Longitudinal analysis of a dominantly inherited Alzheimer disease mutation carrier protected from dementia

  • Llibre-Guerra, Jorge J.
  • Victoria Fernandez, M.
  • Joseph-Mathurin, Nelly
  • Bian, Shijia
  • Carter, Kathleen
  • 외 130명
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초록

We conducted an in-depth longitudinal study on an individual carrying the presenilin 2 p.Asn141Ile mutation, traditionally associated with dominantly inherited Alzheimer's disease (AD), who has remarkably remained asymptomatic past the expected age of clinical onset. This study combines genetic, neuroimaging and biomarker analyses to explore the underpinnings of this resilience. Unlike typical progression in dominantly inherited AD, tau pathology in this case was confined to the occipital region without evidence of spread, potentially explaining the preservation of cognitive functions. Genetic analysis revealed several variants that, although not previously associated with protection against AD, suggest new avenues for understanding disease resistance. Notably, environmental factors such as significant heat exposure and a unique proteomic profile rich in heat shock proteins might indicate adaptive mechanisms contributing to the observed phenotype. This case underscores the complexity of Alzheimer's pathology and suggests that blocking tau deposition could be a promising target for therapeutic intervention. The study highlights the need for further research to identify and validate the mechanisms that could inhibit or localize tau pathology as a strategy to mitigate or delay the onset of Alzheimer's dementia.

키워드

Fluorodeoxyglucose F 18Mucin 3Presenilin 2Presenilin-2Tau ProteinsBiological MarkerComplementary DnaFluorodeoxyglucose F 18Mucin 3Pittsburgh Compound BPresenilin 2Tau ProteinAdaptationAdultAgedAlzheimer DiseaseArticleCase ReportCerebrospinal FluidClinical ArticleClinical Dementia Rating ScaleClinical FeatureCohort AnalysisDementiaDemographicsDigit Symbol Substitution TestDominant InheritanceEnvironmental ExposureFemaleFluid-attenuated Inversion Recovery ImagingGene MutationGenetic AnalysisGenetic VariationGeriatric Depression ScaleHeterozygoteHumanImmune ResponseImmunoassayIn Vivo StudyLate Onset DisorderLeft HippocampusLiquid Chromatography-mass SpectrometryLongitudinal StudyLumbar PunctureMajor Clinical StudyMaleMiddle AgedMini Mental State ExaminationMissense MutationNeuroimagingNeuropathologyNeuropsychiatric InventoryNuclear Magnetic Resonance ImagingOmicsPositron Emission TomographyPostsynaptic DensityProtein LocalizationProteomicsSegregation AnalysisStandardized Uptake Value RatioT1 Weighted ImagingT2 Weighted ImagingThermal ExposureUnified Parkinson Disease Rating ScaleWechsler Adult Intelligence ScaleWechsler Memory ScaleWhole Exome SequencingDominant GeneGeneticsMetabolismMutationPathologyAlzheimer DiseaseDementiaFemaleGenes, DominantHeterozygoteHumansLongitudinal StudiesMaleMiddle AgedMutationPresenilin-2Tau ProteinsTREM2 VARIANTSTAU PATHOLOGYONSETGENE
제목
Longitudinal analysis of a dominantly inherited Alzheimer disease mutation carrier protected from dementia
저자
Llibre-Guerra, Jorge J.Victoria Fernandez, M.Joseph-Mathurin, NellyBian, ShijiaCarter, KathleenLi, YanAschenbrenner, Andrew J.Pottier, CyrilSigurdson, WendyMcDade, EricGordon, Brian A.Renton, Alan E.Benzinger, Tammie L. S.Ibanez, LauraBarthelemy, NicoJohnson, MatthewHassenstab, JasonWang, GuoqiaoGoate, Alison M.Western, DanWang, CiyangHobbs, DianaDaniels, AlishaKarch, CelesteMorris, John C.Cruchaga, CarlosJohnson, Erik C. B.Bateman, Randall J.Aguillon, DavidAllegri, Ricardo F.Baena, AnaBaker, BryceBanks, JessicaBarthelemy, Nicolas R.Bartzel, JamieBateman, RandallBechara, Jacob A.Berman, Sarah B.Bocanegra, YamileBrooks, William S.Cash, David M.Chen, AllisonChen, CharlesChhatwal, Jasmeer P.Chrem Mendez, PatricioCourtney, LauraDaniels, Alisha J.Day, Gregory S.Devenney, EmmaFagan, Anne M.Farlow, MartinFlores, ShaneyFox, Nick C.Franklin, ErinFulton-Howard, BrianGoyal, ManuGraber-Sultan, SusanneGraff-Radford, Neill R.Gremminger, EmilyHellm, CortaigaHoltzman, David M.Hornbeck, RussHuey, Edward D.Ikeuchi, TakeshiIkonomovic, SnezanaIshiguro, TakanobuIshii, KenjiJackson, KelleyJerome, GinaJucker, MathiasKarch, Celeste M.Kasuga, KensakuKeefe, SarahKoudelis, DeborahKuder-Buletta, Elkela Fougere, ChristianLaske, ChristophLee, Jae-HongLevey, Allan I.Levin, JohannesMilena Leon, YudyLopera, FranciscoLu, RuijinMaa, CourtneyMarsh, JacobMartin, MarianaMartins, RalphMassoumzadeh, ParinazMasters, ColinMcCullough, AustinMckay, NicoleMinton, MatthewMori, HiroshiNicklaus, JoyceNie, YuzhengNiimi, YoshikiNoble, James M.Obermueller, UlrikePerrin, Richard J.Picarello, Danielle M.Pulizos, ChristineRamirez, LauraReischl, GeraldRingman, JohnRizzo, JacquelineRoedenbeck, YvonneRoh, Jee HoonRosa-Neto, PedroRyan, Natalie S.Sabaredzovic, EditaSalloway, StephenSanchez-Valle, RaquelSchofield, Peter R.Scott, JalenSenda, MichioSerna, LauraSeyfried, Nicholas T.Simmons, AshleeSkrbec, KarinaSmith, JenniferStauber, JenniferStout, SarahSupnet-Bell, CharleneSurace, EzequielTimofejavaite, RedaVazquez, SilviaVlassenko, AndreiVoeglein, JonathanWang, QingWang, YongXiong, ChengjieXu, XiongXu, JinbinZiegemeier, AngelaZiegemeier, Ellen
DOI
10.1038/s41591-025-03494-0
발행일
2025-02-10
유형
Article; Early Access
저널명
Nature Medicine
31
4
페이지
1267 ~ 1275