Plasma Biomarkers in Neurodegenerative Dementias: Unrevealing the Potential of Serum Oxytocin, BDNF, NPTX1, TREM2, TNF-alpha, IL-1 and Prolactin.

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    • Source:
      Publisher: Bentham Science Publishers Country of Publication: United Arab Emirates NLM ID: 101208441 Publication Model: Print Cited Medium: Internet ISSN: 1875-5828 (Electronic) Linking ISSN: 15672050 NLM ISO Abbreviation: Curr Alzheimer Res Subsets: MEDLINE
    • Publication Information:
      Original Publication: Saif Zone, Sharjah, U.A.E. ; San Francisco, CA : Bentham Science Publishers, c2004-
    • Subject Terms:
    • Abstract:
      Background: Dementia encompasses a range of neurodegenerative disorders characterized by cognitive decline and functional impairment. The identification of reliable biomarkers is essential for accurate diagnosis and gaining insights into the mechanisms underlying diseases.
      Objective: This study aimed to investigate the plasma biomarker profiles associated with Brain- Derived Neurotrophic Factor (BDNF), Oxytocin, Neuronal Pentraxin-1 (NPTX1), Triggering Receptor Expressed on Myeloid Cells 2 (TREM2), Tumor Necrosis Factor-alpha (TNF-alpha), Interleukin- 1 (IL-1) and Prolactin in Alzheimer's disease (AD), dementia with Lewy bodies (DLB), frontotemporal dementias (FTD) and healthy controls.
      Methods: Serum levels of the aforementioned biomarkers were analyzed in 23 AD, 28 DLB, 15 FTD patients recruited from outpatient units and 22 healthy controls. Diagnostic evaluations followed established criteria and standardized clinical tests were conducted. Blood samples were collected and analyzed using ELISA and electrochemiluminescence immunoassay methods.
      Results: Serum BDNF and oxytocin levels did not significantly differ across groups. NPTX1, TREM2, TNF-alpha and IL-1 levels also did not show significant differences among dementia groups. However, prolactin levels exhibited distinct patterns, with lower levels in male DLB patients and higher levels in female AD patients compared to controls.
      Conclusion: The study findings suggest potential shared mechanisms in dementia pathophysiology and highlight the importance of exploring neuroendocrine responses, particularly in AD and DLB. However, further research is warranted to elucidate the role of these biomarkers in dementia diagnosis and disease progression.
      (Copyright© Bentham Science Publishers; For any queries, please email at [email protected].)
    • References:
      Gale S.A.; Acar D.; Daffner K.R.; Dementia. Am J Med 2018,131(10),1161-1169. (PMID: 10.1016/j.amjmed.2018.01.02229425707)
      McGinnis S.; Neuroimaging in neurodegenerative dementias. Semin Neurol 2013,32(4),347-360. (PMID: 10.1055/s-0032-133180823361481)
      Dark H.E.; Duggan M.R.; Walker K.A.; Plasma biomarkers for Alzheimer’s and related dementias: A review and outlook for clinical neuropsychology. Arch Clin Neuropsychol 2024,acae019. (PMID: 10.1093/arclin/acae01938520383)
      Du Y.; Wu H.T.; Qin X.Y.; Cao C.; Liu Y.; Cao Z.Z.; Cheng Y.; Postmortem brain, cerebrospinal fluid and blood neurotrophic factor levels in alzheimer’s disease: a systematic review and meta-analysis. J Mol Neurosci 2018,65(3),289-300. (PMID: 10.1007/s12031-018-1100-829956088)
      Ng TKS; Ho CSH; Tam WWS; Kua EH; Ho RC; Decreased serum brain-derived neurotrophic factor (BDNF) levels in patients with alzheimer's disease (AD): a systematic review and meta-analysis. Int J Mol Sci 2019,20(2),257. (PMID: 10.3390/ijms20020257)
      Tampi R.R.; Maksimowski M.; Ahmed M.; Tampi D.J.; Oxytocin for frontotemporal dementia: a systematic review. Ther Adv Psychopharmacol 2017,7(1),48-53. (PMID: 10.1177/204512531667257428101324)
      Panaro M.A.; Benameur T.; Porro C.; Hypothalamic neuropeptide brain protection: focus on oxytocin. J Clin Med 2020,9(5),1534. (PMID: 10.3390/jcm905153432438751)
      Froemke R.C.; Young L.J.; Oxytocin, neural plasticity and social behavior. Annu Rev Neurosci 2021,44(1),359-381. (PMID: 10.1146/annurev-neuro-102320-10284733823654)
      Kirsch P.; Oxytocin in the socioemotional brain: implications for psychiatric disorders. Dialogues Clin Neurosci 2015,17(4),463-476. (PMID: 10.31887/DCNS.2015.17.4/pkirsch26869847)
      Raskind M.A.; Peskind E.R.; Lampe T.H.; Risse S.C.; Taborsky G.J.; Dorsa D.; Cerebrospinal fluid vasopressin, oxytocin, somatostatin and beta-endorphin in Alzheimer’s disease. Arch Gen Psychiatry 1986,43(4),382-388. (PMID: 10.1001/archpsyc.1986.018000400920132869744)
      Mazurek M.F.; Beal M.F.; Bird E.D.; Martin J.B.; Oxytocin in Alzheimer’s disease. Neurology 1987,37(6),1001-1003. (PMID: 10.1212/WNL.37.6.10013587615)
      North W.G.; Harbaugh R.; Reeder T.; An evaluation of human neurophysin production in Alzheimer’s disease: Preliminary observations. Neurobiol Aging 1992,13(2),261-265. (PMID: 10.1016/0197-4580(92)90038-Y1522943)
      Johnson E.G.; Kuiper W.; Ahmed R.M.; Halliday G.M.; Burrell J.R.; Hodges J.R.; Guastella A.J.; Piguet O.; Kumfor F.; Plasma oxytocin is not associated with social cognition or behavior in frontotemporal dementia and alzheimer’s disease syndromes. Dement Geriatr Cogn Disord 2022,51(3),241-248. (PMID: 10.1159/00052508735705005)
      Figueiro-Silva J.; Gruart A.; Clayton K.B.; Podlesniy P.; Abad M.A.; Gasull X.; Delgado-García J.M.; Trullas R.; Neuronal pentraxin 1 negatively regulates excitatory synapse density and synaptic plasticity. J Neurosci 2015,35(14),5504-5521. (PMID: 10.1523/JNEUROSCI.2548-14.201525855168)
      Abad M.A.; Enguita M.; DeGregorio-Rocasolano N.; Ferrer I.; Trullas R.; Neuronal pentraxin 1 contributes to the neuronal damage evoked by amyloid-beta and is overexpressed in dystrophic neurites in Alzheimer’s brain. J Neurosci 2006,26(49),12735-12747. (PMID: 10.1523/JNEUROSCI.0575-06.200617151277)
      Ma Q.L.; Teng E.; Zuo X.; Jones M.; Teter B.; Zhao E.Y.; Zhu C.; Bilousova T.; Gylys K.H.; Apostolova L.G.; LaDu M.J.; Hossain M.A.; Frautschy S.A.; Cole G.M.; Neuronal pentraxin 1: A synaptic-derived plasma biomarker in Alzheimer’s disease. Neurobiol Dis 2018,114,120-128. (PMID: 10.1016/j.nbd.2018.02.01429501530)
      Krasemann S.; Madore C.; Cialic R.; Baufeld C.; Calcagno N.; El Fatimy R.; Beckers L.; O’Loughlin E.; Xu Y.; Fanek Z.; Greco D.J.; Smith S.T.; Tweet G.; Humulock Z.; Zrzavy T.; Conde-Sanroman P.; Gacias M.; Weng Z.; Chen H.; Tjon E.; Mazaheri F.; Hartmann K.; Madi A.; Ulrich J.D.; Glatzel M.; Worthmann A.; Heeren J.; Budnik B.; Lemere C.; Ikezu T.; Heppner F.L.; Litvak V.; Holtzman D.M.; Lassmann H.; Weiner H.L.; Ochando J.; Haass C.; Butovsky O.; The TREM2-APOE pathway drives the transcriptional phenotype of dysfunctional microglia in neurodegenerative diseases. Immunity 2017,47(3),566-581.e9. (PMID: 10.1016/j.immuni.2017.08.00828930663)
      Jay TR; von Saucken VE; Landreth GE; TREM2 in Neurodegenerative Diseases. Mol Neurodegener 2017,12(1),56. (PMID: 10.1186/s13024-017-0197-5)
      Bekris L.M.; Khrestian M.; Dyne E.; Shao Y.; Pillai J.A.; Rao S.M.; Bemiller S.M.; Lamb B.; Fernandez H.H.; Leverenz J.B.; Soluble TREM2 and biomarkers of central and peripheral inflammation in neurodegenerative disease. J Neuroimmunol 2018,319,19-27. (PMID: 10.1016/j.jneuroim.2018.03.00329685286)
      Culjak M.; Perkovic M.N.; Uzun S.; Strac D.S.; Erjavec G.N.; Leko M.B.; Simic G.; Tudor L.; Konjevod M.; Kozumplik O.; Mimica N.; Pivac N.; The Association between TNF-alpha, IL-1 alpha and IL-10 with Alzheimer’s Disease. Curr Alzheimer Res 2021,17(11),972-984. (PMID: 10.2174/156720501766620113009242733256580)
      Leng F.; Edison P.; Neuroinflammation and microglial activation in Alzheimer disease: where do we go from here? Nat Rev Neurol 2021,17(3),157-172. (PMID: 10.1038/s41582-020-00435-y33318676)
      Leung Y.Y.; Toledo J.B.; Nefedov A.; Polikar R.; Raghavan N.; Xie S.X.; Farnum M.; Schultz T.; Baek Y.; Van Deerlin V.M.; Hu W.T.; Holtzman D.M.; Fagan A.M.; Perrin R.J.; Grossman M.; Soares H.D.; Kling M.A.; Mailman M.; Arnold S.E.; Narayan V.A.; Lee V.M.Y.; Shaw L.M.; Baker D.; Wittenberg G.M.; Trojanowski J.Q.; Wang L.S.; Identifying amyloid pathology–related cerebrospinal fluid biomarkers for Alzheimer’s disease in a multicohort study. Alzheimers Dement 2015,1(3),339-348. (PMID: 10.1016/j.dadm.2015.06.00826693175)
      House A.; Jones J.; Increased response of serum prolactin to metoclopramide in senile dementia of Alzheimer type. Int J Geriatr Psychiat 1989,4(5),279-282. (PMID: 10.1002/gps.930040506)
      Balldin J.; Gottfries C-G.; Karlsson I.; Lindstedt G.; Långström G.; Wålinder J.; Dexamethasone suppression test and serum prolactin in dementia disorders. Br J Psychiatry 1983,143(3),277-281. (PMID: 10.1192/bjp.143.3.2776626841)
      Olğun Y.; Aksoy Poyraz C.; Bozluolçay M.; Poyraz B.Ç.; Quantitative EEG in the differential diagnosis of dementia subtypes. J Geriatr Psychiatry Neurol 2024,08919887241227410. (PMID: 10.1177/0891988724122741038217438)
      Olğun Y.; Aksoy Poyraz C.; Bozluolçay M.; Gündüz A.; Poyraz B.Ç.; A comparative transcranial magnetic stimulation study: Assessing cortical excitability and plasticity in Alzheimer’s disease, dementia with Lewy bodies and Frontotemporal dementia. Psychogeriatrics 2024,24(2),272-280. (PMID: 10.1111/psyg.1307038131520)
      Jack C.R.; Albert M.S.; Knopman D.S.; McKhann G.M.; Sperling R.A.; Carrillo M.C.; Thies B.; Phelps C.H.; Introduction to the recommendations from the National Institute on Aging‐Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement 2011,7(3),257-262. (PMID: 10.1016/j.jalz.2011.03.00421514247)
      McKeith I.G.; Boeve B.F.; Dickson D.W.; Halliday G.; Taylor J.P.; Weintraub D.; Aarsland D.; Galvin J.; Attems J.; Ballard C.G.; Bayston A.; Beach T.G.; Blanc F.; Bohnen N.; Bonanni L.; Bras J.; Brundin P.; Burn D.; Chen-Plotkin A.; Duda J.E.; El-Agnaf O.; Feldman H.; Ferman T.J.; ffytche D.; Fujishiro H.; Galasko D.; Goldman J.G.; Gomperts S.N.; Graff-Radford N.R.; Honig L.S.; Iranzo A.; Kantarci K.; Kaufer D.; Kukull W.; Lee V.M.Y.; Leverenz J.B.; Lewis S.; Lippa C.; Lunde A.; Masellis M.; Masliah E.; McLean P.; Mollenhauer B.; Montine T.J.; Moreno E.; Mori E.; Murray M.; O’Brien J.T.; Orimo S.; Postuma R.B.; Ramaswamy S.; Ross O.A.; Salmon D.P.; Singleton A.; Taylor A.; Thomas A.; Tiraboschi P.; Toledo J.B.; Trojanowski J.Q.; Tsuang D.; Walker Z.; Yamada M.; Kosaka K.; Diagnosis and management of dementia with Lewy bodies. Neurology 2017,89(1),88-100. (PMID: 10.1212/WNL.000000000000405828592453)
      Rascovsky K.; Hodges J.R.; Knopman D.; Mendez M.F.; Kramer J.H.; Neuhaus J.; van Swieten J.C.; Seelaar H.; Dopper E.G.P.; Onyike C.U.; Hillis A.E.; Josephs K.A.; Boeve B.F.; Kertesz A.; Seeley W.W.; Rankin K.P.; Johnson J.K.; Gorno-Tempini M.L.; Rosen H.; Prioleau-Latham C.E.; Lee A.; Kipps C.M.; Lillo P.; Piguet O.; Rohrer J.D.; Rossor M.N.; Warren J.D.; Fox N.C.; Galasko D.; Salmon D.P.; Black S.E.; Mesulam M.; Weintraub S.; Dickerson B.C.; Diehl-Schmid J.; Pasquier F.; Deramecourt V.; Lebert F.; Pijnenburg Y.; Chow T.W.; Manes F.; Grafman J.; Cappa S.F.; Freedman M.; Grossman M.; Miller B.L.; Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 2011,134(9),2456-2477. (PMID: 10.1093/brain/awr17921810890)
      Gorno-Tempini M.L.; Hillis A.E.; Weintraub S.; Kertesz A.; Mendez M.; Cappa S.F.; Ogar J.M.; Rohrer J.D.; Black S.; Boeve B.F.; Manes F.; Dronkers N.F.; Vandenberghe R.; Rascovsky K.; Patterson K.; Miller B.L.; Knopman D.S.; Hodges J.R.; Mesulam M.M.; Grossman M.; Classification of primary progressive aphasia and its variants. Neurology 2011,76(11),1006-1014. (PMID: 10.1212/WNL.0b013e31821103e621325651)
      Folstein M.F.; Folstein S.E.; McHugh P.R.; “Mini-mental state”. J Psychiatr Res 1975,12(3),189-198. (PMID: 10.1016/0022-3956(75)90026-61202204)
      Güngen C.; Ertan T.; Eker E.; Yaşar R.; Engı̇n F.; Reliability and validity of the standardized Mini Mental State Examination in the diagnosis of mild dementia in Turkish population. Turk Psikiyatr Derg 2002,13(4),273-281. (PMID: 12794644)
      Morris J.C.; The Clinical Dementia Rating (CDR): current version and scoring rules. Neurology 1993,43(11),2412-2414. (PMID: 10.1212/WNL.43.11.2412-a8232972)
      Leber I.; Otto M.; Vandenberghe R.; European Reference Network For Rare Neurologıcal Dıseases (ERN-RND), “Scale To Measure Frontotemporal Dementıa CDR® Dementia Staging Instrument Plus NACC FTLD Behavior and Language Domains,” Available from: www.ern-rnd.eu2020.
      Reisberg B.; Ferris S.H.; de Leon M.J.; Crook T.; The Global Deterioration Scale for assessment of primary degenerative dementia. Am J Psychiatry 1982,139(9),1136-1139. (PMID: 10.1176/ajp.139.9.11367114305)
      Garcia Basalo M.M.; Fernandez M.C.; Ojea Quintana M.; Rojas J.I.; Garcia Basalo M.J.; Bogliotti E.; Campora N.; Fernandez M.; Berrios W.; Cristiano E.; Golimstok A.; ALBA Screening Instrument (ASI): A brief screening tool for Lewy Body Dementia. Arch Gerontol Geriatr 2017,70,67-75. (PMID: 10.1016/j.archger.2017.01.00128088604)
      de Medeiros K.; Robert P.; Gauthier S.; Stella F.; Politis A.; Leoutsakos J.; Taragano F.; Kremer J.; Brugnolo A.; Porsteinsson A.P.; Geda Y.E.; Brodaty H.; Gazdag G.; Cummings J.; Lyketsos C.; The neuropsychiatric inventory-clinician rating scale (NPI-C): reliability and validity of a revised assessment of neuropsychiatric symptoms in dementia. Int Psychogeriatr 2010,22(6),984-994. (PMID: 10.1017/S104161021000087620594384)
      Şahi̇n Cankurtaran E.; Danişman M.; Tutar H.; Ulusoy Kaymak S.; The reliability and validity of the turkish version of the neuro psychiatric inventory-clinician. Turk J Med Sci 2015,45(5),1087-1093. (PMID: 10.3906/sag-1405-11126738352)
      Bathina S.; Das U.N.; Brain-derived neurotrophic factor and its clinical implications. Arch Med Sci 2015,6(6),1164-1178. (PMID: 10.5114/aoms.2015.5634226788077)
      Gao L.; Zhang Y.; Sterling K.; Song W.; Brain-derived neurotrophic factor in Alzheimer’s disease and its pharmaceutical potential. Transl Neurodegener 2022,11(1),4. (PMID: 10.1186/s40035-022-00279-035090576)
      Xue B.; Waseem S.M.A.; Zhu Z.; Alshahrani M.A.; Nazam N.; Anjum F.; Habib A.H.; Rafeeq M.M.; Nazam F.; Sharma M.; Brain-derived neurotrophic factor: a connecting link between nutrition, lifestyle and alzheimer’s disease. Front Neurosci 2022,16,925991. (PMID: 10.3389/fnins.2022.92599135692417)
      Angelucci F.; Spalletta G.; Iulio F.; Ciaramella A.; Salani F.; Varsi A.; Gianni W.; Sancesario G.; Caltagirone C.; Bossu P.; Bossù P.; Alzheimer’s disease (AD) and Mild Cognitive Impairment (MCI) patients are characterized by increased BDNF serum levels. Curr Alzheimer Res 2010,7(1),15-20. (PMID: 10.2174/15672051079027447320205668)
      Gómez de San José N.; Massa F.; Halbgebauer S.; Oeckl P.; Steinacker P.; Otto M.; Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration. J Neural Transm 2022,129(2),207-230. (PMID: 10.1007/s00702-021-02411-234460014)
      Ashton NJ; Suárez-Calvet M; Heslegrave A; Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers. Alzheimers Res Ther 2019,11(1),94. (PMID: 10.1186/s13195-019-0545-5)
      Suárez-Calvet M; Kleinberger G; Araque Caballero MÁ; sTREM2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early-stage Alzheimer's disease and associate with neuronal injury markers. EMBO Mol Med 2016,8(5),466-476. (PMID: 10.15252/emmm.201506123)
      Heslegrave A; Heywood W; Paterson R; Increased cerebrospinal fluid soluble TREM2 concentration in Alzheimer's disease. Mol Neurodegener 2016,11,3. (PMID: 10.1186/s13024-016-0071-x)
      Qin Q.; Teng Z.; Liu C.; Li Q.; Yin Y.; Tang Y.; TREM2, microglia and Alzheimer’s disease. Mech Ageing Dev 2021,195,111438. (PMID: 10.1016/j.mad.2021.11143833516818)
      Woollacott IOC; Nicholas JM; Heslegrave A; Cerebrospinal fluid soluble TREM2 levels in frontotemporal dementia differ by genetic and pathological subgroup. Alzheimers Res Ther 2018,10(1),79. (PMID: 10.1186/s13195-018-0405-8)
      Shaftel SS; Griffin WS; O'Banion MK; The role of interleukin-1 in neuroinflammation and Alzheimer disease: an evolving perspective. J Neuroinflammat 2008,5,7. (PMID: 10.1186/1742-2094-5-7)
      Uchida Y; Kan H; Sakurai K; Oishi K; Matsukawa N; Contributions of blood-brain barrier imaging to neurovascular unit pathophysiology of Alzheimer's disease and related dementias. Front Aging Neurosci 2023,15,1111448. (PMID: 10.3389/fnagi.2023.1111448)
    • Grant Information:
      37023,35895 Istanbul Üniversitesi
    • Contributed Indexing:
      Keywords: Alzheimer's disease; BDNF; IL-1; NPTX1; TNF-alpha.; TREM2; dementia with Lewy bodies; frontotemporal dementia; oxytocin; prolactin; serum biomarker
    • Accession Number:
      0 (Receptors, Immunologic)
      9002-62-4 (Prolactin)
      0 (Biomarkers)
      0 (Brain-Derived Neurotrophic Factor)
      0 (Tumor Necrosis Factor-alpha)
      0 (neuronal pentraxin)
      0 (Membrane Glycoproteins)
      0 (Nerve Tissue Proteins)
      50-56-6 (Oxytocin)
      0 (TREM2 protein, human)
      0 (Interleukin-1)
      7171WSG8A2 (BDNF protein, human)
      9007-41-4 (C-Reactive Protein)
    • Publication Date:
      Date Created: 20240528 Date Completed: 20240827 Latest Revision: 20241004
    • Publication Date:
      20241004
    • Accession Number:
      10.2174/0115672050313419240520051751
    • Accession Number:
      38803182