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Nigrostriatal degeneration and serum BDNF levels in patients with “de novo” untreated Parkinson’s disease

G. Marti, N. Saez, M. Corominas, G. Cuberas, C. Lorenzo, O. De Fabregues, J. Alvarez-Sabin, M. Casas, J. Hernandez (Barcelona, Spain)

Meeting: 2016 International Congress

Abstract Number: 1228

Keywords: Neurophysiology, Nigrostriatal dopaminergic synapse deficiency, Parkinsonism, Single-photon emission computed tomography(SPECT)

Session Information

Date: Wednesday, June 22, 2016

Session Title: Parkinson's disease: Neuroimaging and neurophysiology

Session Time: 12:00pm-1:30pm

Location: Exhibit Hall located in Hall B, Level 2

Objective: To evaluate serum Brain-Derived NeurotrophicFactor(BDNF) levels in “de novo” untreated Parkinson’s disease (PD) patients and their relationship to nigrostriatal degeneration measured with [123I]FP-CIT SPECT.

Background: Different factors had been related to develope PD. Among them, some neurotrophic factors like BDNF are involved. It’s thought that low levels of them might play a major role in neural survival and neurodegeneration. Moreover levels of dopamine presynaptic transporter measured with [123I]FP-CIT SPECT had showed a good correlation to severity and progression of PD. Accordingly we hypothesized that lower BDNF will be find in patients with more striatal neurodegeneration.

Methods: Observational and cross-sectional study. “De novo” untreated PDpatients were consecutively recruited. Disease stage was evaluated by the Hoehn-Yahr (H&Y) scale. Disease severity and motor symptoms were rated according to the Unified Parkinson’s disease Rating Scale (UPDRSS) part III. All patients also underwent a psychiatric evaluation including a Structured Clinical Interview for DSM-IV Axis I disorders in order to exclude concomitant psychiatric disorders. Blood samples were collected at the same range of time. BDNF levels were analyzed by ELISA, twice. Furthermore a[123I]FP-CIT SPECT was performed in the PD group using a volumetric quantification of Regions Of Interest(ROI). To determine differences in BDNF levels between PD subjects and healthy controls a Mann-Whitney U test along with linear regression analysis accounting the effect for age and gender was performed. Additionally, the relationship between BDNF levels and the different ratios was assessed by a linear regression model accounting for age, PD duration and severity of motor symptoms. A p value < 0.05 was considered statistically significant.

Results: We recruited 27 PD patients [age 62.85±9.64 yo; 14 (51.85% male)]. Mean UPDRS-III score of 16 (range 12-22). The PDpatients showed significantly lower BDNF levels than healthy controls (54.04±16.68 ng/mL vs 74.25±31.12 ng/mL; p=0.005). Linear regression analysis showed a significant correlation between BDNF levels and average of striatal dopamine transporter binding, especially in contralateral and ipsilateral putamen

[123I]-FP-CIT SPECT and BDNF PD levels correlation
  B IC 95% R² p value
Contralateral Putamen 0,015 (0,008 – 0,022) 0,592 <0,001
Ipsilateral Putamen 0,015 (0,009 – 0,021) 0,586 <0,001
Contralateral Caudate 0,016 (0,007 – 0,026) 0,433 0,004
Ipsilateral Caudate 0,017 (0,008 – 0,026) 0,414 0,006
Linear regression analysis shows a significant correlation between BDNF levels and average of striatal dopamine transporter binding, especially more evident in contralateral and ipsilateral putamen.“(R²= 583; F=34,93; p<0.001; R²= 548; F=30,35; p<0.001)

Conclusions: Low serum BDNF levels are related to the degree of neurodegeneration in the nigrostriatal system.

LXVI Annual Meeting of Spanish Neurology Society.

To cite this abstract in AMA style:

G. Marti, N. Saez, M. Corominas, G. Cuberas, C. Lorenzo, O. De Fabregues, J. Alvarez-Sabin, M. Casas, J. Hernandez. Nigrostriatal degeneration and serum BDNF levels in patients with “de novo” untreated Parkinson’s disease [abstract]. Mov Disord. 2016; 31 (suppl 2). https://www.mdsabstracts.org/abstract/nigrostriatal-degeneration-and-serum-bdnf-levels-in-patients-with-de-novo-untreated-parkinsons-disease/. Accessed May 16, 2025.
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