Review
Copyright ©The Author(s) 2021.
World J Psychiatr. Aug 19, 2021; 11(8): 412-428
Published online Aug 19, 2021. doi: 10.5498/wjp.v11.i8.412
Table 1 Observational studies on hormone therapy and cognition in women
Ref.
Study
Country
Design
n (%)
Age (yr)
Hormone therapy
Main findings
Carlson et al[77], 2001Cache County StudyUnited StatesLongitudinal2073≥ 65ET or EPTHT reduced cognitive decline
Seshadri et al[72], 2001United KingdomCase-controlAD: 59. Controls: 221Mean: 66.7ET or EPTHT was not associated with AD
Kang et al[76], 2004Nurses’ Health StudyUnited StatesLongitudinal13807≥ 70ET or EPTHT was not associated with relevant cognitive benefits
Henderson et al[82], 2005Mirage StudyUnited States, Canada, GermanyCase-controlAD: 426. Controls: 545Mean: 71.1ET or EPTHT reduced the AD risk by 30%
Ryan et al[69], 2009Three City StudyFranceLongitudinal3130≥ 65ET or EPTHT was not associated with dementia or AD, but current users had better cognitive performance in specific domains
Shao et al[79], 2012Cache County Study extendedUnited StatesLongitudinal1768≥ 65ET or EPTHT initiated within five years of menopause decreased the AD risk by 30%
Whitmer et al[80], 2011Kaiser Permanente Medical Care Program of Northern CaliforniaUnited StatesLongitudinal5504Mean in midlife: 48.7ET or EPTThe use of HT only in midlife reduced the dementia risk. On the other hand, the use of HT in late-life increased this risk
Imtiaz et al[70], 2017Kuopio Osteoporosis Risk Factor and Prevention studyFinlandLongitudinal819546 a 56ET or EPTLong-term HT users (> 10 yr) exhibited a 47% reduction in the AD risk
Savolainen-Peltonen et al[83], 2019 FinlandCase-controlAD: 84739. Controls: 84739Mean age at onset of systemic HT: 52ET or EPTHT increased the AD risk by 9%-17%, regardless of the age of onset of use and the type of HT