Volume 25, Issue 6 pp. 367-372
Regular Paper

Age-related changes in BDNF protein levels in human serum: differences between autism cases and normal controls

Ritsuko Katoh-Semba

Corresponding Author

Ritsuko Katoh-Semba

Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan

Corresponding author at: Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi 480-0392, Japan. Tel.: +81 568 88 0811x3563; fax: +81 568 568 88 0829.

E-mail address: [email protected] (R. Katoh-Semba).

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Rie Wakako

Rie Wakako

Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan

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Taku Komori

Taku Komori

Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan

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Hiroko Shigemi

Hiroko Shigemi

Tokai Kinen Hospital, Kasugai, Aichi, Japan

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Noriko Miyazaki

Noriko Miyazaki

Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan

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Hironori Ito

Hironori Ito

Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan

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Toshiyuki Kumagai

Toshiyuki Kumagai

Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan

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Masako Tsuzuki

Masako Tsuzuki

Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan

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Kenji Shigemi

Kenji Shigemi

Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan

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Futoshi Yoshida

Futoshi Yoshida

Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan

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Atsuo Nakayama

Atsuo Nakayama

Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan

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First published: 01 August 2007
Citations: 113

Abstract

Accumulating evidence suggests the possible association between the concentrations of serum brain-derived neurotrophic factor (BDNF) and psychiatric disease with impaired brain development. Yet the reasons remain unclear. We therefore investigated the characteristics of serum BDNF as well as its age-related changes in healthy controls in comparison to autism cases. BDNF was gradually released from platelets at 4 °C, reached a maximal concentration after around 24 h, and remained stable until 42 h. At room temperature, BDNF was found to be immediately degraded. Circadian changes, but not seasonal changes, were found in serum levels of BDNF existing as the mature form with a molecular mass of 14 kDa. In healthy controls, the serum BDNF concentration increased over the first several years, then slightly decreased after reaching the adult level. There were no sex differences between males and females. In the autism cases, mean levels were significantly lower in children 0–9 years old compared to teenagers or adults, or to age-matched healthy controls, indicating a delayed BDNF increase with development. In a separate study of adult rats, a circadian change in serum BDNF was found to be similar to that in the cortex, indicating a possible association with cortical functions.

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