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  1. Article ; Online: Interest in genetic susceptibility testing and disclosure of AD dementia risk in cognitively normal adults: a survey study.

    Waterink, Lisa / Masselink, Larissa A / van der Lee, Sven J / Visser, Leonie N C / Cleutjens, Solange / van der Schaar, Jetske / van Harten, Argonde C / Scheltens, Philip / Sikkes, Sietske A M / van der Flier, Wiesje M / Zwan, Marissa D

    Alzheimer's research & therapy

    2024  Volume 16, Issue 1, Page(s) 1

    Abstract: Background: Apolipoprotein-E (APOE) genetic testing for Alzheimer's disease is becoming more important as clinical trials are increasingly targeting individuals carrying APOE-ε4 alleles. Little is known about the interest in finding out one's genetic ... ...

    Abstract Background: Apolipoprotein-E (APOE) genetic testing for Alzheimer's disease is becoming more important as clinical trials are increasingly targeting individuals carrying APOE-ε4 alleles. Little is known about the interest in finding out one's genetic risk for Alzheimer's disease in the general population. Our objective was to examine this in a sample of cognitively normal (CN) adults within a population-based online research registry with the goal to implement APOE-ε4 status for trial recruitment.
    Methods: An online survey was completed by 442 CN participants between the age of 49 and 75 years (56% female) from the Dutch Brain Research Registry. The survey assessed interest in participation in research into, and disclosure of, genetic risk for dementia. The survey assessed interest in participation in research into, and disclosure of, genetic risk for dementia and knowing their genetic risk in different hypothetical risk scenarios (10%, 30%, and 50% genetic risk for dementia at age 85, corresponding to APOEε2/ε2 or ε2/ε3, APOEε3/ε4 or ε2ε4, and APOE-ε4/ε4 genotypes). Cochran's Q and post hoc McNemar tests were used to analyse differences in frequencies across scenarios.
    Results: Most participants were interested in participating in research into and disclosure of their genetic risk (81%). The most reported reason was to contribute to scientific research (94%). Interest was higher in males, whilst lower-educated participants were more often undecided. When provided with different risk scenarios, interest in knowing their risk was somewhat higher in the scenarios with higher risk, i.e. in the 50% (79%) compared to the 10% scenario (73%;χ
    Conclusions: Our findings indicate that the vast majority of CN adults participating in a research registry expresses interest in AD genetic risk research and disclosure. Interest in genetic risk disclosure is higher in scenarios corresponding to the APOE-ε4 genotype. This suggests APOE-ε4 screening within an online research registry is potentially a well-received method to accelerate inclusion for trials.
    MeSH term(s) Male ; Adult ; Humans ; Female ; Middle Aged ; Aged ; Aged, 80 and over ; Alzheimer Disease/diagnosis ; Alzheimer Disease/genetics ; Alzheimer Disease/epidemiology ; Disclosure ; Genotype ; Apolipoproteins E/genetics ; Genetic Predisposition to Disease/genetics ; Apolipoprotein E4/genetics
    Chemical Substances Apolipoproteins E ; Apolipoprotein E4
    Language English
    Publishing date 2024-01-02
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2506521-X
    ISSN 1758-9193 ; 1758-9193
    ISSN (online) 1758-9193
    ISSN 1758-9193
    DOI 10.1186/s13195-023-01364-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The Role of Age-Related Clonal Hematopoiesis in Genetic Sequencing Studies.

    Holstege, Henne / Hulsman, Marc / van der Lee, Sven J / van den Akker, Erik B

    American journal of human genetics

    2020  Volume 107, Issue 3, Page(s) 575–576

    MeSH term(s) DNA-Binding Proteins ; Dioxygenases ; Hematopoiesis ; High-Throughput Nucleotide Sequencing ; Humans ; Neurodegenerative Diseases ; Proto-Oncogene Proteins
    Chemical Substances DNA-Binding Proteins ; Proto-Oncogene Proteins ; Dioxygenases (EC 1.13.11.-) ; TET2 protein, human (EC 1.13.11.-)
    Language English
    Publishing date 2020-08-08
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 219384-x
    ISSN 1537-6605 ; 0002-9297
    ISSN (online) 1537-6605
    ISSN 0002-9297
    DOI 10.1016/j.ajhg.2020.07.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Quantitative trait loci mapping of circulating metabolites in cerebrospinal fluid to uncover biological mechanisms involved in brain-related phenotypes.

    Reus, Lianne M / Boltz, Toni / Francia, Marcelo / Bot, Merel / Ramesh, Naren / Koromina, Maria / Pijnenburg, Yolande A L / den Braber, Anouk / van der Flier, Wiesje M / Visser, Pieter Jelle / van der Lee, Sven J / Tijms, Betty M / Teunissen, Charlotte E / Loohuis, Loes Olde / Ophoff, Roel A

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Genomic studies of molecular traits have provided mechanistic insights into complex disease, though these lag behind for brain-related traits due to the inaccessibility of brain tissue. We leveraged cerebrospinal fluid (CSF) to study neurobiological ... ...

    Abstract Genomic studies of molecular traits have provided mechanistic insights into complex disease, though these lag behind for brain-related traits due to the inaccessibility of brain tissue. We leveraged cerebrospinal fluid (CSF) to study neurobiological mechanisms
    Language English
    Publishing date 2023-09-27
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.09.26.559021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Association of MGMT and BIN1 genes with Alzheimer's disease risk across sex and APOE ε4 status.

    Le Borgne, Julie / Amouyel, Philippe / Andreassen, Ole / Frikke-Schmidt, Ruth / Hiltunen, Mikko / Ingelsson, Martin / Ramirez, Alfredo / Rossi, Giacomina / Ruiz, Agustin / Sanchez-Juan, Pascual / Sims, Rebecca / Sleegers, Kristel / Tsolaki, Magda / van der Lee, Sven J / Williams, Julie / Lambert, Jean-Charles / Bellenguez, Céline

    Alzheimer's & dementia : the journal of the Alzheimer's Association

    2023  Volume 20, Issue 3, Page(s) 2282–2284

    MeSH term(s) Humans ; Apolipoprotein E4/genetics ; Alzheimer Disease/genetics ; Apolipoproteins E/genetics ; Nuclear Proteins/genetics ; Tumor Suppressor Proteins/genetics ; Adaptor Proteins, Signal Transducing/genetics ; DNA Modification Methylases ; DNA Repair Enzymes
    Chemical Substances Apolipoprotein E4 ; Apolipoproteins E ; BIN1 protein, human ; Nuclear Proteins ; Tumor Suppressor Proteins ; Adaptor Proteins, Signal Transducing ; MGMT protein, human (EC 2.1.1.63) ; DNA Modification Methylases (EC 2.1.1.-) ; DNA Repair Enzymes (EC 6.5.1.-)
    Language English
    Publishing date 2023-12-02
    Publishing country United States
    Document type Letter
    ZDB-ID 2211627-8
    ISSN 1552-5279 ; 1552-5260
    ISSN (online) 1552-5279
    ISSN 1552-5260
    DOI 10.1002/alz.13550
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Mapping the genetic landscape of early-onset Alzheimer's disease in a cohort of 36 families.

    Mol, Merel O / van der Lee, Sven J / Hulsman, Marc / Pijnenburg, Yolande A L / Scheltens, Phillip / Seelaar, Harro / van Swieten, John C / Kaat, Laura Donker / Holstege, Henne / van Rooij, Jeroen G J

    Alzheimer's research & therapy

    2022  Volume 14, Issue 1, Page(s) 77

    Abstract: Background: Many families with clinical early-onset Alzheimer's disease (EOAD) remain genetically unexplained. A combination of genetic factors is not standardly investigated. In addition to monogenic causes, we evaluated the possible polygenic ... ...

    Abstract Background: Many families with clinical early-onset Alzheimer's disease (EOAD) remain genetically unexplained. A combination of genetic factors is not standardly investigated. In addition to monogenic causes, we evaluated the possible polygenic architecture in a large series of families, to assess if genetic testing of familial EOAD could be expanded.
    Methods: Thirty-six pedigrees (77 patients) were ascertained from a larger cohort of patients, with relationships determined by genetic data (exome sequencing data and/or SNP arrays). All families included at least one AD patient with symptom onset <70 years. We evaluated segregating rare variants in known dementia-related genes, and other genes or variants if shared by multiple families. APOE was genotyped and duplications in APP were assessed by targeted test or using SNP array data. We computed polygenic risk scores (PRS) compared with a reference population-based dataset, by imputing SNP arrays or exome sequencing data.
    Results: In eight families, we identified a pathogenic variant, including the genes APP, PSEN1, SORL1, and an unexpected GRN frameshift variant. APOE-ε4 homozygosity was present in eighteen families, showing full segregation with disease in seven families. Eight families harbored a variant of uncertain significance (VUS), of which six included APOE-ε4 homozygous carriers. PRS was not higher in the families combined compared with the population mean (beta 0.05, P = 0.21), with a maximum increase of 0.61 (OR = 1.84) in the GRN family. Subgroup analyses indicated lower PRS in six APP/PSEN1 families compared with the rest (beta -0.22 vs. 0.10; P = 0.009) and lower APOE burden in all eight families with monogenic cause (beta 0.29 vs. 1.15, P = 0.010). Nine families remained without a genetic cause or risk factor identified.
    Conclusion: Besides monogenic causes, we suspect a polygenic disease architecture in multiple families based on APOE and rare VUS. The risk conveyed by PRS is modest across the studied families. Families without any identified risk factor render suitable candidates for further in-depth genetic evaluation.
    MeSH term(s) Alzheimer Disease/genetics ; Alzheimer Disease/pathology ; Apolipoproteins E/genetics ; Cohort Studies ; Heterozygote ; Humans ; LDL-Receptor Related Proteins/genetics ; Membrane Transport Proteins/genetics ; Whole Exome Sequencing
    Chemical Substances Apolipoproteins E ; LDL-Receptor Related Proteins ; Membrane Transport Proteins ; SORL1 protein, human
    Language English
    Publishing date 2022-06-01
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2506521-X
    ISSN 1758-9193 ; 1758-9193
    ISSN (online) 1758-9193
    ISSN 1758-9193
    DOI 10.1186/s13195-022-01018-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Longitudinal Maintenance of Cognitive Health in Centenarians in the 100-plus Study.

    Beker, Nina / Sikkes, Sietske A M / Hulsman, Marc / Tesi, Niccolò / van der Lee, Sven J / Scheltens, Philip / Holstege, Henne

    JAMA network open

    2020  Volume 3, Issue 2, Page(s) e200094

    Abstract: Importance: Some individuals who reach ages beyond 100 years in good cognitive health may be resilient against risk factors associated with cognitive decline. Exploring the processes underlying resilience may contribute to the development of therapeutic ...

    Abstract Importance: Some individuals who reach ages beyond 100 years in good cognitive health may be resilient against risk factors associated with cognitive decline. Exploring the processes underlying resilience may contribute to the development of therapeutic strategies that help to maintain cognitive health while aging.
    Objective: To identify individuals who escape cognitive decline until extreme ages and to investigate the prevalence of associated risk factors.
    Design, setting, and participants: The 100-plus Study is a prospective observational cohort study of community-based Dutch centenarians enrolled between 2013 and 2019 who were visited annually until death or until participation was no longer possible. The centenarians self-reported their cognitive health, as confirmed by a proxy. Of the 1023 centenarians approached for study inclusion, 340 fulfilled the study criteria and were included in analyses. Data analysis was performed from April 2019 to December 2019.
    Main outcomes and measures: Cognition was assessed using the Mini-Mental State Examination (MMSE). To identify centenarians who escape cognitive decline, this study investigated the association of baseline cognition with survivorship and cognitive trajectories for at least 2 years of follow-up using linear mixed models, adjusted for sex, age, and education. This study investigated the prevalence of apolipoprotein E (APOE) genotypes and cardiovascular disease as risk factors associated with cognitive decline.
    Results: At baseline, the median age of 340 centenarians was 100.5 years (range, 100.0-108.2 years); 245 participants (72.1%) were female. The maximum survival estimate plateaued at 82% per year (95% CI, 77% to 87%) across centenarians who scored 26 to 30 points on the baseline MMSE (hazard ratio, 0.56; 95% CI, 0.42 to 0.75; P < .001), suggesting that an MMSE score of 26 or higher is representative of both cognitive and physical health. Among the 79 centenarians who were followed up for 2 years or longer, those with baseline MMSE score less than 26 experienced a decline in MMSE score of 1.68 points per year (95% CI, -2.45 to -0.92 points per year; P = .02), whereas centenarians with MMSE scores of 26 or higher at baseline experienced a decline of 0.71 point per year (95% CI, -1.08 to -0.35 points per year). For 73% of the centenarians with baseline MMSE scores of 26 or higher, no cognitive changes were observed, which often extended to ensuing years or until death. It is estimated that this group is representative of less than 10% of Dutch centenarians. In this group, 18.6% carried at least 1 APOE-ε4 allele, compared with 5.6% of the centenarians with lower and/or declining cognitive performance.
    Conclusions and relevance: Most centenarians who scored 26 or higher on the MMSE at baseline maintained high levels of cognitive performance for at least 2 years, in some cases despite the presence of risk factors associated with cognitive decline. Investigation of this group might reveal the processes underlying resilience against risk factors associated with cognitive decline.
    MeSH term(s) Aged, 80 and over ; Aging/genetics ; Aging/physiology ; Apolipoprotein E4/genetics ; Cognition/physiology ; Female ; Humans ; Longitudinal Studies ; Male ; Mental Status and Dementia Tests/statistics & numerical data ; Prospective Studies
    Chemical Substances Apolipoprotein E4
    Language English
    Publishing date 2020-02-05
    Publishing country United States
    Document type Journal Article ; Observational Study ; Research Support, Non-U.S. Gov't
    ISSN 2574-3805
    ISSN (online) 2574-3805
    DOI 10.1001/jamanetworkopen.2020.0094
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease.

    Peloso, Gina M / van der Lee, Sven J / Destefano, Anita L / Seshardi, Sudha

    Alzheimer's & dementia (Amsterdam, Netherlands)

    2018  Volume 10, Page(s) 595–598

    Abstract: Introduction: There is conflicting evidence whether high-density lipoprotein cholesterol (HDL-C) is a risk factor for Alzheimer's disease (AD) and dementia. Genetic variation in the cholesteryl ester transfer protein (: Methods: Ten single nucleotide ...

    Abstract Introduction: There is conflicting evidence whether high-density lipoprotein cholesterol (HDL-C) is a risk factor for Alzheimer's disease (AD) and dementia. Genetic variation in the cholesteryl ester transfer protein (
    Methods: Ten single nucleotide polymorphisms within the
    Results: Based on 10 single nucleotide polymorphisms distinctly predicting HDL-C in the
    Discussion: Our study does not support the role of HDL-C on risk of AD through HDL-C altered by
    Language English
    Publishing date 2018-09-22
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2832898-X
    ISSN 2352-8729
    ISSN 2352-8729
    DOI 10.1016/j.dadm.2018.08.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Polygenic Risk Score of Longevity Predicts Longer Survival Across an Age Continuum.

    Tesi, Niccolo' / van der Lee, Sven J / Hulsman, Marc / Jansen, Iris E / Stringa, Najada / van Schoor, Natasja M / Scheltens, Philip / van der Flier, Wiesje M / Huisman, Martijn / Reinders, Marcel J T / Holstege, Henne

    The journals of gerontology. Series A, Biological sciences and medical sciences

    2021  Volume 76, Issue 5, Page(s) 750–759

    Abstract: Studying the genome of centenarians may give insights into the molecular mechanisms underlying extreme human longevity and the escape of age-related diseases. Here, we set out to construct polygenic risk scores (PRSs) for longevity and to investigate the ...

    Abstract Studying the genome of centenarians may give insights into the molecular mechanisms underlying extreme human longevity and the escape of age-related diseases. Here, we set out to construct polygenic risk scores (PRSs) for longevity and to investigate the functions of longevity-associated variants. Using a cohort of centenarians with maintained cognitive health (N = 343), a population-matched cohort of older adults from 5 cohorts (N = 2905), and summary statistics data from genome-wide association studies on parental longevity, we constructed a PRS including 330 variants that significantly discriminated between centenarians and older adults. This PRS was also associated with longer survival in an independent sample of younger individuals (p = .02), leading up to a 4-year difference in survival based on common genetic factors only. We show that this PRS was, in part, able to compensate for the deleterious effect of the APOE-ε4 allele. Using an integrative framework, we annotated the 330 variants included in this PRS by the genes they associate with. We find that they are enriched with genes associated with cellular differentiation, developmental processes, and cellular response to stress. Together, our results indicate that an extended human life span is, in part, the result of a constellation of variants each exerting small advantageous effects on aging-related biological mechanisms that maintain overall health and decrease the risk of age-related diseases.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Aging/genetics ; Apolipoproteins E/genetics ; Case-Control Studies ; Cohort Studies ; Cyclin-Dependent Kinase Inhibitor p15/genetics ; Female ; Genome-Wide Association Study ; Humans ; Longevity/genetics ; Male ; Middle Aged ; Polymorphism, Single Nucleotide
    Chemical Substances ApoE protein, human ; Apolipoproteins E ; CDKN2B protein, human ; Cyclin-Dependent Kinase Inhibitor p15
    Language English
    Publishing date 2021-06-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1223643-3
    ISSN 1758-535X ; 1079-5006
    ISSN (online) 1758-535X
    ISSN 1079-5006
    DOI 10.1093/gerona/glaa289
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: SORL1 deficiency in human excitatory neurons causes APP-dependent defects in the endolysosome-autophagy network.

    Hung, Christy / Tuck, Eleanor / Stubbs, Victoria / van der Lee, Sven J / Aalfs, Cora / van Spaendonk, Resie / Scheltens, Philip / Hardy, John / Holstege, Henne / Livesey, Frederick J

    Cell reports

    2021  Volume 35, Issue 11, Page(s) 109259

    Abstract: Dysfunction of the endolysosomal-autophagy network is emerging as an important pathogenic process in Alzheimer's disease. Mutations in the sorting receptor-encoding gene SORL1 cause autosomal-dominant Alzheimer's disease, and SORL1 variants increase risk ...

    Abstract Dysfunction of the endolysosomal-autophagy network is emerging as an important pathogenic process in Alzheimer's disease. Mutations in the sorting receptor-encoding gene SORL1 cause autosomal-dominant Alzheimer's disease, and SORL1 variants increase risk for late-onset AD. To understand the contribution of SORL1 mutations to AD pathogenesis, we analyze the effects of a SORL1 truncating mutation on SORL1 protein levels and endolysosome function in human neurons. We find that truncating mutation results in SORL1 haploinsufficiency and enlarged endosomes in human neurons. Analysis of isogenic SORL1 wild-type, heterozygous, and homozygous null neurons demonstrates that, whereas SORL1 haploinsufficiency results in endosome dysfunction, complete loss of SORL1 leads to additional defects in lysosome function and autophagy. Neuronal endolysosomal dysfunction caused by loss of SORL1 is relieved by extracellular antisense oligonucleotide-mediated reduction of APP protein, demonstrating that PSEN1, APP, and SORL1 act in a common pathway regulating the endolysosome system, which becomes dysfunctional in AD.
    MeSH term(s) Amyloid Precursor Protein Secretases/metabolism ; Amyloid beta-Protein Precursor/metabolism ; Aspartic Acid Endopeptidases/metabolism ; Autophagy ; Dementia/genetics ; Dementia/pathology ; Endosomes/metabolism ; Gene Knockout Techniques ; Humans ; Induced Pluripotent Stem Cells/metabolism ; LDL-Receptor Related Proteins/deficiency ; LDL-Receptor Related Proteins/genetics ; LDL-Receptor Related Proteins/metabolism ; Lysosomes/metabolism ; Membrane Transport Proteins/deficiency ; Membrane Transport Proteins/genetics ; Membrane Transport Proteins/metabolism ; Neurons/metabolism ; Oligonucleotides, Antisense/administration & dosage ; Oligonucleotides, Antisense/pharmacology ; Phenotype ; Protein Binding
    Chemical Substances Amyloid beta-Protein Precursor ; LDL-Receptor Related Proteins ; Membrane Transport Proteins ; Oligonucleotides, Antisense ; SORL1 protein, human ; Amyloid Precursor Protein Secretases (EC 3.4.-) ; Aspartic Acid Endopeptidases (EC 3.4.23.-) ; BACE1 protein, human (EC 3.4.23.46)
    Language English
    Publishing date 2021-06-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2021.109259
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: The Effect of Alzheimer's Disease-Associated Genetic Variants on Longevity.

    Tesi, Niccolò / Hulsman, Marc / van der Lee, Sven J / Jansen, Iris E / Stringa, Najada / van Schoor, Natasja M / Scheltens, Philip / van der Flier, Wiesje M / Huisman, Martijn / Reinders, Marcel J T / Holstege, Henne

    Frontiers in genetics

    2021  Volume 12, Page(s) 748781

    Abstract: Human longevity is influenced by the genetic risk of age-related diseases. As Alzheimer's disease (AD) represents a common condition at old age, an interplay between genetic factors affecting AD and longevity is expected. We explored this interplay by ... ...

    Abstract Human longevity is influenced by the genetic risk of age-related diseases. As Alzheimer's disease (AD) represents a common condition at old age, an interplay between genetic factors affecting AD and longevity is expected. We explored this interplay by studying the prevalence of AD-associated single-nucleotide-polymorphisms (SNPs) in cognitively healthy centenarians, and replicated findings in a parental-longevity GWAS. We found that 28/38 SNPs that increased AD-risk also associated with lower odds of longevity. For each SNP, we express the imbalance between AD- and longevity-risk as an effect-size distribution. Based on these distributions, we grouped the SNPs in three groups: 17 SNPs increased AD-risk more than they decreased longevity-risk, and were enriched for
    Language English
    Publishing date 2021-12-21
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2606823-0
    ISSN 1664-8021
    ISSN 1664-8021
    DOI 10.3389/fgene.2021.748781
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