Early pain in females is linked to late pathological features in murine experimental osteoarthritis

Background Osteoarthritis (OA) is a progressive joint disease and a major cause of chronic pain in adults. The prevalence of OA is higher in female patients, who tend to have worse OA outcomes, partially due to pain. The association between joint pain and OA pathology is often inconclusive. Preclini...

Full description

Bibliographic Details
Main Authors: Natália Valdrighi, Arjen B. Blom, Henk M. van Beuningen, Elly L. Vitters, Monique M. Helsen, Birgitte Walgreen, Peter L.E.M. van Lent, Marije I. Koenders, Peter M. van der Kraan, Fons A.J. van de Loo, Esmeralda N. Blaney Davidson
Format: Article
Language:English
Published: PeerJ Inc. 2023-06-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/15482.pdf
_version_ 1827599256595202048
author Natália Valdrighi
Arjen B. Blom
Henk M. van Beuningen
Elly L. Vitters
Monique M. Helsen
Birgitte Walgreen
Peter L.E.M. van Lent
Marije I. Koenders
Peter M. van der Kraan
Fons A.J. van de Loo
Esmeralda N. Blaney Davidson
author_facet Natália Valdrighi
Arjen B. Blom
Henk M. van Beuningen
Elly L. Vitters
Monique M. Helsen
Birgitte Walgreen
Peter L.E.M. van Lent
Marije I. Koenders
Peter M. van der Kraan
Fons A.J. van de Loo
Esmeralda N. Blaney Davidson
author_sort Natália Valdrighi
collection DOAJ
description Background Osteoarthritis (OA) is a progressive joint disease and a major cause of chronic pain in adults. The prevalence of OA is higher in female patients, who tend to have worse OA outcomes, partially due to pain. The association between joint pain and OA pathology is often inconclusive. Preclinical research studies have largely overlooked sex as a potential determinant in joint pain during OA. This study aimed to investigate the role of sex in joint pain in the collagenase-induced OA (CiOA) model and its link with joint pathology. Methods Multiple aspects of pain were evaluated during identically executed experiments of CiOA in male and female C57BL/6J mice. Cartilage damage, osteophyte formation, synovial thickness, and cellularity were assessed by histology on day 56. The association between pain and pathology was investigated, disaggregated by sex. Results Differences in pain behavior between sexes were found in the majority of the evaluated pain methods. Females displayed lower weight bearing ability in the affected leg compared to males during the early phase of the disease, however, the pathology at the end stage was comparable between sexes. In the second cohort, males displayed increased mechanical sensitivity in the affected joint compared to females but also showed more cartilage damage at the end stage of the model. Within this cohort, gait analysis showed varied results. Males used the affected paw less often and displayed dynamic weight-bearing compensation in the early phase of the model. These differences were not observed in females. Other evaluated parameters displayed comparable gait behavior between males and females. A detailed analysis of individual mice revealed that seven out of 10 pain measurements highly correlated with OA histopathology in females (Pearson r range: 0.642–0.934), whereas in males this measurement was only two (Pearson r range: 0.645–0.748). Conclusion Our data show that sex is a determinant in the link between pain-related behavior with OA features. Therefore, to accurately interpret pain data it is crucial to segregate data analysis by sex to draw the correct mechanistic conclusion.
first_indexed 2024-03-09T04:09:17Z
format Article
id doaj.art-03fdaf6af3ba4d28bb9268a02e580afc
institution Directory Open Access Journal
issn 2167-8359
language English
last_indexed 2024-03-09T04:09:17Z
publishDate 2023-06-01
publisher PeerJ Inc.
record_format Article
series PeerJ
spelling doaj.art-03fdaf6af3ba4d28bb9268a02e580afc2023-12-03T14:01:22ZengPeerJ Inc.PeerJ2167-83592023-06-0111e1548210.7717/peerj.15482Early pain in females is linked to late pathological features in murine experimental osteoarthritisNatália ValdrighiArjen B. BlomHenk M. van BeuningenElly L. VittersMonique M. HelsenBirgitte WalgreenPeter L.E.M. van LentMarije I. KoendersPeter M. van der KraanFons A.J. van de LooEsmeralda N. Blaney DavidsonBackground Osteoarthritis (OA) is a progressive joint disease and a major cause of chronic pain in adults. The prevalence of OA is higher in female patients, who tend to have worse OA outcomes, partially due to pain. The association between joint pain and OA pathology is often inconclusive. Preclinical research studies have largely overlooked sex as a potential determinant in joint pain during OA. This study aimed to investigate the role of sex in joint pain in the collagenase-induced OA (CiOA) model and its link with joint pathology. Methods Multiple aspects of pain were evaluated during identically executed experiments of CiOA in male and female C57BL/6J mice. Cartilage damage, osteophyte formation, synovial thickness, and cellularity were assessed by histology on day 56. The association between pain and pathology was investigated, disaggregated by sex. Results Differences in pain behavior between sexes were found in the majority of the evaluated pain methods. Females displayed lower weight bearing ability in the affected leg compared to males during the early phase of the disease, however, the pathology at the end stage was comparable between sexes. In the second cohort, males displayed increased mechanical sensitivity in the affected joint compared to females but also showed more cartilage damage at the end stage of the model. Within this cohort, gait analysis showed varied results. Males used the affected paw less often and displayed dynamic weight-bearing compensation in the early phase of the model. These differences were not observed in females. Other evaluated parameters displayed comparable gait behavior between males and females. A detailed analysis of individual mice revealed that seven out of 10 pain measurements highly correlated with OA histopathology in females (Pearson r range: 0.642–0.934), whereas in males this measurement was only two (Pearson r range: 0.645–0.748). Conclusion Our data show that sex is a determinant in the link between pain-related behavior with OA features. Therefore, to accurately interpret pain data it is crucial to segregate data analysis by sex to draw the correct mechanistic conclusion.https://peerj.com/articles/15482.pdfOsteoarthritisPainSex differencesSynovitis
spellingShingle Natália Valdrighi
Arjen B. Blom
Henk M. van Beuningen
Elly L. Vitters
Monique M. Helsen
Birgitte Walgreen
Peter L.E.M. van Lent
Marije I. Koenders
Peter M. van der Kraan
Fons A.J. van de Loo
Esmeralda N. Blaney Davidson
Early pain in females is linked to late pathological features in murine experimental osteoarthritis
PeerJ
Osteoarthritis
Pain
Sex differences
Synovitis
title Early pain in females is linked to late pathological features in murine experimental osteoarthritis
title_full Early pain in females is linked to late pathological features in murine experimental osteoarthritis
title_fullStr Early pain in females is linked to late pathological features in murine experimental osteoarthritis
title_full_unstemmed Early pain in females is linked to late pathological features in murine experimental osteoarthritis
title_short Early pain in females is linked to late pathological features in murine experimental osteoarthritis
title_sort early pain in females is linked to late pathological features in murine experimental osteoarthritis
topic Osteoarthritis
Pain
Sex differences
Synovitis
url https://peerj.com/articles/15482.pdf
work_keys_str_mv AT nataliavaldrighi earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT arjenbblom earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT henkmvanbeuningen earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT ellylvitters earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT moniquemhelsen earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT birgittewalgreen earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT peterlemvanlent earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT marijeikoenders earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT petermvanderkraan earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT fonsajvandeloo earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis
AT esmeraldanblaneydavidson earlypaininfemalesislinkedtolatepathologicalfeaturesinmurineexperimentalosteoarthritis