Levels of Angiotensin-Converting Enzyme and Apolipoproteins Are Associated with Alzheimer’s Disease and Cardiovascular Diseases
Open accessAbstract
Angiotensin-converting enzyme-1 (ACE1) and apolipoproteins (APOs) may play important roles in the development of Alzheimer’s disease (AD) and cardiovascular diseases (CVDs). This study aimed to examine the associations of AD, CVD, and endocrine-metabolic diseases (EMDs) with the levels of ACE1 and 9 APO proteins (ApoAI, ApoAII, ApoAIV, ApoB, ApoCI, ApoCIII, ApoD, ApoE, and ApoH). Non-Hispanic white individuals including 109 patients with AD, 356 mild cognitive impairment (MCI), 373 CVD, 198 EMD and controls were selected from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) dataset. Multivariable general linear model (GLM) was used to examine the associations. ApoE ε4 allele was associated with AD, as well as ApoAIV, ApoB and ApoE proteins, but not associated with CVD and EMD. Both AD and CVD were associated with levels of ACE1, ApoB, and ApoH proteins. AD, MCI and EMD were associated with levels of ACE1, ApoAII, and ApoE proteins. This is the first study to report associations of ACE1 and several APO proteins with AD, MCI, CVD and EMD, respectively, including upregulated and downregulated protein levels. In conclusion, as specific or shared biomarkers, the levels of ACE1 and APO proteins are implicated for AD, CVD, EMD and ApoE ε4 allele. Further studies are required for validation to establish reliable biomarkers for these health conditions.
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Higher levels of plasma apoB are associated with AD or cognitive decline.
“Higher levels of plasma apoB are associated with AD or cognitive decline [9, 10]”
From Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants (2023) · cites this paper as [10]
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High performance plasma amyloid-β biomarkers for Alzheimer's disease
Nakamura, A., Kaneko, N., Villemagne, V. L., Kato, T., Doecke, J., Doré, V., Fowler, C., Li, Q.-X., Martins, R., Rowe, C., et al. (2018) · Nature · doi:10.1038/nature25456 · Cited by 1,681 · see citing works
Current understanding of Alzheimer’s disease diagnosis and treatment
Weller, J., & Budson, A. (2018) · F1000Research · doi:10.12688/f1000research.14506.1 · Cited by 1,083 · see citing works
Cerebral amyloid angiopathy and Alzheimer disease — one peptide, two pathways
Greenberg, S. M., Bacskai, B. J., Hernandez-Guillamon, M., Pruzin, J., Sperling, R., & van Veluw, S. J. (2020) · Nature Reviews Neurology · doi:10.1038/s41582-019-0281-2 · Cited by 947 · see citing works
Lipids, apolipoproteins, and their ratios in relation to cardiovascular events with statin treatment
Kastelein, J. J. P., van der Steeg, W. A., Holme, I., Gaffney, M., Cater, N. B., Barter, P., Deedwania, P., Olsson, A. G., Boekholdt, S. M., Demicco, D. A., et al. (2008) · Circulation · doi:10.1161/circulationaha.107.713438 · Cited by 478 · see citing works
Apolipoprotein E isoforms and lipoprotein metabolism
Phillips, M. C. (2014) · IUBMB Life · doi:10.1002/iub.1314 · Cited by 328 · see citing works
Lumsden, A. L., Mulugeta, A., Zhou, A., & Hyppönen, E. (2020) · eBioMedicine · doi:10.1016/j.ebiom.2020.102954 · Cited by 317 · cited 3× · see citing works
“The ApoE ε 3 allele is the most common allele, followed by ε 4 allele [2].”
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Research works printed but not linked: 55
- [3]Huebbe P. Rimbach G. Evolution of human apolipoprotein E (APOE) isoforms: Gene structure, protein function and interaction with dietary factors Ageing Res. Rev. 2017 37 146 161 10.1016/j.arr.2017.06.002 28647612 · DOI
- [4]Kang J.H. Logroscino G. De Vivo I. Hunter D. Grodstein F. Apolipoprotein E, cardiovascular disease and cognitive function in aging women Neurobiol. Aging 2005 26 475 484 10.1016/j.neurobiolaging.2004.05.003 15653176 · DOI
- [6]Riedel B.C. Thompson P.M. Brinton R.D. Age, APOE and sex: Triad of risk of Alzheimer’s disease J. Steroid. Biochem. Mol. Biol. 2016 160 134 147 10.1016/j.jsbmb.2016.03.012 26969397 PMC4905558 · DOI · Paper page
- [7]Wolf A.B. Caselli R.J. Reiman E.M. Valla J. APOE and neuroenergetics: An emerging paradigm in Alzheimer’s disease Neurobiol. Aging 2013 34 1007 1017 10.1016/j.neurobiolaging.2012.10.011 23159550 PMC3545040 · DOI
- [8]Huang Y. Mahley R.W. Apolipoprotein E: Structure and function in lipid metabolism, neurobiology, and Alzheimer’s diseases Neurobiol. Dis. 2014 72 3 12 10.1016/j.nbd.2014.08.025 25173806 PMC4253862 · DOI · Paper page
- [9]Getz G. Reardon C. Apoprotein E and Reverse Cholesterol Transport Int. J. Mol. Sci. 2018 19 3479 10.3390/ijms19113479 PMC6275009 30404132 · DOI
- [10]Mur J. McCartney D.L. Walker R.M. Campbell A. Bermingham M.L. Morris S.W. Porteous D.J. McIntosh A.M. Deary I.J. Evans K.L. DNA methylation in APOE: The relationship with Alzheimer’s and with cardiovascular health Alzheimer’s Dement. Transl. Res. Clin. Interv. 2020 6 e12026 10.1002/trc2.12026 PMC7185210 32346601 · DOI
- [11]Langsted A. Freiberg J.J. Nordestgaard B.G. Fasting and Nonfasting Lipid Levels Circulation 2008 118 2047 2056 10.1161/CIRCULATIONAHA.108.804146 18955664 · DOI · Paper page
- [12]Mahley R.W. Apolipoprotein E: From cardiovascular disease to neurodegenerative disorders J. Mol. Med. 2016 94 739 746 10.1007/s00109-016-1427-y 27277824 PMC4921111 · DOI · Paper page
- [13]Dominiczak M.H. Caslake M.J. Apolipoproteins: Metabolic role and clinical biochemistry applications Ann. Clin. Biochem. Int. J. Lab. Med. 2011 48 498 515 10.1258/acb.2011.011111 22028427 · DOI · Paper page
- [14]Davel A.P. Wenceslau C.F. Akamine E.H. Xavier F.E. Couto G.K. Oliveira H.T. Rossoni L.V. Endothelial dysfunction in cardiovascular and endocrine-metabolic diseases: An update Braz. J. Med. Biol. Res. 2011 44 920 932 10.1590/S0100-879X2011007500104 21956535 · DOI
- [15]Chang T.-Y. Yamauchi Y. Hasan M.T. Chang C. Cellular cholesterol homeostasis and Alzheimer’s disease J. Lipid Res. 2017 58 2239 2254 10.1194/jlr.R075630 28298292 PMC5711498 · DOI · Paper page
- [16]Belloy M.E. Napolioni V. Greicius M.D. A Quarter Century of APOE and Alzheimer’s Disease: Progress to Date and the Path Forward Neuron 2019 101 820 838 10.1016/j.neuron.2019.01.056 30844401 PMC6407643 · DOI · Paper page
- [17]Kotze M.J. Van Rensburg S.J. Pathology supported genetic testing and treatment of cardiovascular disease in middle age for prevention of Alzheimer’s disease Metab. Brain. Dis. 2012 27 255 266 10.1007/s11011-012-9296-8 22552896 PMC3429783 · DOI
- [18]Levi O. Dolev I. Belinson H. Michaelson D.M. Intraneuronal amyloid-β plays a role in mediating the synergistic pathological effects of apoE4 and environmental stimulation J. Neurochem. 2007 103 1031 1040 10.1111/j.1471-4159.2007.04810.x 17666042 · DOI
- [19]Martins I.J. Hone E. Foster J.K. Sünram-Lea S.I. Gnjec A. Fuller S.J. Nolan D. Gandy S.E. Martins R.N. Apolipoprotein E, cholesterol metabolism, diabetes, and the convergence of risk factors for Alzheimer’s disease and cardiovascular disease Mol. Psychiatry 2006 11 721 736 10.1038/sj.mp.4001854 16786033 · DOI · Paper page
- [21]Jochemsen H.M. Teunissen C.E. Ashby E.L. Van der Flier W.M. Jones R.E. Geerlings M.I. Scheltens P. Kehoe P.G. Muller M. The association of angiotensin-converting enzyme with biomarkers for Alzheimer’s disease Alzheimers Res. 2014 6 27 10.1186/alzrt257 PMC4075229 24987467 · DOI · Paper page
- [22]Rusek M. Pluta R. Ułamek-Kozioł M. Czuczwar S.J. Ketogenic Diet in Alzheimer’s Disease Int. J. Mol. Sci. 2019 20 3892 10.3390/ijms20163892 PMC6720297 31405021 · DOI · Paper page
- [24]Poirier J. Apolipoprotein E and Alzheimer’s Disease A Role in Amyloid Catabolism Ann. N. Y. Acad. Sci. 2006 924 81 90 10.1111/j.1749-6632.2000.tb05564.x 11193807 · DOI
- [25]Dlugosz P. Nimpf J. The Reelin Receptors Apolipoprotein E receptor 2 (ApoER2) and VLDL Receptor Int. J. Mol. Sci. 2018 19 3090 10.3390/ijms19103090 PMC6213145 30304853 · DOI · Paper page
- [26]Isbir T. Agaçhan B. Yilmaz H. Aydin M. Kara I. Eker D. Eker E. Interaction between apolipoprotein-E and angiotensin-converting enzyme genotype in Alzheimer’s disease Am. J. Alzheimer’s Dis. Other Dement. 2001 16 205 210 10.1177/153331750101600407 PMC10833823 11501342 · DOI
- [27]Arpa A. Del Ser T. Goda G. Barba R. Bornstein B. Apolipoprotein E, angiotensin-converting enzyme and α-1-antichymotrypsin genotypes are not associated with post-stroke dementia J. Neurol. Sci. 2003 210 77 82 10.1016/S0022-510X(03)00026-1 12736093 · DOI
- [28]Qiu W.W.Q. Lai A. Mon T. Mwamburi M. Taylor W. Rosenzweig J. Kowall N. Stern R. Zhu H. Steffens D.C. Angiotensin Converting Enzyme Inhibitors and Alzheimer Disease in the Presence of the Apolipoprotein E4 Allele Am. J. Geriatr. Psychiatry 2014 22 177 185 10.1016/j.jagp.2012.08.017 23567418 PMC3873370 · DOI
- [29]Renee Ruhaak L. Van Der Laarse A. Cobbaert C.M. Apolipoprotein profiling as a personalized approach to the diagnosis and treatment of dyslipidaemia Ann. Clin. Biochem. Int. J. Lab. Med. 2019 56 338 356 10.1177/0004563219827620 PMC6595551 30889974 · DOI · Paper page
- [30]Tamburus N.Y. Verlengia R. Kunz V.C. César M.C. Silva E. Apolipoprotein B and angiotensin-converting enzyme polymorphisms and aerobic interval training: Randomized controlled trial in coronary artery disease patients Braz. J. Med. Biol. Res. 2018 51 10.1590/1414-431x20186944 PMC5999065 29846435 · DOI
- [31]De Vries M.A. Van Santen S.S. Klop B. Van Der Meulen N. Van Vliet M. Van De Geijn G.-J.M. Van Der Zwan-Van Beek E.M. Birnie E. Liem A.H. De Herder W.W. Erythrocyte-bound apolipoprotein B in atherosclerosis and mortality Eur. J. Clin. Investig. 2017 47 289 296 10.1111/eci.12728 28144944 · DOI
- [32]Hwang Y.-C. Ahn H.-Y. Han K.H. Park S.-W. Park C.-Y. Prediction of future cardiovascular disease with an equation to estimate apolipoprotein B in patients with high cardiovascular risk: An analysis from the TNT and IDEAL study Lipids Health Dis. 2017 16 158 10.1186/s12944-017-0549-8 28830468 PMC5568138 · DOI
- [33]McKhann G. Drachman D. Folstein M. Katzman R. Price D. Stadlan E.M. Clinical diagnosis of Alzheimer’s disease: Report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease Neurology 1984 34 939 944 10.1212/WNL.34.7.939 6610841 · DOI · Paper page
- [34]Iglewicz B. Hoaglin D. The ASQC Basic References in Quality Control: Statistics Techniques How Detect Handle Outliers Mykyta E.F. ASQC Quality Press Milwaukee, WI, USA 1993 Volume 16
- [36]Kehoe P.G. Wong S. Al Mulhim N. Palmer L.E. Miners J.S. Angiotensin-converting enzyme 2 is reduced in Alzheimer’s disease in association with increasing amyloid-β and tau pathology Alzheimer’s Res. Ther. 2016 8 50 10.1186/s13195-016-0217-7 27884212 PMC5123239 · DOI · Paper page
- [37]Yasar S. Varma V.R. Harris G.C. Carlson M.C. Associations of Angiotensin Converting Enzyme-1 and Angiotensin II Blood Levels and Cognitive Function J. Alzheimer’s Dis. 2018 63 655 664 10.3233/JAD-170944 29660936 PMC5998658 · DOI
- [38]Yang Y.-H. Liu C.-K. Angiotensin-Converting Enzyme Gene in Alzheimer’s Disease Tohoku. J. Exp. Med. 2008 215 295 298 10.1620/tjem.215.295 18679002 · DOI
- [39]Hussain A. Tang O. Sun C. Jia X. Selvin E. Nambi V. Folsom A. Heiss G. Zannad F. Mosley T. Soluble Angiotensin-Converting Enzyme 2, Cardiac Biomarkers, Structure, and Function, and Cardiovascular Events (from the Atherosclerosis Risk in Communities Study) Am. J. Cardiol. 2021 146 15 21 10.1016/j.amjcard.2021.01.017 33539861 PMC8038970 · DOI
- [40]Liang Y. Deng H. Bi S. Cui Z. Lata A. Zheng D. Wang Y. Urinary angiotensin converting enzyme 2 increases in patients with type 2 diabetic mellitus Kidney Blood Press. Res. 2015 40 101 110 10.1159/000368486 25791940 · DOI
- [41]Najm R. Jones E.A. Huang Y. Apolipoprotein E4, inhibitory network dysfunction, and Alzheimer’s disease Mol. Neurodegener. 2019 14 24 10.1186/s13024-019-0324-6 31186040 PMC6558779 · DOI · Paper page
- [42]Raman S. Brookhouser N. Brafman D.A. Using human induced pluripotent stem cells (hiPSCs) to investigate the mechanisms by which Apolipoprotein E (APOE) contributes to Alzheimer’s disease (AD) risk Neurobiol. Dis. 2020 138 104788 10.1016/j.nbd.2020.104788 32032733 PMC7098264 · DOI
- [43]Lim W.L. Martins I.J. Martins R.N. The involvement of lipids in Alzheimer’s disease J. Genet. Genom. 2014 41 261 274 10.1016/j.jgg.2014.04.003 24894353 · DOI
- [44]Kajiwara Y. Wang E. Wang M. Sin W.C. Brennand K.J. Schadt E. Naus C.C. Buxbaum J. Zhang B. GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis Acta. Neuropathol. Commun. 2018 6 144 10.1186/s40478-018-0642-x 30577786 PMC6303945 · DOI
- [45]Rawat V. Wang S. Sima J. Bar R. Liraz O. Gundimeda U. Parekh T. Chan J. Johansson J.O. Tang C. ApoE4 Alters ABCA1 Membrane Trafficking in Astrocytes J. Neurosci. 2019 39 9611 9622 10.1523/JNEUROSCI.1400-19.2019 31641056 PMC6880458 · DOI · Paper page
- [46]Liu S. Liu J. Weng R. Gu X. Zhong Z. Apolipoprotein E gene polymorphism and the risk of cardiovascular disease and type 2 diabetes BMC Cardiovasc. Disord. 2019 19 213 10.1186/s12872-019-1194-0 31521122 PMC6744677 · DOI
- [47]Safieh M. Korczyn A.D. Michaelson D.M. ApoE4: An emerging therapeutic target for Alzheimer’s disease BMC Med. 2019 17 64 10.1186/s12916-019-1299-4 30890171 PMC6425600 · DOI · Paper page
- [48]Tzoulaki I. Castagné R. Boulangé C.L. Karaman I. Chekmeneva E. Evangelou E. Ebbels T.M.D. Kaluarachchi M.R. Chadeau-Hyam M. Mosen D. Serum metabolic signatures of coronary and carotid atherosclerosis and subsequent cardiovascular disease Eur. Heart J. 2019 40 2883 2896 10.1093/eurheartj/ehz235 31102408 PMC7963131 · DOI
- [49]Soares H.D. Plasma Biomarkers Associated With the Apolipoprotein E Genotype and Alzheimer Disease Arch. Neurol. 2012 69 1310 10.1001/archneurol.2012.1070 22801723 PMC3683865 · DOI · Paper page
- [50]Gigante B. Leander K. Vikstrom M. Frumento P. Carlsson A.C. Bottai M. De Faire U. Elevated ApoB serum levels strongly predict early cardiovascular events Heart 2012 98 1242 1245 10.1136/heartjnl-2012-301852 22760866 · DOI
- [51]Walldius G. Jungner I. Holme I. Aastveit A.H. Kolar W. Steiner E. High apolipoprotein B, low apolipoprotein A-I, and improvement in the prediction of fatal myocardial infarction (AMORIS study): A prospective study Lancet 2001 358 2026 2033 10.1016/S0140-6736(01)07098-2 11755609 · DOI
- [53]Sniderman A.D. Thanassoulis G. Glavinovic T. Navar A.M. Pencina M. Catapano A. Ference B.A. Apolipoprotein B Particles and Cardiovascular Disease JAMA Cardiol. 2019 4 1287 10.1001/jamacardio.2019.3780 31642874 PMC7369156 · DOI · Paper page
- [54]Shih Y.H. Tsai K.J. Lee C.W. Shiesh S.C. Chen W.T. Pai M.C. Kuo Y.M. Apolipoprotein C-III is an amyloid-β-binding protein and an early marker for Alzheimer’s disease J. Alzheimer’s Dis. 2014 41 855 865 10.3233/JAD-140111 24685634 · DOI
- [55]Rehiman S.H. Lim S.M. Neoh C.F. Majeed A.B.A. Chin A.V. Tan M.P. Kamaruzzaman S.B. Ramasamy K. Proteomics as a reliable approach for discovery of blood-based Alzheimer’s disease biomarkers: A systematic review and meta-analysis Ageing Res. Rev. 2020 60 101066 10.1016/j.arr.2020.101066 32294542 · DOI
- [56]Bahrami A. Barreto G.E. Lombardi G. Pirro M. Sahebkar A. Emerging roles for high-density lipoproteins in neurodegenerative disorders Biofactors 2019 45 725 739 10.1002/biof.1541 31301192 · DOI
- [57]Guo T. Yin R.X. Li H. Wang Y.M. Wu J.Z. Yang D.Z. Association of the Trp316Ser variant (rs1801690) near the apolipoprotein H (β2-glycoprotein-I) gene and serum lipid levels Int. J. Clin. Exp. Pathol. 2015 8 7291 7304 26261630 PMC4525964
- [58]Mather K.A. Thalamuthu A. Oldmeadow C. Song F. Armstrong N.J. Poljak A. Holliday E.G. McEvoy M. Kwok J.B. Assareh A.A. Genome-wide significant results identified for plasma apolipoprotein H levels in middle-aged and older adults Sci. Rep. 2016 6 23675 10.1038/srep23675 27030319 PMC4814826 · DOI
- [59]Mattsson N. Insel P. Nosheny R. Trojanowski J.Q. Shaw L.M. Jack C.R. Tosun D. Weiner M. Effects of cerebrospinal fluid proteins on brain atrophy rates in cognitively healthy older adults Neurobiol. Aging 2014 35 614 622 10.1016/j.neurobiolaging.2013.08.027 24094581 PMC3864623 · DOI
- [60]Ding Q. Shults N.V. Gychka S.G. Harris B.T. Suzuki Y.J. Protein Expression of Angiotensin-Converting Enzyme 2 (ACE2) is Upregulated in Brains with Alzheimer’s Disease Int. J. Mol. Sci. 2021 22 1687 10.3390/ijms22041687 33567524 PMC7914443 · DOI
- [61]Ignjatovic V. Geyer P.E. Palaniappan K.K. Chaaban J.E. Omenn G.S. Baker M.S. Deutsch E.W. Schwenk J.M. Mass Spectrometry-Based Plasma Proteomics: Considerations from Sample Collection to Achieving Translational Data J. Proteome Res. 2019 18 4085 4097 10.1021/acs.jproteome.9b00503 31573204 PMC6898750 · DOI
- [62]Hsieh H. Boehm J. Sato C. Iwatsubo T. Tomita T. Sisodia S. Malinow R. AMPAR Removal Underlies Aβ-Induced Synaptic Depression and Dendritic Spine Loss Neuron 2006 52 831 843 10.1016/j.neuron.2006.10.035 17145504 PMC1850952 · DOI · Paper page
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Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants
He, K. Y., Khramtsova, E. A., Cabrera-Socorro, A., Zhang, Y., Li, S., Sarver, B. A. J., Smets, B., Li, Q. S., De Muynck, L., Parrado, A. R., et al. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00684-7 · Cited by 8 · see citing works
- Authors
- Xu, C., Garcia, D., Lu, Y., Ozuna, K., Adjeroh, D. A., Wang, K., & Initiative, O. B. O. T. A. D. N.
- Affiliations
- The University of Texas Rio Grande Valley (US)
- Marshall University (US)
- West Virginia University (US)
- Corresponding author
- Xu, Chun
- Wang, Kesheng
- Venue
- Cells
- Publisher
- MDPI AG
- Published
- 2021-12-23
- Volume
- 11
- Issue
- 1
- Pages
- 29
- ISSN
- 2073-4409 (ISSN-L)
- PMC
- PMC8744784
- OpenAlex
- W4200480175
- Cited by
- 19
- References
- 6
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 4 · 2023: 5 · 2022: 3 · 2021: 1
- FWCI
- 2.33
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Cells (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- ScholarWorks @ UTRGV (The University of Texas Rio Grande Valley) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- U.S. Department of Defense (U01 AG024904, W81XWH, W81XWH-12-2-, W81XWH1220012, AG024904)
- Foundation for the National Institutes of Health (W81XWH-12-2-0012, U01AG024904, Grant U01 AG024904, AG024904)
- Alzheimer's Association (U01 AG024904, W81XWH-12-2-0012)
- Bristol-Myers Squibb (U01 AG024904, AG024904, W81XWH-12-2-0012)
- Eli Lilly and Company (U01 AG024904, AG024904, W81XWH-12-2-0012)
- Pfizer (AG024904, W81XWH-12-2-0012, U01 AG024904)
- Biogen (W81XWH-12-2-0012, U01 AG024904, AG024904)
- University of Southern California (W81XWH-12-2-0012, U01 AG024904)
- F. Hoffmann-La Roche (W81XWH-12-2-0012, AG024904, U01 AG024904)
- Meso Scale Diagnostics (U01 AG024904, AG024904, W81XWH-12-2-0012)
- Alzheimer's Disease Neuroimaging Initiative (W81XWH-12-2–0012, U01AG024904, AG024904, W81XWH-12-2-, Department of Defense award number W81XWH-12-2-0012)
- BioClinica (U01 AG024904, W81XWH-12-2-0012, AG024904)
- Novartis Pharmaceuticals Corporation (W81XWH-12-2-0012, U01 AG024904, AG024904)
- Northern California Institute for Research and Education (U01 AG024904, W81XWH-12-2-0012)
- Eisai (W81XWH-12-2-0012, U01 AG024904, AG024904)
- Servier (AG024904, W81XWH-12-2-0012, U01 AG024904)
- H. Lundbeck A/S (U01 AG024904, AG024904, W81XWH-12-2-0012)
- IXICO (AG024904, W81XWH-12-2-0012, U01 AG024904)
- National Institutes of Health (3u01ag024904-10s2, W81XWH, W81XWH-12-2-0012, U01-AG024904, Grant U01 AG024904, AG024904)
- Genentech (W81XWH-12-2-0012, AG024904, U01 AG024904)
- Canadian Institutes of Health Research (U01 AG024904, W81XWH-12-2-0012)
- National Institute on Aging (U01-AG-024904, W81XWH-12-2–0012, AG 024904)
- National Institute of Biomedical Imaging and Bioengineering (W81XWH-12-2-0012, U01 AG024904, AG024904)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- angiotensin-converting enzyme, apolipoproteins, Alzheimer's disease, cardiovascular disease, endocrine and metabolic diseases, mild cognitive impairment, APOE ε4, apolipoprotein B, beta2-glycoprotein I, biomarkers, protein abundance
- MeSH terms
- Aged, Alzheimer Disease, Apolipoproteins, Cardiovascular Diseases, Female, Humans, Peptidyl-Dipeptidase A, Male, Multivariate Analysis, Cluster Analysis, Linear Models
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