Skip to main content
Erschienen in: Brain Structure and Function 8/2016

01.12.2015 | Original Article

Modulation effect of the SORL1 gene on functional connectivity density in healthy young adults

verfasst von: Junlin Shen, Peng Zhang, Huaigui Liu, Lixue Xu, Jiayuan Xu, Wen Qin, Bing Liu, Tianzi Jiang, Chunshui Yu

Erschienen in: Brain Structure and Function | Ausgabe 8/2016

Einloggen, um Zugang zu erhalten

Abstract

The sortilin-related receptor 1 (SORL1) gene has been associated with late-onset Alzheimer’s disease (LOAD) and structural impairments in several ethnic populations. However, how this gene affects brain function properties remains unclear. We investigated associations of SORL1 rs2070045 with functional connectivity density (FCD) in healthy young adults. This single-nucleotide polymorphism was selected because it is the SORL1 variant that has been frequently associated with LOAD in several populations, including the Chinese Han population. A total of 275 healthy young Chinese Han subjects with successful genotyping and MRI examinations were included. The effect of SORL1 rs2070045 was explored using a voxel-wise FCD analysis. A significant effect of SORL1 rs2070045 on the FCD was found in the right inferior temporal gyrus. The risk G allele carriers of the rs2070045 exhibited a lower FCD than the protective TT carriers. This effect was independent of the status of apolipoprotein E. This study provides the first evidence that the SORL1 gene is associated with brain FCD differences in healthy young adults. In the genetic risk subjects, connectivity impairment already starts during young adulthood, which may predispose the risk allele carriers to be susceptible to LOAD after several decades.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
Zurück zum Zitat Assareh AA, Piguet O, Lye TC, Mather KA, Broe GA, Schofield PR, Sachdev PS, Kwok JB (2014) Association of SORL1 gene variants with hippocampal and cerebral atrophy and Alzheimer’s disease. Curr Alzheimer Res 11:558–563CrossRefPubMed Assareh AA, Piguet O, Lye TC, Mather KA, Broe GA, Schofield PR, Sachdev PS, Kwok JB (2014) Association of SORL1 gene variants with hippocampal and cerebral atrophy and Alzheimer’s disease. Curr Alzheimer Res 11:558–563CrossRefPubMed
Zurück zum Zitat Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA (2009) Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. Am J Hum Genet 84:35–43CrossRefPubMedPubMedCentral Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA (2009) Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. Am J Hum Genet 84:35–43CrossRefPubMedPubMedCentral
Zurück zum Zitat Bettens K, Brouwers N, Engelborghs S, De Deyn PP, Van Broeckhoven C, Sleegers K (2008) SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population. Hum Mutat 29:769–770CrossRefPubMed Bettens K, Brouwers N, Engelborghs S, De Deyn PP, Van Broeckhoven C, Sleegers K (2008) SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population. Hum Mutat 29:769–770CrossRefPubMed
Zurück zum Zitat Braak H, Braak E (1991) Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol 82:239–259CrossRefPubMed Braak H, Braak E (1991) Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol 82:239–259CrossRefPubMed
Zurück zum Zitat Bralten J, Arias-Vasquez A, Makkinje R, Veltman JA, Brunner HG, Fernandez G, Rijpkema M, Franke B (2011) Association of the Alzheimer’s gene SORL1 with hippocampal volume in young, healthy adults. Am J Psychiatry 168:1083–1089CrossRefPubMed Bralten J, Arias-Vasquez A, Makkinje R, Veltman JA, Brunner HG, Fernandez G, Rijpkema M, Franke B (2011) Association of the Alzheimer’s gene SORL1 with hippocampal volume in young, healthy adults. Am J Psychiatry 168:1083–1089CrossRefPubMed
Zurück zum Zitat Cellini E, Tedde A, Bagnoli S, Pradella S, Piacentini S, Sorbi S, Nacmias B (2009) Implication of sex and SORL1 variants in Italian patients with Alzheimer disease. Arch Neurol 66:1260–1266CrossRefPubMed Cellini E, Tedde A, Bagnoli S, Pradella S, Piacentini S, Sorbi S, Nacmias B (2009) Implication of sex and SORL1 variants in Italian patients with Alzheimer disease. Arch Neurol 66:1260–1266CrossRefPubMed
Zurück zum Zitat Convit A, de Asis J, de Leon MJ, Tarshish CY, De Santi S, Rusinek H (2000) Atrophy of the medial occipitotemporal, inferior, and middle temporal gyri in non-demented elderly predict decline to Alzheimer’s disease. Neurobiol Aging 21:19–26CrossRefPubMed Convit A, de Asis J, de Leon MJ, Tarshish CY, De Santi S, Rusinek H (2000) Atrophy of the medial occipitotemporal, inferior, and middle temporal gyri in non-demented elderly predict decline to Alzheimer’s disease. Neurobiol Aging 21:19–26CrossRefPubMed
Zurück zum Zitat Cousin E, Mace S, Rocher C, Dib C, Muzard G, Hannequin D, Pradier L, Deleuze JF, Genin E, Brice A, Campion D (2011) No replication of genetic association between candidate polymorphisms and Alzheimer’s disease. Neurobiol Aging 32:1443–1451CrossRefPubMed Cousin E, Mace S, Rocher C, Dib C, Muzard G, Hannequin D, Pradier L, Deleuze JF, Genin E, Brice A, Campion D (2011) No replication of genetic association between candidate polymorphisms and Alzheimer’s disease. Neurobiol Aging 32:1443–1451CrossRefPubMed
Zurück zum Zitat Cuenco KT, Lunetta KL, Baldwin CT, McKee AC, Guo J, Cupples LA, Green RC, St George-Hyslop PH, Chui H, DeCarli C, Farrer LA (2008) Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease. Arch Neurol 65:1640–1648CrossRefPubMedCentral Cuenco KT, Lunetta KL, Baldwin CT, McKee AC, Guo J, Cupples LA, Green RC, St George-Hyslop PH, Chui H, DeCarli C, Farrer LA (2008) Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease. Arch Neurol 65:1640–1648CrossRefPubMedCentral
Zurück zum Zitat Felsky D, Szeszko P, Yu L, Honer WG, De Jager PL, Schneider JA, Malhotra AK, Lencz T, Ikuta T, Pipitone J, Chakravarty MM, Lobaugh NJ, Mulsant BH, Pollock BG, Kennedy JL, Bennett DA, Voineskos AN (2014) The SORL1 gene and convergent neural risk for Alzheimer’s disease across the human lifespan. Mol Psychiatry 19:1125–1132CrossRefPubMed Felsky D, Szeszko P, Yu L, Honer WG, De Jager PL, Schneider JA, Malhotra AK, Lencz T, Ikuta T, Pipitone J, Chakravarty MM, Lobaugh NJ, Mulsant BH, Pollock BG, Kennedy JL, Bennett DA, Voineskos AN (2014) The SORL1 gene and convergent neural risk for Alzheimer’s disease across the human lifespan. Mol Psychiatry 19:1125–1132CrossRefPubMed
Zurück zum Zitat Feng X, Hou D, Deng Y, Li W, Tian M, Yu Z (2015) SORL1 gene polymorphism association with late-onset Alzheimer’s disease. Neurosci Lett 584:382–389CrossRefPubMed Feng X, Hou D, Deng Y, Li W, Tian M, Yu Z (2015) SORL1 gene polymorphism association with late-onset Alzheimer’s disease. Neurosci Lett 584:382–389CrossRefPubMed
Zurück zum Zitat Feulner TM, Laws SM, Friedrich P, Wagenpfeil S, Wurst SH, Riehle C, Kuhn KA, Krawczak M, Schreiber S, Nikolaus S, Forstl H, Kurz A, Riemenschneider M (2010) Examination of the current top candidate genes for AD in a genome-wide association study. Mol Psychiatry 15:756–766CrossRefPubMed Feulner TM, Laws SM, Friedrich P, Wagenpfeil S, Wurst SH, Riehle C, Kuhn KA, Krawczak M, Schreiber S, Nikolaus S, Forstl H, Kurz A, Riemenschneider M (2010) Examination of the current top candidate genes for AD in a genome-wide association study. Mol Psychiatry 15:756–766CrossRefPubMed
Zurück zum Zitat Jin C, Zhang L, Xian Y, Liu X, Wu Y, Zhang F, Zhu J, Zhang G, Chen C, Gong R, Zhang L, Yuan J, Zhang F, Tian L, Wang G, Cheng Z (2014) The SORL1 polymorphism rs985421 may confer the risk for amnestic mild cognitive impairment and Alzheimer’s disease in the Han Chinese population. Neurosci Lett 563:80–84CrossRefPubMed Jin C, Zhang L, Xian Y, Liu X, Wu Y, Zhang F, Zhu J, Zhang G, Chen C, Gong R, Zhang L, Yuan J, Zhang F, Tian L, Wang G, Cheng Z (2014) The SORL1 polymorphism rs985421 may confer the risk for amnestic mild cognitive impairment and Alzheimer’s disease in the Han Chinese population. Neurosci Lett 563:80–84CrossRefPubMed
Zurück zum Zitat Kimura R, Yamamoto M, Morihara T, Akatsu H, Kudo T, Kamino K, Takeda M (2009) SORL1 is genetically associated with Alzheimer disease in a Japanese population. Neurosci Lett 461:177–180CrossRefPubMed Kimura R, Yamamoto M, Morihara T, Akatsu H, Kudo T, Kamino K, Takeda M (2009) SORL1 is genetically associated with Alzheimer disease in a Japanese population. Neurosci Lett 461:177–180CrossRefPubMed
Zurück zum Zitat Kolsch H, Jessen F, Wiltfang J, Lewczuk P, Dichgans M, Teipel SJ, Kornhuber J, Frolich L, Heuser I, Peters O, Wiese B, Kaduszkiewicz H, van den Bussche H, Hull M, Kurz A, Ruther E, Henn FA, Maier W (2009) Association of SORL1 gene variants with Alzheimer’s disease. Brain Res 1264:1–6CrossRefPubMed Kolsch H, Jessen F, Wiltfang J, Lewczuk P, Dichgans M, Teipel SJ, Kornhuber J, Frolich L, Heuser I, Peters O, Wiese B, Kaduszkiewicz H, van den Bussche H, Hull M, Kurz A, Ruther E, Henn FA, Maier W (2009) Association of SORL1 gene variants with Alzheimer’s disease. Brain Res 1264:1–6CrossRefPubMed
Zurück zum Zitat Lee JH, Cheng R, Schupf N, Manly J, Lantigua R, Stern Y, Rogaeva E, Wakutani Y, Farrer L, St George-Hyslop P, Mayeux R (2007) The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort. Arch Neurol 64:501–506CrossRefPubMedPubMedCentral Lee JH, Cheng R, Schupf N, Manly J, Lantigua R, Stern Y, Rogaeva E, Wakutani Y, Farrer L, St George-Hyslop P, Mayeux R (2007) The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort. Arch Neurol 64:501–506CrossRefPubMedPubMedCentral
Zurück zum Zitat Lee JH, Cheng R, Honig LS, Vonsattel JP, Clark L, Mayeux R (2008) Association between genetic variants in SORL1 and autopsy-confirmed Alzheimer disease. Neurology 70:887–889CrossRefPubMed Lee JH, Cheng R, Honig LS, Vonsattel JP, Clark L, Mayeux R (2008) Association between genetic variants in SORL1 and autopsy-confirmed Alzheimer disease. Neurology 70:887–889CrossRefPubMed
Zurück zum Zitat Li Y, Rowland C, Catanese J, Morris J, Lovestone S, O’Donovan MC, Goate A, Owen M, Williams J, Grupe A (2008) SORL1 variants and risk of late-onset Alzheimer’s disease. Neurobiol Dis 29:293–296CrossRefPubMed Li Y, Rowland C, Catanese J, Morris J, Lovestone S, O’Donovan MC, Goate A, Owen M, Williams J, Grupe A (2008) SORL1 variants and risk of late-onset Alzheimer’s disease. Neurobiol Dis 29:293–296CrossRefPubMed
Zurück zum Zitat Liang Y, Li H, Lv C, Shu N, Chen K, Li X, Zhang J, Hu L, Zhang Z (2015) Sex moderates the effects of the Sorl1 gene rs2070045 polymorphism on cognitive impairment and disruption of the cingulum integrity in healthy elderly. Neuropsychopharmacology 40:1519–1527CrossRefPubMedPubMedCentral Liang Y, Li H, Lv C, Shu N, Chen K, Li X, Zhang J, Hu L, Zhang Z (2015) Sex moderates the effects of the Sorl1 gene rs2070045 polymorphism on cognitive impairment and disruption of the cingulum integrity in healthy elderly. Neuropsychopharmacology 40:1519–1527CrossRefPubMedPubMedCentral
Zurück zum Zitat Liu F, Ikram MA, Janssens AC, Schuur M, de Koning I, Isaacs A, Struchalin M, Uitterlinden AG, den Dunnen JT, Sleegers K, Bettens K, Van Broeckhoven C, van Swieten J, Hofman A, Oostra BA, Aulchenko YS, Breteler MM, van Duijn CM (2009) A study of the SORL1 gene in Alzheimer’s disease and cognitive function. J Alzheimers Dis 18:51–64PubMed Liu F, Ikram MA, Janssens AC, Schuur M, de Koning I, Isaacs A, Struchalin M, Uitterlinden AG, den Dunnen JT, Sleegers K, Bettens K, Van Broeckhoven C, van Swieten J, Hofman A, Oostra BA, Aulchenko YS, Breteler MM, van Duijn CM (2009) A study of the SORL1 gene in Alzheimer’s disease and cognitive function. J Alzheimers Dis 18:51–64PubMed
Zurück zum Zitat Louwersheimer E, Ramirez A, Cruchaga C, Becker T, Kornhuber J, Peters O, Heilmann S, Wiltfang J, Jessen F, Visser PJ, Scheltens P, Pijnenburg YA, Teunissen CE, Barkhof F, van Swieten JC, Holstege H, Van der Flier WM (2015) The influence of genetic variants in SORL1 gene on the manifestation of Alzheimer’s disease. Neurobiol Aging 36:1605.e13–1605.e20CrossRef Louwersheimer E, Ramirez A, Cruchaga C, Becker T, Kornhuber J, Peters O, Heilmann S, Wiltfang J, Jessen F, Visser PJ, Scheltens P, Pijnenburg YA, Teunissen CE, Barkhof F, van Swieten JC, Holstege H, Van der Flier WM (2015) The influence of genetic variants in SORL1 gene on the manifestation of Alzheimer’s disease. Neurobiol Aging 36:1605.e13–1605.e20CrossRef
Zurück zum Zitat Meng Y, Lee JH, Cheng R, St George-Hyslop P, Mayeux R, Farrer LA (2007) Association between SORL1 and Alzheimer’s disease in a genome-wide study. NeuroReport 18:1761–1764CrossRefPubMedPubMedCentral Meng Y, Lee JH, Cheng R, St George-Hyslop P, Mayeux R, Farrer LA (2007) Association between SORL1 and Alzheimer’s disease in a genome-wide study. NeuroReport 18:1761–1764CrossRefPubMedPubMedCentral
Zurück zum Zitat Miyashita Y (1993) Inferior temporal cortex: where visual perception meets memory. Annu Rev Neurosci 16:245–263CrossRefPubMed Miyashita Y (1993) Inferior temporal cortex: where visual perception meets memory. Annu Rev Neurosci 16:245–263CrossRefPubMed
Zurück zum Zitat Ning M, Yang Y, Zhang Z, Chen Z, Zhao T, Zhang D, Zhou D, Xu J, Liu Z, Wang Y, Liu Y, Zhao X, Li W, Li S, He L (2010) Amyloid-beta-related genes SORL1 and ACE are genetically associated with risk for late-onset Alzheimer disease in the Chinese population. Alzheimer Dis Assoc Disord 24:390–396CrossRefPubMed Ning M, Yang Y, Zhang Z, Chen Z, Zhao T, Zhang D, Zhou D, Xu J, Liu Z, Wang Y, Liu Y, Zhao X, Li W, Li S, He L (2010) Amyloid-beta-related genes SORL1 and ACE are genetically associated with risk for late-onset Alzheimer disease in the Chinese population. Alzheimer Dis Assoc Disord 24:390–396CrossRefPubMed
Zurück zum Zitat Okamura N, Arai H, Higuchi M, Tashiro M, Matsui T, Itoh M, Iwatsubo T, Tomita T, Sasaki H (1999) Cerebrospinal fluid levels of amyloid beta-peptide 1-42, but not tau have positive correlation with brain glucose metabolism in humans. Neurosci Lett 273:203–207CrossRefPubMed Okamura N, Arai H, Higuchi M, Tashiro M, Matsui T, Itoh M, Iwatsubo T, Tomita T, Sasaki H (1999) Cerebrospinal fluid levels of amyloid beta-peptide 1-42, but not tau have positive correlation with brain glucose metabolism in humans. Neurosci Lett 273:203–207CrossRefPubMed
Zurück zum Zitat Olgiati P, Politis A, Albani D, Rodilossi S, Polito L, Zisaki A, Piperi C, Liappas I, Stamouli E, Mailis A, Batelli S, Forloni G, Marsano A, Balestri M, Soldatos CR, De Ronchi D, Kalofoutis A, Serretti A (2013) Effects of SORL1 gene on Alzheimer’s disease. Focus on gender, neuropsychiatric symptoms and pro-inflammatory cytokines. Curr Alzheimer Res 10:154–164CrossRefPubMed Olgiati P, Politis A, Albani D, Rodilossi S, Polito L, Zisaki A, Piperi C, Liappas I, Stamouli E, Mailis A, Batelli S, Forloni G, Marsano A, Balestri M, Soldatos CR, De Ronchi D, Kalofoutis A, Serretti A (2013) Effects of SORL1 gene on Alzheimer’s disease. Focus on gender, neuropsychiatric symptoms and pro-inflammatory cytokines. Curr Alzheimer Res 10:154–164CrossRefPubMed
Zurück zum Zitat Piscopo P, Tosto G, Belli C, Talarico G, Galimberti D, Gasparini M, Canevelli M, Poleggi A, Crestini A, Albani D, Forloni G, Lucca U, Quadri P, Tettamanti M, Fenoglio C, Scarpini E, Bruno G, Vanacore N, Confaloni A (2015) SORL1 gene is associated with the conversion from mild cognitive impairment to Alzheimer’s disease. J Alzheimers Dis 46:771–776CrossRefPubMed Piscopo P, Tosto G, Belli C, Talarico G, Galimberti D, Gasparini M, Canevelli M, Poleggi A, Crestini A, Albani D, Forloni G, Lucca U, Quadri P, Tettamanti M, Fenoglio C, Scarpini E, Bruno G, Vanacore N, Confaloni A (2015) SORL1 gene is associated with the conversion from mild cognitive impairment to Alzheimer’s disease. J Alzheimers Dis 46:771–776CrossRefPubMed
Zurück zum Zitat Power JD, Barnes KA, Snyder AZ, Schlaggar BL, Petersen SE (2012) Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. Neuroimage 59:2142–2154CrossRefPubMed Power JD, Barnes KA, Snyder AZ, Schlaggar BL, Petersen SE (2012) Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. Neuroimage 59:2142–2154CrossRefPubMed
Zurück zum Zitat Power JD, Barnes KA, Snyder AZ, Schlaggar BL, Petersen SE (2013) Steps toward optimizing motion artifact removal in functional connectivity MRI; a reply to Carp. Neuroimage 76:439–441CrossRefPubMed Power JD, Barnes KA, Snyder AZ, Schlaggar BL, Petersen SE (2013) Steps toward optimizing motion artifact removal in functional connectivity MRI; a reply to Carp. Neuroimage 76:439–441CrossRefPubMed
Zurück zum Zitat Reiman EM, Chen K, Alexander GE, Caselli RJ, Bandy D, Osborne D, Saunders AM, Hardy J (2004) Functional brain abnormalities in young adults at genetic risk for late-onset Alzheimer’s dementia. Proc Natl Acad Sci USA 101:284–289CrossRefPubMed Reiman EM, Chen K, Alexander GE, Caselli RJ, Bandy D, Osborne D, Saunders AM, Hardy J (2004) Functional brain abnormalities in young adults at genetic risk for late-onset Alzheimer’s dementia. Proc Natl Acad Sci USA 101:284–289CrossRefPubMed
Zurück zum Zitat Reynolds CA, Hong MG, Eriksson UK, Blennow K, Johansson B, Malmberg B, Berg S, Gatz M, Pedersen NL, Bennet AM, Prince JA (2010) Sequence variation in SORL1 and dementia risk in Swedes. Neurogenetics 11:139–142CrossRefPubMed Reynolds CA, Hong MG, Eriksson UK, Blennow K, Johansson B, Malmberg B, Berg S, Gatz M, Pedersen NL, Bennet AM, Prince JA (2010) Sequence variation in SORL1 and dementia risk in Swedes. Neurogenetics 11:139–142CrossRefPubMed
Zurück zum Zitat Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, Katayama T, Baldwin CT, Cheng R, Hasegawa H, Chen F, Shibata N, Lunetta KL, Pardossi-Piquard R, Bohm C, Wakutani Y, Cupples LA, Cuenco KT, Green RC, Pinessi L, Rainero I, Sorbi S, Bruni A, Duara R, Friedland RP, Inzelberg R, Hampe W, Bujo H, Song YQ, Andersen OM, Willnow TE, Graff-Radford N, Petersen RC, Dickson D, Der SD, Fraser PE, Schmitt-Ulms G, Younkin S, Mayeux R, Farrer LA, St George-Hyslop P (2007) The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet 39:168–177CrossRefPubMedPubMedCentral Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, Katayama T, Baldwin CT, Cheng R, Hasegawa H, Chen F, Shibata N, Lunetta KL, Pardossi-Piquard R, Bohm C, Wakutani Y, Cupples LA, Cuenco KT, Green RC, Pinessi L, Rainero I, Sorbi S, Bruni A, Duara R, Friedland RP, Inzelberg R, Hampe W, Bujo H, Song YQ, Andersen OM, Willnow TE, Graff-Radford N, Petersen RC, Dickson D, Der SD, Fraser PE, Schmitt-Ulms G, Younkin S, Mayeux R, Farrer LA, St George-Hyslop P (2007) The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet 39:168–177CrossRefPubMedPubMedCentral
Zurück zum Zitat Scherzer CR, Offe K, Gearing M, Rees HD, Fang G, Heilman CJ, Schaller C, Bujo H, Levey AI, Lah JJ (2004) Loss of apolipoprotein E receptor LR11 in Alzheimer disease. Arch Neurol 61:1200–1205CrossRefPubMed Scherzer CR, Offe K, Gearing M, Rees HD, Fang G, Heilman CJ, Schaller C, Bujo H, Levey AI, Lah JJ (2004) Loss of apolipoprotein E receptor LR11 in Alzheimer disease. Arch Neurol 61:1200–1205CrossRefPubMed
Zurück zum Zitat Shibata N, Ohnuma T, Baba H, Higashi S, Nishioka K, Arai H (2008) Genetic association between SORL1 polymorphisms and Alzheimer’s disease in a Japanese population. Dement Geriatr Cogn Disord 26:161–164PubMed Shibata N, Ohnuma T, Baba H, Higashi S, Nishioka K, Arai H (2008) Genetic association between SORL1 polymorphisms and Alzheimer’s disease in a Japanese population. Dement Geriatr Cogn Disord 26:161–164PubMed
Zurück zum Zitat Tan EK, Lee J, Chen CP, Teo YY, Zhao Y, Lee WL (2009) SORL1 haplotypes modulate risk of Alzheimer’s disease in Chinese. Neurobiol Aging 30:1048–1051CrossRefPubMed Tan EK, Lee J, Chen CP, Teo YY, Zhao Y, Lee WL (2009) SORL1 haplotypes modulate risk of Alzheimer’s disease in Chinese. Neurobiol Aging 30:1048–1051CrossRefPubMed
Zurück zum Zitat Thal DR, Rub U, Orantes M, Braak H (2002) Phases of Aβ-deposition in the human brain and its relevance for the development of AD. Neurology 58:1791–1800CrossRefPubMed Thal DR, Rub U, Orantes M, Braak H (2002) Phases of Aβ-deposition in the human brain and its relevance for the development of AD. Neurology 58:1791–1800CrossRefPubMed
Zurück zum Zitat Thomas G, Sinville R, Sutton S, Farquar H, Hammer RP, Soper SA, Cheng YW, Barany F (2004) Capillary and microelectrophoretic separations of ligase detection reaction products produced from low-abundant point mutations in genomic DNA. Electrophoresis 25:1668–1677CrossRefPubMed Thomas G, Sinville R, Sutton S, Farquar H, Hammer RP, Soper SA, Cheng YW, Barany F (2004) Capillary and microelectrophoretic separations of ligase detection reaction products produced from low-abundant point mutations in genomic DNA. Electrophoresis 25:1668–1677CrossRefPubMed
Zurück zum Zitat Webster JA, Myers AJ, Pearson JV, Craig DW, Hu-Lince D, Coon KD, Zismann VL, Beach T, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Huentelman MJ, Joshipura K, Walker D, Heward CB, Ravid R, Rogers J, Papassotiropoulos A, Hardy J, Reiman EM, Stephan DA (2008) Sorl1 as an Alzheimer’s disease predisposition gene? Neurodegener Dis 5:60–64CrossRefPubMed Webster JA, Myers AJ, Pearson JV, Craig DW, Hu-Lince D, Coon KD, Zismann VL, Beach T, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Huentelman MJ, Joshipura K, Walker D, Heward CB, Ravid R, Rogers J, Papassotiropoulos A, Hardy J, Reiman EM, Stephan DA (2008) Sorl1 as an Alzheimer’s disease predisposition gene? Neurodegener Dis 5:60–64CrossRefPubMed
Zurück zum Zitat Wen Y, Miyashita A, Kitamura N, Tsukie T, Saito Y, Hatsuta H, Murayama S, Kakita A, Takahashi H, Akatsu H, Yamamoto T, Kosaka K, Yamaguchi H, Akazawa K, Ihara Y, Kuwano R (2013) SORL1 is genetically associated with neuropathologically characterized late-onset Alzheimer’s disease. J Alzheimers Dis 35:387–394PubMed Wen Y, Miyashita A, Kitamura N, Tsukie T, Saito Y, Hatsuta H, Murayama S, Kakita A, Takahashi H, Akatsu H, Yamamoto T, Kosaka K, Yamaguchi H, Akazawa K, Ihara Y, Kuwano R (2013) SORL1 is genetically associated with neuropathologically characterized late-onset Alzheimer’s disease. J Alzheimers Dis 35:387–394PubMed
Zurück zum Zitat Xue X, Zhang M, Lin Y, Xu E, Jia J (2014) Association between the SORL1 rs2070045 polymorphism and late-onset Alzheimer’s disease: interaction with the ApoE genotype in the Chinese Han population. Neurosci Lett 559:94–98CrossRefPubMed Xue X, Zhang M, Lin Y, Xu E, Jia J (2014) Association between the SORL1 rs2070045 polymorphism and late-onset Alzheimer’s disease: interaction with the ApoE genotype in the Chinese Han population. Neurosci Lett 559:94–98CrossRefPubMed
Zurück zum Zitat Yi P, Chen Z, Zhao Y, Guo J, Fu H, Zhou Y, Yu L, Li L (2009) PCR/LDR/capillary electrophoresis for detection of single-nucleotide differences between fetal and maternal DNA in maternal plasma. Prenat Diagn 29:217–222CrossRefPubMed Yi P, Chen Z, Zhao Y, Guo J, Fu H, Zhou Y, Yu L, Li L (2009) PCR/LDR/capillary electrophoresis for detection of single-nucleotide differences between fetal and maternal DNA in maternal plasma. Prenat Diagn 29:217–222CrossRefPubMed
Zurück zum Zitat Yuan X, Shan B, Ma Y, Tian J, Jiang K, Cao Q, Wang R (2010) Multi-center study on Alzheimer’s disease using FDG PET: group and individual analyses. J Alzheimers Dis 19:927–935PubMed Yuan X, Shan B, Ma Y, Tian J, Jiang K, Cao Q, Wang R (2010) Multi-center study on Alzheimer’s disease using FDG PET: group and individual analyses. J Alzheimers Dis 19:927–935PubMed
Zurück zum Zitat Zhang F, Liu X, Wang B, Cheng Z, Zhao X, Zhu J, Wang D, Wang Y, Dong A, Li P, Jin C (2015) An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer’s disease in the Han Chinese population. Neuropsychiatr Dis Treat 11:1443–1448PubMedPubMedCentral Zhang F, Liu X, Wang B, Cheng Z, Zhao X, Zhu J, Wang D, Wang Y, Dong A, Li P, Jin C (2015) An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer’s disease in the Han Chinese population. Neuropsychiatr Dis Treat 11:1443–1448PubMedPubMedCentral
Zurück zum Zitat Zhong Y, Huang L, Cai S, Zhang Y, von Deneen KM, Ren A, Ren J (2014) Altered effective connectivity patterns of the default mode network in Alzheimer’s disease: an fMRI study. Neurosci Lett 578:171–175CrossRefPubMed Zhong Y, Huang L, Cai S, Zhang Y, von Deneen KM, Ren A, Ren J (2014) Altered effective connectivity patterns of the default mode network in Alzheimer’s disease: an fMRI study. Neurosci Lett 578:171–175CrossRefPubMed
Metadaten
Titel
Modulation effect of the SORL1 gene on functional connectivity density in healthy young adults
verfasst von
Junlin Shen
Peng Zhang
Huaigui Liu
Lixue Xu
Jiayuan Xu
Wen Qin
Bing Liu
Tianzi Jiang
Chunshui Yu
Publikationsdatum
01.12.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Brain Structure and Function / Ausgabe 8/2016
Print ISSN: 1863-2653
Elektronische ISSN: 1863-2661
DOI
https://doi.org/10.1007/s00429-015-1149-x

Weitere Artikel der Ausgabe 8/2016

Brain Structure and Function 8/2016 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.