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Mov Disord Clin Pract ; 11(7): 808-813, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38661486

RESUMO

BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) has been linked to an increased risk of early-onset Parkinson's disease. However, the pathophysiological mechanisms underlying parkinsonism remain poorly understood. OBJECTIVE: The objective is to investigate salivary total α-synuclein levels in 22q11.2DS patients with and without parkinsonian motor signs. METHODS: This cross-sectional study included 10 patients with 22q11.2DS with parkinsonism (Park+), ten 22q11.2DS patients without parkinsonism (Park-), and 10 age and sex-comparable healthy subjects (HS). Salivary and serum α-synuclein levels were measured using enzyme-linked immunosorbent assay. RESULTS: Salivary total α-synuclein concentration was significantly lower in Park (+) patients than in Park (-) patients and HS (P = 0.007). In addition, salivary α-synuclein showed good accuracy in discriminating Park (+) from Park (-) patients (area under the curve = 0.86) and correlated with motor severity and cognitive impairment. CONCLUSION: This exploratory study suggests that the parkinsonian phenotype of 22q11.2DS is associated with a reduced concentration of monomeric α-synuclein in biological fluids.


Assuntos
Biomarcadores , Síndrome de DiGeorge , Transtornos Parkinsonianos , Saliva , alfa-Sinucleína , Humanos , Masculino , Feminino , Estudos Transversais , alfa-Sinucleína/metabolismo , alfa-Sinucleína/genética , Saliva/química , Saliva/metabolismo , Biomarcadores/sangue , Biomarcadores/metabolismo , Biomarcadores/análise , Transtornos Parkinsonianos/metabolismo , Transtornos Parkinsonianos/genética , Transtornos Parkinsonianos/diagnóstico , Transtornos Parkinsonianos/sangue , Adulto , Síndrome de DiGeorge/genética , Síndrome de DiGeorge/metabolismo , Síndrome de DiGeorge/diagnóstico , Síndrome de DiGeorge/sangue , Adulto Jovem , Pessoa de Meia-Idade , Adolescente
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