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Neuroimage Clin ; 23: 101905, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31279240

RESUMO

OBJECTIVE: To evaluate, in vivo, the impact of ongoing chronic migraine (CM) attacks on the endogenous µ-opioid neurotransmission. BACKGROUND: CM is associated with cognitive-emotional dysfunction. CM is commonly associated with frequent acute medication use, including opioids. METHODS: We scanned 15 migraine patients during the spontaneous headache attack (ictal phase): 7 individuals with CM and 8 with episodic migraine (EM), as well as 7 healthy controls (HC), using positron emission tomography (PET) with the selective µ-opioid receptor (µOR) radiotracer [11C]carfentanil. Migraineurs were scanned in two paradigms, one with thermal pain threshold challenge applied to the site of the headache, and one without thermal challenge. Multivariable analysis was performed between the µ-opioid receptor availability and the clinical data. RESULTS: µOR availability, measured with [11C]carfentanil nondisplaceable binding potential (BPND), in the left thalamus (P-value = 0.005) and left caudate (P-value = 0.003) were decreased in CM patients with thermal pain threshold during the ictal phase relative to HC. Lower µOR BPND in the right parahippocampal region (P-value = 0.001) and right amygdala (P-value = 0.002) were seen in CM relative to EM patients. Lower µOR BPND values indicate either a decrease in µOR concentration or an increase in endogenous µ-opioid release in CM patients. In the right amygdala, 71% of the overall variance in µOR BPND levels was explained by the type of migraine (CM vs. EM: partial-R2 = 0.47, P-value<0.001, Cohen's effect size d = 2.6SD), the severity of the attack (pain area and intensity number summation [P.A.I.N.S.]: partial-R2 = 0.16, P-value = 0.031), and the thermal pain threshold (allodynia: partial-R2 = 0.08). CONCLUSIONS: Increased endogenous µ-opioid receptor-mediated neurotransmission is seen in the limbic system of CM patients, especially in right amygdala, which is highly modulated by the attack frequency, pain severity, and sensitivity. This study demonstrates for the first time the negative impact of chronification and exacerbation of headache attacks on the endogenous µ-opioid mechanisms of migraine patients. ClinicalTrials.gov identifier: NCT03004313.


Assuntos
Tonsila do Cerebelo/metabolismo , Transtornos de Enxaqueca/metabolismo , Transtornos de Enxaqueca/fisiopatologia , Nociceptividade/fisiologia , Limiar da Dor/fisiologia , Giro Para-Hipocampal/metabolismo , Receptores Opioides mu/metabolismo , Adulto , Tonsila do Cerebelo/diagnóstico por imagem , Analgésicos Opioides/farmacocinética , Núcleo Caudado/diagnóstico por imagem , Núcleo Caudado/metabolismo , Doença Crônica , Feminino , Fentanila/análogos & derivados , Fentanila/farmacocinética , Humanos , Masculino , Pessoa de Meia-Idade , Transtornos de Enxaqueca/diagnóstico por imagem , Giro Para-Hipocampal/diagnóstico por imagem , Estimulação Física , Tomografia por Emissão de Pósitrons , Compostos Radiofarmacêuticos/farmacocinética , Índice de Gravidade de Doença , Tálamo/diagnóstico por imagem , Tálamo/metabolismo , Adulto Jovem
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