Plasma calcitonin gene-related peptide (CGRP) in migraine and endometriosis during the menstrual cycle.


Journal

Annals of clinical and translational neurology
ISSN: 2328-9503
Titre abrégé: Ann Clin Transl Neurol
Pays: United States
ID NLM: 101623278

Informations de publication

Date de publication:
06 2021
Historique:
revised: 18 03 2021
received: 16 01 2021
accepted: 23 03 2021
pubmed: 3 5 2021
medline: 13 1 2022
entrez: 2 5 2021
Statut: ppublish

Résumé

Migraine, endometriosis, and the comorbidity of both are frequent pain disorders of special relevance for women. The neuropeptide calcitonin gene-related peptide (CGRP) is critically involved in migraine, and circumstantial evidence suggests a role in endometriosis. We assessed CGRP levels at different times of menstrual cycle in four groups: healthy women, women with migraine or endometriosis and with the comorbidity of both. Women with episodic migraine and women with a histologically confirmed endometriosis were recruited from specialized centers. For CGRP determination with a commercial enzyme immunoassay kit, cubital vein blood samples were collected on menstrual cycle day 2 ± 2 (during menstruation) and on day 15 ± 2 (periovulatory period). The primary endpoint of the study was the absolute difference of CGRP plasma levels between the menstrual and the periovulatory phase of all study groups. Groups were compared using nonparametric test procedures. A total of 124 women were included in the study. The change of CGRP plasma levels between menstruation and the periovulatory period was different between groups (p = 0.007). Women with comorbid migraine and endometriosis showed an increase of CGRP in the menstrual phase of +6.32 (interquartile range, IQR -3.64-13.60) compared to the periovulatory time, while healthy controls had a decrease of -10.14 (-22.54-0.91, p = 0.004). CGRP levels were different in the periovulatory phase among groups (p = 0.008), with highest values in healthy controls. CGRP levels change significantly during the menstrual cycle. Different patterns in women with the comorbidity point to a deviant regulation of CGRP release.

Identifiants

pubmed: 33934575
doi: 10.1002/acn3.51360
pmc: PMC8164854
doi:

Substances chimiques

Peptide Fragments 0
calcitonin gene related peptide (1-7) 0
Calcitonin Gene-Related Peptide JHB2QIZ69Z

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1251-1259

Informations de copyright

© 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

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Auteurs

Bianca Raffaelli (B)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.
Clinician Scientist Program, Berlin Institute of Health (BIH), Berlin, Germany.

Lucas Hendrik Overeem (LH)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Jasper Mecklenburg (J)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Maxi Dana Hofacker (MD)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Henriette Knoth (H)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Claus Peter Nowak (CP)

Institute of Biometry and Clinical Epidemiology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Lars Neeb (L)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Andreas Dietmar Ebert (AD)

Praxis für Frauengesundheit, Gynäkologie und Geburtshilfe, Endometriosezentrum, Berlin, Germany.

Jalid Sehouli (J)

Department of Gynecology with Center of Oncological Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Sylvia Mechsner (S)

Department of Gynecology with Center of Oncological Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Uwe Reuter (U)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

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Classifications MeSH