Regional atrophy of the insular cortex is associated with neuropsychiatric symptoms in Alzheimer's disease patients
Abstract
BACKGROUND: Alzheimer's disease (AD) is a devastating illness that results in progressive cognitive decline and neuropsychiatric symptoms. The neuropsychiatric symptoms are associated with a rapid decline in cognition and activities of daily living and increased mortality, however the neuroanatomical localisation involved in the development of neuropsychiatric symptoms remains poorly understood. The aim of this study was to identify the association with the regional volume of the insular cortex and each neuropsychiatric symptom in patients with AD. METHODS: Subjects diagnosed with AD (n = 40) were evaluated. Magnetic resonance images were obtained and the insular cortex was subdivided into four subregions through the central sulcus of the insula and bilaterally: right anterior insular cortex, right posterior insular cortex, left anterior insular cortex and left posterior insular cortex. The neuropsychiatric symptoms were assessed using the Neuropsychiatric Inventory. A partial correlation analysis was performed. RESULTS: A significant negative correlation existed between apathy, the irritability subscale score and the volume ratio of the bilateral anterior insular cortex and right posterior insular cortex (r = -0.457, -0.433 and -0.572, respectively, p = 0.032, 0.044 and 0.005, respectively). CONCLUSION: The findings suggest that the regional atrophy of the insular cortex is associated with neuropsychiatric symptoms in AD patients.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Apathy in Alzheimer's disease is associated with decreased insula volume.
“Two studies report an association of apathy with decreased insula volume (Moon et al., 2014; Stanton et al., 2013) although they disagree on whether this is bilateral or unilateral.”
From Neuropsychiatric symptoms in Alzheimer's disease: what might be associated brain circuits? (2015) · cites this paper as Moon et al., 2014
Cites
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D., & Stadlan, E. M. (1984) · Neurology · doi:10.1212/wnl.34.7.939 · Cited by 27,915 · see citing works
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657 · see citing works
Stereotaxic Display of Brain Lesions
Rorden, C., & Brett, M. (2000) · Behavioural Neurology · doi:10.1155/2000/421719 · Cited by 2,573 · see citing works
Folate, Vitamin B12, and Serum Total Homocysteine Levels in Confirmed Alzheimer Disease
Clarke, R., Smith, A. D., Jobst, K. A., Refsum, H., Sutton, L., & Ueland, P. M. (1998) · Archives of Neurology · doi:10.1001/archneur.55.11.1449 · Cited by 1,408 · see citing works
Decreased volume of left and total anterior insular lobule in schizophrenia
Makris, N., Goldstein, J. M., Kennedy, D. N., Hodge, S. M., Caviness, V. S., Faraone, S. V., Tsuang, M. T., & Seidman, L. J. (2006) · Schizophrenia Research · doi:10.1016/j.schres.2005.11.020 · Cited by 743 · see citing works
Frontal-subcortical circuits and neuropsychiatric disorders
Mega, M. S., & Cummings, J. L. (1994) · Journal of Neuropsychiatry · doi:10.1176/jnp.6.4.358 · Cited by 726 · see citing works
Global and local gray matter loss in mild cognitive impairment and Alzheimer's disease
Karas, G. B., Scheltens, P., Rombouts, S. A. R. B., Visser, P. J., van Schijndel, R. A., Fox, N. C., & Barkhof, F. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.006 · Cited by 613 · see citing works
Neuroanatomical correlates of behavioural disorders in dementia
Rosen, H. J., Allison, S. C., Schauer, G. F., Gorno-Tempini, M. L., Weiner, M. W., & Miller, B. L. (2005) · Brain · doi:10.1093/brain/awh628 · Cited by 497 · see citing works
Voxel-based mapping of brain gray matter volume and glucose metabolism profiles in normal aging
Kalpouzos, G., Chételat, G., Baron, J.-C., Landeau, B., Mevel, K., Godeau, C., Barré, L., Constans, J.-M., Viader, F., Eustache, F., et al. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.05.019 · Cited by 392 · see citing works
Neuroanatomical correlates of neuropsychiatric symptoms in Alzheimer's disease
Bruen, P. D., McGeown, W. J., Shanks, M. F., & Venneri, A. (2008) · Brain · doi:10.1093/brain/awn151 · Cited by 374 · see citing works
Insular cortex and neuropsychiatric disorders: A review of recent literature
Nagai, M., Kishi, K., & Kato, S. (2007) · European Psychiatry · doi:10.1016/j.eurpsy.2007.02.006 · Cited by 332 · see citing works
Functional organization of the human anterior insular cortex
Mutschler, I., Wieckhorst, B., Kowalevski, S., Derix, J., Wentlandt, J., Schulze‐Bonhage, A., & Ball, T. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.03.101 · Cited by 238 · see citing works
Association between blood pressure, white matter lesions, and atrophy of the medial temporal lobe
den Heijer, T., Launer, L. J., Prins, N. D., van Dijk, E. J., Vermeer, S. E., Albert Hofman, D., Koudstaal, P. J., & Breteler, M. M. B. (2005) · Neurology · doi:10.1212/01.wnl.0000149641.55751.2e · Cited by 237 · see citing works
Disrupted Functional Connectivity of the Pain Network in Fibromyalgia
Cifré, I., Sitges, C., Fraiman, D., Muñoz, M. Á., Balenzuela, P., González‐Roldán, A. M., Martínez-Jauand, M., Birbaumer, N., Chialvo, D. R., & Montoya, P. (2011) · Psychosomatic Medicine · doi:10.1097/psy.0b013e3182408f04 · Cited by 212 · see citing works
Structural correlates of apathy in Alzheimer's disease
Apostolova, L. G., Akopyan, G. G., Partiali, N., Steiner, C. A., Dutton, R. A., Hayashi, K. M., Dinov, I. D., Toga, A. W., Cummings, J. L., & Thompson, P. M. (2007) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000103914 · Cited by 190 · see citing works
Kasai, K., Shenton, M. E., Salisbury, D. F., Onitsuka, T., Toner, S. K., Yurgelun-Todd, D. A., Kikinis, R., Jolesz, F. A., & McCarley, R. W. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.11.1069 · Cited by 172 · see citing works
The neuropsychological impact of insular cortex lesions
Jones, C. L., Ward, J., & Critchley, H. D. (2010) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.2009.193672 · Cited by 158 · see citing works
A SPECT study of apathy in Alzheimer's disease
Lanctôt, K. L., Moosa, S., Herrmann, N., Leibovitch, F. S., Rothenburg, L., Cotter, A., & Black, S. E. (2007) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000103633 · Cited by 126 · see citing works
Striatal dopamine transporter levels correlate with apathy in neurodegenerative diseases
David, R., Koulibaly, M., Benoit, M., Garcia, R., Caci, H., Darcourt, J., & Robert, P. (2008) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2007.08.007 · Cited by 117 · see citing works
DeCarli, C. S., Reed, T., Miller, B. L., Wolf, P. A., Swan, G. E., & Carmelli, D. (1999) · Stroke · doi:10.1161/01.str.30.8.1548 · Cited by 111 · see citing works
Serum lipids and hippocampal volume: The link to Alzheimer's disease?
Wolf, H., Hensel, A., Arendt, T., Kivipelto, M., Winblad, B. G., & Gertz, H. (2004) · Annals of Neurology · doi:10.1002/ana.20289 · Cited by 110 · see citing works
Psychopathology of very mild dementia of the Alzheimer type
Rubin, E. H., & Kinscherf, D. A. (1989) · American Journal of Psychiatry · doi:10.1176/ajp.146.8.1017 · Cited by 109 · see citing works
Caputo, M., Monastero, R., Mariani, E., Santucci, A., Mangialasche, F., Camarda, R., Senin, U., & Mecocci, P. (2008) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2008.01175.x · Cited by 84 · see citing works
Effects of demographic factors on cortical thickness in Alzheimer's disease
Seo, S. W., Im, K., Lee, J. M., Kim, S. T., Ahn, H. J., Go, S. M., Kim, S.-H., & Na, D. L. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.02.004 · Cited by 78 · see citing works
LAM, L. C. W., Tam, C. W. C., Chiu, H. F. K., & Lui, V. W.-C. (2006) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.1694 · Cited by 54 · see citing works
Taki, Y., Thyreau, B., Kinomura, S., Sato, K., Goto, R., Wu, K., Kawashima, R., & Fukuda, H. (2012) · Human Brain Mapping · doi:10.1002/hbm.22067 · Cited by 52 · see citing works
Variations in estrogen receptor α gene and risk of dementia, and brain volumes on MRI
den Heijer, T., Schuit, S. C. E., Pols, H. A. P., van Meurs, J. B. J., Albert Hofman, D., Koudstaal, P. J., van Duijn, C. M., Uitterlinden, A. G., & Breteler, M. M. B. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001553 · Cited by 43 · see citing works
Cardiovascular Risk Factors Cause Cortical Thinning in Cognitively Impaired Patients
Seo, S. W., Lee, J., Im, K., Park, J.-S., Kim, S.-H., Kim, S. T., Ahn, J., Kim, M.-J., Kim, G. H., Kim, J., et al. (2011) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0b013e31822e0831 · Cited by 42 · see citing works
Inheritance of the ApoE ε4 Allele Increases the Rate of Brain Atrophy in Dementia Patients
Wahlund, L., Julin, P., Lannfelt, L., et al. (1999) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000017130 · Cited by 34 · see citing works
Matsuoka, T., Narumoto, J., Shibata, K., Okamura, A., Nakamura, K., Okuyama, C., Nishimura, T., & Fukui, K. (2010) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000295115 · Cited by 32 · see citing works
Tezuka, K., Meguro, K., Akanuma, K., Tanaka, N., Ishii, H., & Yamaguchi, S. (2011) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2011.05.019 · Cited by 11 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Neuropsychiatric symptoms in Alzheimer's disease: what might be associated brain circuits?
Rosenberg, P. B., Nowrangi, M. A., & Lyketsos, C. G. (2015) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2015.05.005 · Cited by 302 · see citing works
Diseases, Disorders, and Comorbidities of Interoception
Bonaz, B., Lane, R. D., Oshinsky, M. L., Kenny, P. J., Sinha, R., Mayer, E. A., & Critchley, H. D. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.009 · Cited by 260 · see citing works
Kos, C., van Tol, M.-J., Marsman, J.-B. C., Knegtering, H., & Aleman, A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.08.012 · Cited by 101 · see citing works
Naudin, M., Mondon, K., El-Hage, W., Perriot, E., Boudjarane, M., Desmidt, T., Lorette, A., Belzung, C., Hommet, C., & Atanasova, B. (2015) · Psychiatry Research · doi:10.1016/j.psychres.2015.03.021 · Cited by 19 · see citing works
- Authors
- Moon, Y., Moon, W.-J., Kim, H., & Han, S.-H.
- Affiliations
- Konkuk University (KR)
- Pediatrics and Genetics (US)
- Venue
- European Neurology
- Publisher
- S. Karger AG
- Published
- 2014
- Volume
- 71
- Issue
- 5-6
- Pages
- 223-229
- ISSN
- 0014-3022 (ISSN-L)
- 1421-9913
- OpenAlex
- W1989919992
- Cited by
- 56
- References
- 31
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 3 · 2023: 11 · 2022: 4 · 2021: 6 · 2020: 6 · 2019: 1 · 2018: 5 · 2017: 2 · 2016: 9 · 2015: 3
- FWCI
- 3.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Neurology (publishedVersion)
- PubMed (publishedVersion)
- 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 › Cognitive Neuroscience › Neurobiology of Language and Bilingualism
- Keywords
- Alzheimer's disease, insula, regional brain atrophy, neuropsychiatric symptoms, apathy, irritability, anterior insula, posterior insular cortex, cortical volume, Neuropsychiatric Inventory
- MeSH terms
- Aged, Alzheimer Disease, Atrophy, Cerebral Cortex, Female, Humans, Irritable Mood, Functional Laterality, Magnetic Resonance Imaging, Male, Neuropsychological Tests, Organ Size, Retrospective Studies, Severity of Illness Index, Apathy
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review