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DOI 10.1159/000147479

Медицинская библиотека · Dementia and geriatric cognitive disorders · 2008

Sugar chains of cerebrospinal fluid transferrin as a new biological marker of Alzheimer's disease.

Taniguchi Miyako, Okayama Yuka, Hashimoto Yuki, Kitaura Miki, Jimbo Daiki, Wakutani Yosuke, Wada-Isoe Kenji, Nakashima Kenji, Akatsu Hiroyasu, Furukawa Katsutoshi, Arai Hiroyuki, Urakami Katsuya

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND/AIMS: Alzheimer's disease (AD) is a well-known type of dementia. However, it remains difficult to identify AD in the early stage and to distinguish it from other dementing disorders. We examined glycoproteins in cerebrospinal fluid (CSF) as potential biological markers of AD.

METHODS

CSF samples were collected from AD, other dementia and nondemented patients. Glycoproteins in CSF were detected by lectin blotting using wheat germ agglutinin (WGA), and sugar chain analysis was performed by isoelectric focusing.

RESULTS

In Alzheimer's CSF, several glycoproteins had lower WGA-binding activities, one of which was sufficiently sensitive and specific to distinguish AD from nondemented controls and other dementias. Further analysis identified this glycosylated protein as transferrin, and altered sugar chain composition of transferrin isoforms was observed despite normal protein levels in CSF.

CONCLUSION

The decreased WGA-binding activity of transferrin in AD is probably due to altered glycosylation of transferrin molecules. Transferrin glycosylation is thus a potential biological marker for AD diagnosis, and changes in this glycosylation may play an important role in the pathophysiology of AD.

Для цитирования: Taniguchi Miyako, Okayama Yuka, Hashimoto Yuki, Kitaura Miki, Jimbo Daiki, Wakutani Yosuke, Wada-Isoe Kenji, Nakashima Kenji, Akatsu Hiroyasu, Furukawa Katsutoshi, Arai Hiroyuki, Urakami Katsuya. Sugar chains of cerebrospinal fluid transferrin as a new biological marker of Alzheimer's disease.. Dementia and geriatric cognitive disorders. 2008. DOI: 10.1159/000147479.

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