» Articles » PMID: 31624776

Blood Platelet Research in Autism Spectrum Disorders: In Search of Biomarkers

Overview
Publisher Elsevier
Date 2019 Oct 19
PMID 31624776
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Autism spectrum disorder (ASD) is a clinically heterogeneous neurodevelopmental disorder that is caused by gene-environment interactions. To improve its diagnosis and treatment, numerous efforts have been undertaken to identify reliable biomarkers for autism. None of them have delivered the holy grail that represents a reproducible, quantifiable, and sensitive biomarker. Though blood platelets are mainly known to prevent bleeding, they also play pivotal roles in cancer, inflammation, and neurological disorders. Platelets could serve as a peripheral biomarker or cellular model for autism as they share common biological and molecular characteristics with neurons. In particular, platelet-dense granules contain neurotransmitters such as serotonin and gamma-aminobutyric acid. Molecular players controlling granule formation and secretion are similarly regulated in platelets and neurons. The major platelet integrin receptor αIIbβ3 has recently been linked to ASD as a regulator of serotonin transport. Though many studies revealed associations between platelet markers and ASD, there is an important knowledge gap in linking these markers with autism and explaining the altered platelet phenotypes detected in autism patients. The present review enumerates studies of different biomarkers detected in ASD using platelets and highlights the future needs to bring this research to the next level and advance our understanding of this complex disorder.

Citing Articles

The link between BDNF and platelets in neurological disorders.

Bouhaddou N, Mabrouk M, Atifi F, Bouyahya A, Zaid Y Heliyon. 2024; 10(21):e39278.

PMID: 39568824 PMC: 11577193. DOI: 10.1016/j.heliyon.2024.e39278.


Zinc signaling controls astrocyte-dependent synapse modulation via the PAF receptor pathway.

Stanton J, Hans S, Zabetakis I, Grabrucker A J Neurochem. 2024; 169(2):e16252.

PMID: 39450676 PMC: 11808829. DOI: 10.1111/jnc.16252.


A Systematic Review on Autism and Hyperserotonemia: State-of-the-Art, Limitations, and Future Directions.

Esposito D, Cruciani G, Zaccaro L, di Carlo E, Spitoni G, Manti F Brain Sci. 2024; 14(5).

PMID: 38790459 PMC: 11119126. DOI: 10.3390/brainsci14050481.


Dysregulation of platelet serotonin, 14-3-3, and GPIX in sudden infant death syndrome.

Frelinger 3rd A, Haynes R, Goldstein R, Berny-Lang M, Gerrits A, Riehs M Sci Rep. 2024; 14(1):11092.

PMID: 38750089 PMC: 11096399. DOI: 10.1038/s41598-024-61949-9.


The intriguing role of platelets as custodians of brain-derived neurotrophic factor.

Boukhatem I, Fleury S, Jourdi G, Lordkipanidze M Res Pract Thromb Haemost. 2024; 8(3):102398.

PMID: 38706782 PMC: 11066552. DOI: 10.1016/j.rpth.2024.102398.


References
1.
Asor E, Ben-Shachar D . Platelets: A possible glance into brain biological processes in schizophrenia. World J Psychiatry. 2013; 2(6):124-33. PMC: 3782191. DOI: 10.5498/wjp.v2.i6.124. View

2.
Yip P, Zhao X, Montgomery A, Siu C . The Arg-Gly-Asp motif in the cell adhesion molecule L1 promotes neurite outgrowth via interaction with the alphavbeta3 integrin. Mol Biol Cell. 1998; 9(2):277-90. PMC: 25251. DOI: 10.1091/mbc.9.2.277. View

3.
Lintas C, Persico A . Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist. J Med Genet. 2008; 46(1):1-8. PMC: 2603481. DOI: 10.1136/jmg.2008.060871. View

4.
Boullin D, Coleman M, OBrien R . Abnormalities in platelet 5-hydroxytryptamine efflux in patients with infantile autism. Nature. 1970; 226(5243):371-2. DOI: 10.1038/226371a0. View

5.
Dhossche D, Applegate H, Abraham A, Maertens P, Bland L, Bencsath A . Elevated plasma gamma-aminobutyric acid (GABA) levels in autistic youngsters: stimulus for a GABA hypothesis of autism. Med Sci Monit. 2002; 8(8):PR1-6. View