Brain Lipids and Lipid Droplet Dysregulation in Alzheimer’s Disease and Neuropsychiatric Disorders
Open accessAbstract
Background: Lipids are essential components of the structure and for the function of brain cells. The intricate balance of lipids, including phospholipids, glycolipids, cholesterol, cholesterol ester, and triglycerides, is crucial for maintaining normal brain function. The roles of lipids and lipid droplets and their relevance to neurodegenerative and neuropsychiatric disorders (NPDs) remain largely unknown. Summary: Here, we reviewed the basic role of lipid components as well as a specific lipid organelle, lipid droplets, in brain function, highlighting the potential impact of altered lipid metabolism in the pathogenesis of Alzheimer’s disease (AD) and NDPs. Key Messages: Brain lipid dysregulation plays a pivotal role in the pathogenesis and progression of neurodegenerative and NPDs including AD and schizophrenia. Understanding the cell type-specific mechanisms of lipid dysregulation in these diseases is crucial for identifying better diagnostic biomarkers and for developing therapeutic strategies aiming at restoring lipid homeostasis.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Lipid droplets (LDs) have important roles in ageing and Alzheimer's disease (AD).
“Moreover, LDs—cellular organelles containing lipids such as glycerolipids and cholesterol—were recently found to have important roles in ageing and Alzheimer's disease (AD)10–15.”
From PICALM Alzheimer’s risk allele causes aberrant lipid droplets in microglia (2025) · cites this paper as [15]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 226 · Cited by 54
Research works printed but not linked: 196
- [1]Arias D, Saxena S, Verguet S. Quantifying the global burden of mental disorders and their economic value. EClinicalMedicine. 2022; 54: 101675. 36193171 PMC9526145
- [3]2021 Alzheimer’s disease facts and figures. Alzheimers Dement. 2021; 17(3): 327– 406. 33756057
- [4]Scheltens P, Blennow K, Breteler MM, de Strooper B, Frisoni GB, Salloway S,. Alzheimer’s disease. Lancet. 2016; 388(10043): 505– 17. 26921134
- [5]Shi J, Levinson DF, Duan J, Sanders AR, Zheng Y, Pe’er I,. Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature. 2009; 460(7256): 753– 7. 19571809 PMC2775422
- [6]International Schizophrenia Consortium; Purcell SM, Wray NR, Stone JL, Visscher PM, O’Donovan MC,. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature. 2009; 460(7256): 748– 52. 19571811 PMC3912837
- [8]Schizophrenia Psychiatric Genome-Wide Association Study GWAS Consortium. Genome-wide association study identifies five new schizophrenia loci. Nat Genet. 2011; 43(10): 969– 76. 21926974 PMC3303194
- [10]Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature. 2014; 511(7510): 421– 7. 25056061 PMC4112379
- [11]Mullins N, Forstner AJ, O’Connell KS, Coombes B, Coleman JRI, Qiao Z,. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nat Genet. 2021; 53(6): 817– 29. 34002096 PMC8192451
- [12]Ripke S, Walters JT, O’Donovan MC. Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia. medRxiv. 2020.
- [16]Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V,. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nat Genet. 2019; 51(5): 793– 803. 31043756 PMC6956732
- [17]Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E,. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat Genet. 2019; 51(1): 63– 75. 30478444 PMC6481311
- [18]Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM,. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease. Nat Genet. 2011; 43(5): 429– 35. 21460840 PMC3084173
- [20]Karch CM, Goate AM. Alzheimer’s disease risk genes and mechanisms of disease pathogenesis. Biol Psychiatry. 2015; 77(1): 43– 51. 24951455 PMC4234692
- [21]Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C,. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet. 2013; 45(12): 1452– 8. 24162737 PMC3896259
- [22]Jansen IE, Savage JE, Watanabe K, Bryois J, Williams DM, Steinberg S,. Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk. Nat Genet. 2019; 51(3): 404– 13. 30617256 PMC6836675
- [23]Bellenguez C, Küçükali F, Jansen IE, Kleineidam L, Moreno-Grau S, Amin N,. New insights into the genetic etiology of Alzheimer’s disease and related dementias. Nat Genet. 2022; 54(4): 412– 36. 35379992 PMC9005347
- [24]Snyder SH. The dopamine hypothesis of schizophrenia: focus on the dopamine receptor. Am J Psychiatry. 1976; 133(2): 197– 202. 1251927
- [25]Hamilton JA, Hillard CJ, Spector AA, Watkins PA. Brain uptake and utilization of fatty acids, lipids and lipoproteins: application to neurological disorders. J Mol Neurosci. 2007; 33(1): 2– 11. 17901539
- [26]Sastry PS. Lipids of nervous tissue: composition and metabolism. Prog Lipid Res. 1985; 24(2): 69– 176. 3916238
- [27]Kao YC, Ho PC, Tu YK, Jou IM, Tsai KJ. Lipids and alzheimer’s disease. Int J Mol Sci. 2020; 21(4): 1505. 32098382 PMC7073164
- [28]Yang AC, Tsai SJ. New targets for schizophrenia treatment beyond the dopamine hypothesis. Int J Mol Sci. 2017; 18(8): 1689. 28771182 PMC5578079
- [30]Lyssenko NN, Praticò D. ABCA7 and the altered lipidostasis hypothesis of Alzheimer’s disease. Alzheimers Dement. 2021; 17(2): 164– 74. 33336544 PMC7986801
- [31]Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC,. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nat Genet. 2019; 51(3): 414– 30. 30820047 PMC6463297
- [32]Wingo TS, Cutler DJ, Wingo AP, Le NA, Rabinovici GD, Miller BL,. Association of early-onset alzheimer disease with elevated low-density lipoprotein cholesterol levels and rare genetic coding variants of APOB. JAMA Neurol. 2019; 76(7): 809– 17. 31135820 PMC6547122
- [33]Liu Y, Thalamuthu A, Mather KA, Crawford J, Ulanova M, Wong MWK,. Plasma lipidome is dysregulated in Alzheimer’s disease and is associated with disease risk genes. Transl Psychiatry. 2021; 11(1): 344. 34092785 PMC8180517
- [34]Piñero J, Bravo À, Queralt-Rosinach N, Gutiérrez-Sacristán A, Deu-Pons J, Centeno E,. DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants. Nucleic Acids Res. 2016; 45(D1): D833– D9. 27924018 PMC5210640
- [35]Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S,. Discovery and refinement of loci associated with lipid levels. Nat Genet. 2013; 45(11): 1274– 83. 24097068 PMC3838666
- [37]Sun BB, Kurki MI, Foley CN, Mechakra A, Chen CY, Marshall E,. Genetic associations of protein-coding variants in human disease. Nature. 2022; 603(7899): 95– 102. 35197637 PMC8891017
- [38]Han W, Shepard RD, Lu W. Regulation of GABAARs by transmembrane accessory proteins. Trends Neurosci. 2021; 44(2): 152– 65. 33234346 PMC7855156
- [39]Yang T, Wei P, Pan W. Integrative analysis of multi-omics data for discovering low-frequency variants associated with low-density lipoprotein cholesterol levels. Bioinformatics. 2021; 36(21): 5223– 8. 33070182 PMC7850048
- [40]Luo Y, Eran A, Palmer N, Avillach P, Levy-Moonshine A, Szolovits P,. A multidimensional precision medicine approach identifies an autism subtype characterized by dyslipidemia. Nat Med. 2020; 26(9): 1375– 9. 32778826
- [41]Bieberich E. Sphingolipids and lipid rafts: novel concepts and methods of analysis. Chem Phys Lipids. 2018; 216: 114– 31. 30194926 PMC6196108
- [42]Hannun YA, Obeid LM. Sphingolipids and their metabolism in physiology and disease. Nat Rev Mol Cell Biol. 2018; 19(3): 175– 91. 29165427 PMC5902181
- [43]Bouscary A, Quessada C, René F, Spedding M, Turner BJ, Henriques A,. Sphingolipids metabolism alteration in the central nervous system: amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases. Semin Cell Dev Biol. 2021; 112: 82– 91. 33160824
- [44]Farooqui AA, Horrocks LA, Farooqui T. Glycerophospholipids in brain: their metabolism, incorporation into membranes, functions, and involvement in neurological disorders. Chem Phys Lipids. 2000; 106(1): 1– 29. 10878232
- [45]Schulze H, Sandhoff K. Lysosomal lipid storage diseases. Cold Spring Harb Perspect Biol. 2011; 3(6): a004804. 21502308 PMC3098676
- [46]Papayannopoulos V, Co C, Prehoda KE, Snapper S, Taunton J, Lim WA. A polybasic motif allows N-WASP to act as a sensor of PIP(2) density. Mol Cell. 2005; 17(2): 181– 91. 15664188
- [47]Peter BJ, Kent HM, Mills IG, Vallis Y, Butler PJ, Evans PR,. BAR domains as sensors of membrane curvature: the amphiphysin BAR structure. Science. 2004; 303(5657): 495– 9. 14645856
- [48]Zeniou-Meyer M, Zabari N, Ashery U, Chasserot-Golaz S, Haeberlé AM, Demais V,. Phospholipase D1 production of phosphatidic acid at the plasma membrane promotes exocytosis of large dense-core granules at a late stage. J Biol Chem. 2007; 282(30): 21746– 57. 17540765
- [49]Schaeren-Wiemers N, van der Bijl P, Schwab ME. The UDP-galactose:ceramide galactosyltransferase: expression pattern in oligodendrocytes and Schwann cells during myelination and substrate preference for hydroxyceramide. J Neurochem. 1995; 65(5): 2267– 78. 7595516
- [50]West RJH, Briggs L, Perona Fjeldstad M, Ribchester RR, Sweeney ST. Sphingolipids regulate neuromuscular synapse structure and function in Drosophila. J Comp Neurol. 2018; 526(13): 1995– 2009. 29761896 PMC6175220
- [51]Yu RK, Tsai YT, Ariga T. Functional roles of gangliosides in neurodevelopment: an overview of recent advances. Neurochem Res. 2012; 37(6): 1230– 44. 22410735 PMC3895947
- [52]Tang FL, Wang J, Itokazu Y, Yu RK. Ganglioside GD3 regulates dendritic growth in newborn neurons in adult mouse hippocampus via modulation of mitochondrial dynamics. J Neurochem. 2021; 156(6): 819– 33. 32743804 PMC8460354
- [53]Cuello AC. Gangliosides, NGF, brain aging and disease: a mini-review with personal reflections. Neurochem Res. 2012; 37(6): 1256– 60. 22484968
- [54]Ferrari G, Greene LA. Promotion of neuronal survival by GM1 ganglioside. Phenomenology and mechanism of action. Ann N Y Acad Sci. 1998; 845: 263– 73. 9668360
- [55]Hemmings BA, Restuccia DF. PI3K-PKB/Akt pathway. Cold Spring Harb Perspect Biol. 2012; 4(9): a011189. 22952397 PMC3428770
- [56]Won JS, Singh AK, Singh I. Lactosylceramide: a lipid second messenger in neuroinflammatory disease. J Neurochem. 2007; 103(Suppl 1): 180– 91. 17986153
- [58]Olsen ASB, Færgeman NJ. Sphingolipids: membrane microdomains in brain development, function and neurological diseases. Open Biol. 2017; 7(5): 170069. 28566300 PMC5451547
- [59]Fabiani C, Antollini SS. Alzheimer’s disease as a membrane disorder: spatial cross-talk among beta-amyloid peptides, nicotinic acetylcholine receptors and lipid rafts. Front Cell Neurosci. 2019; 13: 309. 31379503 PMC6657435
- [61]Drolle E, Negoda A, Hammond K, Pavlov E, Leonenko Z. Changes in lipid membranes may trigger amyloid toxicity in Alzheimer's disease. PLoS One. 2017; 12(8): e0182194. 28767712 PMC5540602
- [62]Frisardi V, Panza F, Seripa D, Farooqui T, Farooqui AA. Glycerophospholipids and glycerophospholipid-derived lipid mediators: a complex meshwork in Alzheimer’s disease pathology. Prog Lipid Res. 2011; 50(4): 313– 30. 21703303
- [63]Williams TL, Serpell LC. Membrane and surface interactions of Alzheimer’s Aβ peptide-insights into the mechanism of cytotoxicity. FEBS J. 2011; 278(20): 3905– 17. 21722314
- [64]Niu Z, Zhang Z, Zhao W, Yang J. Interactions between amyloid beta peptide and lipid membranes. Biochim Biophys Acta Biomembr. 2018; 1860(9): 1663– 9. 29679539
- [65]Cazzaniga E, Bulbarelli A, Lonati E, Orlando A, Re F, Gregori M,. Abeta peptide toxicity is reduced after treatments decreasing phosphatidylethanolamine content in differentiated neuroblastoma cells. Neurochem Res. 2011; 36(5): 863– 9. 21287268
- [66]Sanchez-Mejia RO, Mucke L. Phospholipase A2 and arachidonic acid in Alzheimer’s disease. Biochim Biophys Acta. 2010; 1801(8): 784– 90. 20553961 PMC3024142
- [67]Jesko H, Stepien A, Lukiw WJ, Strosznajder RP. The cross-talk between sphingolipids and insulin-like growth factor signaling: significance for aging and neurodegeneration. Mol Neurobiol. 2019; 56(5): 3501– 21. 30140974 PMC6476865
- [68]Mencarelli C, Martinez-Martinez P. Ceramide function in the brain: when a slight tilt is enough. Cell Mol Life Sci. 2013; 70(2): 181– 203. 22729185 PMC3535405
- [69]Katsel P, Li C, Haroutunian V. Gene expression alterations in the sphingolipid metabolism pathways during progression of dementia and Alzheimer’s disease: a shift toward ceramide accumulation at the earliest recognizable stages of Alzheimer’s disease? Neurochem Res. 2007; 32(4–5): 845– 56. 17342407
- [70]Czubowicz K, Jesko H, Wencel P, Lukiw WJ, Strosznajder RP. The role of ceramide and sphingosine-1-phosphate in alzheimer’s disease and other neurodegenerative disorders. Mol Neurobiol. 2019; 56(8): 5436– 55. 30612333 PMC6614129
- [71]Custodia A, Romaus-Sanjurjo D, Aramburu-Núñez M, Alvarez-Rafael D, Vázquez-Vázquez L, Camino-Castiñeiras J,. Ceramide/sphingosine 1-phosphate Axis as a key target for diagnosis and treatment in alzheimer’s disease and other neurodegenerative diseases. Int J Mol Sci. 2022; 23(15): 8082. 35897658 PMC9331765
- [72]Hur JY. γ-Secretase in Alzheimer’s disease. Exp Mol Med. 2022; 54(4): 433– 46. 35396575 PMC9076685
- [73]Hicks DA, Nalivaeva NN, Turner AJ. Lipid rafts and Alzheimer’s disease: protein-lipid interactions and perturbation of signaling. Front Physiol. 2012; 3: 189. 22737128 PMC3381238
- [74]Hensley K. Neuroinflammation in Alzheimer’s disease: mechanisms, pathologic consequences, and potential for therapeutic manipulation. J Alzheimers Dis. 2010; 21(1): 1– 14. 20182045 PMC3792565
- [75]Ghosh S, Dyer RA, Beasley CL. Evidence for altered cell membrane lipid composition in postmortem prefrontal white matter in bipolar disorder and schizophrenia. J Psychiatr Res. 2017; 95: 135– 42. 28843843
- [76]Schwarz E, Prabakaran S, Whitfield P, Major H, Leweke FM, Koethe D,. High throughput lipidomic profiling of schizophrenia and bipolar disorder brain tissue reveals alterations of free fatty acids, phosphatidylcholines, and ceramides. J Proteome Res. 2008; 7(10): 4266– 77. 18778095
- [77]Shimamoto-Mitsuyama C, Nakaya A, Esaki K, Balan S, Iwayama Y, Ohnishi T,. Lipid pathology of the corpus callosum in schizophrenia and the potential role of abnormal gene regulatory networks with reduced microglial marker expression. Cereb Cortex. 2021; 31(1): 448– 62. 32924060 PMC7727339
- [78]Berger GE, Smesny S, Amminger GP. Bioactive lipids in schizophrenia. Int Rev Psychiatry. 2006; 18(2): 85– 98. 16777663
- [79]Noponen M, Sanfilipo M, Samanich K, Ryer H, Ko G, Angrist B,. Elevated PLA2 activity in schizophrenics and other psychiatric patients. Biol Psychiatry. 1993; 34(9): 641– 9. 8292693
- [80]Yu Q, He Z, Zubkov D, Huang S, Kurochkin I, Yang X,. Lipidome alterations in human prefrontal cortex during development, aging, and cognitive disorders. Mol Psychiatry. 2020; 25(11): 2952– 69. 30089790 PMC7577858
- [81]Karege F, Perroud N, Burkhardt S, Fernandez R, Ballmann E, La Harpe R,. Alterations in phosphatidylinositol 3-kinase activity and PTEN phosphatase in the prefrontal cortex of depressed suicide victims. Neuropsychobiology. 2011; 63(4): 224– 31. 21422769
- [82]Dwivedi Y, Rizavi HS, Teppen T, Zhang H, Mondal A, Roberts RC,. Lower phosphoinositide 3-kinase (PI 3-kinase) activity and differential expression levels of selective catalytic and regulatory PI 3-kinase subunit isoforms in prefrontal cortex and hippocampus of suicide subjects. Neuropsychopharmacology. 2008; 33(10): 2324– 40. 18075493
- [84]Gracia-Garcia P, Rao V, Haughey NJ, Bandaru VV, Smith G, Rosenberg PB,. Elevated plasma ceramides in depression. J Neuropsychiatry Clin Neurosci. 2011; 23(2): 215– 8. 21677254 PMC3121176
- [85]Turri M, Marchi C, Adorni MP, Calabresi L, Zimetti F. Emerging role of HDL in brain cholesterol metabolism and neurodegenerative disorders. Biochim Biophys Acta Mol Cell Biol Lipids. 2022; 1867(5): 159123. 35151900
- [86]Grundy SM. Absorption and metabolism of dietary cholesterol. Annu Rev Nutr. 1983; 3: 71– 96. 6357243
- [88]Luo J, Yang H, Song BL. Mechanisms and regulation of cholesterol homeostasis. Nat Rev Mol Cell Biol. 2020; 21(4): 225– 45. 31848472
- [89]Fünfschilling U, Saher G, Xiao L, Möbius W, Nave KA. Survival of adult neurons lacking cholesterol synthesis in vivo. BMC Neurosci. 2007; 8: 1. 17199885 PMC1769390
- [90]Nieweg K, Schaller H, Pfrieger FW. Marked differences in cholesterol synthesis between neurons and glial cells from postnatal rats. J Neurochem. 2009; 109(1): 125– 34. 19166509
- [91]Essayan-Perez S, Südhof TC. Neuronal γ-secretase regulates lipid metabolism, linking cholesterol to synaptic dysfunction in Alzheimer’s disease. Neuron. 2023; 111(20): 3176– 94.e7. 37543038 PMC10592349
- [92]Berghoff SA, Spieth L, Sun T, Hosang L, Depp C, Sasmita AO,. Neuronal cholesterol synthesis is essential for repair of chronically demyelinated lesions in mice. Cell Rep. 2021; 37(4): 109889. 34706227
- [95]Gamba P, Giannelli S, Staurenghi E, Testa G, Sottero B, Biasi F,. The controversial role of 24-S-hydroxycholesterol in alzheimer’s disease. Antioxidants. 2021; 10(5): 740. 34067119 PMC8151638
- [96]Hughes TM, Rosano C, Evans RW, Kuller LH. Brain cholesterol metabolism, oxysterols, and dementia. J Alzheimers Dis. 2013; 33(4): 891– 911. 23076077 PMC4354887
- [97]Sodero AO. 24S-hydroxycholesterol: cellular effects and variations in brain diseases. J Neurochem. 2021; 157(4): 899– 918. 33118626
- [98]Corraliza-Gomez M, Sanchez D, Ganfornina MD. Lipid-binding proteins in brain health and disease. Front Neurol. 2019; 10: 1152. 31787919 PMC6854030
- [100]Raulin AC, Martens YA, Bu G. Lipoproteins in the central nervous system: from biology to pathobiology. Annu Rev Biochem. 2022; 91: 731– 59. 35303786 PMC9634960
- [101]Kim WS, Guillemin GJ, Glaros EN, Lim CK, Garner B. Quantitation of ATP-binding cassette subfamily-A transporter gene expression in primary human brain cells. Neuroreport. 2006; 17(9): 891– 6. 16738483
- [102]Koldamova RP, Lefterov IM, Ikonomovic MD, Skoko J, Lefterov PI, Isanski BA,. 22R-hydroxycholesterol and 9-cis-retinoic acid induce ATP-binding cassette transporter A1 expression and cholesterol efflux in brain cells and decrease amyloid beta secretion. J Biol Chem. 2003; 278(15): 13244– 56. 12547833
- [103]Jin U, Park SJ, Park SM. Cholesterol metabolism in the brain and its association with Parkinson’s disease. Exp Neurobiol. 2019; 28(5): 554– 67. 31698548 PMC6844833
- [104]Borràs C, Mercer A, Sirisi S, Alcolea D, Escolà-Gil JC, Blanco-Vaca F,. HDL-like-mediated cell cholesterol trafficking in the central nervous system and alzheimer’s disease pathogenesis. Int J Mol Sci. 2022; 23(16): 9356. 36012637 PMC9409363
- [106]Berghoff SA, Spieth L, Sun T, Hosang L, Schlaphoff L, Depp C,. Microglia facilitate repair of demyelinated lesions via post-squalene sterol synthesis. Nat Neurosci. 2021; 24(1): 47– 60. 33349711 PMC7116742
- [107]Saher G, Brügger B, Lappe-Siefke C, Möbius W, Tozawa R, Wehr MC,. High cholesterol level is essential for myelin membrane growth. Nat Neurosci. 2005; 8(4): 468– 75. 15793579
- [109]Serrano-Pozo A, Qian J, Monsell SE, Betensky RA, Hyman BT. APOEε2 is associated with milder clinical and pathological Alzheimer disease. Ann Neurol. 2015; 77(6): 917– 29. 25623662 PMC4447539
- [111]Wennberg AM, Tosakulwong N, Lesnick TG, Murray ME, Whitwell JL, Liesinger AM,. Association of apolipoprotein E ε4 with transactive response DNA-binding protein 43. JAMA Neurol. 2018; 75(11): 1347– 54. 30422173 PMC6248121
- [114]Wang H, Kulas JA, Wang C, Holtzman DM, Ferris HA, Hansen SB. Regulation of beta-amyloid production in neurons by astrocyte-derived cholesterol. Proc Natl Acad Sci USA. 2021; 118(33): e2102191118. 34385305 PMC8379952
- [117]Lee SI, Jeong W, Lim H, Cho S, Lee H, Jang Y,. APOE4-carrying human astrocytes oversupply cholesterol to promote neuronal lipid raft expansion and Aβ generation. Stem Cell Rep. 2021; 16(9): 2128– 37. PMC8452535 34450034
- [118]Bandaru VV, Troncoso J, Wheeler D, Pletnikova O, Wang J, Conant K,. ApoE4 disrupts sterol and sphingolipid metabolism in Alzheimer’s but not normal brain. Neurobiol Aging. 2009; 30(4): 591– 9. 17888544 PMC2758772
- [120]Moulton MJ, Barish S, Ralhan I, Chang J, Goodman LD, Harland JG,. Neuronal ROS-induced glial lipid droplet formation is altered by loss of Alzheimer’s disease-associated genes. Proc Natl Acad Sci USA. 2021; 118(52): e2112095118. 34949639 PMC8719885
- [121]Wang N, Wang M, Jeevaratnam S, Rosenberg C, Ikezu TC, Shue F,. Opposing effects of apoE2 and apoE4 on microglial activation and lipid metabolism in response to demyelination. Mol Neurodegener. 2022; 17(1): 75. 36419137 PMC9682675
- [123]Yerbury JJ, Poon S, Meehan S, Thompson B, Kumita JR, Dobson CM,. The extracellular chaperone clusterin influences amyloid formation and toxicity by interacting with prefibrillar structures. FASEB J. 2007; 21(10): 2312– 22. 17412999
- [124]Yuste-Checa P, Trinkaus VA, Riera-Tur I, Imamoglu R, Schaller TF, Wang H,. The extracellular chaperone Clusterin enhances Tau aggregate seeding in a cellular model. Nat Commun. 2021; 12(1): 4863. 34381050 PMC8357826
- [125]De Roeck A, Van Broeckhoven C, Sleegers K. The role of ABCA7 in Alzheimer’s disease: evidence from genomics, transcriptomics and methylomics. Acta Neuropathol. 2019; 138(2): 201– 20. 30903345 PMC6660495
- [126]Dib S, Pahnke J, Gosselet F. Role of ABCA7 in human health and in alzheimer’s disease. Int J Mol Sci. 2021; 22(9): 4603. 33925691 PMC8124837
- [127]Tanaka N, Abe-Dohmae S, Iwamoto N, Fitzgerald ML, Yokoyama S. Helical apolipoproteins of high-density lipoprotein enhance phagocytosis by stabilizing ATP-binding cassette transporter A7. J Lipid Res. 2010; 51(9): 2591– 9. 20495215 PMC2918442
- [128]Shepardson NE, Shankar GM, Selkoe DJ. Cholesterol level and statin use in alzheimer disease: I. Review of epidemiological and preclinical studies. Arch Neurol. 2011; 68(10): 1239– 44. 21987540 PMC3211071
- [129]Iwagami M, Qizilbash N, Gregson J, Douglas I, Johnson M, Pearce N,. Blood cholesterol and risk of dementia in more than 1·8 million people over two decades: a retrospective cohort study. Lancet Healthy Longev. 2021; 2(8): e498– 506. 36097999
- [130]Walker AJ, Kim Y, Borissiouk I, Rehder R, Dodd S, Morris G,. Statins: neurobiological underpinnings and mechanisms in mood disorders. Neurosci Biobehav Rev. 2021; 128: 693– 708. 34265321
- [131]Markovic VM, Cupic Z, Macesic S, Stanojevic A, Vukojevic V, Kolar-Anic L. Modelling cholesterol effects on the dynamics of the hypothalamic-pituitary-adrenal (HPA) axis. Math Med Biol. 2016; 33(1): 1– 28. 25332212
- [132]Martins-De-Souza D, Wobrock T, Zerr I, Schmitt A, Gawinecka J, Schneider-Axmann T,. Different apolipoprotein E, apolipoprotein A1 and prostaglandin-H2 D-isomerase levels in cerebrospinal fluid of schizophrenia patients and healthy controls. World J Biol Psychiatry. 2010; 11(5): 719– 28. 20446881
- [133]Dean B, Digney A, Sundram S, Thomas E, Scarr E. Plasma apolipoprotein E is decreased in schizophrenia spectrum and bipolar disorder. Psychiatry Res. 2008; 158(1): 75– 8. 18096247
- [134]Jonas K, Clouston S, Li K, Fochtmann LJ, Lencz T, Malhotra AK,. Apolipoprotein E-ε4 allele predicts escalation of psychotic symptoms in late adulthood. Schizophr Res. 2019; 206: 82– 8. 30584027 PMC6525644
- [135]González-Castro TB, Tovilla-Zárate CA, Hernández-Díaz Y, Fresán A, Juárez-Rojop IE, Ble-Castillo JL,. No association between ApoE and schizophrenia: evidence of systematic review and updated meta-analysis. Schizophr Res. 2015; 169(1–3): 355– 68. 26372448
- [136]Yang Y, Wan C, Li H, Zhu H, La Y, Xi Z,. Altered levels of acute phase proteins in the plasma of patients with schizophrenia. Anal Chem. 2006; 78(11): 3571– 6. 16737209
- [137]Huang JT, Wang L, Prabakaran S, Wengenroth M, Lockstone HE, Koethe D,. Independent protein-profiling studies show a decrease in apolipoprotein A1 levels in schizophrenia CSF, brain and peripheral tissues. Mol Psychiatry. 2008; 13(12): 1118– 28. 17938634
- [138]Saari K, Jokelainen J, Veijola J, Koponen H, Jones PB, Savolainen M,. Serum lipids in schizophrenia and other functional psychoses: a general population northern Finland 1966 birth cohort survey. Acta Psychiatr Scand. 2004; 110(4): 279– 85. 15352929
- [139]Kim DD, Barr AM, Fredrikson DH, Honer WG, Procyshyn RM. Association between serum lipids and antipsychotic response in schizophrenia. Curr Neuropharmacol. 2019; 17(9): 852– 60. 30819084 PMC7052836
- [140]Pillinger T, McCutcheon RA, Howes OD. Variability of glucose, insulin, and lipid disturbances in first-episode psychosis: a meta-analysis. Psychol Med. 2023; 53(7): 3150– 6. 37449481 PMC10235663
- [141]Qiu Y, Li S, Teng Z, Tan Y, Xu X, Yang M,. Association between abnormal glycolipid level and cognitive dysfunction in drug-naïve patients with bipolar disorder. J Affect Disord. 2022; 297: 477– 85. 34715186
- [142]Torsvik A, Brattbakk HR, Trentani A, Holdhus R, Stansberg C, Bartz-Johannessen CA,. Patients with schizophrenia and bipolar disorder display a similar global gene expression signature in whole blood that reflects elevated proportion of immature neutrophil cells with association to lipid changes. Transl Psychiatry. 2023; 13(1): 147. 37147304 PMC10163263
- [143]Das D, Peng X, Lam ATN, Bader JS, Avramopoulos D. Transcriptome analysis of human induced excitatory neurons supports a strong effect of clozapine on cholesterol biosynthesis. Schizophr Res. 2021; 228: 324– 6. 33497908 PMC7987755
- [144]Olzmann JA, Carvalho P. Dynamics and functions of lipid droplets. Nat Rev Mol Cell Biol. 2019; 20(3): 137– 55. 30523332 PMC6746329
- [145]Gluchowski NL, Becuwe M, Walther TC, Farese RV Jr. Lipid droplets and liver disease: from basic biology to clinical implications. Nat Rev Gastroenterol Hepatol. 2017; 14(6): 343– 55. 28428634 PMC6319657
- [146]Cohen S. Lipid droplets as organelles. Int Rev Cell Mol Biol. 2018; 337: 83– 110. 29551163 PMC6241319
- [147]Walther TC, Farese RV Jr. Lipid droplets and cellular lipid metabolism. Annu Rev Biochem. 2012; 81: 687– 714. 22524315 PMC3767414
- [148]Unger RH, Orci L. Lipoapoptosis: its mechanism and its diseases. Biochim Biophys Acta. 2002; 1585(2–3): 202– 12. 12531555
- [149]Farmer BC, Walsh AE, Kluemper JC, Johnson LA. Lipid droplets in neurodegenerative disorders. Front Neurosci. 2020; 14: 742. 32848541 PMC7403481
- [151]Guttenplan KA, Weigel MK, Prakash P, Wijewardhane PR, Hasel P, Rufen-Blanchette U,. Neurotoxic reactive astrocytes induce cell death via saturated lipids. Nature. 2021; 599(7883): 102– 7. 34616039 PMC12054010
- [152]Fader Kaiser CM, Romano PS, Vanrell MC, Pocognoni CA, Jacob J, Caruso B,. Biogenesis and breakdown of lipid droplets in pathological conditions. Front Cell Dev Biol. 2021; 9: 826248. 35198567 PMC8860030
- [153]Yang C, Wang X, Wang J, Wang X, Chen W, Lu N,. Rewiring neuronal glycerolipid metabolism determines the extent of axon regeneration. Neuron. 2020; 105(2): 276– 92.e5. 31786011 PMC6975164
- [156]Loats AE, Carrera S, Fleming AF, Roberts ARE, Sherrard A, Toska E,. Cholesterol is required for transcriptional repression by BASP1. Proc Natl Acad Sci USA. 2021; 118(29): e2101671118. 34266955 PMC8307447
- [157]Islimye E, Girard V, Gould AP. Functions of stress-induced lipid droplets in the nervous system. Front Cell Dev Biol. 2022; 10: 863907. 35493070 PMC9047859
- [158]Bruce KD, Zsombok A, Eckel RH. Lipid processing in the brain: a key regulator of systemic metabolism. Front Endocrinol. 2017; 8: 60. PMC5378716 28421037
- [159]Weightman Potter PG, Vlachaki Walker JM, Robb JL, Chilton JK, Williamson R, Randall AD,. Basal fatty acid oxidation increases after recurrent low glucose in human primary astrocytes. Diabetologia. 2019; 62(1): 187– 98. 30293112 PMC6290858
- [160]He M, Pei Z, Mohsen AW, Watkins P, Murdoch G, Van Veldhoven PP,. Identification and characterization of new long chain acyl-CoA dehydrogenases. Mol Genet Metab. 2011; 102(4): 418– 29. 21237683 PMC3073726
- [161]Ebert D, Haller RG, Walton ME. Energy contribution of octanoate to intact rat brain metabolism measured by 13C nuclear magnetic resonance spectroscopy. J Neurosci. 2003; 23(13): 5928– 35. 12843297 PMC6741266
- [162]Shimabukuro MK, Langhi LG, Cordeiro I, Brito JM, Batista CM, Mattson MP,. Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes. Sci Rep. 2016; 6: 23795. 27029648 PMC4814830
- [163]Harkins D, Cooper HM, Piper M. The role of lipids in ependymal development and the modulation of adult neural stem cell function during aging and disease. Semin Cell Dev Biol. 2021; 112: 61– 8. 32771376
- [164]Capilla-Gonzalez V, Cebrian-Silla A, Guerrero-Cazares H, Garcia-Verdugo JM, Quiñones-Hinojosa A. Age-related changes in astrocytic and ependymal cells of the subventricular zone. Glia. 2014; 62(5): 790– 803. 24677590 PMC4322944
- [165]Hamilton LK, Dufresne M, Joppé SE, Petryszyn S, Aumont A, Calon F,. Aberrant lipid metabolism in the forebrain niche suppresses adult neural stem cell proliferation in an animal model of alzheimer’s disease. Cell Stem Cell. 2015; 17(4): 397– 411. 26321199
- [167]Bailey AP, Koster G, Guillermier C, Hirst EM, MacRae JI, Lechene CP,. Antioxidant role for lipid droplets in a stem cell niche of Drosophila. Cell. 2015; 163(2): 340– 53. 26451484 PMC4601084
- [168]Kis V, Barti B, Lippai M, Sass M. Specialized cortex glial cells accumulate lipid droplets in Drosophila melanogaster. PLoS One. 2015; 10(7): e0131250. 26148013 PMC4493057
- [169]Liu L, Zhang K, Sandoval H, Yamamoto S, Jaiswal M, Sanz E,. Glial lipid droplets and ROS induced by mitochondrial defects promote neurodegeneration. Cell. 2015; 160(1–2): 177– 90. 25594180 PMC4377295
- [170]Smolic T, Tavcar P, Horvat A, Cerne U, Haluzan Vasle A, Tratnjek L,. Astrocytes in stress accumulate lipid droplets. Glia. 2021; 69(6): 1540– 62. 33609060 PMC8248329
- [171]Lee LL, Aung HH, Wilson DW, Anderson SE, Rutledge JC, Rutkowsky JM. Triglyceride-rich lipoprotein lipolysis products increase blood-brain barrier transfer coefficient and induce astrocyte lipid droplets and cell stress. Am J Physiol Cell Physiol. 2017; 312(4): C500– 16. 28077357 PMC5407020
- [172]Etschmaier K, Becker T, Eichmann TO, Schweinzer C, Scholler M, Tam-Amersdorfer C,. Adipose triglyceride lipase affects triacylglycerol metabolism at brain barriers. J Neurochem. 2011; 119(5): 1016– 28. 21951135
- [174]Alzheimer A, Stelzmann RA, Schnitzlein HN, Murtagh FR. An English translation of alzheimer’s 1907 paper, “über eine eigenartige erkankung der hirnrinde”. Clin Anat. 1995; 8(6): 429– 31. 8713166
- [176]Jauhar S, Johnstone M, McKenna PJ. Schizophrenia. Lancet. 2022; 399(10323): 473– 86. 35093231
- [177]Hussain G, Wang J, Rasul A, Anwar H, Imran A, Qasim M,. Role of cholesterol and sphingolipids in brain development and neurological diseases. Lipids Health Dis. 2019; 18(1): 26. 30683111 PMC6347843
- [179]Peruzzolo TL, Pinto JV, Roza TH, Shintani AO, Anzolin AP, Gnielka V,. Inflammatory and oxidative stress markers in post-traumatic stress disorder: a systematic review and meta-analysis. Mol Psychiatry. 2022; 27(8): 3150– 63. 35477973
- [180]Xie Z, Jones A, Deeney JT, Hur SK, Bankaitis VA. Inborn errors of long-chain fatty acid β-oxidation link neural stem cell self-renewal to autism. Cell Rep. 2016; 14(5): 991– 9. 26832401 PMC4749429
- [181]Ramosaj M, Madsen S, Maillard V, Scandella V, Sudria-Lopez D, Yuizumi N,. Lipid droplet availability affects neural stem/progenitor cell metabolism and proliferation. Nat Commun. 2021; 12(1): 7362. 34934077 PMC8692608
- [182]Clark D, Dedova I, Cordwell S, Matsumoto I. A proteome analysis of the anterior cingulate cortex gray matter in schizophrenia. Mol Psychiatry. 2006; 11(5): 459– 70, 423. 16491132
- [183]Krohn J, Domart F, Do TT, Dresbach T. The synaptic vesicle protein Mover/TPRG1L is associated with lipid droplets in astrocytes. Glia. 2023; 71(12): 2799– 814. 37539560
- [184]Muhtaseb AW, Duan J. Modeling common and rare genetic risk factors of neuropsychiatric disorders in human induced pluripotent stem cells. Schizophr Res. 2022. PMC9735430 35459617
- [185]Lee SJ, Zhang J, Choi AM, Kim HP. Mitochondrial dysfunction induces formation of lipid droplets as a generalized response to stress. Oxid Med Cell Longev. 2013; 2013: 327167. 24175011 PMC3794647
- [186]Benador IY, Veliova M, Liesa M, Shirihai OS. Mitochondria bound to lipid droplets: where mitochondrial dynamics regulate lipid storage and utilization. Cell Metab. 2019; 29(4): 827– 35. 30905670 PMC6476311
- [187]Zhang S, Zhang H, Forrest MP, Zhou Y, Sun X, Bagchi VA,. Multiple genes in a single GWAS risk locus synergistically mediate aberrant synaptic development and function in human neurons. Cell Genom. 2023; 3(9): 100399. 37719141 PMC10504676
- [188]Link JC, Reue K. Genetic basis for sex differences in obesity and lipid metabolism. Annu Rev Nutr. 2017; 37(1): 225– 45. 28628359 PMC5759759
- [189]Kanoni S, Graham SE, Wang Y, Surakka I, Ramdas S, Zhu X,. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biol. 2022; 23(1): 268. 36575460 PMC9793579
- [190]2020 Alzheimer’s disease facts and figures. Alzheimers Dement. 2020. 32157811
- [191]Guo L, Zhong MB, Zhang L, Zhang B, Cai D. Sex differences in Alzheimer’s disease: insights from the multiomics landscape. Biol Psychiatry. 2022; 91(1): 61– 71. 33896621 PMC8996342
- [192]Wang JM, Irwin RW, Brinton RD. Activation of estrogen receptor alpha increases and estrogen receptor beta decreases apolipoprotein E expression in hippocampus in vitro and in vivo. Proc Natl Acad Sci USA. 2006; 103(45): 16983– 8. 17077142 PMC1636565
- [193]Ratnakumar A, Zimmerman SE, Jordan BA, Mar JC. Estrogen activates Alzheimer's disease genes. Alzheimers Dement. 2019; 5: 906– 17. PMC6926344 31890855
- [194]Nathan BP, Barsukova AG, Shen F, McAsey M, Struble RG. Estrogen facilitates neurite extension via apolipoprotein E in cultured adult mouse cortical neurons. Endocrinology. 2004; 145(7): 3065– 73. 15033916
- [195]Corder EH, Ghebremedhin E, Taylor MG, Thal DR, Ohm TG, Braak H. The biphasic relationship between regional brain senile plaque and neurofibrillary tangle distributions: modification by age, sex, and APOE polymorphism. Ann N Y Acad Sci. 2004; 1019: 24– 8. 15246987
- [196]Fisher DW, Bennett DA, Dong H. Sexual dimorphism in predisposition to Alzheimer’s disease. Neurobiol Aging. 2018; 70: 308– 24. 29754747 PMC6368179
- [197]Beydoun MA, Boueiz A, Abougergi MS, Kitner-Triolo MH, Beydoun HA, Resnick SM,. Sex differences in the association of the apolipoprotein E epsilon 4 allele with incidence of dementia, cognitive impairment, and decline. Neurobiol Aging. 2012; 33(4): 720– 31.e4. 20619505 PMC2974952
- [198]Fleisher A, Grundman M, Jack CR Jr, Petersen RC, Taylor C, Kim HT,. Sex, apolipoprotein E epsilon 4 status, and hippocampal volume in mild cognitive impairment. Arch Neurol. 2005; 62(6): 953– 7. 15956166
- [199]Brown CM, Choi E, Xu Q, Vitek MP, Colton CA. The APOE4 genotype alters the response of microglia and macrophages to 17beta-estradiol. Neurobiol Aging. 2008; 29(12): 1783– 94. 17553597 PMC2597534
- [200]Hsu M, Dedhia M, Crusio WE, Delprato A. Sex differences in gene expression patterns associated with the APOE4 allele. F1000Res. 2019; 8: 387. 31448102 PMC6685458
- [201]Prakash P, Manchanda P, Paouri E, Bisht K, Sharma K, Wijewardhane PR,. Amyloid β induces lipid droplet-mediated microglial dysfunction in Alzheimer’s disease. bioRxiv. 2023: 2023.06.04.543525. PMC12168635 40393454
- [202]Green T, Flash S, Reiss AL. Sex differences in psychiatric disorders: what we can learn from sex chromosome aneuploidies. Neuropsychopharmacology. 2019; 44(1): 9– 21. 30127341 PMC6235860
- [203]Stoney CM, Matthews KA, Mcdonald RH, Johnson CA. Sex differences in lipid, lipoprotein, cardiovascular, and neuroendocrine responses to acute stress. Psychophysiology. 1988; 25(6): 645– 56. 3241852
- [204]Ramos-Loyo J, Medina-Hernández V, Estarrón-Espinosa M, Canales-Aguirre A, Gómez-Pinedo U, Cerdán-Sánchez LF. Sex differences in lipid peroxidation and fatty acid levels in recent onset schizophrenia. Prog Neuro-Psychopharmacol Biol Psychiatry. 2013; 44: 154– 61. 23421976
- [205]Brivio E, Kos A, Ulivi AF, Karamihalev S, Ressle A, Stoffel R,. Sex shapes cell-type-specific transcriptional signatures of stress exposure in the mouse hypothalamus. Cell Rep. 2023; 42(8): 112874. 37516966
- [206]Millett CE, Phillips BE, Saunders EFH. The sex-specific effects of LPS on depressive-like behavior and oxidative stress in the Hippocampus of the mouse. Neuroscience. 2019; 399: 77– 88. 30553795
- [207]McNamara RK, Jandacek R, Rider T, Tso P, Hahn C-G, Richtand NM,. Abnormalities in the fatty acid composition of the postmortem orbitofrontal cortex of schizophrenic patients: gender differences and partial normalization with antipsychotic medications. Schizophr Res. 2007; 91(1–3): 37– 50. 17236749 PMC1853256
- [208]Kale A, Naphade N, Sapkale S, Kamaraju M, Pillai A, Joshi S,. Reduced folic acid, vitamin B12 and docosahexaenoic acid and increased homocysteine and cortisol in never-medicated schizophrenia patients: implications for altered one-carbon metabolism. Psychiatry Res. 2010; 175(1–2): 47– 53. 19969375
- [209]Yin F. Lipid metabolism and Alzheimer’s disease: clinical evidence, mechanistic link and therapeutic promise. FEBS J. 2023; 290(6): 1420– 53. 34997690 PMC9259766
- [210]Fassbender K, Simons M, Bergmann C, Stroick M, Lutjohann D, Keller P,. Simvastatin strongly reduces levels of Alzheimer’s disease beta -amyloid peptides Abeta 42 and Abeta 40 in vitro and in vivo. Proc Natl Acad Sci USA. 2001; 98(10): 5856– 61. 11296263 PMC33303
- [211]Refolo LM, Malester B, LaFrancois J, Bryant-Thomas T, Wang R, Tint GS,. Hypercholesterolemia accelerates the Alzheimer’s amyloid pathology in a transgenic mouse model. Neurobiol Dis. 2000; 7(4): 321– 31. 10964604
- [214]Dagliati A, Peek N, Brinton RD, Geifman N. Sex and APOE genotype differences related to statin use in the aging population. Alzheimers Dement. 2021; 7(1): e12156. PMC8088592 33969178
- [215]Kim JM, Stewart R, Kang HJ, Bae KY, Kim SW, Shin IS,. A prospective study of statin use and poststroke depression. J Clin Psychopharmacol. 2014; 34(1): 72– 9. 24304857
- [216]Kim SW, Kang HJ, Bae KY, Shin IS, Hong YJ, Ahn YK,. Interactions between pro-inflammatory cytokines and statins on depression in patients with acute coronary syndrome. Prog Neuro-Psychopharmacol Biol Psychiatry. 2018; 80(Pt C): 250– 4. 28689006
- [217]Rej S, Schulte SW, Rajji TK, Gildengers AG, Miranda D, Menon M,. Statins and cognition in late-life bipolar disorder. Int J Geriatr Psychiatry. 2018; 33(10): 1355– 60. 30022520
- [218]Nomura I, Kishi T, Ikuta T, Iwata N. Statin add-on therapy in the antipsychotic treatment of schizophrenia: a meta-analysis. Psychiatry Res. 2018; 260: 41– 7. 29172097
- [219]Sommer IE, Gangadin SS, de Witte LD, Koops S, van Baal C, Bahn S,. Simvastatin augmentation for patients with early-phase schizophrenia-spectrum disorders: a double-blind, randomized placebo-controlled trial. Schizophr Bull. 2021; 47(4): 1108– 15. 33608711 PMC8266622
- [220]Fotso Soh J, Beaulieu S, Trepiccione F, Linnaranta O, Torres-Platas G, Platt RW,. A double-blind, randomized, placebo-controlled pilot trial of atorvastatin for nephrogenic diabetes insipidus in lithium users. Bipolar Disord. 2021; 23(1): 66– 75. 32621644
- [221]Köhler-Forsberg O, Gasse C, Petersen L, Nierenberg AA, Mors O, Østergaard SD. Statin treatment and the risk of depression. J Affect Disord. 2019; 246: 706– 15. 30611914
- [222]Okereke OI, Vyas CM, Mischoulon D, Chang G, Cook NR, Weinberg A,. Effect of long-term supplementation with marine omega-3 fatty acids vs placebo on risk of depression or clinically relevant depressive symptoms and on change in mood scores: a randomized clinical trial. JAMA. 2021; 326(23): 2385– 94. 34932079 PMC8693224
- [223]Liang CS, Tseng PT, Su KP. Effect of long-term supplementation with marine omega-3 fatty acids vs placebo on risk of depression. JAMA. 2022; 327(13): 1290– 1. 35380588
- [224]Papsdorf K, Brunet A. Linking lipid metabolism to chromatin regulation in aging. Trends Cell Biol. 2019; 29(2): 97– 116. 30316636 PMC6340780
- [225]Parnell E, Culotta L, Forrest MP, Jalloul HA, Eckman BL, Loizzo DD,. Excitatory dysfunction drives network and calcium handling deficits in 16p11.2 duplication schizophrenia induced pluripotent stem cell-derived neurons. Biol Psychiatry. 2023; 94(2): 153– 63. 36581494 PMC10166768
- [226]Zhang S, Sanders AR, Duan J. Modeling PTSD neuronal stress responses in a dish. Nat Neurosci. 2022; 25(11): 1402– 4. 36266472 PMC9721095
- [227]Kozlova A, Zhang S, Kotlar AV, Jamison B, Zhang H, Shi S,. Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. Am J Hum Genet. 2022; 109(8): 1500– 19. 35931052 PMC9388388
- [228]Yue W, Huang H, Duan J. Potential diagnostic biomarkers for schizophrenia. Med Rev Berl. 2022; 2(4): 385– 416. PMC10388817 37724326
- [230]Butler Iii RR, Kozlova A, Zhang H, Zhang S, Streit M, Sanders AR,. The genetic relevance of human induced pluripotent stem cell-derived microglia to alzheimer’s disease and major neuropsychiatric disorders. Mol Neuropsychiatry. 2020; 5(Suppl 1): 85– 96. 32399472 PMC7206606
- [231]Barretto N, Zhang H, Powell SK, Fernando MB, Zhang S, Flaherty EK,. ASCL1- and DLX2-induced GABAergic neurons from hiPSC-derived NPCs. J Neurosci Methods. 2020; 334: 108548. 32065989 PMC7426253
- Authors
- Zhao, X., Zhang, S., Sanders, A. R., & Duan, J.
- Affiliations
- Endeavor Health (US)
- Corresponding author
- Duan, Jubao
- Venue
- Complex Psychiatry
- Publisher
- S. Karger AG
- Published
- 2023
- Volume
- 9
- Issue
- 1-4
- Pages
- 154-171
- ISSN
- 2673-298X (ISSN-L)
- 2673-3005
- PMC
- PMC10697751
- OpenAlex
- W4388517796
- Cited by
- 54
- References
- 226
- Citations by year
- 2026: 19 · 2025: 22 · 2024: 13
- FWCI
- 5.43
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Complex Psychiatry (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (R01AG063175, R01AG081374)
- National Institute of Mental Health (R01MH116281, R01MH106575)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
- Keywords
- brain lipids, lipid droplets, Alzheimer's disease, neuropsychiatric disorders, lipid metabolism, neurodegenerative diseases, schizophrenia, lipid homeostasis, phospholipids, cholesterol, triglycerides, diagnostic biomarkers
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