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Serum cystatin C and the risk of Alzheimer disease in elderly men

Sundelöf, Johan (author)
Uppsala universitet,Geriatrik
Ärnlöv, Johan (author)
Högskolan Dalarna,Medicinsk vetenskap
Ingelsson, E. (author)
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Sundström, J. (author)
Uppsala universitet,Institutionen för medicinska vetenskaper
Basu, Samar (author)
Uppsala universitet,Klinisk nutrition och metabolism
Zethelius, Björn (author)
Uppsala universitet,Geriatrik
Larsson, Anders (author)
Uppsala universitet,Klinisk kemi
Irizarry, M. C. (author)
Giedraitis, Vilmantas (author)
Uppsala universitet,Geriatrik
Rönnemaa, Elina (author)
Uppsala universitet,Geriatrik
Degerman-Gunnarsson, Malin (author)
Uppsala universitet,Geriatrik
Hyman, B. T. (author)
Basun, Hans (author)
Uppsala universitet,Geriatrik
Kilander, Lena (author)
Uppsala universitet,Geriatrik
Lannfelt, Lars (author)
Uppsala universitet,Geriatrik
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 (creator_code:org_t)
2008-09-29
2008
English.
In: Neurology. - : Ovid Technologies (Wolters Kluwer Health). - 0028-3878 .- 1526-632X. ; 71:14, s. 1072-1079
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Multiple lines of research suggest that increased cystatin C activity in the brain protects against the development of Alzheimer disease (AD). METHODS: Serum cystatin C levels were analyzed at two examinations of the Uppsala Longitudinal Study of Adult Men, a longitudinal, community-based study of elderly men (age 70 years, n = 1,153 and age 77 years, n = 761, a subset of the age 70 examination). Cox regressions were used to examine associations between serum cystatin C and incident AD. AD cases were identified by cognitive screening and comprehensive medical chart review in all subjects. RESULTS: On follow-up (median 11.3 years), 82 subjects developed AD. At age 70 years, lower cystatin C was associated with higher risk of AD independently of age, APOE4 genotype, glomerular filtration rate, diabetes, hypertension, stroke, cholesterol, body mass index, smoking, education level, and plasma amyloid-beta protein 40 and 42 levels (hazard ratio [HR] for lowest [<1.12 micromol/L] vs highest [>1.30 micromol/L] tertile = 2.67, 95% CI 1.22-5.83, p < 0.02). The results were similar at age 77 years (43 participants developed AD during follow-up). Furthermore, a 0.1-mumol/L decrease of cystatin C between ages 70 and 77 years was associated with a 29% higher risk of incident AD (HR 1.29, 95% CI 1.03-1.63, p < 0.03). CONCLUSIONS: Low levels of serum cystatin C precede clinically manifest Alzheimer disease (AD) in elderly men free of dementia at baseline and may be a marker of future risk of AD. These findings strengthen the evidence for a role for cystatin C in the development of clinical AD.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

MEDICINE
MEDICIN
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