Serum homocysteine and risk of dementia in Japan

被引:31
作者
Chen, Sanmei [1 ]
Honda, Takanori [1 ]
Ohara, Tomoyuki [1 ,2 ]
Hata, Jun [1 ,3 ,4 ]
Hirakawa, Yoichiro [1 ,4 ]
Yoshida, Daigo [1 ]
Shibata, Mao [1 ,3 ]
Sakata, Satoko [1 ,3 ,4 ]
Oishi, Emi [1 ,4 ]
Furuta, Yoshihiko [1 ,4 ]
Kitazono, Takanari [3 ,4 ]
Ninomiya, Toshiharu [1 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Epidemiol & Publ Hlth, Fukuoka, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Neuropsychiat, Fukuoka, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Ctr Cohort Studies, Fukuoka, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Med & Clin Sci, Fukuoka, Japan
关键词
PLASMA HOMOCYSTEINE; ALZHEIMER-DISEASE; METAANALYSIS; PATHOLOGY; CRITERIA; MODELS; TRENDS; FOLATE;
D O I
10.1136/jnnp-2019-322366
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To examine the association between serum total homocysteine levels (tHcy) and dementia risk. Methods A total of 1588 Japanese adults aged >= 60 years without dementia were prospectively followed from 2002 to 2012. Cox proportional hazards models and restricted cubic splines were used to estimate the HRs of tHcy levels on the risk of dementia. Results During the follow-up, 372 subjects developed all-cause dementia; 247 had Alzheimer's disease (AD) and 98 had vascular dementia (VaD). Compared with the lowest tHcy quintile (<= 6.4 mu mol/L), the multivariable-adjusted HRs (95% CI) of the highest quintile (>= 11.5 mu mol/L) were 2.28 (1.51-3.43) for all-cause dementia, 1.96 (1.19-3.24) for AD and 2.51 (1.14-5.51) for VaD. In restricted cubic splines, the risk of all-cause dementia steadily increased between approximately 8-15 mu mol/L and plateaued thereafter, with a similar non-linear shape observed for AD and VaD (all p for non-linearity <= 0.02). In stratified analyses by the most recognised genetic polymorphism affecting tHcy concentrations (methylenetetrahydrofolate reductase C677T), the positive association of tHcy with all-cause dementia persisted in both non-carriers and carriers of the risk allele, and even tended to be stronger in the former (p for heterogeneity=0.07). Conclusion High serum tHcy levels are associated with an elevated risk of dementia, AD and VaD in a non-linear manner, such that an exposure-response association is present only within a relatively high range of tHcy levels. Non-genetic factors affecting serum tHcy concentrations may play important roles in tHcy-dementia associations irrespective of the genetic susceptibility for raised tHcy.
引用
收藏
页码:540 / 546
页数:7
相关论文
共 41 条
[1]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[2]   Genetic and environmental influences on plasma homocysteine: Results from a Danish twin study [J].
Bathum, Lise ;
Petersen, Inge ;
Christiansen, Lene ;
Konieczna, Agnieszka ;
Sorensen, Thorkild I. A. ;
Kyvik, Kirsten O. .
CLINICAL CHEMISTRY, 2007, 53 (05) :971-979
[3]   Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database [J].
Bertram, Lars ;
McQueen, Matthew B. ;
Mullin, Kristina ;
Blacker, Deborah ;
Tanzi, Rudolph E. .
NATURE GENETICS, 2007, 39 (01) :17-23
[4]  
Brattström L, 1998, BMJ-BRIT MED J, V316, P894, DOI 10.1136/bmj.316.7135.894
[5]   Folate, vitamin B12, and serum total homocysteine levels in confirmed Alzheimer disease [J].
Clarke, R ;
Smith, AD ;
Jobst, KA ;
Refsum, H ;
Sutton, L ;
Ueland, PM .
ARCHIVES OF NEUROLOGY, 1998, 55 (11) :1449-1455
[6]   Homocysteine and risk of ischemic heart disease and stroke -: A meta-analysis [J].
Clarke, R ;
Collins, R ;
Lewington, S ;
Donald, A ;
Alfthan, G ;
Tuomilehto, J ;
Arnesen, E ;
Bonaa, K ;
Blacher, J ;
Boers, GHJ ;
Bostom, A ;
Bots, ML ;
Grobee, DE ;
Brattström, L ;
Breteler, MMB ;
Hofman, A ;
Chambers, JC ;
Kooner, JS ;
Coull, BM ;
Evans, RW ;
Kuller, LH ;
Evers, S ;
Folsom, AR ;
Freyburger, G ;
Parrot, F ;
Genst, J ;
Dalery, K ;
Graham, IM ;
Daly, L ;
Hoogeveen, EK ;
Kostense, PJ ;
Stehouwer, CDA ;
Hopknis, PN ;
Jacques, P ;
Selhub, J ;
Luft, FC ;
Jungers, P ;
Lindgren, A ;
Lolin, YI ;
Loehrer, F ;
Fowler, B ;
Mansoor, MA ;
Malinow, MR ;
Ducimetiere, P ;
Nygard, O ;
Refsum, H ;
Vollset, SE ;
Ueland, PM ;
Omenn, GS ;
Beresford, SAA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (16) :2015-2022
[7]   FLEXIBLE REGRESSION-MODELS WITH CUBIC-SPLINES [J].
DURRLEMAN, S ;
SIMON, R .
STATISTICS IN MEDICINE, 1989, 8 (05) :551-561
[8]   Plasma homocysteine and MTHFRC677T polymorphism as risk factors for incident dementia [J].
Ford, Andrew H. ;
Flicker, Leon ;
Alfonso, Helman ;
Hankey, Graeme J. ;
Norman, Paul E. ;
van Bockxmeer, Frank M. ;
Almeida, Osvaldo P. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2012, 83 (01) :70-75
[9]   A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[10]   Clinicopathological outline of dementia with Lewy bodies applying the revised criteria: The hisayama study [J].
Fujimi, Kouhei ;
Sasaki, Kensuke ;
Noda, Kazuhito ;
Wakisaka, Yoshinobu ;
Tanizaki, Yumihiro ;
Matsui, Yukiko ;
Sekita, Atsuko ;
Iida, Mitsuo ;
Kiyohara, Yutaka ;
Kanba, Shigenobu ;
Iwaki, Toru .
BRAIN PATHOLOGY, 2008, 18 (03) :317-325