TY - JOUR
T1 - Serum homocysteine and risk of dementia in Japan
AU - Chen, Sanmei
AU - Honda, Takanori
AU - Ohara, Tomoyuki
AU - Hata, Jun
AU - Hirakawa, Yoichiro
AU - Yoshida, Daigo
AU - Shibata, Mao
AU - Sakata, Satoko
AU - Oishi, Emi
AU - Furuta, Yoshihiko
AU - Kitazono, Takanari
AU - Ninomiya, Toshiharu
N1 - Funding Information:
Funding This study was supported in part by grants-in-aid for scientific research (a) (JP16h02692) and (B) (JP16h05850, JP17h04126 and JP18h02737) and (c) (JP17K09114, JP17K09113, JP17K01853, JP18K07565, JP18K09412 and JP19K07890) and grants-in-aid for early career scientists (JP18K17925, JP18K17382 and JP19K19474) from the Ministry of education, culture, sports, science and Technology of Japan; by health and labour sciences research grants of the Ministry of health, labour and Welfare of Japan (h29-Junkankitou-ippan-003 and h30-shokuhin-[sitei]-005) and by the Japan agency for Medical research and Development (JP19dk0207025, JP19ek0210082, JP19ek0210083, JP19km0405202, JP19ek0210080 and JP19fk0108075).
Publisher Copyright:
© Author(s) (or their employer(s)) 2020.
PY - 2020/5/1
Y1 - 2020/5/1
N2 - 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 μmol/L), the multivariable-adjusted HRs (95% CI) of the highest quintile (≥11.5 μmol/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 μmol/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.
AB - 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 μmol/L), the multivariable-adjusted HRs (95% CI) of the highest quintile (≥11.5 μmol/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 μmol/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.
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U2 - 10.1136/jnnp-2019-322366
DO - 10.1136/jnnp-2019-322366
M3 - Article
C2 - 32234968
AN - SCOPUS:85082619440
SN - 0022-3050
VL - 91
SP - 540
EP - 546
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
IS - 5
ER -