Amanda E. Nelson , Liubov Arbeeva , Kelly Johnson , Serena Savage-Guin , Tessa Walker , Masataka Enomoto , Christina Stevens , Milja Koskinen , Tracey Cole , Savannah Aker , Connor Thonen-Fleck , M. Andrea Azcarate-Peril , Richard F. Loeser , Jordan B. Renner , Yvonne M. Golightly , B. Duncan X. Lascelles
{"title":"多关节骨性关节炎与症状、实验室值和肠道微生物群的横断面相关性:一项针对人类和宠物狗的多模式研究","authors":"Amanda E. Nelson , Liubov Arbeeva , Kelly Johnson , Serena Savage-Guin , Tessa Walker , Masataka Enomoto , Christina Stevens , Milja Koskinen , Tracey Cole , Savannah Aker , Connor Thonen-Fleck , M. Andrea Azcarate-Peril , Richard F. Loeser , Jordan B. Renner , Yvonne M. Golightly , B. Duncan X. Lascelles","doi":"10.1016/j.ocarto.2025.100682","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To describe the frequency of multiple joint osteoarthritis (MJOA) and symptoms, and associations with fecal microbial diversity and composition, in cohorts of humans and dogs.</div></div><div><h3>Design</h3><div>Human participants enrolled in the community-based Johnston County Health Study (JoCoHS), and an independent cohort of pet dogs, were included. Questionnaires, functional assessments, standardized multiple joint radiographs, and pain assessments, blood and fecal samples were obtained. Microbiome analysis was done by 16S rRNA amplicon sequencing. MJOA was defined as ≥3 unique joint sites involved; symptom burden was based on self-reported/proxy measures of pain. Descriptive statistics and Spearman correlations with Benjamini-Hochberg correction were used to determine relationships among lab tests, pain, and microbiome diversity measures.</div></div><div><h3>Results</h3><div>Human participants (n = 100, 63 % women, mean age 56 years, mean body mass index 34 kg/m<sup>2</sup>) and 115 pet dogs (40 % spayed females, 57 % neutered males, mean age 8 years, mean weight 27 kg) were included; 20 % had radiographic MJOA (rMJOA). Microbial α-diversity did not differ between participants with or without rMJOA. However, lower levels of the <em>Christensenellaceae R-7 group</em> and <em>Lachnoclostridium</em> in humans, and the butyrate-producing bacterium, <em>Faecalibacterium</em> in dogs, were moderately correlated with greater pain severity, as were higher levels of <em>Escherichia-Shigella</em> in dogs. <em>Faecalibacterium</em> was more abundant in humans without rMJOA.</div></div><div><h3>Conclusions</h3><div>These two cohorts demonstrated remarkably similar frequencies of rMJOA (∼20 %), supporting the use of dogs to model naturally occurring MJOA. Taxa potentially related to rMJOA and pain were identified in this preliminary analysis, providing new insights into links between dysbiosis and MJOA.</div></div>","PeriodicalId":74377,"journal":{"name":"Osteoarthritis and cartilage open","volume":"7 4","pages":"Article 100682"},"PeriodicalIF":2.8000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cross-sectional associations of radiographic multiple joint osteoarthritis and symptoms, laboratory values and the gut microbiota: A multimodal study in humans and pet dogs\",\"authors\":\"Amanda E. Nelson , Liubov Arbeeva , Kelly Johnson , Serena Savage-Guin , Tessa Walker , Masataka Enomoto , Christina Stevens , Milja Koskinen , Tracey Cole , Savannah Aker , Connor Thonen-Fleck , M. Andrea Azcarate-Peril , Richard F. Loeser , Jordan B. Renner , Yvonne M. Golightly , B. Duncan X. Lascelles\",\"doi\":\"10.1016/j.ocarto.2025.100682\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>To describe the frequency of multiple joint osteoarthritis (MJOA) and symptoms, and associations with fecal microbial diversity and composition, in cohorts of humans and dogs.</div></div><div><h3>Design</h3><div>Human participants enrolled in the community-based Johnston County Health Study (JoCoHS), and an independent cohort of pet dogs, were included. Questionnaires, functional assessments, standardized multiple joint radiographs, and pain assessments, blood and fecal samples were obtained. Microbiome analysis was done by 16S rRNA amplicon sequencing. MJOA was defined as ≥3 unique joint sites involved; symptom burden was based on self-reported/proxy measures of pain. Descriptive statistics and Spearman correlations with Benjamini-Hochberg correction were used to determine relationships among lab tests, pain, and microbiome diversity measures.</div></div><div><h3>Results</h3><div>Human participants (n = 100, 63 % women, mean age 56 years, mean body mass index 34 kg/m<sup>2</sup>) and 115 pet dogs (40 % spayed females, 57 % neutered males, mean age 8 years, mean weight 27 kg) were included; 20 % had radiographic MJOA (rMJOA). Microbial α-diversity did not differ between participants with or without rMJOA. However, lower levels of the <em>Christensenellaceae R-7 group</em> and <em>Lachnoclostridium</em> in humans, and the butyrate-producing bacterium, <em>Faecalibacterium</em> in dogs, were moderately correlated with greater pain severity, as were higher levels of <em>Escherichia-Shigella</em> in dogs. <em>Faecalibacterium</em> was more abundant in humans without rMJOA.</div></div><div><h3>Conclusions</h3><div>These two cohorts demonstrated remarkably similar frequencies of rMJOA (∼20 %), supporting the use of dogs to model naturally occurring MJOA. Taxa potentially related to rMJOA and pain were identified in this preliminary analysis, providing new insights into links between dysbiosis and MJOA.</div></div>\",\"PeriodicalId\":74377,\"journal\":{\"name\":\"Osteoarthritis and cartilage open\",\"volume\":\"7 4\",\"pages\":\"Article 100682\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Osteoarthritis and cartilage open\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2665913125001189\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Osteoarthritis and cartilage open","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2665913125001189","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cross-sectional associations of radiographic multiple joint osteoarthritis and symptoms, laboratory values and the gut microbiota: A multimodal study in humans and pet dogs
Objective
To describe the frequency of multiple joint osteoarthritis (MJOA) and symptoms, and associations with fecal microbial diversity and composition, in cohorts of humans and dogs.
Design
Human participants enrolled in the community-based Johnston County Health Study (JoCoHS), and an independent cohort of pet dogs, were included. Questionnaires, functional assessments, standardized multiple joint radiographs, and pain assessments, blood and fecal samples were obtained. Microbiome analysis was done by 16S rRNA amplicon sequencing. MJOA was defined as ≥3 unique joint sites involved; symptom burden was based on self-reported/proxy measures of pain. Descriptive statistics and Spearman correlations with Benjamini-Hochberg correction were used to determine relationships among lab tests, pain, and microbiome diversity measures.
Results
Human participants (n = 100, 63 % women, mean age 56 years, mean body mass index 34 kg/m2) and 115 pet dogs (40 % spayed females, 57 % neutered males, mean age 8 years, mean weight 27 kg) were included; 20 % had radiographic MJOA (rMJOA). Microbial α-diversity did not differ between participants with or without rMJOA. However, lower levels of the Christensenellaceae R-7 group and Lachnoclostridium in humans, and the butyrate-producing bacterium, Faecalibacterium in dogs, were moderately correlated with greater pain severity, as were higher levels of Escherichia-Shigella in dogs. Faecalibacterium was more abundant in humans without rMJOA.
Conclusions
These two cohorts demonstrated remarkably similar frequencies of rMJOA (∼20 %), supporting the use of dogs to model naturally occurring MJOA. Taxa potentially related to rMJOA and pain were identified in this preliminary analysis, providing new insights into links between dysbiosis and MJOA.