Part II: Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients

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Part II : Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients. / Guo, Song; Vollesen, Anne Luise Haulund; Hansen, Young Bae Lee; Frandsen, Erik; Andersen, Malene Rohr; Amin, Faisal Mohammad; Fahrenkrug, Jan; Olesen, Jes; Ashina, Messoud.

I: Cephalalgia : an international journal of headache, Bind 37, Nr. 2, 02.2017, s. 136-147.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Guo, S, Vollesen, ALH, Hansen, YBL, Frandsen, E, Andersen, MR, Amin, FM, Fahrenkrug, J, Olesen, J & Ashina, M 2017, 'Part II: Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients', Cephalalgia : an international journal of headache, bind 37, nr. 2, s. 136-147. https://doi.org/10.1177/0333102416639517

APA

Guo, S., Vollesen, A. L. H., Hansen, Y. B. L., Frandsen, E., Andersen, M. R., Amin, F. M., Fahrenkrug, J., Olesen, J., & Ashina, M. (2017). Part II: Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients. Cephalalgia : an international journal of headache, 37(2), 136-147. https://doi.org/10.1177/0333102416639517

Vancouver

Guo S, Vollesen ALH, Hansen YBL, Frandsen E, Andersen MR, Amin FM o.a. Part II: Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients. Cephalalgia : an international journal of headache. 2017 feb.;37(2):136-147. https://doi.org/10.1177/0333102416639517

Author

Guo, Song ; Vollesen, Anne Luise Haulund ; Hansen, Young Bae Lee ; Frandsen, Erik ; Andersen, Malene Rohr ; Amin, Faisal Mohammad ; Fahrenkrug, Jan ; Olesen, Jes ; Ashina, Messoud. / Part II : Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients. I: Cephalalgia : an international journal of headache. 2017 ; Bind 37, Nr. 2. s. 136-147.

Bibtex

@article{2870643c300d40c183ae254b3c033a2d,
title = "Part II: Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients",
abstract = "Background Intravenous infusion of pituitary adenylate cyclase-activating polypeptide-38 (PACAP38) provokes migraine attacks in 65-70% of migraine without aura (MO) patients. We investigated whether PACAP38 infusion causes changes in the endogenous production of PACAP38, vasoactive intestinal polypeptide (VIP), calcitonin gene-related peptide (CGRP), tumour necrosis factor alpha (TNFα), S100 calcium binding protein B (S100B), neuron-specific enolase and pituitary hormones in migraine patients. Methods We allocated 32 previously genotyped MO patients to receive intravenous infusion PACAP38 (10 pmol/kg/minute) for 20 minutes and recorded migraine-like attacks. Sixteen of the patients were carriers of the risk allele rs2274316 ( MEF2D), which confers increased risk of MO and may regulate PACAP38 expression, and 16 were non-carriers. We collected blood samples at baseline and 20, 30, 40, 60 and 90 minutes after the start of the infusion. A control group of six healthy volunteers received intravenous saline. Results PACAP38 infusion caused significant changes in plasma concentrations of VIP ( p = 0.026), prolactin ( p = 0.011), S100B ( p < 0.001) and thyroid-stimulating hormone (TSH; p = 0.015), but not CGRP ( p = 0.642) and TNFα ( p = 0.535). We found no difference in measured biochemical variables after PACAP38 infusion in patients who later developed migraine-like attacks compared to those who did not ( p > 0.05). There was no difference in the changes of biochemical variables between patients with and without the MEF2D-associated gene variant ( p > 0.05). Conclusion PACAP38 infusion elevated the plasma levels of VIP, prolactin, S100B and TSH, but not CGRP and TNFα. Development of delayed migraine-like attacks or the presence of the MEF2D gene variant was not associated with pre-ictal changes in plasma levels of neuropeptides, TNFα and pituitary hormones.",
keywords = "Adult, Cohort Studies, Denmark, Double-Blind Method, Female, Humans, Infusions, Intravenous, Male, Middle Aged, Migraine Disorders, Neuropeptides, Pituitary Adenylate Cyclase-Activating Polypeptide, Surveys and Questionnaires, Tumor Necrosis Factor-alpha, Journal Article",
author = "Song Guo and Vollesen, {Anne Luise Haulund} and Hansen, {Young Bae Lee} and Erik Frandsen and Andersen, {Malene Rohr} and Amin, {Faisal Mohammad} and Jan Fahrenkrug and Jes Olesen and Messoud Ashina",
year = "2017",
month = feb,
doi = "10.1177/0333102416639517",
language = "English",
volume = "37",
pages = "136--147",
journal = "Cephalalgia",
issn = "0800-1952",
publisher = "SAGE Publications",
number = "2",

}

RIS

TY - JOUR

T1 - Part II

T2 - Biochemical changes after pituitary adenylate cyclase-activating polypeptide-38 infusion in migraine patients

AU - Guo, Song

AU - Vollesen, Anne Luise Haulund

AU - Hansen, Young Bae Lee

AU - Frandsen, Erik

AU - Andersen, Malene Rohr

AU - Amin, Faisal Mohammad

AU - Fahrenkrug, Jan

AU - Olesen, Jes

AU - Ashina, Messoud

PY - 2017/2

Y1 - 2017/2

N2 - Background Intravenous infusion of pituitary adenylate cyclase-activating polypeptide-38 (PACAP38) provokes migraine attacks in 65-70% of migraine without aura (MO) patients. We investigated whether PACAP38 infusion causes changes in the endogenous production of PACAP38, vasoactive intestinal polypeptide (VIP), calcitonin gene-related peptide (CGRP), tumour necrosis factor alpha (TNFα), S100 calcium binding protein B (S100B), neuron-specific enolase and pituitary hormones in migraine patients. Methods We allocated 32 previously genotyped MO patients to receive intravenous infusion PACAP38 (10 pmol/kg/minute) for 20 minutes and recorded migraine-like attacks. Sixteen of the patients were carriers of the risk allele rs2274316 ( MEF2D), which confers increased risk of MO and may regulate PACAP38 expression, and 16 were non-carriers. We collected blood samples at baseline and 20, 30, 40, 60 and 90 minutes after the start of the infusion. A control group of six healthy volunteers received intravenous saline. Results PACAP38 infusion caused significant changes in plasma concentrations of VIP ( p = 0.026), prolactin ( p = 0.011), S100B ( p < 0.001) and thyroid-stimulating hormone (TSH; p = 0.015), but not CGRP ( p = 0.642) and TNFα ( p = 0.535). We found no difference in measured biochemical variables after PACAP38 infusion in patients who later developed migraine-like attacks compared to those who did not ( p > 0.05). There was no difference in the changes of biochemical variables between patients with and without the MEF2D-associated gene variant ( p > 0.05). Conclusion PACAP38 infusion elevated the plasma levels of VIP, prolactin, S100B and TSH, but not CGRP and TNFα. Development of delayed migraine-like attacks or the presence of the MEF2D gene variant was not associated with pre-ictal changes in plasma levels of neuropeptides, TNFα and pituitary hormones.

AB - Background Intravenous infusion of pituitary adenylate cyclase-activating polypeptide-38 (PACAP38) provokes migraine attacks in 65-70% of migraine without aura (MO) patients. We investigated whether PACAP38 infusion causes changes in the endogenous production of PACAP38, vasoactive intestinal polypeptide (VIP), calcitonin gene-related peptide (CGRP), tumour necrosis factor alpha (TNFα), S100 calcium binding protein B (S100B), neuron-specific enolase and pituitary hormones in migraine patients. Methods We allocated 32 previously genotyped MO patients to receive intravenous infusion PACAP38 (10 pmol/kg/minute) for 20 minutes and recorded migraine-like attacks. Sixteen of the patients were carriers of the risk allele rs2274316 ( MEF2D), which confers increased risk of MO and may regulate PACAP38 expression, and 16 were non-carriers. We collected blood samples at baseline and 20, 30, 40, 60 and 90 minutes after the start of the infusion. A control group of six healthy volunteers received intravenous saline. Results PACAP38 infusion caused significant changes in plasma concentrations of VIP ( p = 0.026), prolactin ( p = 0.011), S100B ( p < 0.001) and thyroid-stimulating hormone (TSH; p = 0.015), but not CGRP ( p = 0.642) and TNFα ( p = 0.535). We found no difference in measured biochemical variables after PACAP38 infusion in patients who later developed migraine-like attacks compared to those who did not ( p > 0.05). There was no difference in the changes of biochemical variables between patients with and without the MEF2D-associated gene variant ( p > 0.05). Conclusion PACAP38 infusion elevated the plasma levels of VIP, prolactin, S100B and TSH, but not CGRP and TNFα. Development of delayed migraine-like attacks or the presence of the MEF2D gene variant was not associated with pre-ictal changes in plasma levels of neuropeptides, TNFα and pituitary hormones.

KW - Adult

KW - Cohort Studies

KW - Denmark

KW - Double-Blind Method

KW - Female

KW - Humans

KW - Infusions, Intravenous

KW - Male

KW - Middle Aged

KW - Migraine Disorders

KW - Neuropeptides

KW - Pituitary Adenylate Cyclase-Activating Polypeptide

KW - Surveys and Questionnaires

KW - Tumor Necrosis Factor-alpha

KW - Journal Article

U2 - 10.1177/0333102416639517

DO - 10.1177/0333102416639517

M3 - Journal article

C2 - 26994298

VL - 37

SP - 136

EP - 147

JO - Cephalalgia

JF - Cephalalgia

SN - 0800-1952

IS - 2

ER -

ID: 184914524