Moderately Elevated Plasma Homocysteine, Methylenetetrahydrofolate Reductase Genotype, and Risk for Stroke, Vascular Dementia, and Alzheimer Disease in Northern Ireland
Background and Purpose— Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this amino acid has been shown to be due to nutritional status and methylenetetrahydrofolate reductase (MTHFR) genotype. Metho...
Saved in:
Published in | Stroke (1970) Vol. 33; no. 10; pp. 2351 - 2356 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Hagerstown, MD
Lippincott Williams & Wilkins
01.10.2002
American Heart Association, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0039-2499 1524-4628 1524-4628 |
DOI | 10.1161/01.STR.0000032550.90046.38 |
Cover
Abstract | Background and Purpose—
Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this amino acid has been shown to be due to nutritional status and methylenetetrahydrofolate reductase (MTHFR) genotype.
Methods—
Under a case-control design we compared fasting levels of homocysteine and MTHFR genotypes in groups of subjects consisting of stroke, vascular dementia (VaD), and Alzheimer disease patients and normal controls from Northern Ireland.
Results—
A significant increase in plasma homocysteine was observed in all 3 disease groups compared with controls. This remained significant after allowance for confounding factors (age, sex, hypertension, cholesterol, smoking, creatinine, and nutritional measures). MTHFR genotype was not found to influence homocysteine levels, although the T allele was found to increase risk for VaD and perhaps dementia after stroke.
Conclusions—
We report that moderately high plasma levels of homocysteine are associated with stroke, VaD, and Alzheimer disease. This is not due to vascular risk factors, nutritional status, or MTHFR genotype. |
---|---|
AbstractList | Background and Purpose—
Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this amino acid has been shown to be due to nutritional status and methylenetetrahydrofolate reductase (MTHFR) genotype.
Methods—
Under a case-control design we compared fasting levels of homocysteine and MTHFR genotypes in groups of subjects consisting of stroke, vascular dementia (VaD), and Alzheimer disease patients and normal controls from Northern Ireland.
Results—
A significant increase in plasma homocysteine was observed in all 3 disease groups compared with controls. This remained significant after allowance for confounding factors (age, sex, hypertension, cholesterol, smoking, creatinine, and nutritional measures). MTHFR genotype was not found to influence homocysteine levels, although the T allele was found to increase risk for VaD and perhaps dementia after stroke.
Conclusions—
We report that moderately high plasma levels of homocysteine are associated with stroke, VaD, and Alzheimer disease. This is not due to vascular risk factors, nutritional status, or MTHFR genotype. Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this amino acid has been shown to be due to nutritional status and methylenetetrahydrofolate reductase (MTHFR) genotype.BACKGROUND AND PURPOSEElevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this amino acid has been shown to be due to nutritional status and methylenetetrahydrofolate reductase (MTHFR) genotype.Under a case-control design we compared fasting levels of homocysteine and MTHFR genotypes in groups of subjects consisting of stroke, vascular dementia (VaD), and Alzheimer disease patients and normal controls from Northern Ireland.METHODSUnder a case-control design we compared fasting levels of homocysteine and MTHFR genotypes in groups of subjects consisting of stroke, vascular dementia (VaD), and Alzheimer disease patients and normal controls from Northern Ireland.A significant increase in plasma homocysteine was observed in all 3 disease groups compared with controls. This remained significant after allowance for confounding factors (age, sex, hypertension, cholesterol, smoking, creatinine, and nutritional measures). MTHFR genotype was not found to influence homocysteine levels, although the T allele was found to increase risk for VaD and perhaps dementia after stroke.RESULTSA significant increase in plasma homocysteine was observed in all 3 disease groups compared with controls. This remained significant after allowance for confounding factors (age, sex, hypertension, cholesterol, smoking, creatinine, and nutritional measures). MTHFR genotype was not found to influence homocysteine levels, although the T allele was found to increase risk for VaD and perhaps dementia after stroke.We report that moderately high plasma levels of homocysteine are associated with stroke, VaD, and Alzheimer disease. This is not due to vascular risk factors, nutritional status, or MTHFR genotype.CONCLUSIONSWe report that moderately high plasma levels of homocysteine are associated with stroke, VaD, and Alzheimer disease. This is not due to vascular risk factors, nutritional status, or MTHFR genotype. Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this amino acid has been shown to be due to nutritional status and methylenetetrahydrofolate reductase (MTHFR) genotype. Under a case-control design we compared fasting levels of homocysteine and MTHFR genotypes in groups of subjects consisting of stroke, vascular dementia (VaD), and Alzheimer disease patients and normal controls from Northern Ireland. A significant increase in plasma homocysteine was observed in all 3 disease groups compared with controls. This remained significant after allowance for confounding factors (age, sex, hypertension, cholesterol, smoking, creatinine, and nutritional measures). MTHFR genotype was not found to influence homocysteine levels, although the T allele was found to increase risk for VaD and perhaps dementia after stroke. We report that moderately high plasma levels of homocysteine are associated with stroke, VaD, and Alzheimer disease. This is not due to vascular risk factors, nutritional status, or MTHFR genotype. BACKGROUND AND PURPOSE: Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this amino acid has been shown to be due to nutritional status and methylenetetrahydrofolate reductase (MTHFR) genotype. METHODS: Under a case-control design we compared fasting levels of homocysteine and MTHFR genotypes in groups of subjects consisting of stroke, vascular dementia (VaD), and Alzheimer disease patients and normal controls from Northern Ireland. RESULTS: A significant increase in plasma homocysteine was observed in all 3 disease groups compared with controls. This remained significant after allowance for confounding factors (age, sex, hypertension, cholesterol, smoking, creatinine, and nutritional measures). MTHFR genotype was not found to influence homocysteine levels, although the T allele was found to increase risk for VaD and perhaps dementia after stroke. CONCLUSIONS: We report that moderately high plasma levels of homocysteine are associated with stroke, VaD, and Alzheimer disease. This is not due to vascular risk factors, nutritional status, or MTHFR genotype. |
Author | Passmore, A. Peter Dynan, Kevin B. McIlroy, Stephen P. Lawson, John T. Patterson, Christopher C. |
Author_xml | – sequence: 1 givenname: Stephen P. surname: McIlroy fullname: McIlroy, Stephen P. organization: From the Departments of Geriatric Medicine (S.P.M., K.B.D., A.P.P.) and Epidemiology and Public Health (C.C.P), Queen’s University Belfast, and Department of Radiology, Belfast City Hospital Trust Group (J.T.L.), Belfast, Northern Ireland – sequence: 2 givenname: Kevin B. surname: Dynan fullname: Dynan, Kevin B. organization: From the Departments of Geriatric Medicine (S.P.M., K.B.D., A.P.P.) and Epidemiology and Public Health (C.C.P), Queen’s University Belfast, and Department of Radiology, Belfast City Hospital Trust Group (J.T.L.), Belfast, Northern Ireland – sequence: 3 givenname: John T. surname: Lawson fullname: Lawson, John T. organization: From the Departments of Geriatric Medicine (S.P.M., K.B.D., A.P.P.) and Epidemiology and Public Health (C.C.P), Queen’s University Belfast, and Department of Radiology, Belfast City Hospital Trust Group (J.T.L.), Belfast, Northern Ireland – sequence: 4 givenname: Christopher C. surname: Patterson fullname: Patterson, Christopher C. organization: From the Departments of Geriatric Medicine (S.P.M., K.B.D., A.P.P.) and Epidemiology and Public Health (C.C.P), Queen’s University Belfast, and Department of Radiology, Belfast City Hospital Trust Group (J.T.L.), Belfast, Northern Ireland – sequence: 5 givenname: A. Peter surname: Passmore fullname: Passmore, A. Peter organization: From the Departments of Geriatric Medicine (S.P.M., K.B.D., A.P.P.) and Epidemiology and Public Health (C.C.P), Queen’s University Belfast, and Department of Radiology, Belfast City Hospital Trust Group (J.T.L.), Belfast, Northern Ireland |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13974369$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/12364720$$D View this record in MEDLINE/PubMed |
BookMark | eNqF0t1uFCEUAGBiaux29RUMaaJXzgoD8-eVTa1tk1bNtnpLWDiTpWVgBcZkfCIfU9ZdbdIbuYEcPg4ncI7QgfMOEDqmZEFpTd8Suri5XS7IdrCyqsiiI4TXC9Y-QTNalbzgddkeoFne7oqSd90hOorxLvOStdUzdEhLVvOmJDP069prCDKBnfCZhR95pfEXK-Mg8YUfvJpiAuPgDb6GtJ4sOEiQglxPOvje2-zxEvSokoyAz8H5NG2ylk7jpYn3uPcB36Tg73Pwm4xqtDLgDzCAS0bu3In9uQYzQI6bCNs8xuFPPqQ1BIcvA9isnqOnvbQRXuznOfr68ez29KK4-nx-eXpyVSjekVSsWsJ6KSuyqjVtoFas7zgtS85Vr0lVar6CpuetrllTU5XxiitZdaqRREkt2Ry93uXdBP99hJjEYKICm2sAP0bRlLRirKMZHj-Cd34MLtcmaNc0TVVnOEcv92hcDaDFJphBhkn8_YAMXu1Bfhtp-yCdMvHBsa7hrO6ye79zKvgYA_RCmSST8S5_hrGCErHtDUGoyL0hHnpD_OkNwdqc4t2jFP9u-f_h34KFwMo |
CODEN | SJCCA7 |
CitedBy_id | crossref_primary_10_1093_ajcn_86_6_1581 crossref_primary_10_1016_j_bpsc_2016_09_005 crossref_primary_10_1007_s00702_010_0383_x crossref_primary_10_1212_WNL_0000000000000185 crossref_primary_10_1002_gps_2197 crossref_primary_10_1111_j_1468_1331_2011_03534_x crossref_primary_10_3233_JAD_220760 crossref_primary_10_1038_s41598_019_57199_9 crossref_primary_10_1159_000076348 crossref_primary_10_1093_ageing_afm006 crossref_primary_10_1016_j_jns_2004_05_012 crossref_primary_10_3109_00207454_2011_578778 crossref_primary_10_1016_j_pnpbp_2005_06_026 crossref_primary_10_1192_apt_11_3_176 crossref_primary_10_1016_j_pbb_2010_05_003 crossref_primary_10_1177_15648265080292S119 crossref_primary_10_1016_j_jalz_2008_12_003 crossref_primary_10_1016_j_nut_2014_06_016 crossref_primary_10_1016_j_clinbiochem_2007_04_007 crossref_primary_10_1002_ddr_10360 crossref_primary_10_1016_j_jns_2010_04_001 crossref_primary_10_2165_00002512_200522060_00003 crossref_primary_10_1016_j_expneurol_2005_07_003 crossref_primary_10_1159_000072812 crossref_primary_10_1212_01_wnl_0000295996_54210_69 crossref_primary_10_1016_S1474_4422_06_70598_1 crossref_primary_10_1016_j_seizure_2016_11_016 crossref_primary_10_1179_016164106X130470 crossref_primary_10_3390_biom11121865 crossref_primary_10_1074_jbc_M413895200 crossref_primary_10_3390_ijms20112757 crossref_primary_10_1002_ana_20869 crossref_primary_10_3923_crn_2016_1_15 crossref_primary_10_1007_s12264_013_1381_4 crossref_primary_10_3109_10408361003791520 crossref_primary_10_1177_1533317513505131 crossref_primary_10_3389_fnins_2021_661198 crossref_primary_10_1515_CCLM_2003_221 crossref_primary_10_1007_s11940_015_0367_0 crossref_primary_10_1002_mnfr_200700353 crossref_primary_10_1016_j_brainresbull_2005_09_020 crossref_primary_10_3945_an_112_002535 crossref_primary_10_1093_ajcn_80_1_114 crossref_primary_10_1016_j_mrgentox_2018_03_001 crossref_primary_10_1016_j_arr_2024_102278 crossref_primary_10_1515_CCLM_2005_191 crossref_primary_10_1093_bmb_ldp020 crossref_primary_10_1515_CCLM_2005_193 crossref_primary_10_1016_j_jalz_2005_06_001 crossref_primary_10_1017_S1092852900002819 crossref_primary_10_3233_JAD_170687 crossref_primary_10_1016_S0246_0378_06_28794_3 crossref_primary_10_1007_s12035_016_9722_8 crossref_primary_10_1007_s13410_013_0154_y crossref_primary_10_1146_annurev_genom_5_061903_175935 crossref_primary_10_1152_ajpheart_00598_2010 crossref_primary_10_1146_annurev_nutr_071715_050947 crossref_primary_10_1159_000076359 crossref_primary_10_3233_JAD_150977 crossref_primary_10_2217_fnl_2016_0002 crossref_primary_10_1210_jc_2013_3262 crossref_primary_10_1007_s00401_006_0136_y crossref_primary_10_1007_s10522_005_2622_3 crossref_primary_10_1016_S0749_0690_03_00073_9 crossref_primary_10_1097_01_WNF_0000236763_16032_60 crossref_primary_10_35440_hutfd_1063465 crossref_primary_10_1016_j_gene_2013_09_066 crossref_primary_10_3390_nu16081155 crossref_primary_10_1002_ana_20645 crossref_primary_10_1093_ajcn_86_5_1581 crossref_primary_10_1093_jn_137_2_407 crossref_primary_10_1177_102490791001700103 crossref_primary_10_2217_14622416_8_1_41 crossref_primary_10_1111_j_1528_1167_2012_03671_x crossref_primary_10_1016_S1474_4422_03_00438_1 crossref_primary_10_1016_j_neulet_2014_11_049 crossref_primary_10_1515_CCLM_2008_301 crossref_primary_10_4061_2009_632489 crossref_primary_10_1155_2017_6216205 crossref_primary_10_1016_j_arr_2020_101126 crossref_primary_10_1016_j_exger_2010_11_032 crossref_primary_10_1016_S1474_4422_03_00258_8 crossref_primary_10_1016_j_neuint_2006_07_007 crossref_primary_10_1111_j_1468_1331_2009_02590_x crossref_primary_10_1186_1756_0500_7_194 crossref_primary_10_1007_s12291_017_0646_5 crossref_primary_10_1038_nrneurol_2012_27 crossref_primary_10_1111_j_1460_9568_2010_07434_x crossref_primary_10_1097_00001504_200311000_00008 crossref_primary_10_1093_ajcn_83_4_905 crossref_primary_10_18705_1607_419X_2013_19_4_326_333 crossref_primary_10_1111_j_1399_0004_2011_01673_x crossref_primary_10_1038_mp_2011_18 crossref_primary_10_1111_j_1468_1331_2004_00915_x crossref_primary_10_1007_s11064_006_9207_7 crossref_primary_10_1111_j_1600_0404_2005_00556_x crossref_primary_10_1016_S1634_7072_07_70557_3 crossref_primary_10_1002_mds_22522 crossref_primary_10_1016_j_dadm_2017_01_005 crossref_primary_10_1002_glia_20185 crossref_primary_10_1086_430409 crossref_primary_10_1016_j_jstrokecerebrovasdis_2015_11_041 crossref_primary_10_1016_j_bbadis_2015_12_016 crossref_primary_10_3390_biomedicines10112741 crossref_primary_10_1080_00207454_2020_1733554 crossref_primary_10_1177_026988110401800415 crossref_primary_10_1159_000077812 crossref_primary_10_1111_cns_14502 crossref_primary_10_1017_S1092852900027589 crossref_primary_10_1038_s12276_019_0216_4 crossref_primary_10_3389_fpsyt_2022_754165 crossref_primary_10_2174_1871527319666200303121016 crossref_primary_10_1016_j_mehy_2009_01_050 crossref_primary_10_1016_j_nutres_2018_07_012 crossref_primary_10_3923_jms_2017_89_94 crossref_primary_10_1093_gerona_60_9_1190 crossref_primary_10_3233_JAD_143102 crossref_primary_10_3390_genes15121509 crossref_primary_10_1016_j_neurobiolaging_2007_12_010 crossref_primary_10_1155_2013_524106 crossref_primary_10_1016_j_neures_2010_06_011 crossref_primary_10_2298_JMB0504225S crossref_primary_10_1016_j_ntt_2013_05_002 crossref_primary_10_1177_0269881104047285 crossref_primary_10_1016_j_bandc_2009_07_007 crossref_primary_10_1186_s12986_017_0233_z crossref_primary_10_1002_gps_5458 crossref_primary_10_1016_j_clnu_2008_08_006 crossref_primary_10_1016_j_archger_2008_03_009 crossref_primary_10_1007_s12013_014_0166_3 crossref_primary_10_1111_j_1365_2990_2005_00678_x crossref_primary_10_1002_gps_784 crossref_primary_10_1016_j_mad_2016_04_005 crossref_primary_10_3233_JAD_150140 crossref_primary_10_1007_s12291_015_0512_2 crossref_primary_10_1007_s11940_010_0080_y crossref_primary_10_1111_j_1749_6632_2005_tb06138_x |
Cites_doi | 10.1016/0165-0270(94)90168-6 10.1097/00002093-199601040-00003 10.1001/jama.1993.03510220049033 10.1016/0022-3956(75)90026-6 10.1016/0304-3940(93)90175-K 10.1111/j.1749-6632.1997.tb48471.x 10.1161/str.29.7.1401 10.1161/str.31.7.1494 10.1016/S0140-6736(95)92407-8 10.1136/jnnp.53.12.1080 10.1001/archneur.1996.00550080033010 10.1038/ng0595-111 10.1146/annurev.med.49.1.31 10.1161/circ.94.10.2410 10.1161/01.CIR.93.1.7 10.1212/WNL.54.2.397 10.1172/JCI113343 10.1001/jama.1997.03540460039030 10.1111/j.1471-4159.1981.tb00426.x 10.1016/S0140-6736(00)04008-3 10.1111/j.1399-0004.1997.tb04362.x 10.1046/j.1440-1819.1999.00619.x 10.1001/archneur.55.11.1449 10.1161/str.28.4.785 10.1001/jama.1995.03530190040032 10.1007/s004390050488 10.1016/0378-4347(91)80407-4 10.1001/jama.1995.03530130055028 10.1016/0006-291X(81)91224-9 |
ContentType | Journal Article |
Copyright | 2002 INIST-CNRS Copyright American Heart Association, Inc. Oct 2002 |
Copyright_xml | – notice: 2002 INIST-CNRS – notice: Copyright American Heart Association, Inc. Oct 2002 |
DBID | AAYXX CITATION IQODW CGR CUY CVF ECM EIF NPM K9. NAPCQ 7X8 |
DOI | 10.1161/01.STR.0000032550.90046.38 |
DatabaseName | CrossRef Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Premium MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Premium MEDLINE - Academic |
DatabaseTitleList | CrossRef MEDLINE - Academic MEDLINE ProQuest Health & Medical Complete (Alumni) |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1524-4628 |
EndPage | 2356 |
ExternalDocumentID | 212599801 12364720 13974369 10_1161_01_STR_0000032550_90046_38 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GeographicLocations | Northern Ireland |
GeographicLocations_xml | – name: Northern Ireland |
GroupedDBID | --- .3C .55 .GJ .XZ .Z2 01R 0R~ 123 1J1 2WC 3O- 40H 4Q1 4Q2 4Q3 53G 5RE 5VS 6PF 71W 77Y 7O~ A9M AAAAV AAAXR AAGIX AAHPQ AAIQE AAJCS AAMOA AAMTA AAQKA AAQQT AARTV AASCR AASOK AAUEB AAXQO AAYEP AAYJJ AAYXX ABASU ABBUW ABDIG ABJNI ABPXF ABQRW ABVCZ ABXVJ ABXYN ABZAD ABZZY ACCJW ACDDN ACDOF ACEWG ACGFS ACGOD ACILI ACLDA ACWDW ACWRI ACXJB ACXNZ ACZKN ADBBV ADFPA ADGGA ADGHP ADHPY ADNKB AE3 AE6 AEBDS AEETU AENEX AFBFQ AFDTB AFEXH AFFNX AFMBP AFNMH AFSOK AFUWQ AGINI AHMBA AHOMT AHQNM AHQVU AHRYX AHVBC AIJEX AINUH AJCLO AJIOK AJNWD AJNYG AJZMW AKCTQ AKULP ALKUP ALMA_UNASSIGNED_HOLDINGS ALMTX AMJPA AMKUR AMNEI AOHHW AOQMC AYCSE BAWUL BCGUY BOYCO BQLVK BS7 C45 CITATION CS3 DIK DIWNM DU5 DUNZO E.X E3Z EBS EEVPB EJD ERAAH EX3 F2K F2L F2M F2N F5P FCALG FL- FW0 GNXGY GQDEL GX1 H0~ H13 HLJTE HZ~ IKREB IKYAY IN~ IPNFZ J5H JF9 JG8 JK3 JK8 K8S KD2 KMI KQ8 L-C L7B M18 N4W N9A N~7 N~B N~M O9- OAG OAH OB3 OCUKA ODA ODMTH OGROG OHYEH OK1 OL1 OLG OLH OLU OLV OLY OLZ OPUJH ORVUJ OUVQU OVD OVDNE OVIDH OVLEI OVOZU OWBYB OWU OWV OWW OWX OWY OWZ OXXIT P-K P2P PQQKQ R58 RAH RIG RLZ S4R S4S T8P TEORI TSPGW V2I VVN W3M W8F WH7 WOQ WOW X3V X3W X7M XXN XYM YFH YHZ YQJ YYP ZB8 ZGI ZZMQN IQODW ACIJW AWKKM CGR CUY CVF ECM EIF NPM OJAPA OLW RHF YCJ K9. NAPCQ 7X8 ADKSD |
ID | FETCH-LOGICAL-c490t-b803faa50b6d17e6c3f9412244cfd052d4be7f48d63761c03fb4ca59c7a0cada3 |
ISSN | 0039-2499 1524-4628 |
IngestDate | Mon Sep 08 17:27:47 EDT 2025 Thu Aug 21 12:41:37 EDT 2025 Wed Feb 19 02:33:01 EST 2025 Mon Jul 21 09:15:58 EDT 2025 Thu Apr 24 23:12:01 EDT 2025 Tue Jul 01 01:13:41 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Keywords | Methylenetetrahydrofolate reductase (NADPH) homocyst(e)ine Alzheimer disease Cardiovascular disease Blood plasma Vascular disease genetics Homocystein Apolipoprotein E Degenerative disease Fast Cerebrovascular disease Human Nervous system diseases Stroke Thiol Vascular dementia Enzyme Genotype Cerebral disorder Sulfur containing aminoacid Allele Central nervous system disease Risk factor dementia Oxidoreductases cerebrovascular disorders Elderly Comparative study |
Language | English |
License | CC BY 4.0 |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c490t-b803faa50b6d17e6c3f9412244cfd052d4be7f48d63761c03fb4ca59c7a0cada3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
OpenAccessLink | https://www.ahajournals.org/doi/pdf/10.1161/01.STR.0000032550.90046.38 |
PMID | 12364720 |
PQID | 197775615 |
PQPubID | 35232 |
PageCount | 6 |
ParticipantIDs | proquest_miscellaneous_72153391 proquest_journals_197775615 pubmed_primary_12364720 pascalfrancis_primary_13974369 crossref_citationtrail_10_1161_01_STR_0000032550_90046_38 crossref_primary_10_1161_01_STR_0000032550_90046_38 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2002-10-01 |
PublicationDateYYYYMMDD | 2002-10-01 |
PublicationDate_xml | – month: 10 year: 2002 text: 2002-10-01 day: 01 |
PublicationDecade | 2000 |
PublicationPlace | Hagerstown, MD |
PublicationPlace_xml | – name: Hagerstown, MD – name: United States – name: Hagerstown |
PublicationTitle | Stroke (1970) |
PublicationTitleAlternate | Stroke |
PublicationYear | 2002 |
Publisher | Lippincott Williams & Wilkins American Heart Association, Inc |
Publisher_xml | – name: Lippincott Williams & Wilkins – name: American Heart Association, Inc |
References | e_1_3_2_26_2 (e_1_3_2_13_2) 1993 e_1_3_2_27_2 e_1_3_2_28_2 (e_1_3_2_17_2) 1984; 24 e_1_3_2_20_2 e_1_3_2_21_2 e_1_3_2_22_2 e_1_3_2_24_2 e_1_3_2_25_2 (e_1_3_2_7_2) 1988; 43 e_1_3_2_9_2 e_1_3_2_15_2 e_1_3_2_8_2 e_1_3_2_16_2 e_1_3_2_6_2 e_1_3_2_18_2 e_1_3_2_19_2 (e_1_3_2_29_2) 1997; 52 e_1_3_2_1_2 e_1_3_2_30_2 e_1_3_2_32_2 e_1_3_2_10_2 e_1_3_2_31_2 e_1_3_2_5_2 e_1_3_2_11_2 e_1_3_2_4_2 e_1_3_2_12_2 e_1_3_2_33_2 e_1_3_2_3_2 e_1_3_2_2_2 e_1_3_2_14_2 (e_1_3_2_23_2) 1996; 54 12364715 - Stroke. 2002 Oct;33(10):2343-4 12663871 - Stroke. 2003 Apr;34(4):833-44; author reply 833-44 |
References_xml | – volume: 43 start-page: 414 year: 1988 ident: e_1_3_2_7_2 publication-title: Am J Hum Genet – ident: e_1_3_2_25_2 doi: 10.1016/0165-0270(94)90168-6 – ident: e_1_3_2_28_2 doi: 10.1097/00002093-199601040-00003 – ident: e_1_3_2_10_2 doi: 10.1001/jama.1993.03510220049033 – ident: e_1_3_2_18_2 doi: 10.1016/0022-3956(75)90026-6 – ident: e_1_3_2_12_2 doi: 10.1016/0304-3940(93)90175-K – ident: e_1_3_2_32_2 doi: 10.1111/j.1749-6632.1997.tb48471.x – ident: e_1_3_2_30_2 doi: 10.1161/str.29.7.1401 – ident: e_1_3_2_20_2 doi: 10.1161/str.31.7.1494 – ident: e_1_3_2_1_2 doi: 10.1016/S0140-6736(95)92407-8 – ident: e_1_3_2_21_2 doi: 10.1136/jnnp.53.12.1080 – ident: e_1_3_2_22_2 doi: 10.1001/archneur.1996.00550080033010 – ident: e_1_3_2_6_2 doi: 10.1038/ng0595-111 – ident: e_1_3_2_3_2 doi: 10.1146/annurev.med.49.1.31 – volume: 24 start-page: 939 year: 1984 ident: e_1_3_2_17_2 publication-title: Neurology – ident: e_1_3_2_5_2 doi: 10.1161/circ.94.10.2410 – ident: e_1_3_2_8_2 doi: 10.1161/01.CIR.93.1.7 – ident: e_1_3_2_33_2 doi: 10.1212/WNL.54.2.397 – ident: e_1_3_2_4_2 doi: 10.1172/JCI113343 – ident: e_1_3_2_2_2 doi: 10.1001/jama.1997.03540460039030 – ident: e_1_3_2_14_2 doi: 10.1111/j.1471-4159.1981.tb00426.x – ident: e_1_3_2_27_2 doi: 10.1016/S0140-6736(00)04008-3 – volume: 52 start-page: 408 year: 1997 ident: e_1_3_2_29_2 publication-title: Clin Genet doi: 10.1111/j.1399-0004.1997.tb04362.x – ident: e_1_3_2_31_2 doi: 10.1046/j.1440-1819.1999.00619.x – ident: e_1_3_2_26_2 doi: 10.1001/archneur.55.11.1449 – start-page: 430 year: 1993 ident: e_1_3_2_13_2 publication-title: Science – ident: e_1_3_2_19_2 doi: 10.1161/str.28.4.785 – ident: e_1_3_2_9_2 doi: 10.1001/jama.1995.03530190040032 – ident: e_1_3_2_16_2 doi: 10.1007/s004390050488 – ident: e_1_3_2_24_2 doi: 10.1016/0378-4347(91)80407-4 – ident: e_1_3_2_11_2 doi: 10.1001/jama.1995.03530130055028 – volume: 54 start-page: S59 year: 1996 ident: e_1_3_2_23_2 publication-title: Nutr Rev – ident: e_1_3_2_15_2 doi: 10.1016/0006-291X(81)91224-9 – reference: 12663871 - Stroke. 2003 Apr;34(4):833-44; author reply 833-44 – reference: 12364715 - Stroke. 2002 Oct;33(10):2343-4 |
SSID | ssj0002385 |
Score | 2.1853037 |
Snippet | Background and Purpose—
Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in... Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in the levels of this... BACKGROUND AND PURPOSE: Elevated plasma homocysteine level has been associated with increased risk for cardiovascular and cerebrovascular disease. Variation in... |
SourceID | proquest pubmed pascalfrancis crossref |
SourceType | Aggregation Database Index Database Enrichment Source |
StartPage | 2351 |
SubjectTerms | Aged Alleles Alzheimer Disease - blood Alzheimer Disease - epidemiology Apolipoproteins E - genetics Biological and medical sciences Case-Control Studies Comorbidity Dementia, Vascular - blood Dementia, Vascular - epidemiology Female Gene Frequency Genotype Homocysteine - blood Humans Hyperhomocysteinemia - blood Hyperhomocysteinemia - epidemiology Hyperhomocysteinemia - genetics Male Medical sciences Methylenetetrahydrofolate Reductase (NADPH2) Neurology Northern Ireland - epidemiology Nutritional Status Odds Ratio Oxidoreductases Acting on CH-NH Group Donors - genetics Reference Values Risk Assessment Risk Factors Statistical Distributions Stroke - blood Stroke - epidemiology Vascular diseases and vascular malformations of the nervous system |
Title | Moderately Elevated Plasma Homocysteine, Methylenetetrahydrofolate Reductase Genotype, and Risk for Stroke, Vascular Dementia, and Alzheimer Disease in Northern Ireland |
URI | https://www.ncbi.nlm.nih.gov/pubmed/12364720 https://www.proquest.com/docview/197775615 https://www.proquest.com/docview/72153391 |
Volume | 33 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3ZbtNAFB2FIiEkhFhLKJR54K1x8DIex48VixqqIERTqW_WeMZWIyVO1DgP6RfxLXwV985iO4JIhZck8jKWco_nLnPmXELeh2FQsnKUwoskc48VQeylpYw8xREjUZQXmvI_-cbPLtnXq_iq1_vVYS1t6nwob_-6r-R_rArHwK64S_YfLNsMCgfgN9gXPsHC8HknG-tGZhAszrcnuE1cYPS4gnB4IU6ul4ulRJXmmSlZYqfoLXgYiJFrmF-2CuZfyGpr7JqCkq_gzLCb8hJLso7RqWnnSENc1zdWmLMhripdVjRMW7z2dH57XcwW2G_cLPlgIUUvCmGrtTFumal2eoJe6DG1TlSa-J2CxESOXYXQUtDaPWiftrad8jn486rTMVqv_TpqcUv8_m7UQx2zoNFRsLVhV-0IG94cOCs7Q4fMww213SncaGk4qPrdCTkyerZ_egoe6N0PQ_gLrYglZFf-MMWKwdAoznQgtFpoDAVGb99vvWfDaXSn7pH7YZIYysD4vIkKIDSKregtPPrD_gejjK0daidWerQCC4t5afqt7E-IdGA0fUIe24yGnhp4PiW9onpGHkwsZ-M5-dmilDqUUoNS2kXpgO7FKG0wSh1GBxTwRBGhFBBKDUIH1OGTOnya6xp0UotOOquoQye16HxBLr98nn4882x_EE-y1K-9fORHpRCxn3MVJAWXUZkyXClmslR-HCoGM03JRoqDFw0kXJwzKeJUJsKXQonoJTmollXxilCp4rxgnIsQvkZhDuPkgDGl0DwF532SOktk0ornYw-XeaaTaB5kfpBdTH9krUEzbdAsGvVJ1Ny7MhIyd7rreMfg7a2QQbCIp31y5BCQ2TlpncEbmySQEsV98q45Cw4DVwFFVSw36ywJMcVLgz45NLBpR7awe733zBF52L6Ub8hBfbMp3kJQXufHGu2_Ae3M4jY |
linkProvider | Flying Publisher |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Moderately+elevated+plasma+homocysteine%2C+methylenetetrahydrofolate+reductase+genotype%2C+and+risk+for+stroke%2C+vascular+dementia%2C+and+Alzheimer+disease+in+Northern+Ireland&rft.jtitle=Stroke+%281970%29&rft.au=McIlroy%2C+Stephen+P&rft.au=Dynan%2C+Kevin+B&rft.au=Lawson%2C+John+T&rft.au=Patterson%2C+Christopher+C&rft.date=2002-10-01&rft.eissn=1524-4628&rft.volume=33&rft.issue=10&rft.spage=2351&rft_id=info:doi/10.1161%2F01.str.0000032550.90046.38&rft_id=info%3Apmid%2F12364720&rft.externalDocID=12364720 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0039-2499&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0039-2499&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0039-2499&client=summon |