Abstract
On 11 September 2001 the World Trade Center (WTC) in New York was attacked by terrorists, causing the collapse of multiple buildings including the iconic 110-story ‘Twin Towers’. Thousands of people died that day from the collapse of the buildings, fires, falling from the buildings, falling debris, or other related accidents. Survivors of the attacks, those who worked in search and rescue during and after the buildings collapsed, and those working in recovery and clean-up operations were exposed to severe psychological stressors. Concurrently, these ‘WTC-affected’ individuals breathed and ingested a mixture of organic and particulate neurotoxins and pro-inflammogens generated as a result of the attack and building collapse. Twenty years later, researchers have documented neurocognitive and motor dysfunctions that resemble the typical features of neurodegenerative disease in some WTC responders at midlife. Cortical atrophy, which usually manifests later in life, has also been observed in this population. Evidence indicates that neurocognitive symptoms and corresponding brain atrophy are associated with both physical exposures at the WTC and chronic post-traumatic stress disorder, including regularly re-experiencing traumatic memories of the events while awake or during sleep. Despite these findings, little is understood about the long-term effects of these physical and mental exposures on the brain health of WTC-affected individuals, and the potential for neurocognitive disorders. Here, we review the existing evidence concerning neurological outcomes in WTC-affected individuals, with the aim of contextualizing this research for policymakers, researchers and clinicians and educating WTC-affected individuals and their friends and families. We conclude by providing a rationale and recommendations for monitoring the neurological health of WTC-affected individuals.
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References
Ground Zero stops burning, after 100 days. Guardian (Lond.) https://www.theguardian.com/world/2001/dec/20/september11.usa (2001).
Plumer, B. Nine facts about terrorism in the United States since 9/11. Washington Post https://www.washingtonpost.com/news/wonk/wp/2013/09/11/nine-facts-about-terrorism-in-the-united-states-since-911/ (2013).
September 11 terror attacks fast facts. CNN https://www.cnn.com/2013/07/27/us/september-11-anniversary-fast-facts/ (2020).
Dahlgren, J., Cecchini, M., Takhar, H. & Paepke, O. Persistent organic pollutants in 9/11 World Trade Center rescue workers: reduction following detoxification. Chemosphere 69, 1320–1325 (2007).
Lippmann, M., Cohen, M. D. & Chen, L. C. Health effects of World Trade Center (WTC) dust: an unprecedented disaster’s inadequate risk management. Crit. Rev. Toxicol. 45, 492–530 (2015).
Toom, V. Whose body is it? Technolegal materialization of victims’ bodies and remains after the World Trade Center terrorist attacks. Sci. Technol. Hum. Values 41, 686–708 (2015).
Lioy, P. J. et al. Characterization of the dust/smoke aerosol that settled east of the World Trade Center (WTC) in lower Manhattan after the collapse of the WTC 11 September 2001. Env. Health Perspect. 110, 703–714 (2002).
Kahn, L. G. et al. Adolescents exposed to the World Trade Center collapse have elevated serum dioxin and furan concentrations more than 12 years later. Env. Int. 111, 268–278 (2018).
Dick, F. D. Solvent neurotoxicity. Occup. Env. Med. 63, 221–226, 179 (2006).
Rao, D. B., Jortner, B. S. & Sills, R. C. Animal models of peripheral neuropathy due to environmental toxicants. ILAR J. 54, 315–323 (2014).
Wilkenfeld, M., Fazzari, M., Segelnick, J. & Stecker, M. Neuropathic symptoms in World Trade Center disaster survivors and responders. J. Occup. Env. Med. 58, 83–86 (2016).
Marmor, M. et al. Paresthesias among community members exposed to the World Trade Center disaster. J. Occup. Env. Med. 59, 389–396 (2017).
Thawani, S., Wang, B., Shao, Y., Reibman, J. & Marmor, M. Time to onset of paresthesia among community members exposed to the World Trade Center disaster. Int. J. Env. Res. Public. Health 16, 1429 (2019).
Colbeth, H. L. et al. Post-9/11 peripheral neuropathy symptoms among World Trade Center-exposed firefighters and emergency medical service workers. Int. J. Environ. Res. Public Health 16, 1727 (2019).
Galea, S. et al. Psychological sequelae of the September 11 terrorist attacks in New York City. N. Engl. J. Med. 346, 982–987 (2002).
Diagnostic and Statistical Manual of Mental Disorders: DSM-5 5th edn (American Psychiatric Association, 2013).
Liu, B., Tarigan, L. H., Bromet, E. J. & Kim, H. World Trade Center disaster exposure-related probable posttraumatic stress disorder among responders and civilians: a meta-analysis. PLoS ONE 9, e101491 (2014).
Stern, Y. et al. Whitepaper: Defining and investigating cognitive reserve, brain reserve, and brain maintenance. Alzheimers Dement. 16, 1305–1311 (2020).
Spiro, A. III, Schnurr, P. P. & Aldwin, C. M. Combat-related posttraumatic stress disorder symptoms in older men. Psychol. Aging 9, 17–26 (1994).
Haghani, A., Morgan, T. E., Forman, H. J. & Finch, C. E. Air pollution neurotoxicity in the adult brain: emerging concepts from experimental findings. J. Alzheimers Dis. 76, 773–797 (2020).
Lucchini, R. G. et al. Neurofunctional dopaminergic impairment in elderly after lifetime exposure to manganese. Neurotoxicology 45, 309–317 (2014).
Lucchini, R. G., Dorman, D. C., Elder, A. & Veronesi, B. Neurological impacts from inhalation of pollutants and the nose–brain connection. Neurotoxicology 33, 838–841 (2012).
Landrigan, P. J. et al. Health and environmental consequences of the World Trade Center disaster. Env. Health Perspect. 112, 731–739 (2004).
Forman, H. J. & Finch, C. E. A critical review of assays for hazardous components of air pollution. Free Radic. Biol. Med. 117, 202–217 (2018).
Riediker, M. et al. Particle toxicology and health — where are we? Part. Fibre Toxicol. 16, 19 (2019).
Mumaw, C. L. et al. Microglial priming through the lung–brain axis: the role of air pollution-induced circulating factors. FASEB J. 30, 1880–1891 (2016).
Zeliger, H. I. Exposure to lipophilic chemicals as a cause of neurological impairments, neurodevelopmental disorders and neurodegenerative diseases. Interdiscip. Toxicol. 6, 103–110 (2013).
Best, E. A. et al. Biomarkers of exposure to polycyclic aromatic hydrocarbons and cognitive function among elderly in the United States (National Health and Nutrition Examination Survey: 2001–2002). PLoS ONE 11, e0147632 (2016).
Jedrychowski, W. A. et al. Prenatal exposure to polycyclic aromatic hydrocarbons and cognitive dysfunction in children. Env. Sci. Pollut. Res. Int. 22, 3631–3639 (2015).
Peterson, B. S. et al. Effects of prenatal exposure to air pollutants (polycyclic aromatic hydrocarbons) on the development of brain white matter, cognition, and behavior in later childhood. JAMA Psychiat. 72, 531–540 (2015).
Perera, F. P. et al. Prenatal airborne polycyclic aromatic hydrocarbon exposure and child IQ at age 5 years. Pediatrics 124, e195–e202 (2009).
Perera, F. P. et al. Early-life exposure to polycyclic aromatic hydrocarbons and ADHD behavior problems. PLoS ONE 9, e111670 (2014).
Bromet, E. et al. DSM-IV post-traumatic stress disorder among World Trade Center responders 11–13 years after the disaster of 11 September 2001 (9/11). Psychol. Med. 46, 771–783 (2016).
Hall, K. S., Hoerster, K. D. & Yancy, W. S. Jr Post-traumatic stress disorder, physical activity, and eating behaviors. Epidemiol. Rev. 37, 103–115 (2015).
Bonanno, G. A. Resilience in the face of potential trauma. Curr. Dir. Psychol. Sci. 14, 135–138 (2005).
Kornfield, S. L., Klaus, J., McKay, C., Helstrom, A. & Oslin, D. Subsyndromal posttraumatic stress disorder symptomatology in primary care military veterans: treatment implications. Psychol. Serv. 9, 383–389 (2012).
Shelby, R. A., Golden-Kreutz, D. M. & Andersen, B. L. PTSD diagnoses, subsyndromal symptoms, and comorbidities contribute to impairments for breast cancer survivors. J. Trauma. Stress. 21, 165–172 (2008).
Wallace, D., Moss, A. S. & Hodges, S. Sub-syndromal PTSD: what is important to know in military personnel and veterans? Australas. Psychiat. 28, 254–256 (2019).
Pietrzak, R. H., Goldstein, M. B., Malley, J. C., Johnson, D. C. & Southwick, S. M. Subsyndromal posttraumatic stress disorder is associated with health and psychosocial difficulties in veterans of operations Enduring Freedom and Iraqi Freedom. Depress. Anxiety 26, 739–744 (2009).
Abdallah, C. G. et al. The neurobiology and pharmacotherapy of posttraumatic stress disorder. Annu. Rev. Pharmacol. Toxicol. 59, 171–189 (2019).
Sherin, J. E. & Nemeroff, C. B. Post-traumatic stress disorder: the neurobiological impact of psychological trauma. Dialogues Clin. Neurosci. 13, 263–278 (2011).
Pitman, R. K. et al. Biological studies of post-traumatic stress disorder. Nat. Rev. Neurosci. 13, 769–787 (2012).
Malikowska-Racia, N. & Salat, K. Recent advances in the neurobiology of posttraumatic stress disorder: a review of possible mechanisms underlying an effective pharmacotherapy. Pharmacol. Res. 142, 30–49 (2019).
Livingston, G. et al. Dementia prevention, intervention, and care: 2020 report of the Lancet Commission. Lancet 396, 413–446 (2020).
Chen, J. C. et al. Ambient air pollution and neurotoxicity on brain structure: evidence from Women’s Health Initiative Memory Study. Ann. Neurol. 78, 466–476 (2015).
Ailshire, J. A. & Clarke, P. Fine particulate matter air pollution and cognitive function among U.S. older adults. J. Gerontol. B 70, 322–328 (2015).
Gatto, N. M. et al. Components of air pollution and cognitive function in middle-aged and older adults in Los Angeles. Neurotoxicology 40, 1–7 (2014).
Gonzalez-Maciel, A., Reynoso-Robles, R., Torres-Jardon, R., Mukherjee, P. S. & Calderon-Garciduenas, L. Combustion-derived nanoparticles in key brain target cells and organelles in young urbanites: culprit hidden in plain sight in Alzheimer’s disease development. J. Alzheimers Dis. 59, 189–208 (2017).
Wilker, E. H. et al. Long-term exposure to fine particulate matter, residential proximity to major roads and measures of brain structure. Stroke 46, 1161–1166 (2015).
Wallin, C. et al. Alzheimer’s disease and cigarette smoke components: effects of nicotine, PAHs, and Cd(II), Cr(III), Pb(II), Pb(IV) ions on amyloid-beta peptide aggregation. Sci. Rep. 7, 14423 (2017).
Shaffer, R. M. et al. Fine particulate matter exposure and cerebrospinal fluid markers of vascular injury. J. Alzheimers Dis. 71, 1015–1025 (2019).
Campbell, A. et al. Particulate matter in polluted air may increase biomarkers of inflammation in mouse brain. Neurotoxicology 26, 133–140 (2005).
Cacciottolo, M. et al. Traffic-related air pollutants (TRAP-PM) promote neuronal amyloidogenesis through oxidative damage to lipid rafts. Free Radic. Biol. Med. 147, 242–251 (2020).
Justice, N. J. et al. Posttraumatic stress disorder-like induction elevates β-amyloid levels, which directly activates corticotropin-releasing factor neurons to exacerbate stress responses. J. Neurosci. 35, 2612–2623 (2015).
Filiano, A. J., Gadani, S. P. & Kipnis, J. Interactions of innate and adaptive immunity in brain development and function. Brain Res. 1617, 18–27 (2015).
Andrews, J. A. & Neises, K. D. Cells, biomarkers, and post-traumatic stress disorder: evidence for peripheral involvement in a central disease. J. Neurochem. 120, 26–36 (2012).
Glaser, R. & Kiecolt-Glaser, J. K. Stress-induced immune dysfunction: implications for health. Nat. Rev. Immunol. 5, 243–251 (2005).
Kuan, P. F. et al. Cell type-specific gene expression patterns associated with posttraumatic stress disorder in World Trade Center responders. Transl. Psychiat. 9, 1 (2019).
Deslauriers, J., Powell, S. & Risbrough, V. B. Immune signaling mechanisms of PTSD risk and symptom development: insights from animal models. Curr. Opin. Behav. Sci. 14, 123–132 (2017).
Felmingham, K. et al. Duration of posttraumatic stress disorder predicts hippocampal grey matter loss. Neuroreport 20, 1402–1406 (2009).
Ousdal, O. T. et al. The association of PTSD symptom severity with amygdala nuclei volumes in traumatized youths. Translat. Psychiat. 10, 1–10 (2020).
Yehuda, R. Advances in understanding neuroendocrine alterations in PTSD and their therapeutic implications. Ann. N. Y. Acad. Sci. 1071, 137–166 (2006).
Wingenfeld, K. & Wolf, O. T. HPA axis alterations in mental disorders: impact on memory and its relevance for therapeutic interventions. CNS Neurosci. Ther. 17, 714–722 (2011).
Yehuda, R. Post-traumatic stress disorder. N. Engl. J. Med. 346, 108–114 (2002).
Gill, J. M., Saligan, L., Woods, S. & Page, G. PTSD is associated with an excess of inflammatory immune activities. Perspect. Psychiatr. Care 45, 262–277 (2009).
Akiyama, H. et al. Cell mediators of inflammation in the Alzheimer disease brain. Alzheimer Dis. Assoc. Disord. 14, S47–S53 (2000).
Leyns, C. E. G. & Holtzman, D. M. Glial contributions to neurodegeneration in tauopathies. Mol. Neurodegener. 12, 50 (2017).
Clouston, S. A. et al. Cognitive impairment among World Trade Center responders: long-term implications of re-experiencing the 9/11 terrorist attacks. Alzheimers Dement. 4, 67–75 (2016).
Alzheimer’s Disease Fact Sheet https://www.nia.nih.gov/health/alzheimers-disease-fact-sheet (National Institute on Aging, 2021)
Daviglus, M. L. et al. National Institutes of Health State-of-the-Science Conference statement: preventing Alzheimer disease and cognitive decline. Ann. Intern. Med. 153, 176–181 (2010).
Clouston, S. et al. Traumatic exposures, posttraumatic stress disorder, and cognitive functioning in World Trade Center responders. Alzheimers Dement. 3, 593–602 (2017).
Clouston, S. A. P. et al. Reduced cortical thickness in World Trade Center responders with cognitive impairment. Alzheimers Dement. 12, e12059 (2020).
Chen, A. P. F. et al. A deep learning approach for monitoring parietal-dominant Alzheimer’s disease in World Trade Center responders at midlife. Brain Commun. 3, fcab145 (2021).
Singh, A. et al. World Trade Center exposure, post-traumatic stress disorder, and subjective cognitive concerns in a cohort of rescue/recovery workers. Acta Psychiat. Scand. 141, 275–284 (2020).
Singh, A. et al. PTSD and depressive symptoms as potential mediators of the association between World Trade Center exposure and subjective cognitive concerns in rescue/recovery workers. Int. J. Environ. Res. Public Health 17, 5683 (2020).
Seil, K., Yu, S. & Alper, H. A cognitive reserve and social support-focused latent class analysis to predict self-reported confusion or memory loss among middle-aged World Trade Center health registry enrollees. Int. J. Environ. Res. Public Health 16, 1401 (2019).
Clouston, S. A. P. et al. Incidence of mild cognitive impairment in World Trade Center responders: long-term consequences of re-experiencing the events on 9/11/2001. Alzheimers Dement. 11, 628–636 (2019).
Huang, C. et al. White matter connectivity in incident mild cognitive impairment: a diffusion spectrum imaging study of world trade center responders at midlife. J. Alzheimers Dis. 80, 1209–1219 (2021).
Deri, Y. et al. Neuroinflammation and mild cognitive impairment in World Trade Center responders at midlife: a pilot study using [18F]-FEPPA PET imaging. Brain Behav. Immun. Health 16, 100287 (2021).
Mukherjee, S., Clouston, S., Kotov, R., Bromet, E. & Luft, B. Handgrip strength of World Trade Center (WTC) responders: the role of re-experiencing posttraumatic stress disorder (PTSD) symptoms. Int. J. Environ. Res. Public Health 16, 1128 (2019).
Clouston, S. A. P., Guralnik, J. M., Kotov, R., Bromet, E. J. & Luft, B. J. Functional limitations among responders to the World Trade Center attacks 14 years after the disaster: implications of chronic posttraumatic stress disorder. J. Trauma. Stress. 30, 443–452 (2017).
Diminich, E. D. et al. Chronic posttraumatic stress disorder and comorbid cognitive and physical impairments in World Trade Center responders. J. Trauma. Stress. 34, 616–627 (2020).
Massy-Westropp, N. M., Gill, T. K., Taylor, A. W., Bohannon, R. W. & Hill, C. L. Hand grip strength: age and gender stratified normative data in a population-based study. BMC Res. Notes 4, 127 (2011).
Ling, C. H. et al. Handgrip strength and mortality in the oldest old population: the Leiden 85-plus study. CMAJ 182, 429–435 (2010).
Taekema, D. G., Gussekloo, J., Maier, A. B., Westendorp, R. G. & de Craen, A. J. Handgrip strength as a predictor of functional, psychological and social health. A prospective population-based study among the oldest old. Age Ageing 39, 331–337 (2010).
Fukumori, N. et al. Association between hand-grip strength and depressive symptoms: locomotive syndrome and health outcomes in Aizu Cohort Study (LOHAS). Age Ageing 44, 592–598 (2015).
Lino, V. T. et al. Handgrip strength and factors associated in poor elderly assisted at a primary care unit in Rio de Janeiro, Brazil. PLoS ONE 11, e0166373 (2016).
Firth, J. et al. Association between muscular strength and cognition in people with major depression or bipolar disorder and healthy controls. JAMA Psychiat. 75, 740–746 (2018).
Firth, J. et al. Grip strength is associated with cognitive performance in schizophrenia and the general population: a UK Biobank study of 476559 participants. Schizophr. Bull. 44, 728–736 (2018).
Ganzel, B., Casey, B., Glover, G., Voss, H. U. & Temple, E. The aftermath of 9/11: effect of intensity and recency of trauma on outcome. Emotion 7, 227 (2007).
Ganzel, B. L., Kim, P., Glover, G. H. & Temple, E. Resilience after 9/11: multimodal neuroimaging evidence for stress-related change in the healthy adult brain. NeuroImage 40, 788–795 (2008).
Deri, Y. et al. Neuroinflammation in World Trade Center responders at midlife: A pilot study using [18F]-FEPPA PET imaging. Brain Behav. Immun. Health 16, 100287 (2021).
Deri, Y. et al. Selective hippocampal subfield volume reductions in World Trade Center responders with cognitive impairment. Alzheimer’s & dementia: diagnosis. Assess. Dis. Monit. 13, e12165 (2021).
Potvin, O., Dieumegarde, L., Duchesne, S. & Initiative, A. S. D. N. Normative morphometric data for cerebral cortical areas over the lifetime of the adult human brain. Neuroimage 156, 315–339 (2017).
Clouston, S. A. P. et al. A cortical thinning signature to identify World Trade Center responders with possible dementia. Intelligence-based Medicine 5, 100032 (2021).
Aldrich, T. K. et al. Lung function in rescue workers at the World Trade Center after 7 years. N. Engl. J. Med. 362, 1263–1272 (2010).
Rosen, R. L. et al. Elevated C-reactive protein and posttraumatic stress pathology among survivors of the 9/11 World Trade Center attacks. J. Psychiatr. Res. 89, 14–21 (2017).
Bello, G. A. et al. Development of a physiological frailty index for the World Trade Center general responder cohort. Curr. Gerontol. Geriatr. Res. 2018, 3725926 (2018).
Clouston, S. A., Edelman, N. H., Aviv, A., Stewart, C. & Luft, B. J. Shortened leukocyte telomere length is associated with reduced pulmonary function and greater subsequent decline in function in a sample of World Trade Center responders. Sci. Rep. 9, 8148 (2019).
Kuan, P. F. et al. Gene expression associated with PTSD in World Trade Center responders: an RNA sequencing study. Transl. Psychiat. 7, 1297 (2017).
Kuan, P.-F. et al. Molecular linkage between post-traumatic stress disorder and cognitive impairment: a targeted proteomics study of World Trade Center responders. Transl. Psychiat. 10, 269 (2020).
Jack, C. R. Jr. et al. NIA-AA Research Framework: toward a biological definition of Alzheimer’s disease. Alzheimers Dement. 14, 535–562 (2018).
Albert, M. S. et al. The diagnosis of mild cognitive impairment due to Alzheimer’s disease: recommendations from the National Institute on Aging–Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement. 7, 270–279 (2011).
McKhann, G. M. et al. The diagnosis of dementia due to Alzheimer’s disease: recommendations from the National Institute on Aging–Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement. 7, 263–269 (2011).
Ismail, Z. et al. The Mild Behavioral Impairment Checklist (MBI-C): a rating scale for neuropsychiatric symptoms in pre-dementia populations. J. Alzheimers Dis. 56, 929–938 (2017).
Zammit, A. R. et al. A coordinated multi-study analysis of the longitudinal association between handgrip strength and cognitive function in older adults. J. Gerontol. B 76, 229–241 (2021).
Duggan, E. C. et al. A multi-study coordinated meta-analysis of pulmonary function and cognition in aging. J. Gerontol. A. 74, 1793–1804 (2019).
Association, A. S. 2019 Alzheimer’s disease facts and figures. Alzheimers Dement. 15, 321–387 (2019).
Gorelick, P. B. et al. Vascular contributions to cognitive impairment and dementia: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 42, 2672–2713 (2011).
Lim, E. W. et al. Amyloid-β and Parkinson’s disease. J. Neurol. 266, 2605–2619 (2019).
Chin, K. S., Yassi, N., Churilov, L., Masters, C. L. & Watson, R. Prevalence and clinical associations of tau in Lewy body dementias: a systematic review and meta-analysis. Parkinsonism Relat. Disord. 80, 184–193 (2020).
Crary, J. F. et al. Primary age-related tauopathy (PART): a common pathology associated with human aging. Acta Neuropathol. 128, 755–766 (2014).
Jack, C. R. Jr. et al. Suspected non-Alzheimer disease pathophysiology — concept and controversy. Nat. Rev. Neurol. 12, 117–124 (2016).
Power, M. C. et al. Combined neuropathological pathways account for age-related risk of dementia. Ann. Neurol. 84, 10–22 (2018).
Jack, C. R. Jr. et al. Tracking pathophysiological processes in Alzheimer’s disease: an updated hypothetical model of dynamic biomarkers. Lancet Neurol. 12, 207–216 (2013).
Bäckman, L., Jones, S., Berger, A.-K., Laukka, E. J. & Small, B. J. Cognitive impairment in preclinical Alzheimer’s disease: a meta-analysis. Neuropsychology 19, 520 (2005).
Li, G. et al. Cerebrospinal fluid biomarkers for Alzheimer’s and vascular disease vary by age, gender, and APOE genotype in cognitively normal adults. Alzheimers Res. Ther. 9, 48 (2017).
Petersen, R. Mild cognitive impairment: transition between aging and Alzheimer’s disease. Neurologia 15, 93–101 (2000).
Bondi, M. W. et al. Neuropsychological criteria for mild cognitive impairment improves diagnostic precision, biomarker associations, and progression rates. J. Alzheimers Dis. 42, 275–289 (2014).
Lopez, O. L., Becker, J. T. & Sweet, R. A. Non-cognitive symptoms in mild cognitive impairment subjects. Neurocase 11, 65–71 (2005).
Martin, E. & Velayudhan, L. Neuropsychiatric symptoms in mild cognitive impairment: a literature review. Dement. Geriatr. Cogn. Disord. 49, 146–155 (2020).
Roberto, N. et al. Neuropsychiatric profiles and conversion to dementia in mild cognitive impairment, a latent class analysis. Sci. Rep. 11, 6448 (2021).
US Preventive Services Task Force. Screening for cognitive impairment in older adults: US Preventive Services Task Force recommendation statement. JAMA 323, 757–763 (2020).
Liss, J. L. et al. Practical recommendations for timely, accurate diagnosis of symptomatic Alzheimer’s disease (MCI and dementia) in primary care: a review and synthesis. J. Intern. Med. 290, 310–334 (2021).
Sliwinski, M. J. et al. Reliability and validity of ambulatory cognitive assessments. Assessment 25, 14–30 (2018).
Luis, C. A., Keegan, A. P. & Mullan, M. Cross validation of the Montreal Cognitive Assessment in community dwelling older adults residing in the southeastern US. Int. J. Geriatr. Psychiat. 24, 197–201 (2009).
Wittich, W., Phillips, N., Nasreddine, Z. S. & Chertkow, H. Sensitivity and specificity of the Montreal Cognitive Assessment modified for individuals who are visually impaired. J. Vis. Impair. Blind. 104, 360–368 (2010).
Deri, Y. et al. Selective hippocampal subfield volume reductions in World Trade Center responders with cognitive impairment. Alzheimers Dement. 13, e12165 (2021).
Chen, A. P. F. et al. A deep learning approach for monitoring parietal-dominant Alzheimer’s disease in World Trade Center responders at midlife. Brain Commun. 3, fcab145 (2021).
Yoncheva, Y. N. et al. Computerized cognitive training for children with neurofibromatosis type 1 (NF1): a pilot study. Psychiat. Res. Neuroimag. 266, 53–78 (2017).
Stricker, N. H. et al. Longitudinal comparison of in clinic and at home administration of the Cogstate Brief Battery and demonstrated practice effects in the Mayo Clinic Study Of Aging. J. Prev. Alzheimers Dis. 7, 21–28 (2020).
Sanderson, W. C. & Scherbov, S. Measuring the speed of aging across population subgroups. PLoS ONE 9, e96289 (2014).
Clouston, S. et al. Posttraumatic stress-related cognitive and physical impairment: clinical characterization of a novel disorder. J. Trauma. Stress. 34, 616–627 (2020).
Anor, C. J. et al. Neuropsychiatric symptoms in Alzheimer disease, vascular dementia, and mixed dementia. Neurodegener. Dis. 17, 127–134 (2017).
Mavounza, C., Ouellet, M.-C. & Hudon, C. Caregivers’ emotional distress due to neuropsychiatric symptoms of persons with amnestic mild cognitive impairment or Alzheimer’s disease. Aging Ment. Health 24, 423–430 (2020).
Isik, A. T., Soysal, P., Solmi, M. & Veronese, N. Bidirectional relationship between caregiver burden and neuropsychiatric symptoms in patients with Alzheimer’s disease: a narrative review. Int. J. Geriatr. Psychiat. 34, 1326–1334 (2019).
Hongisto, K. et al. Quality of life in relation to neuropsychiatric symptoms in Alzheimer’s disease: 5-year prospective ALSOVA cohort study. Int. J. Geriatr. Psychiat. 33, 47–57 (2018).
Coughlan, G., Laczó, J., Hort, J., Minihane, A.-M. & Hornberger, M. Spatial navigation deficits — overlooked cognitive marker for preclinical Alzheimer disease? Nat. Rev. Neurol. 14, 496–506 (2018).
Babulal, G. M. et al. A naturalistic study of driving behavior in older adults and preclinical Alzheimer disease: a pilot study. J. Appl. Gerontol. 38, 277–289 (2017).
Lichtenberg, P. A. Financial exploitation, financial capacity, and Alzheimer’s disease. Am. Psychol. 71, 312 (2016).
Richards, M. & Brayne, C. What do we mean by Alzheimer’s disease? BMJ 341, c4670 (2010).
Pampuscenko, K. et al. Extracellular tau induces microglial phagocytosis of living neurons in cell cultures. J. Neurochem. 154, 316–329 (2020).
Reimand, J. et al. PET and CSF amyloid-β status are differently predicted by patient features: information from discordant cases. Alzheimers Res. Ther. 11, 100 (2019).
Lowe, V. J. et al. Widespread brain tau and its association with ageing, Braak stage and Alzheimer’s dementia. Brain 141, 271–287 (2017).
Therriault, J. et al. Topographic distribution of amyloid-β, tau, and atrophy in patients with behavioral/dysexecutive Alzheimer disease. Neurology 96, e81–e92 (2021).
Weigand, A. J. et al. Is tau in the absence of amyloid on the Alzheimer’s continuum?: A study of discordant PET positivity. Brain Commun. 2, fcz046 (2020).
Abe, K. et al. A new serum biomarker set to detect mild cognitive impairment and Alzheimer’s disease by peptidome technology. J. Alzheimers Dis. 73, 217–227 (2020).
Bogoslovsky, T. et al. Increases of plasma levels of glial fibrillary acidic protein, tau, and amyloid beta up to 90 days after traumatic brain injury. J. Neurotrauma 34, 66–73 (2017).
Fossati, S. et al. Differential value of plasma tau as a biomarker for Alzheimer’s disease and chronic traumatic brain injury. Alzheimers Dement. 13, P1307 (2017).
Mattsson, N. et al. Plasma tau in Alzheimer disease. Neurology 87, 1827–1835 (2016).
Pase, M. et al. Plasma tau corresponds to preclinical Alzheimer’s disease and is a strong predictor of future dementia. Neurology 90(Suppl. 15), S48.001 (2018).
Thijssen, E. H. et al. Diagnostic value of plasma phosphorylated tau181 in Alzheimer’s disease and frontotemporal lobar degeneration. Nat. Med. 26, 387–397 (2020).
Janelidze, S. et al. Plasma p-tau181 in Alzheimer’s disease: relationship to other biomarkers, differential diagnosis, neuropathology and longitudinal progression to Alzheimer’s dementia. Nat. Med. 26, 379–386 (2020).
Barthélemy, N. R., Horie, K., Sato, C. & Bateman, R. J. Blood plasma phosphorylated-tau isoforms track CNS change in Alzheimer’s disease. J. Exp. Med. 217, e20200861 (2020).
Mielke, M. M. et al. Plasma phospho-tau181 increases with Alzheimer’s disease clinical severity and is associated with tau- and amyloid-positron emission tomography. Alzheimers Dement. 14, 989–997 (2018).
Kritikos, M. et al. Pathway analysis for plasma β-amyloid, tau and neurofilament light (ATN) in World Trade Center responders at midlife. Neurol. Ther. 9, 159–171 (2020).
Savjani, R. R., Taylor, B. A., Acion, L., Wilde, E. A. & Jorge, R. E. Accelerated changes in cortical thickness measurements with age in military service members with traumatic brain injury. J. Neurotrauma 34, 3107–3116 (2017).
Whitwell, J. L. et al. Patterns of atrophy differ among specific subtypes of mild cognitive impairment. Arch. Neurol. 64, 1130–1138 (2007).
O’Donnell, L. J. & Westin, C. F. An introduction to diffusion tensor image analysis. Neurosurg. Clin. N. Am. 22, 185–196 (2011).
Faria Dde, P., Copray, S., Buchpiguel, C., Dierckx, R. & de Vries, E. PET imaging in multiple sclerosis. J. Neuroimmune Pharmacol. 9, 468–482 (2014).
Ciccarelli, O. et al. Pathogenesis of multiple sclerosis: insights from molecular and metabolic imaging. Lancet Neurol. 13, 807–822 (2014).
Mielke, M. M. et al. Plasma and CSF neurofilament light. Relat. Longitud. Neuroimaging Cogn. Measures 93, e252–e260 (2019).
Boyle, P. A. et al. Much of late life cognitive decline is not due to common neurodegenerative pathologies. Ann. Neurol. 74, 478–489 (2013).
Wilson, R. S. et al. Neural reserve, neuronal density in the locus ceruleus, and cognitive decline. Neurology 80, 1202–1208 (2013).
Honer, W. et al. Cognitive reserve, presynaptic proteins and dementia in the elderly. Transl. Psychiat. 2, e114–e114 (2012).
Eisenstein, M. Genetics: finding risk factors. Nature 475, S20–S22 (2011).
Montagne, A. et al. APOE4 leads to blood–brain barrier dysfunction predicting cognitive decline. Nature 581, 71–76 (2020).
Kritikos, M., Gandy, S. E., Meliker, J. R., Luft, B. J. & Clouston, S. A. P. Acute versus chronic exposures to inhaled particulate matter and neurocognitive dysfunction: pathways to Alzheimer’s disease or a related dementia. J. Alzheimers Dis. 78, 871–886 (2020).
Plassman, B. L. et al. Intelligence and education as predictors of cognitive state in late life: a 50-year follow-up. Neurology 45, 1446–1450 (1995).
Deary, I. J., Whalley, L. J., Lemmon, H., Crawford, J. R. & Starr, J. M. The stability of individual differences in mental ability from childhood to old age: follow-up of the 1932 Scottish Mental Survey. Intelligence 28, 49–55 (2000).
Snowdon, D. A. et al. Linguistic ability in early life and cognitive function and Alzheimer’s disease in late life: findings from the Nun Study. JAMA 275, 528–532 (1996).
Clouston, S. A. P. et al. Benefits of educational attainment on adult fluid cognition: international evidence from three birth cohorts. Int. J. Epidemiol. 41, 1729–1736 (2012).
Vňuková, M., Richards, M. & Cadar, D. How do our decisions to smoke and drink in midlife affect our cognitive performance in later life? Findings from the 1946 British Birth Cohort. J. Aging Geriatr. Med. 1, 2 (2017).
Rawle, M. J. et al. Apolipoprotein-E (APOE) ε4 and cognitive decline over the adult life course. Transl. Psychiat. 8, 1–8 (2018).
Yu, J.-T. et al. Evidence-based prevention of Alzheimer’s disease: systematic review and meta-analysis of 243 observational prospective studies and 153 randomised controlled trials. J. Neurol. Neurosurg. Psychiat. 91, 1201–1209 (2020).
The SPRINT MIND Investigators for the SPRINT Research Group. Effect of intensive vs standard blood pressure control on probable dementia: a randomized clinical trial. JAMA 321, 553–561 (2019).
Mintun, M. A. et al. Donanemab in early Alzheimer’s disease. N. Engl. J. Med. 384, 1691–1704 (2021).
Xu, H. et al. Long term effects of cholinesterase inhibitors on cognitive decline and mortality. Neurology 96, e2220–e22230 (2021).
Richards, M. et al. Identifying the lifetime cognitive and socioeconomic antecedents of cognitive state: seven decades of follow-up in a British birth cohort study. BMJ Open 9, e024404 (2019).
Northey, J. M., Cherbuin, N., Pumpa, K. L., Smee, D. J. & Rattray, B. Exercise interventions for cognitive function in adults older than 50: a systematic review with meta-analysis. Br. J. Sports Med. 52, 154–160 (2018).
Stern, Y. et al. Effect of aerobic exercise on cognition in younger adults: a randomized clinical trial. Neurology 92, e905–e916 (2019).
Sloan, R. P. et al. Aerobic exercise training and inducible inflammation: results of a randomized controlled trial in healthy, young adults. J. Am. Heart Assoc. 7, e010201 (2018).
Berg, A. et al. Treatment of PTSD: An Assessment of the Evidence (National Academies Press, 2007).
Hoskins, M. et al. Pharmacotherapy for post-traumatic stress disorder: systematic review and meta-analysis. Br. J. Psychiat. 206, 93–100 (2015).
Berger, W. et al. Pharmacologic alternatives to antidepressants in posttraumatic stress disorder: a systematic review. Prog. Neuropsychopharmacol. Biol. Psychiat. 33, 169–180 (2009).
Feder, A. et al. Efficacy of intravenous ketamine for treatment of chronic posttraumatic stress disorder: a randomized clinical trial. JAMA Psychiat. 71, 681–688 (2014).
Kelmendi, B. et al. PTSD: from neurobiology to pharmacological treatments. Eur. J. Psychotraumatol. 7, 31858 (2016).
Raskind, M. A. et al. A parallel group placebo controlled study of prazosin for trauma nightmares and sleep disturbance in combat veterans with post-traumatic stress disorder. Biol. Psychiat. 61, 928–934 (2007).
Peskind, E. R., Bonner, L. T., Hoff, D. J. & Raskind, M. A. Prazosin reduces trauma-related nightmares in older men with chronic posttraumatic stress disorder. J. Geriatr. Psychiat. Neurol. 16, 165–171 (2003).
Ahmadpanah, M. et al. Comparing the effect of prazosin and hydroxyzine on sleep quality in patients suffering from posttraumatic stress disorder. Neuropsychobiology 69, 235–242 (2014).
Germain, A. et al. Placebo-controlled comparison of prazosin and cognitive-behavioral treatments for sleep disturbances in US military veterans. J. Psychosom. Res. 72, 89–96 (2012).
Taylor, F. B. et al. Prazosin effects on objective sleep measures and clinical symptoms in civilian trauma posttraumatic stress disorder: a placebo-controlled study. Biol. Psychiat. 63, 629–632 (2008).
Raskind, M. A. et al. Trial of prazosin for post-traumatic stress disorder in military veterans. N. Engl. J. Med. 378, 507–517 (2018).
Raskind, M. A. et al. A trial of prazosin for combat trauma PTSD with nightmares in active-duty soldiers returned from Iraq and Afghanistan. Am. J. Psychiat. 170, 1003–1010 (2013).
Raskind, M. A. et al. Reduction of nightmares and other PTSD symptoms in combat veterans by prazosin: a placebo-controlled study. Am. J. Psychiat. 160, 371–373 (2003).
Monson, C. M. & Shnaider, P. Treating PTSD With Cognitive–Behavioral Therapies Interventions That Work (American Psychological Association, 2014).
Difede, J. & Eskra, D. Cognitive processing therapy for PTSD in a survivor of the World Trade Center bombing. J. Trauma. Pract. 1, 155–165 (2002).
Wachen, J. S. et al. Implementing cognitive processing therapy for posttraumatic stress disorder with active duty U.S. military personnel: special considerations and case examples. Cogn. Behav. Pract. 23, 133–147 (2016).
Waltman, S. H. Functional analysis in differential diagnosis: using cognitive processing therapy to treat PTSD. Clin. Case Stud. 14, 422–433 (2015).
Ehlers, A. & Clark, D. M. A cognitive model of posttraumatic stress disorder. Behav. Res. Ther. 38, 319–345 (2000).
Ehlers, A. et al. A randomized controlled trial of 7-day intensive and standard weekly cognitive therapy for PTSD and emotion-focused supportive therapy. Am. J. Psychiat. 171, 294–304 (2014).
Foa, E., Hembree, E. A., Rothbaum, B. O. & Rauch, S. Prolonged Exposure Therapy for PTSD — Therapist Guide: Emotional Processing of Traumatic Experiences (Oxford University Press, 2019).
Bahar-Fuchs, A., Clare, L. & Woods, B. Cognitive training and cognitive rehabilitation for mild to moderate Alzheimer’s disease and vascular dementia. Cochrane Database Syst. Rev. 2013, CD003260 (2013).
Mowszowski, L., Batchelor, J. & Naismith, S. L. Early intervention for cognitive decline: can cognitive training be used as a selective prevention technique? Int. Psychogeriatr. 22, 537–548 (2010).
Bahar-Fuchs, A., Martyr, A., Goh, A. M., Sabates, J. & Clare, L. Cognitive training for people with mild to moderate dementia. Cochrane Database Syst. Rev. 3, CD013069 (2019).
Belleville, S., Mellah, S., de Boysson, C., Demonet, J. F. & Bier, B. The pattern and loci of training-induced brain changes in healthy older adults are predicted by the nature of the intervention. PLoS ONE 9, e102710 (2014).
Belleville, S. et al. Training-related brain plasticity in subjects at risk of developing Alzheimer’s disease. Brain 134, 1623–1634 (2011).
Hampstead, B. M. et al. Activation and effective connectivity changes following explicit-memory training for face–name pairs in patients with mild cognitive impairment: a pilot study. Neurorehabil Neural Repair. 25, 210–222 (2011).
Edwards, J. D., Fausto, B. A., Tetlow, A. M., Corona, R. T. & Valdés, E. G. Systematic review and meta-analyses of useful field of view cognitive training. Neurosci. Biobehav. Rev. 84, 72–91 (2018).
Edwards, J. D. et al. Speed of processing training results in lower risk of dementia. Alzheimers Dement. Transl. Res. Clin. Interv. 3, 603–611 (2017).
Vasterling, J. J., Verfaellie, M. & Sullivan, K. D. Mild traumatic brain injury and posttraumatic stress disorder in returning veterans: perspectives from cognitive neuroscience. Clin. Psychol. Rev. 29, 674–684 (2009).
H.R.847 – James Zadroga 9/11 Health and Compensation Act of 2010. Report 111-560 (House of Representatives, 2010).
World Trade Center Health Effects program at a glance. https://www.cdc.gov/wtc/ataglance.html (NIOSH, Centers for Disease Control and Prevention, 2021).
Farfel, M. et al. An overview of 9/11 experiences and respiratory and mental health conditions among World Trade Center Health Registry enrollees. J. Urban. Health 85, 880–909 (2008).
Acknowledgements
We thank R. D. Daniels, T. Kubale and D. Reismann for their assistance in planning and participating in the meeting that led to this Perspective. We would also like to acknowledge funding from the National Institute for Occupational Safety and Health (CDC/NIOSH: 200-2011-39361; U01 OH011314; U01 OH010718), and from the National Institute on Aging (NIH/NIA: R01 AG049953; P50 AG005138).
Review criteria
A comprehensive literature review was completed in advance of the 2019 US National Institute for Occupational Safety and Health (NIOSH) meeting using a database of papers published about World Trade Center (WTC) exposures and outcomes maintained by the NIOSH programme. Speakers were invited by two WTC researchers and asked to provide two representative papers of their own work to be briefly discussed during the meeting to educate audience members about their research. In preparation for this Perspective, a scoping literature search was also conducted using PubMed, including articles published in the areas of cognition, ageing, neurobiology, neuroimaging or neurodegeneration in survivor and responder populations affected by WTC attacks from 11 September 2001 to 1 May 2021 (search terms: “World Trade Center” AND (cogniti* OR aging OR neurobiology OR neuroimage* OR neurodegener*). The search resulted in 70 non-overlapping citations; relevant studies were retained and cited in this Perspective and studies specific to the topics of interest in this Perspective were highlighted. Attendees were also asked to discuss the relevance of MCI in this cohort and highlight important aspects that merited further investigation. The meeting was recorded and transcribed. Each presenter was asked to review transcripts for errors and for clarity, and all presenters were asked to review this manuscript for accuracy and to ensure final agreement with these materials. A writing team was tasked with capturing meeting materials and relevant background in this paper, and all authors were provided with opportunities to edit, modify and update sections in the final manuscript.
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S.A.P.C., M.K. and Y.D. researched data for the article, made substantial contributions to discussion of content, wrote the article, and reviewed and edited the manuscript before submission. C.B.H., C.F., E.R.P., A.S. and E.D.D. made substantial contributions to discussion of content, wrote the article, and reviewed and edited the manuscript before submission. J.E. wrote the article, and reviewed and edited the manuscript before submission. All other authors made substantial contributions to discussion of content, and reviewed and edited the manuscript before submission.
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Nature Reviews Neurology thanks B. Snitz, who co-reviewed with B. Shaaban; D. Cory-Sletcha and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
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Glossary
- Cognitive reserve theory
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The theory that individual differences in the cognitive processes or neural networks underlying task performance enable some individuals to cope better with brain damage than other individuals
- Healthy worker effect
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The tendency for those who are working to be healthier, on average, than those who were unemployed or who do not participate in the workforce, leading to a consistent under-estimation of the impact of occupational exposures
- Re-experiencing symptoms
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Having sudden and unwanted traumatic memories that intrude into or even seem to replace what is happening in the current moment
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Clouston, S.A.P., Hall, C.B., Kritikos, M. et al. Cognitive impairment and World Trade Centre-related exposures. Nat Rev Neurol 18, 103–116 (2022). https://doi.org/10.1038/s41582-021-00576-8
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DOI: https://doi.org/10.1038/s41582-021-00576-8
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