (Nepal - 7.2; India - 16.0; Bhutan - 12.1; Pakistan - 2.5; Bangladesh - 6.0; Maldives - 11.0; Afghanistan 7.1 per 100,000 population). Road traffic deaths (road traffic accidents [RTAs]) have also been steadily raising in Sri Lanka and considered as the third leading cause of injury deaths after suicide and collective violence (war-related deaths) and the annual death rate of RTAs is approximately 12.1/100,000 population. Although death counts due to RTAs are high between the ages of 20 and 55 years, which is likely a result of population age structure, the death rates continue to increase with age and are highest in elderly people. These are serious public health issues in Sri Lanka as well as in other LMICs; however, it has not been received priority by the government healthcare sectors and it has not been studied extensively by the healthcare professionals. Taken together, our findings suggest that forensic autopsy should include neuropathological examination to the brains of elderly injury deaths caused by fatal accidents aged ≥60 years. Further, it is important for primary carers and healthcare professionals to have an awareness of a possible link between cognitive impairment or early stages AD and cause of death in the elderly. This provides an opportunity to reduce the risk of injury deaths in this age group.
We greatly acknowledge the funding agencies: Sri Lanka Council for Agricultural Research Policy (CARP Project Grant No- 12/684/515), National Science Foundation, Sri Lanka (Grant No- RG 2004/M/16), University of Sri Jayewardenepura, Sri Lanka (Grant No- ASP/06/RE/2010/07), University of New South Wales, Australia, and International Brain Research Organization-Asia Pacific Regional Committee (IBRO-APRC): IBRO-APRC Exchange Fellowship for their financial assistance to carry out the research study in elderly Sri Lankan samples. We sincerely acknowledge Prof. Gabor Kato and Prof. Ann Kato, Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland, for their significant contribution in the language structure of the manuscript. We would also like to mention our special thanks to donors and their families for their substantial contribution in this research. We duly acknowledge Mrs. W. J. M Fernando (Technical Officer) and other staff of the Department of Pathology, University of Sri Jayewardenepura, and the staff of Judicial Medical Office, Colombo South Teaching Hospital, for their kind assistance in this work.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Kumar S, Verma AK. A study of elderly unnatural deaths in medico-legal autopsies at Lucknow locality. Med Sci Law 2014;54:127-31.
Eilertsen HH, Lilleng PK, Mæhle BO, Morild I. Unnatural death in the elderly: A forensic study from Western Norway. Forensic Sci Med Pathol 2007;3:23-31.
Rohde K, Peskind ER, Raskind MA. Suicide in two patients with Alzheimer's disease. J Am Geriatr Soc 1995;43:187-9.
Lesco PA. Murder-suicide in Alzheimer's disease. J Am Geriatr Soc 1989;37:167-8.
Rubio A, Vestner AL, Stewart JM, Forbes NT, Conwell Y, Cox C, et al.
Suicide and Alzheimer's pathology in the elderly: A case-control study. Biol Psychiatry 2001;49:137-45.
Peisah C, Snowdon J, Gorrie C, Kril J, Rodriguez M. Investigation of Alzheimer's disease-related pathology in community dwelling older subjects who committed suicide. J Affect Disord 2007;99:127-32.
Viitanen M, Johansson K, Bogdanovic N, Berkowicz A, Druid H, Eriksson A, et al.
Alzheimer changes are common in aged drivers killed in single car crashes and at intersections. Forensic Sci Int 1998;96:115-27.
Gorrie CA, Rodriguez M, Sachdev P, Duflou J, Waite PM. Increased neurofibrillary tangles in the brains of older pedestrians killed in traffic accidents. Dement Geriatr Cogn Disord 2006;22:20-6.
Gorrie CA, Rodriguez M, Sachdev P, Duflou J, Waite PM. Mild neuritic changes are increased in the brains of fatally injured older motor vehicle drivers. Accid Anal Prev 2007;39:1114-20.
Montine TJ, Phelps CH, Beach TG, Bigio EH, Cairns NJ, Dickson DW, et al
. National Institute on Aging-Alzheimer's Association guidelines for the neuropathological assessment of Alzheimer's disease: Practical approach. Acta Neuropathol 2012;123:1-11.
Mirra SS, Heyman A, McKeel D, Sumi SM, Crain BJ, Brownlee LM, et al.
The consortium to establish a registry for Alzheimer's disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease. Neurology 1991;41:479-86.
Braak H, Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol 1991;82:239-59.
Braak H, Alafuzoff I, Arzberger T, Kretzschmar H, Del Tredici K. Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry. Acta Neuropathol 2006;112:389-404.
Nagy Z, Yilmazer-Hanke DM, Braak H, Braak E, Schultz C, Hanke J, et al.
Assessment of the pathological stages of Alzheimer's disease in thin paraffin sections: A comparative study. Dement Geriatr Cogn Disord 1998;9:140-4.
Thal DR, Rüb U, Orantes M, Braak H. Phases of A beta-deposition in the human brain and its relevance for the development of AD. Neurology 2002;58:1791-800.
Purohit DP, Batheia NO, Sano M, Jashnani KD, Kalaria RN, Karunamurthy A, et al
. Profile of Alzheimer's disease-related pathology in an aging urban population sample in India. J Alzheimers Dis 2011;24:187-96.
McKeith IG, Dickson DW, Lowe J, Emre M, O'Brien JT, Feldman H, et al
. Consortium on DLB. Diagnosis and management of dementia with Lewy bodies: Third report of the DLB Consortium. Neurology 2005;65:1863-72.
Braak H, Del Tredici K, Rub U, de Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol Aging 2003;24:197-211.
McKeith IG, Galasko D, Kosaka K, Perry EK, Dickson DW, Hansen LA, et al
. Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the consortium on DLB international workshop. Neurology 1996;47:1113-24.
Greenberg SM, Vonsattel JP. Diagnosis of cerebral amyloid angiopathy. Sensitivity and specificity of cortical biopsy. Stroke 1997;28:1418-22.
Classification of atherosclerotic lesions; a report of a study group. World Health Organ Tech Rep Ser 1958;57:1-20.
Beach TG, Wilson JR, Sue LI, Newell A, Poston M, Cisneros R, et al.
Circle of Willis atherosclerosis: Association with Alzheimer's disease, neuritic plaques and neurofibrillary tangles. Acta Neuropathol 2007;113:13-21.
Grinberg LT, Thal DR. Vascular pathology in the aged human brain. Acta Neuropathol 2010;119:277-90.
Gorelick PB, Scuteri A, Black SE, Decarli C, Greenberg SM, Iadecola C, et al.
Vascular contributions to cognitive impairment and dementia: A statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2011;42:2672-713.
Jellinger KA. Challenges in the neuropathological diagnosis of dementias. Int J Neuropathol 2013;1:8-52.
Alafuzoff I, Gelpi E, Al-Sarraj S, Arzberger T, Attems J, Bodi I, et al.
The need to unify neuropathological assessments of vascular alterations in the ageing brain: Multicentre survey by the BrainNet Europe consortium. Exp Gerontol 2012;47:825-33.
van Hoesen GW, Hyman BT, Damasio AR. Entorhinal cortex pathology in Alzheimer's disease. Hippocampus 1991;1:1-8.
Purandare N, Voshaar RC, Rodway C, Bickley H, Burns A, Kapur N, et al.
Suicide in dementia: 9-year national clinical survey in England and Wales. Br J Psychiatry 2009;194:175-80.
Aalten P, de Vugt ME, Jaspers N, Jolles J, Verhey FR. The course of neuropsychiatric symptoms in dementia. Part I: Findings from the two-year longitudinal Maasbed study. Int J Geriatr Psychiatry 2005;20:523-30.
Lim WS, Rubin EH, Coats M, Morris JC. Early-stage Alzheimer disease represents increased suicidal risk in relation to later stages. Alzheimer Dis Assoc Disord 2005;19:214-9.
Conwell Y, Duberstein PR, Caine ED. Risk factors for suicide in later life. Biol Psychiatry 2002;52:193-204.
Wijesinghe P, Shankar SK, Yasha TC, Gorrie CA, Amaratunga D, Hulathduwa SR, et al
. Cytoskeletal pathologies of age related diseases between elderly Sri Lankan and Indian brain samples. Curr Alzheimer Res 2016;13:268-80.
Wijesinghe P, Shankar SK, Yasha TC, Gorrie CA, Amaratunga D, Hulathduwa SR, et al
. Vascular contributions in Alzheimer related neuropathological changes:First autopsy evidence from a South Asian ageing population. J Alzheimers Dis 2016;54:1607-18.
Yasha TC, Shankar L, Santosh V, Das S, Shankar SK. Histopathological & immunohistochemical evaluation of ageing changes in normal human brain. Indian J Med Res 1997;105:141-50.
Satishchandra P, Yasha TC, Shankar L, Santosh V, Das S, Swamy HS, et al.
Familial Alzheimer disease:First report from India. Alzheimer Dis Assoc Disord 1997;11:107-9.
Barodawala SA, Ghadi PS. A progress report on the prevalence of Alzheimer's lesions in Bombay hospital population. Curr Sci 1992;63:449-55.
Shankar SK, Chandra PS, Rao TS. Alzheimer's disease – Histological, ultrastructural, and immunochemical study of an autopsy proven case. Indian J Psychiatry 1988;30:291-8.
] [Full text]
Somasundaram O. Alzheimer's disease. J Indian Med Assoc 1974;63:66-8.
Dani SU, Pittella JE, Boehme A, Hori A, Schneider B. Progressive formation of neuritic plaques and neurofibrillary tangles is exponentially related to age and neuronal size. A morphometric study of three geographically distinct series of aging people. Dement Geriatr Cogn Disord 1997;8:217-27.
Ogeng'o JA, Cohen DL, Sayi JG, Matuja WB, Chande HM, Kitinya JN, et al.
Cerebral amyloid beta protein deposits and other Alzheimer lesions in non-demented elderly East Africans. Brain Pathol 1996;6:101-7.
Osuntokun BO, Ogunniyi A, Junaid TA, Lekwauwa UG. Autopsy survey for Alzheimer's disease in Nigerian Africans: A preliminary report. Afr J Med Med Sci 1995;24:75-9.
Osuntokun BO, Ogunniyi A, Akang EE, Aghadiuno PU, Ilori A, Bamgboye EA, et al.
Beta A4-amyloid in the brains of non-demented Nigerian Africans. Lancet 1994;343:56.
Alzheimer Disease International. World Alzheimer Report 2010: The Global Economic Impact of Dementia. London: Alzheimer Disease International; 2010.
World Health Organization. World Health Statistics 2013. Geneva: World Health Organization Press; 2013.
de Silva HA, Gunatilake SB, Smith AD. Prevalence of dementia in a semi-urban population in Sri Lanka: Report from a regional survey. Int J Geriatr Psychiatry 2003;18:711-5.
Kalaria RN, Maestre GE, Arizaga R, Friedland RP, Galasko D, Hall K, et al.
Alzheimer's disease and vascular dementia in developing countries: Prevalence, management, and risk factors. Lancet Neurol 2008;7:812-26.
Palmer K, Kabir ZN, Ahmed T, Hamadani JD, Cornelius C, Kivipelto M, et al.
Prevalence of dementia and factors associated with dementia in rural Bangladesh: Data from a cross-sectional, population-based study. Int Psychogeriatr 2014;26:1905-15.
Government of Sri Lanka: Statistical Abstract 2008: Transport and Communication. Department of Census and Statistics, Sri Lanka; 2008.
Prof. K Ranil D. De Silva
Department of Anatomy, Faculty of Medical Sciences, Genetic Diagnostic and Research Laboratory and Human Brain Bank Tissue Repository, University of Sri Jayewardenepura, Nugegoda 10250
Source of Support: None, Conflict of Interest: None
[Figure 1], [Figure 2]
[Table 1], [Table 2]