{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T22:16:32Z","timestamp":1777932992210,"version":"3.51.4"},"reference-count":44,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2022,2,1]],"date-time":"2022-02-01T00:00:00Z","timestamp":1643673600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Rejuvenation Research"],"published-print":{"date-parts":[[2022,2]]},"abstract":"<jats:p>\n                    Alzheimer's disease (AD) has no cure, mainly because of late diagnosis. Early diagnostic biomarkers are crucial. Phospholipases A\n                    <jats:sub>2<\/jats:sub>\n                    (PLA\n                    <jats:sub>2<\/jats:sub>\n                    ) are hydrolases with several functions in the brain, nevertheless their deregulation contributes to neurodegeneration. We evaluated platelet total PLA\n                    <jats:sub>2<\/jats:sub>\n                    activity (p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    ) in healthy elderly subjects (HE,\n                    <jats:italic toggle=\"yes\">n<\/jats:italic>\n                    \u2009=\u2009102), patients suffering from mild cognitive impairment (MCI,\n                    <jats:italic toggle=\"yes\">n<\/jats:italic>\n                    \u2009=\u200990) and AD (\n                    <jats:italic toggle=\"yes\">n<\/jats:italic>\n                    \u2009=\u200991). Platelets are considered \u201ccirculating neurons\u201d and p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    appears to mirror the cerebral activity. p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    of the three cohorts was similar, but in MCI the higher p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    the worse the global cognitive status (Mini Mental State Examination score [MMSE]) and in AD the lower p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    the more severe the pathology stage (Clinical Dementia Rating [CDR]). Accordingly, MCI with MMSE \u226526 overlapped HE, in MCI with MMSE &lt;26 and in AD with CDR 1 p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    increased, in AD with CDR 2 p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    decreased. In MCI p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    positively correlated with blood oxidation and inflammation, in AD it was the opposite. Finally, Discrimination Index (DI)\u2014calculated multiplying p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    , oxidative level and Cu\/Zn ratio (an inflammation parameter)\u2014differentiated MCI patients who progressed to dementia in the following 24 months and AD patients with the worse pathology development. Summarizing, p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    changes during MCI and AD progression, is linked, in opposite way, to oxidative\/inflammatory status in MCI and AD and might help, when included in DI, to identify MCI converters to dementia and AD patients with the more severe prognosis. p\n                    <jats:sub>tot<\/jats:sub>\n                    PLA\n                    <jats:sub>2<\/jats:sub>\n                    may have a diagnostic\/prognostic value and be a potential therapeutic target.\n                  <\/jats:p>","DOI":"10.1089\/rej.2021.0020","type":"journal-article","created":{"date-parts":[[2021,12,16]],"date-time":"2021-12-16T08:50:05Z","timestamp":1639644605000},"page":"16-24","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":3,"title":["Platelet Total PLA\n                    <sub>2<\/sub>\n                    Activity, Serum Oxidative Level, and Plasma Cu\/Zn Ratio: A Vicious Cycle with a Potential Role to Monitor MCI and Alzheimer's Disease Progression"],"prefix":"10.1177","volume":"25","author":[{"given":"Marta","family":"Balietti","sequence":"first","affiliation":[{"name":"Center for Neurobiology of Aging, IRCCS INRCA, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tiziana","family":"Casoli","sequence":"additional","affiliation":[{"name":"Center for Neurobiology of Aging, IRCCS INRCA, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Robertina","family":"Giacconi","sequence":"additional","affiliation":[{"name":"Advanced Technology Center for Aging Research, IRCCS INRCA, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cinzia","family":"Giuli","sequence":"additional","affiliation":[{"name":"Geriatrics Operative Unit, IRCCS INRCA, Fermo, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2022,2,15]]},"reference":[{"key":"e_1_3_6_2_2","doi-asserted-by":"publisher","DOI":"10.1002\/jnr.24805"},{"key":"e_1_3_6_3_2","doi-asserted-by":"publisher","DOI":"10.18632\/aging.101925"},{"key":"e_1_3_6_4_2","doi-asserted-by":"publisher","DOI":"10.1021\/acschemneuro.5b00073"},{"key":"e_1_3_6_5_2","doi-asserted-by":"publisher","DOI":"10.1615\/CritRevImmunol.v37.i2-6.20"},{"key":"e_1_3_6_6_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0090-6980(02)00020-5"},{"key":"e_1_3_6_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.pnpbp.2010.08.019"},{"key":"e_1_3_6_8_2","doi-asserted-by":"publisher","DOI":"10.1007\/s00702-006-0597-0"},{"key":"e_1_3_6_9_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.neulet.2005.12.014"},{"key":"e_1_3_6_10_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1471-4159.1997.69020704.x"},{"key":"e_1_3_6_11_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1749-6632.1996.tb34438.x"},{"key":"e_1_3_6_12_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.neurobiolaging.2011.11.008"},{"key":"e_1_3_6_13_2","doi-asserted-by":"publisher","DOI":"10.1007\/s00213-008-1092-0"},{"key":"e_1_3_6_14_2","first-page":"1727","article-title":"Platelets in Alzheimer's disease-associated cellular senescence and inflammation","volume":"19","author":"Casoli T","year":"2013","unstructured":"Casoli T, , Balietti M, , Giorgetti B, , Solazzi M, , Scarpino O, , Fattoretti P. Platelets in Alzheimer's disease-associated cellular senescence and inflammation. 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