Serum level of brain-derived neurotrophic factor in Parkinson's disease: a meta-analysis

Brain-derived neurotrophic factor (BDNF), a critical modulator in the neurodevelopment and maintenance of both central and peripheral nervous systems, is regarded as a potential therapeutic target of Parkinson's disease (PD). However, its association with PD remains unclear and the data are inc...

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Veröffentlicht in:Progress in neuro-psychopharmacology & biological psychiatry 2019-01, Vol.88, p.168-174
Hauptverfasser: Jiang, Lina, Zhang, Hainan, Wang, Chunyu, Ming, Fengyu, Shi, Xiaoliu, Yang, Mei
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Sprache:eng
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Zusammenfassung:Brain-derived neurotrophic factor (BDNF), a critical modulator in the neurodevelopment and maintenance of both central and peripheral nervous systems, is regarded as a potential therapeutic target of Parkinson's disease (PD). However, its association with PD remains unclear and the data are inconsistent. To explore the correlation, studies reporting BDNF levels in PD patients and healthy controls are searched and a sample of 1496 participants are pooled in the meta-analysis, demonstrating significantly decreased serum levels of BDNF in PD patients when compared with the healthy controls (SMD = −1.03; 95% CI [−1.83, −0.23]; P = .012). Meta-regression analysis indicates gender is an important confounding factor (Adj R2 = 69.20%, p = .004, I2 res = 90.64%), whereas age (Adj R2 = 11.91%, P = .95, I2 res = 96.86%), H-Y stages of PD progression (Adj R2 = −30.18%, P = .612, I2 res = 96.62%) and MoCA score assessed cognitive impairment (Adj R2 = 2.18%, P = .517, I2 res = 64.41%) show few moderating effects. The research provides evidence of moderate quality that blood levels of BDNF are decreased in PD patients despite various influencing factors, supporting an association between decreased level of peripheral BDNF and PD. •Serum level of BDNF declines in PD patients.•Gender affects peripheral BDNF decline in PD patients.•Age and disease severity do not affect peripheral BDNF decline in PD patients.
ISSN:0278-5846
1878-4216
DOI:10.1016/j.pnpbp.2018.07.010