• This record comes from PubMed

Sex differences in brain atrophy in dementia with Lewy bodies

. 2024 Mar ; 20 (3) : 1815-1826. [epub] 20231222

Language English Country United States Media print-electronic

Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural

Grant support
R37-AG011378 NIH HHS - United States
R01 AG041851 NIA NIH HHS - United States
C06 RR018898 NCRR NIH HHS - United States
U01-AG006786 NIH HHS - United States
R01-AG040042 NIH HHS - United States
P50 AG016574 NIA NIH HHS - United States
R01 AG040042 NIA NIH HHS - United States
R01 AG011378 NIA NIH HHS - United States
R01 NS080820 NINDS NIH HHS - United States
P30 AG062677 NIA NIH HHS - United States
R01-NS080820 NIH HHS - United States
U01 NS100620 NINDS NIH HHS - United States
R01-AG041851 NIH HHS - United States
P50-AG016574 NIH HHS - United States
R37 AG011378 NIA NIH HHS - United States
U01-NS100620 NIH HHS - United States
C06-RR018898 NIH HHS - United States
U01 AG006786 NIA NIH HHS - United States

INTRODUCTION: Sex influences neurodegeneration, but it has been poorly investigated in dementia with Lewy bodies (DLB). We investigated sex differences in brain atrophy in DLB using magnetic resonance imaging (MRI). METHODS: We included 436 patients from the European-DLB consortium and the Mayo Clinic. Sex differences and sex-by-age interactions were assessed through visual atrophy rating scales (n = 327; 73 ± 8 years, 62% males) and automated estimations of regional gray matter volume and cortical thickness (n = 165; 69 ± 9 years, 72% males). RESULTS: We found a higher likelihood of frontal atrophy and smaller volumes in six cortical regions in males and thinner olfactory cortices in females. There were significant sex-by-age interactions in volume (six regions) and cortical thickness (seven regions) across the entire cortex. DISCUSSION: We demonstrate that males have more widespread cortical atrophy at younger ages, but differences tend to disappear with increasing age, with males and females converging around the age of 75. HIGHLIGHTS: Male DLB patients had higher odds for frontal atrophy on radiological visual rating scales. Male DLB patients displayed a widespread pattern of cortical gray matter alterations on automated methods. Sex differences in gray matter measures in DLB tended to disappear with increasing age.

Alzheimer Center Amsterdam Neurology Vrije Universiteit Amsterdam Amsterdam UMC location Vumc Amsterdam The Netherlands

Amsterdam Neuroscience Neurodegeneration Vrije Universiteit Amsterdam Amsterdam UMC location Vumc Amsterdam The Netherlands

Brain and Mind Research Central European Institute of Technology Masaryk University Brno Czech Republic

Center for Age Related Medicine Stavanger University Hospital Stavanger Norway

Department of Medicine and Aging Sciences University G d'Annunzio of Chieti Pescara Chieti Chieti Italy

Department of Neurology Mayo Clinic Rochester USA

Department of Neurology University Medical Center Ljubljana Slovenia

Department of Neuroscience Rehabilitation Ophthalmology Genetics Maternal and Child Health University of Genova Genova Italy

Department of Old Age Psychiatry Institute of Psychiatry Psychology and Neuroscience King's College London London UK

Department of Quality and Health Technology Faculty of Health Sciences University of Stavanger Stavanger Norway

Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA

Department of Radiology and Nuclear Medicine Amsterdam UMC Vrije Universiteit Amsterdam the Netherlands

Department of Radiology Mayo Clinic Rochester Minnesota USA

Division of Clinical Geriatrics Center for Alzheimer Research Department of Neurobiology Care Sciences and Society Karolinska Institutet Stockholm Sweden

Division of Psychiatry University College London London UK

Facultad de Ciencias de la Salud Universidad Fernando Pessoa Canarias Las Palmas España

Geriatrics and Neurology Units Research and Resources Memory Center Hôpitaux Universitaires de Strasbourg Strasbourg France

ICube Laboratory Strasbourg France

Institute of Biomedical Research August Pi i Sunyer Barcelona Catalonia Spain

Medical Psychology Unit Department of Medicine Institute of Neuroscience University of Barcelona Barcelona Catalonia Spain

Memory Clinic Department of Neurology Charles University 2nd Faculty of Medicine and Motol University Hospital Prague Czech Republic

Memory Clinic Landspitali Reykjavik Iceland

Network Center for Biomedical Research in Neurodegenerative Diseases Barcelona Catalonia Spain

Neurology Unit Department of Clinical and Experimental Sciences University of Brescia Brescia Italy

Parkinson and Movement Disorders Unit Study Center on Neurodegeneration Padova Italy

Queen Square Institute of Neurology and Centre for Medical Image Computing University College London London UK

St Margaret's Hospital Essex Partnership University NHS Foundation Trust Essex UK

Stavanger Medical Imaging Laboratory Department of Radiology Stavanger University Hospital Stavanger Norway

The Norwegian Centre for Movement Disorders Stavanger University Hospital Stavanger Norway

Translational and Clinical Research Institute Faculty of Medical Sciences Newcastle University Newcastle upon Tyne UK

University Hospital of Psychiatry and Psychotherapy Bern University of Bern Bern Switzerland

Update Of

PubMed

See more in PubMed

Podcasy JL, Epperson CN. Considering sex and gender in Alzheimer disease and other dementias. Dialogues Clin Neurosci. 2016;18(4):437‐446. doi:10.31887/DCNS.2016.18.4/cepperson PubMed DOI PMC

Cerri S, Mus L, Blandini F. Parkinson's disease in women and men: what's the difference? J Parkinsons Dis. 2019;9(3):501‐515. doi:10.3233/JPD-191683 PubMed DOI PMC

Fereshtehnejad SM, Religa D, Westman E, Aarsland D, Lökk J, Eriksdotter M. Demography, diagnostics, and medication in dementia with Lewy bodies and Parkinson's disease with dementia: data from the Swedish Dementia Quality Registry (SveDem). Neuropsychiatr Dis Treat. 2013;9:927‐935. doi:10.2147/NDT.S45840 PubMed DOI PMC

Kane JPM, Surendranathan A, Bentley A, et al. Clinical prevalence of Lewy body dementia. Alzheimer's Res Ther. 2018;10:19. doi:10.1186/s13195-018-0350-6 PubMed DOI PMC

Gan J, Chen Z, Shi Z, et al. Sex differences in clinical cognitive impairment with Lewy bodies: a Chinese multicenter study. Biol Sex Differ. 2022;13(55). doi:10.1186/s13293-022-00464-w PubMed DOI PMC

Mouton A, Blanc F, Gros A, et al. Sex ratio in dementia with Lewy bodies balanced between Alzheimer's disease and Parkinson's disease dementia: a cross‐sectional study. Alzheimer's Res Ther. 2018;10:92. doi:10.1186/s13195-018-0417-4 PubMed DOI PMC

Utsumi K, Fukatsu R, Yamada R, Takamaru Y, Hara Y, Yasumura S. Characteristics of initial symptoms and symptoms at diagnosis in probable dementia with Lewy body disease: incidence of symptoms and gender differences. Psychogeriatrics. 2020;20(5):737‐745. doi:10.1111/psyg.12586 PubMed DOI

Bayram E, Coughlin DG, Banks SJ, Litvan I. Sex differences for phenotype in pathologically defined dementia with Lewy bodies. J Neurol Neurosurg Psychiatry. 2021;92(7):745‐750. doi:10.1136/jnnp-2020-325668 PubMed DOI PMC

Chiu PY, Teng PR, Wei CY, Wang CW, Tsai CT. Gender difference in the association and presentation of visual hallucinations in dementia with Lewy bodies: a cross‐sectional study. Int J Geriatr Psychiatry. 2018;33(1):193‐199. doi:10.1002/gps.4706 PubMed DOI

van de Beek M, Babapour Mofrad R, van Steenoven I, et al. Sex‐specific associations with cerebrospinal fluid biomarkers in dementia with Lewy bodies. Alzheimer's Res Ther. 2020;12:44. doi:10.1186/s13195-020-00610-9 PubMed DOI PMC

Barnes LL, Lamar M, Schneider JA. Sex differences in mixed neuropathologies in community‐dwelling older adults. Brain Res. 2019;1719:11‐16. doi:10.1016/j.brainres.2019.05.028 PubMed DOI PMC

Fujimi K, Sasaki K, Noda K, et al. Clinicopathological outline of dementia with Lewy bodies applying the revised criteria: the Hisayama study. Brain Pathol. 2008;18(3):317‐325. doi:10.1111/j.1750-3639.2008.00169.x PubMed DOI PMC

Chiu SY, Wyman‐Chick KA, Ferman TJ, et al. Sex differences in dementia with Lewy bodies: focused review of available evidence and future directions. Parkinsonism Relat Disord. 2023;107:105285. doi:10.1016/j.parkreldis.2023.105285 PubMed DOI PMC

Ferreira D, Przybelski SA, Lesnick TG, et al. β‐Amyloid and tau biomarkers and clinical phenotype in dementia with Lewy bodies. Neurology. 2020;95(24):e3257‐e3268. doi:10.1212/WNL.0000000000010943 PubMed DOI PMC

Ghebremedhin E, Rosenberger A, Rüb U, et al. Inverse relationship between cerebrovascular lesions and severity of Lewy body pathology in patients with Lewy body diseases. J Neuropathol Exp Neurol. 2010;69(5):442‐448. doi:10.1097/NEN.0b013e3181d88e63 PubMed DOI

Ferreira D, Nedelska Z, Graff‐Radford J, et al. Cerebrovascular disease, neurodegeneration, and clinical phenotype in dementia with Lewy bodies. Neurobiol Aging. 2021;105:252‐261. doi:10.1016/j.neurobiolaging.2021.04.029 PubMed DOI PMC

Ferreira D, Przybelski SA, Lesnick TG, et al. Cross‐sectional associations of β‐Amyloid, tau, and cerebrovascular biomarkers with neurodegeneration in probable dementia with Lewy bodies. Neurology. 2023;100(8):e846‐e859. doi:10.1212/WNL.0000000000201579. Published online 2022. PubMed DOI PMC

Bayram E, Coughlin DG, Litvan I. Sex differences for clinical correlates of Alzheimer's pathology in people with Lewy body pathology. Mov Disord. 2022;37(7):1505‐1515. doi:10.1002/mds.29044 PubMed DOI PMC

Boccalini C, Nicastro N, Peretti DE, Caminiti SP, Perani D, Garibotto V. Sex differences in dementia with Lewy bodies: an imaging study of neurotransmission pathways. Eur J Nucl Med Mol Imaging. 2023;50(7):2036‐2046. doi:10.1007/s00259-023-06132-4 PubMed DOI PMC

Caminiti SP, Boccalini C, Nicastro N, Garibotto V, Perani D. Sex differences in brain metabolic connectivity architecture in probable dementia with Lewy bodies. Neurobiol Aging. 2023;126:14‐24. doi:10.1016/j.neurobiolaging.2023.02.004 PubMed DOI

Ballmaier M, O'Brien JT, Burton EJ, et al. Comparing gray matter loss profiles between dementia with Lewy bodies and Alzheimer's disease using cortical pattern matching: diagnosis and gender effects. Neuroimage. 2004;23(1):325‐335. doi:10.1016/j.neuroimage.2004.04.026 PubMed DOI

Oppedal K, Borda MG, Ferreira D, Westman E, Aarsland D. European DLB consortium: diagnostic and prognostic biomarkers in dementia with Lewy bodies, a multicenter international initiative. Neurodegener Dis Manag. 2019;9(5):247‐250. doi:10.2217/nmt-2019-0016 PubMed DOI

Abdelnour C, Ferreira D, Oppedal K, et al. The combined effect of amyloid‐β and tau biomarkers on brain atrophy in dementia with Lewy bodies. Neuroimage Clin. 2020;27:102333. doi:10.1016/j.nicl.2020.102333 PubMed DOI PMC

Kantarci K, Lowe VJ, Boeve BF, et al. AV‐1451 tau and β‐amyloid positron emission tomography imaging in dementia with Lewy bodies. Ann Neurol. 2017;81(1):58‐67. doi:10.1002/ana.24825 PubMed DOI PMC

McKeith IG, Dickson DW, Lowe J, et al. Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium. Neurology. 2005;65(12):1863‐1872. doi:10.1212/01.wnl.0000187889.17253.b1 PubMed DOI

Fazekas F, Chawluk JB, Alavi A, Hurtig HI, Zimmerman RA. MR signal abnormalities at 1.5 T in Alzheimer's dementia and normal aging. AJNR. 1987;8(3):421‐426. PubMed

Kantarci K, Petersen RC, Przybelski SA, et al. Hippocampal volumes, proton magnetic resonance spectroscopy metabolites, and cerebrovascular disease in mild cognitive impairment subtypes. Arch Neurol. 2008;65(12):1621‐1628. doi:10.1001/archneur.65.12.1621 PubMed DOI PMC

Oppedal K, Ferreira D, Cavallin L, et al. A signature pattern of cortical atrophy in dementia with Lewy bodies: a study on 333 patients from the European DLB consortium. Alzheimers Dement. 2019;15(3):400‐409. doi:10.1016/j.jalz.2018.09.011 PubMed DOI

Ferreira D, Verhagen C, Hernández‐Cabrera JA, et al. Distinct subtypes of Alzheimer's disease based on patterns of brain atrophy: longitudinal trajectories and clinical applications. Sci Rep. 2017;7:46263. doi:10.1038/srep46263 PubMed DOI PMC

Ferreira D, Cavallin L, Larsson EM, et al. Practical cut‐offs for visual rating scales of medial temporal, frontal and posterior atrophy in Alzheimer's disease and mild cognitive impairment. J Intern Med. 2015;278(3):277‐290. doi:10.1111/joim.12358 PubMed DOI

Ferreira D, Cavallin L, Granberg T, et al. Quantitative validation of a visual rating scale for frontal atrophy: associations with clinical status, APOE e4, CSF biomarkers and cognition. Eur Radiol. 2016;26(8):2597‐2610. doi:10.1007/s00330-015-4101-9 PubMed DOI

Scheltens P, Leys D, Barkhof F, et al. Atrophy of medial temporal lobes on MRI in “probable” Alzheimer's disease and normal ageing: diagnostic value and neuropsychological correlates. J Neurol Neurosurg Psychiatry. 1992;55(10):967‐972. doi:10.1136/jnnp.55.10.967 PubMed DOI PMC

Koedam ELGE, Lehmann M, van der Flier WM, et al. Visual assessment of posterior atrophy development of a MRI rating scale. Eur Radiol. 2011;21(12):2618‐2625. doi:10.1007/s00330-011-2205-4 PubMed DOI PMC

Schwarz CG, Gunter JL, Wiste HJ, et al. A large‐scale comparison of cortical thickness and volume methods for measuring Alzheimer's disease severity. Neuroimage Clin. 2016;11:802‐812. doi:10.1016/j.nicl.2016.05.017 PubMed DOI PMC

Schwarz CG, Gunter JL, Ward CP, et al. The mayo clinic adult lifespan template: better quantification across the lifespan. In: Alzheimer's Association International Conference (AAIC): Poster Presentations . 2017;13:792. doi:10.1016/j.jalz.2017.06.1071 DOI

Avants BB, Epstein CL, Grossman M, Gee JC. Symmetric diffeomorphic image registration with cross‐correlation: evaluating automated labeling of elderly and neurodegenerative brain. Med Image Anal. 2008;12(1):26‐41. doi:10.1016/j.media.2007.06.004 PubMed DOI PMC

Das SR, Avants BB, Grossman M, Gee JC. Registration based cortical thickness measurement. Neuroimage. 2009;45(3):867‐879. doi:10.1016/j.neuroimage.2008.12.016 PubMed DOI PMC

Genovese CR, Lazar NA, Nichols T. Thresholding of statistical maps in functional neuroimaging using the false discovery rate. Neuroimage. 2002;15(4):870‐878. doi:10.1006/nimg.2001.1037 PubMed DOI

Ferreira D. Structural imaging in dementia with Lewy bodies: the potential of multivariate data analysis. Psychiatry Res Neuroimaging. 2020;306:111180. doi:10.1016/j.pscychresns.2020.111180 PubMed DOI

Williams SS, Williams J, Combrinck M, Christie S, Smith AD, McShane R. Olfactory impairment is more marked in patients with mild dementia with Lewy bodies than those with mild Alzheimer disease. J Neurol Neurosurg Psychiatry. 2009;80(6):667‐670. doi:10.1136/jnnp.2008.155895 PubMed DOI

Beach TG, Adler CH, Zhang N, et al. Severe hyposmia distinguishes neuropathologically confirmed dementia with Lewy bodies from Alzheimer's disease dementia. PLoS One. 2020;15(4):e0231720. doi:10.1371/journal.pone.0231720 PubMed DOI PMC

Thomas AJ, Hamilton CA, Barker S, et al. Olfactory impairment in mild cognitive impairment with Lewy bodies and Alzheimer's disease. Int Psychogeriatr. 2022;34(6):585‐592. doi:10.1017/S1041610221001265 PubMed DOI

McKeith IG, Boeve BF, Dickson DW, et al. Diagnosis and management of dementia with Lewy bodies: fourth consensus report of the DLB Consortium. Neurology. 2017;89(1):88‐100. doi:10.1212/WNL.0000000000004058 PubMed DOI PMC

Inguanzo A, Poulakis K, Mohanty R, et al. MRI data‐driven clustering reveals different subtypes of Dementia with Lewy bodies. npj Parkinsons Dis. 2023;9(1):5. doi:10.1038/s41531-023-00448-6 PubMed DOI PMC

Garcia‐Falgueras A, Junque C, Giménez M, Caldú X, Segovia S, Guillamon A. Sex differences in the human olfactory system. Brain Res. 2006;1116:103‐111. doi:10.1016/j.brainres.2006.07.115 PubMed DOI

Alotaibi MM, De Marco M, Venneri A. Sex differences in olfactory cortex neuronal loss in aging. Front Hum Neurosci. 2023;17:1130200. doi:10.3389/fnhum.2023.1130200 PubMed DOI PMC

Campabadal A, Segura B, Junque C, Iranzo A. Structural and functional magnetic resonance imaging in isolated REM sleep behavior disorder: a systematic review of studies using neuroimaging software. Sleep Med Rev. 2021;59:101495. doi:10.1016/j.smrv.2021.101495 PubMed DOI

Bustamante‐Barrientos FA, Méndez‐Ruette M, Ortloff A, et al. The impact of estrogen and estrogen‐like molecules in neurogenesis and neurodegeneration: beneficial or harmful? Front Cell Neurosci. 2021;15:636176. doi:10.3389/fncel.2021.636176 PubMed DOI PMC

Kantarci K, Tosakulwong N, Lesnick TG, et al. Brain structure and cognition 3 years after the end of an early menopausal hormone therapy trial. Neurology. 2018;90(16):e1404‐e1412. doi:10.1212/WNL.0000000000005325 PubMed DOI PMC

Pezzoli S, Cagnin A, Antonini A, Venneri A. Frontal and subcortical contribution to visual hallucinations in dementia with Lewy bodies and Parkinson's disease. Postgrad Med. 2019;131(7):509‐522. doi:10.1080/00325481.2019.1656515 PubMed DOI

Ritchie SJ, Cox SR, Shen X, et al. Sex differences in the adult human brain: evidence from 5216 UK biobank participants. Cereb Cortex. 2018;28(8):2959‐2975. doi:10.1093/cercor/bhy109 PubMed DOI PMC

Christova P, Georgopoulos AP. Differential reduction of gray matter volume with age in 35 cortical areas in men (more) and women (less). J Neurophysiol. 2023;129(4):894‐899. doi:10.1152/jn.00066.2023 PubMed DOI PMC

Yadav SK, Kathiresan N, Mohan S, et al. Gender‐based analysis of cortical thickness and structural connectivity in Parkinson's disease. J Neurol. 2016;263(11):2308‐2318. doi:10.1007/s00415-016-8265-2 PubMed DOI PMC

Tremblay C, Abbasi N, Zeighami Y, et al. Sex effects on brain structure in de novo Parkinson's disease: a multimodal neuroimaging study. Brain. 2020;143(10):3052‐3066. doi:10.1093/brain/awaa234 PubMed DOI

Oltra J, Uribe C, Campabadal A, et al. Sex differences in brain and cognition in de novo Parkinson's Disease. Front Aging Neurosci. 2021;13:791532. doi:10.3389/fnagi.2021.791532 PubMed DOI PMC

Oltra J, Segura B, Uribe C, et al. Sex differences in brain atrophy and cognitive impairment in Parkinson's disease patients with and without probable rapid eye movement sleep behavior disorder. J Neurol. 2022;269:1591‐1599. doi:10.1007/s00415-021-10728-x PubMed DOI PMC

Li H, Jia X, Chen M, Jia X, Yang Q. Sex differences in brain structure in de novo Parkinson's disease: a cross‐sectional and longitudinal neuroimaging study. J Parkinsons Dis. doi:10.3233/JPD-225125. Published online 2023. PubMed DOI PMC

Kurasz AM, Smith GE, McFarland MG, Armstrong MJ, O'Bryant S. Ethnoracial differences in Lewy body diseases with cognitive impairment. J Alzheimer's Dis. 2020;77(1):165‐174. doi:10.3233/JAD-200395 PubMed DOI PMC

Newest 20 citations...

See more in
Medvik | PubMed

Grey matter networks in women and men with dementia with Lewy bodies

. 2024 Apr 13 ; 10 (1) : 84. [epub] 20240413

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...