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Tytuł pozycji:

Experimental evaluation of central pain processes in young women with primary dysmenorrhea.

Tytuł:
Experimental evaluation of central pain processes in young women with primary dysmenorrhea.
Autorzy:
Payne LA; Pediatric Pain and Palliative Care Program, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Seidman LC; Pediatric Pain and Palliative Care Program, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Sim MS; Departments of Medicine Statistics Core and.
Rapkin AJ; Obstetrics and Gynecology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Naliboff BD; G Oppenheimer Center for Neurobiology of Stress and Resilience (CNSR), David Geffen School of Medicine at UCLA Los Angeles, CA, United States.
Zeltzer LK; Pediatric Pain and Palliative Care Program, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Źródło:
Pain [Pain] 2019 Jun; Vol. 160 (6), pp. 1421-1430.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
Język:
English
Imprint Name(s):
Publication: 2015- : Hagerstown, MD : Lippincott Williams & Wilkins
Original Publication: Amsterdam, Elsevier/North-Holland.
MeSH Terms:
Pain Measurement*
Dysmenorrhea/*drug therapy
Menstrual Cycle/*drug effects
Neuralgia/*drug therapy
Adolescent ; Central Nervous System Sensitization/drug effects ; Female ; Humans ; Male ; Pain Threshold/drug effects ; Young Adult
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Grant Information:
K23 HD077042 United States HD NICHD NIH HHS; KL2 TR000122 United States TR NCATS NIH HHS
Entry Date(s):
Date Created: 20190206 Date Completed: 20200511 Latest Revision: 20221005
Update Code:
20240105
PubMed Central ID:
PMC6527468
DOI:
10.1097/j.pain.0000000000001516
PMID:
30720583
Czasopismo naukowe
Primary dysmenorrhea (PD; menstrual pain without an underlying medical condition) is associated with enhanced pain sensitivity and temporal summation (TS) in adult women, which may reflect the presence of central pain processes. Research in this area has been limited by focusing on only adult populations and incomplete assessments of central sensitization. The current study explored both excitatory and inhibitory measures of pain processing in girls and young adult women with and without PD. Thirty-two young women with PD and 34 healthy controls underwent laboratory pain testing during each of 3 menstrual cycle phases (menstrual, ovulatory, and midluteal), which included measures of pain tolerance and threshold, TS, and conditioned pain modulation. Results indicated enhanced pain sensitivity in young women with PD as measured by heat pain tolerance and Average Pain50 (P50), compared with healthy controls. These group differences were evident at all phases of the menstrual cycle. No group differences in cold pain tolerance, TS, or conditioned pain modulation were evident at any phase of the menstrual cycle. These data suggest some evidence of central sensitization in young women with PD, although no evidence of enhanced excitatory or deficient inhibitory mechanisms were observed. Future research should focus on identifying other potential phenotypes for PD to determine those at risk of developing other pain problems.

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