Evaluation of Selection Bias in an Incident-Based Dementia Autopsy Case Series
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Neuropathological (np) relative frequency estimates of dementia may be biased if the autopsied subjects are not representative of all dementia subjects within a target population. We identified characteristics that differed between autopsied and non-autopsied subjects from an incident-based dementia case series and compared autopsy-based estimates of the relative frequency of np diagnoses before and after adjusting for potential selection bias. Clinically demented subjects who were autopsied (n = 206), had died but were not autopsied (n = 271), were still alive (n = 71), or had dropped out of the study (n = 82) were included. Compared with non-autopsied subjects, autopsied subjects were more likely to be Caucasian, educated beyond high school, and married. They also tended to have a lower baseline Mini-Mental State Examination score and were more likely to have a clinical diagnosis of Alzheimer disease (AD) than non-autopsied subjects. Neuropathological AD with Lewy bodies (LB) had the largest crude relative frequency estimate at 38% of the autopsy sample, followed by 25% for AD with vascular lesions, 13% for pure AD, 13% for LB (with or without vascular lesions), and 8% for pure vascular pathologies. Adjustment for potential sources of selection bias had little effect on relative frequency estimates, suggesting that np diagnoses in the autopsied subjects provide reasonable dementia relative frequency estimates among all clinically demented cases in this series.
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One study has reported no evident selection bias between autopsied and non-autopsied subjects among an incident community-diagnosed dementia series, suggesting that dementia case composition may not be substantially different in different settings.
“However, one study has reported no evident selection bias between autopsied and non-autopsied subjects among an incident community-diagnosed dementia series, suggesting that dementia case composition may not be substantially different in different settings (48).”
From Accuracy of the Clinical Diagnosis of Alzheimer Disease at National Institute on Aging Alzheimer Disease Centers, 2005–2010 (2012) · cites this paper as [48]
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Experimental — accuracy not yet measuredSample selection in incident-based dementia autopsy series has an effect (a caveat).
“A specific caveat in this respect is the effect of sample selection in incident-bases dementia autopsy series [164].”
From The overlap between vascular disease and Alzheimer’s disease - lessons from pathology (2014) · cites this paper as [164]
Community samples tend to show greater degrees of cerebrovascular pathology compared to hospital-based samples.
“Community samples tend to show greater degrees of cerebrovascular pathology as compared to hospital based samples; and the prevalence of mixed AD/CVD was higher in the community-based RUSH Memory and Aging Project (44%) than in the RUSH Religious Order Study (28%).”
From The overlap between vascular disease and Alzheimer’s disease - lessons from pathology (2014) · cites this paper as [164]
The prevalence of mixed AD/CVD was higher in the community-based RUSH Memory and Aging Project (44%) than in the RUSH Religious Order Study (28%).
“Community samples tend to show greater degrees of cerebrovascular pathology as compared to hospital based samples; and the prevalence of mixed AD/CVD was higher in the community-based RUSH Memory and Aging Project (44%) than in the RUSH Religious Order Study (28%).”
From The overlap between vascular disease and Alzheimer’s disease - lessons from pathology (2014) · cites this paper as [164]
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- Authors
- Tsuang, D., Simpson, K. L., Li, G., Barnhart, R. L., Edland, S. D., Bowen, J., McCormick, W., Teri, L., Nochlin, D., Larson, E. B., Thompson, M. L., & Leverenz, J. B.
- Affiliations
- University of Washington (US)
- Mayo Clinic (US)
- Mental Illness Research, Education and Clinical Centers (US)
- Corresponding author
- Tsuang, Debby
- Simpson, Kate L
- Li, Gail
- Teri, Linda
- Leverenz, James B
- Venue
- Alzheimer Disease & Associated Disorders
- Published
- 2005-04
- Volume
- 19
- Issue
- 2
- Pages
- 67-73
- ISSN
- 0893-0341 (ISSN-L)
- PMC
- PMC1524825
- OpenAlex
- W2063879864
- Cited by
- 37
- References
- 20
- Citations by year
- 2024: 1 · 2023: 2 · 2022: 3 · 2021: 2 · 2020: 2 · 2019: 3 · 2016: 1 · 2015: 3 · 2014: 1 · 2013: 2 · 2012: 2
- FWCI
- 1.60
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Alzheimer Disease & Associated Disorders (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (AG 05136, U01AG006781, AG-06781, P50AG005136)
- National Institute of Neurological Disorders and Stroke (R01NS048595, R01 NS48595)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- selection bias, dementia, neuropathological diagnosis, autopsy, Alzheimer's disease, Lewy bodies, vascular dementia, sample representativeness
- MeSH terms
- Aged, Aged, 80 and over, Analysis of Variance, Autopsy, Dementia, Female, Humans, Male, Registries, Selection Bias, Incidence, Chi-Square Distribution
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