Adhvaryu KP, Karthikbabu S, Rao PTJC, Pediatrics E (2022) Motor performance of children with attention deficit hyperactivity disorder: focus on the Bruininks-Oseretsky Test of Motor Proficiency. 65:512
Ahn KH, Kim SK, Choi JM, Jung SY, Won JH, Back MJ, Fu Z, Jang JM, Ha HC, Kim DK (2013) Identification of heat shock protein 60 as a Regulator of Neutral Sphingomyelinase 2 and its role in dopamine uptake. PLoS ONE 8:e67216
Article CAS PubMed PubMed Central Google Scholar
Ariga T, Jarvis WD, Yu RK (1998) Role of sphingolipid-mediated cell death in neurodegenerative diseases. J Lipid Res 39:1–16
Article CAS PubMed Google Scholar
Austerman J (2015) ADHD and behavioral disorders: Assessment, management, and an update from DSM-5. Cleve Clin J Med 82:S2–7
Barrier L, Page G, Barc S, Piriou A, Portoukalian J (2003) Sulfatide and GM1 Ganglioside modulate the high-affinity dopamine uptake in rat striatal synaptosomes: evidence for the involvement of their ionic charges. Neurochem Int 42:305–313
Article CAS PubMed Google Scholar
Ben-David O, Futerman AH (2010) The role of the ceramide acyl chain length in neurodegeneration: involvement of ceramide synthases. Neuromol Med 12:341–350
Bradbury AM, Bongarzone ER, Sands MS (2021) Krabbe disease: New hope for an old disease. Neurosci Lett 752:135841
Article CAS PubMed PubMed Central Google Scholar
Brunkhorst-Kanaan N, Trautmann S, Schreiber Y, Thomas D, Kittel-Schneider S, Gurke R, Geisslinger G, Reif A, Tegeder IJB (2021a) Sphingolipid and endocannabinoid profiles in adult attention deficit hyperactivity disorder. 9:1173
Brunkhorst-Kanaan N, Trautmann S, Schreiber Y, Thomas D, Kittel-Schneider S, Gurke R, Geisslinger G, Reif A, Tegeder I (2021b) Sphingolipid and endocannabinoid profiles in adult attention deficit hyperactivity disorder. Biomedicines 9
Buccinnà B, Piccinini M, Prinetti A, Scandroglio F, Prioni S, Valsecchi M, Votta B, Grifoni S, Lupino E, Ramondetti C et al (2009) Alterations of myelin-specific proteins and sphingolipids characterize the brains of acid sphingomyelinase-deficient mice, an animal model of Niemann-pick disease type A. J Neurochem 109:105–115
Cho S-C, Kim H-W, Kim B-N, Kim J-W, Shin M-S, Chung S, Cho D-Y, Jung S-W, Yoo HJ (2010) Chung I-WJPi: gender-specific association of the brain-derived neurotrophic factor gene with attention-deficit/hyperactivity disorder. 7:285
Cole W, Mostofsky S, Larson JG, Denckla M, Mahone EJN (2008) Age-related changes in motor subtle signs among girls and boys with ADHD. 71:1514–1520
Copeland B, Vogelsberg V, Neff N, Hadjiconstantinou MJJP, Therapeutics E (1996) Protein kinase C activators decrease dopamine uptake into striatal synaptosomes. 277:1527–1532
Crasta JE, Zhao Y, Seymour KE, Suskauer SJ, Mostofsky SH, Rosch KSJCN (2021) Developmental trajectory of subtle motor signs in attention-deficit/hyperactivity disorder: a longitudinal study from childhood to adolescence. 27:317–332
da Silva BS, Grevet EH, Silva LCF, Ramos JKN, Rovaris DL, Bau CHDJD (2023) Discover Mental Health 3:2
Article PubMed PubMed Central Google Scholar
Darwish AH, Elgohary TM, Nosair NA (2019) Serum Interleukin-6 level in children with attention-deficit hyperactivity disorder (ADHD). J Child Neurol 34:61–67
de Wit NM, den Hoedt S, Martinez-Martinez P, Rozemuller AJ, Mulder MT, de Vries HE (2019) Astrocytic ceramide as possible indicator of neuroinflammation. J Neuroinflamm 16:48
Detrick JA, Zink C, Rosch KS, Horn PS, Huddleston DA, Crocetti D, Wu SW, Pedapati EV, Wassermann EM, Mostofsky SHJBC (2021) Motor cortex modulation and reward in children with attention-deficit/hyperactivity disorder. 3:fcab093
Drechsler R, Brem S, Brandeis D, Grünblatt E, Berger G, Walitza SJN (2020) ADHD: current concepts and treatments in children and adolescents. 51:315–335
El Ghamry R, El-Sheikh M, Abdel Meguid M, Nagib S (2021) Aly El Gabry DJMECP: plasma brain-derived neurotrophic factor (BDNF) in Egyptian children with attention deficit hyperactivity disorder. 28:1–9
Ercan E, Amado S, Somer O (2001) Çıkoğlu SJÇvGRSD: Dikkat eksikliği hiperaktivite bozukluğu ve yıkıcı davranım bozuklukları için bir test bataryası geliştirme çabası. 8:132–144
Faltraco F, Palm D, Uzoni A, Borchert L, Simon F, Tucha O, Thome J (1996) Dopamine adjusts the circadian gene expression of Per2 and Per3 in human dermal fibroblasts from ADHD patients. Journal of neural transmission (Vienna, Austria: 2021, 128:1135–1145
Fliers E, Rommelse N, Vermeulen S, Altink M, Buschgens C, Faraone S, Sergeant J, Franke B (2008) Buitelaar JJJont: Motor coordination problems in children and adolescents with ADHD rated by parents and teachers: effects of age and gender. 115:211–220
Franke B, Michelini G, Asherson P, Banaschewski T, Bilbow A, Buitelaar JK, Cormand B, Faraone SV, Ginsberg Y, Haavik J et al (2018) Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan. Eur Neuropsychopharmacology: J Eur Coll Neuropsychopharmacol 28:1059–1088
Gokler BJTJCAMH (2004) Reliability and validity of schedule for affective disorders and Schizophrenia for school age children-present and lifetime version-turkish version (K-SADS-PL-T)[in Turkish]. 11:109–116
Güleç A, Güler HA, Türkoğlu SJCI (2024) Relationship between traumatic experiences, circadian preference and ADHD symptoms in adolescents with ADHD residing in Institutional Care: a controlled study.:1–9
Han X, Rozen S, Boyle SH, Hellegers C, Cheng H, Burke JR, Welsh-Bohmer KA, Doraiswamy PM, Kaddurah-Daouk R (2011) Metabolomics in early Alzheimer’s disease: identification of altered plasma sphingolipidome using shotgun lipidomics. PLoS ONE 6:e21643
Article CAS PubMed PubMed Central Google Scholar
Haughey NJ, Bandaru VV, Bae M, Mattson MP (2010) Roles for dysfunctional sphingolipid metabolism in Alzheimer’s disease neuropathogenesis. Biochim Biophys Acta 1801:878–886
Article CAS PubMed PubMed Central Google Scholar
Henriquez-Henriquez M, Acosta MT, Martinez AF, Vélez JI, Lopera F, Pineda D, Palacio JD, Quiroga T, Worgall TS (2020a) Deckelbaum RJJTp: mutations in sphingolipid metabolism genes are associated with ADHD. 10:231
Henriquez-Henriquez M, Acosta MT, Martinez AF, Vélez JI, Lopera F, Pineda D, Palacio JD, Quiroga T, Worgall TS, Deckelbaum RJ et al (2020b) Mutations in sphingolipid metabolism genes are associated with ADHD. Translational Psychiatry 10:231
Article CAS PubMed PubMed Central Google Scholar
Henríquez-Henríquez MP, Solari S, Quiroga T, Kim BI, Deckelbaum RJ (2015) Worgall TSJFin: low serum sphingolipids in children with attention deficit-hyperactivity disorder. 9:300
Hess JL, Radonjić NV, Patak J, Glatt SJ, Faraone SV (2021) Autophagy, apoptosis, and neurodevelopmental genes might underlie selective brain region vulnerability in attention-deficit/hyperactivity disorder. Mol Psychiatry 26:6643–6654
Article CAS PubMed Google Scholar
Iacono S, Del Giudice E, Leon A, La Bella V, Spataro R (2022) A novel compound heterozygous mutation in GALC associated with adult-onset Krabbe disease: case report and literature review. Neurogenetics 23:157–165
Article CAS PubMed Google Scholar
Ishii T, Warabi E, Mann GE (2019) Circadian control of BDNF-mediated Nrf2 activation in astrocytes protects dopaminergic neurons from ferroptosis. Free Radic Biol Med 133:169–178
Article CAS PubMed Google Scholar
Jové M, Cabré R, Mota-Martorell N, Martin-Garí M, Obis È, Ramos P, Canales I, Galo-Licona JD, Sol J, Nogueras L et al (2021) Age-related changes in Lipidome of Rat Frontal Cortex and Cerebellum are partially reversed by Methionine Restriction Applied in Old Age. Int J Mol Sci 22
Kaufman J, Birmaher B, Brent D, Rao U, Flynn C, Moreci P, Williamson D, Ryan NJJotAAoC, Psychiatry A (1997) Schedule for affective disorders and schizophrenia for school-age children-present and lifetime version (K-SADS-PL): initial reliability and validity data. 36:980–988
Kharitonova M, Martin RE, Gabrieli JD, Sheridan MAJD (2013) Cortical gray-matter thinning is associated with age-related improvements on executive function tasks. 6:61–71
Kuperberg SJ, Wadgaonkar R (2017) Sepsis-Associated Encephalopathy: the blood-brain barrier and the Sphingolipid Rheostat. Front Immunol 8:597
Article PubMed PubMed Central Google Scholar
Leffa DT, Bellaver B, de Oliveira C, de Macedo IC, de Freitas JS, Grevet EH, Caumo W, Rohde LA, Quincozes-Santos A, Torres ILS (2017) Increased oxidative parameters and decreased cytokine levels in an animal model of Attention-Deficit/Hyperactivity disorder. Neurochem Res 42:3084–3092
Article CAS PubMed Google Scholar
Lequin RM (2005) Enzyme immunoassay (EIA)/enzyme-linked immunosorbent assay (ELISA). Clin Chem 51:2415–2418
Article CAS PubMed Google Scholar
Lintas C, Cassano I, Azzarà A, Stigliano MG, Gregorj C, Sacco R, Stoccoro A, Coppedè F, Gurrieri FJG (2023) Maternal epigenetic dysregulation as a possible risk factor for neurodevelopmental disorders. 14:585
Loft LM, Moseholm KF, Pedersen KK, Jensen MK, Koch M (2022) Cronje HTJCOiL: sphingomyelins and ceramides: possible biomarkers for dementia? 33:57–67
Marian OC, Teo JD, Lee JY, Song H, Kwok JB, Landin-Romero R, Halliday G, Don AS (2023) Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations. Acta Neuropathol Commun 11:52
Article CAS PubMed PubMed Central Google Scholar
Marín T, Dulcey AE, Campos F, de la Fuente C, Acuña M, Castro J, Pinto C, Yañez MJ, Cortez C, McGrath DW et al (2022) c-Abl activation linked to autophagy-lysosomal dysfunction contributes to neurological impairment in Niemann-pick type a Disease. Front cell Dev Biology 10:844297
Marks N, Berg MJ, Saito M, Saito M (2008) Glucosylceramide synthase decrease in frontal cortex of Alzheimer brain correlates with abnormal increase in endogenous ceramides: consequences to morphology and viability on enzyme suppression in cultured primary neurons. Brain Res 1191:136–147
Article CAS PubMed Google Scholar
Martins IP, Lauterbach M, Luís H, Amaral H, Rosenbaum G, Slade PD, Townes BDJCN (2013) Neurological subtle signs and cognitive development: a study in late childhood and adolescence. 19:466–478
Mielke MM, Maetzler W, Haughey NJ, Bandaru VV, Savica R, Deuschle C, Gasser T, Hauser AK, Gräber-Sultan S, Schleicher E et al (2013) Plasma ceramide and glucosylceramide metabolism is altered in sporadic Parkinson’s disease and associated with cognitive impairment: a pilot study. PLoS ONE 8:e73094
Article CAS PubMed PubMed Central Google Scholar
Mondal K, Del Mar NA, Gary AA, Grambergs RC, Yousuf M, Tahia F, Stephenson B, Stephenson DJ, Chalfant CE, Reiner A, Mandal N (2024) Sphingolipid changes in mouse brain and plasma after mild traumatic brain injury at the acute phases. Lipids Health Dis 23:200
Article CAS PubMed PubMed Central Google Scholar
Mostofsky M SH, Newschaffer CJ, Denckla MBJP, skills (2003) Overflow movements predict impaired response inhibition in children with ADHD. 97:1315–1331
Nagel BJ, Bathula D, Herting M, Schmitt C, Kroenke CD, Fair D (2011) Nigg JTJJotAAoC, Psychiatry A: altered white matter microstructure in children with attention-deficit/hyperactivity disorder. 50:283–292
Nakajima K, Tohyama Y, Kohsaka S, Kurihara TJJ (2002) Ceramide activates microglia to enhance the production/secretion of brain-derived neurotrophic factor (BDNF) without induction of deleterious factors in vitro. 80:697–705
Notaras M, van den Buuse MJTN (2019) Brain-derived neurotrophic factor (BDNF): novel insights into regulation and genetic variation. 25:434–454
Oizumi H, Sugimura Y, Totsune T, Kawasaki I, Ohshiro S, Baba T, Kimpara T, Sakuma H, Hasegawa T, Kawahata I et al (2022) Plasma sphingolipid abnormalities in neurodegenerative diseases. PLoS ONE 17:e0279315
Comments (0)