Association of soluble cell adhesion molecules and lipid levels in rheumatoid arthritis patients

Objectives To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP). Methods Cross-sectional study nested of a RA cohort....

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Published inClinical rheumatology Vol. 42; no. 3; pp. 731 - 739
Main Authors Colunga-Pedraza, Iris J., Galarza-Delgado, Dionicio A., Guajardo-Jauregui, Natalia, Cardenas-de la Garza, Jesus A., Garcia-Arellano, Gisela, Arvizu-Rivera, Rosa I., Garza-Cisneros, Andrea N., Garcia-Heredia, Alexis, Balderas-Palacios, Mario A., Azpiri-Lopez, Jose R.
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.03.2023
Springer Nature B.V
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ISSN0770-3198
1434-9949
1434-9949
DOI10.1007/s10067-022-06395-6

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Abstract Objectives To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP). Methods Cross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins’ therapy, aged 40–75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman’s correlation coefficient (rs). Results We included 71 RA patients, 37 with CP and 34 without CP. RA ( n  = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs =  − 0.366, p  = 0.002) and low-density lipoprotein (LDL) (rs =  − 0.316, p  = 0.007), and a small negative correlation with high-density lipoprotein (rs =  − 0.250, p  = 0.036). ESR showed a small negative correlation with LDL (rs =  − 0.247, p  = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs =  − 0.405, p  = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs =  − 0.364, p  = 0.034) and LDL (rs =  − 0.352, p  = 0.041), and sICAM with VLDL (rs =  − 0.343, p  = 0.047). Conclusions RA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA. Key Points • In RA patients with and without atherosclerosis, higher sVCAM-1 titers were associated with lower TC, LDL and HDL, and higher levels of ESR associated with lower LDL. • Higher levels of sVCAM-1 were associated with lower TC in RA patients with atherosclerosis, and with lower TC and LDL in RA patients without atherosclerosis. • There was an inverse association of sICAM-1 with VLDL, in RA patients without atherosclerosis. • sVCAM-1 may have a role in the detection of paradoxical lipid levels in RA, but more research is needed to validate our findings.
AbstractList To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP). Cross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins' therapy, aged 40-75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman's correlation coefficient (rs). We included 71 RA patients, 37 with CP and 34 without CP. RA (n = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs =  - 0.366, p = 0.002) and low-density lipoprotein (LDL) (rs =  - 0.316, p = 0.007), and a small negative correlation with high-density lipoprotein (rs =  - 0.250, p = 0.036). ESR showed a small negative correlation with LDL (rs =  - 0.247, p = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs =  - 0.405, p = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs =  - 0.364, p = 0.034) and LDL (rs =  - 0.352, p = 0.041), and sICAM with VLDL (rs =  - 0.343, p = 0.047). RA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA.
OBJECTIVES: To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP). METHODS: Cross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins’ therapy, aged 40–75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman’s correlation coefficient (rs). RESULTS: We included 71 RA patients, 37 with CP and 34 without CP. RA (n = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs = − 0.366, p = 0.002) and low-density lipoprotein (LDL) (rs = − 0.316, p = 0.007), and a small negative correlation with high-density lipoprotein (rs = − 0.250, p = 0.036). ESR showed a small negative correlation with LDL (rs = − 0.247, p = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs = − 0.405, p = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs = − 0.364, p = 0.034) and LDL (rs = − 0.352, p = 0.041), and sICAM with VLDL (rs = − 0.343, p = 0.047). CONCLUSIONS: RA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA.
ObjectivesTo evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP).MethodsCross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins’ therapy, aged 40–75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman’s correlation coefficient (rs).ResultsWe included 71 RA patients, 37 with CP and 34 without CP. RA (n = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs =  − 0.366, p = 0.002) and low-density lipoprotein (LDL) (rs =  − 0.316, p = 0.007), and a small negative correlation with high-density lipoprotein (rs =  − 0.250, p = 0.036). ESR showed a small negative correlation with LDL (rs =  − 0.247, p = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs =  − 0.405, p = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs =  − 0.364, p = 0.034) and LDL (rs =  − 0.352, p = 0.041), and sICAM with VLDL (rs =  − 0.343, p = 0.047).ConclusionsRA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA.Key Points• In RA patients with and without atherosclerosis, higher sVCAM-1 titers were associated with lower TC, LDL and HDL, and higher levels of ESR associated with lower LDL.• Higher levels of sVCAM-1 were associated with lower TC in RA patients with atherosclerosis, and with lower TC and LDL in RA patients without atherosclerosis.• There was an inverse association of sICAM-1 with VLDL, in RA patients without atherosclerosis.• sVCAM-1 may have a role in the detection of paradoxical lipid levels in RA, but more research is needed to validate our findings.
To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP).OBJECTIVESTo evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP).Cross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins' therapy, aged 40-75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman's correlation coefficient (rs).METHODSCross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins' therapy, aged 40-75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman's correlation coefficient (rs).We included 71 RA patients, 37 with CP and 34 without CP. RA (n = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs =  - 0.366, p = 0.002) and low-density lipoprotein (LDL) (rs =  - 0.316, p = 0.007), and a small negative correlation with high-density lipoprotein (rs =  - 0.250, p = 0.036). ESR showed a small negative correlation with LDL (rs =  - 0.247, p = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs =  - 0.405, p = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs =  - 0.364, p = 0.034) and LDL (rs =  - 0.352, p = 0.041), and sICAM with VLDL (rs =  - 0.343, p = 0.047).RESULTSWe included 71 RA patients, 37 with CP and 34 without CP. RA (n = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs =  - 0.366, p = 0.002) and low-density lipoprotein (LDL) (rs =  - 0.316, p = 0.007), and a small negative correlation with high-density lipoprotein (rs =  - 0.250, p = 0.036). ESR showed a small negative correlation with LDL (rs =  - 0.247, p = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs =  - 0.405, p = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs =  - 0.364, p = 0.034) and LDL (rs =  - 0.352, p = 0.041), and sICAM with VLDL (rs =  - 0.343, p = 0.047).RA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA.CONCLUSIONSRA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA.
Objectives To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP). Methods Cross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins’ therapy, aged 40–75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman’s correlation coefficient (rs). Results We included 71 RA patients, 37 with CP and 34 without CP. RA ( n  = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs =  − 0.366, p  = 0.002) and low-density lipoprotein (LDL) (rs =  − 0.316, p  = 0.007), and a small negative correlation with high-density lipoprotein (rs =  − 0.250, p  = 0.036). ESR showed a small negative correlation with LDL (rs =  − 0.247, p  = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs =  − 0.405, p  = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs =  − 0.364, p  = 0.034) and LDL (rs =  − 0.352, p  = 0.041), and sICAM with VLDL (rs =  − 0.343, p  = 0.047). Conclusions RA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA. Key Points • In RA patients with and without atherosclerosis, higher sVCAM-1 titers were associated with lower TC, LDL and HDL, and higher levels of ESR associated with lower LDL. • Higher levels of sVCAM-1 were associated with lower TC in RA patients with atherosclerosis, and with lower TC and LDL in RA patients without atherosclerosis. • There was an inverse association of sICAM-1 with VLDL, in RA patients without atherosclerosis. • sVCAM-1 may have a role in the detection of paradoxical lipid levels in RA, but more research is needed to validate our findings.
Author Arvizu-Rivera, Rosa I.
Guajardo-Jauregui, Natalia
Galarza-Delgado, Dionicio A.
Cardenas-de la Garza, Jesus A.
Garcia-Arellano, Gisela
Garcia-Heredia, Alexis
Balderas-Palacios, Mario A.
Garza-Cisneros, Andrea N.
Colunga-Pedraza, Iris J.
Azpiri-Lopez, Jose R.
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  surname: Arvizu-Rivera
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  organization: Rheumatology Service, Internal Medicine Department, Hospital Universitario “Dr, Jose Eleuterio Gonzalez”, Universidad Autonoma de Nuevo Leon
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  surname: Garcia-Heredia
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  organization: Cardiology Service, Internal Medicine Department, Hospital Universitario “Dr, Jose Eleuterio Gonzalez”, Universidad Autonoma de Nuevo Leon, Francisco I. Madero Y Gonzalitos S/N
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crossref_primary_10_3390_ijms252212425
crossref_primary_10_1021_acs_jproteome_3c00574
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2022. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).
Copyright_xml – notice: The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR) 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
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IEDL.DBID 7X7
ISSN 0770-3198
1434-9949
IngestDate Fri Jul 11 16:51:11 EDT 2025
Mon Jul 21 09:57:42 EDT 2025
Fri Jul 25 06:28:22 EDT 2025
Thu Apr 03 07:07:04 EDT 2025
Thu Apr 24 23:01:16 EDT 2025
Tue Jul 01 04:05:20 EDT 2025
Fri Feb 21 02:46:24 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords Lipids
Rheumatoid arthritis
Atherosclerosis
Cardiovascular risk
Vascular cell adhesion molecule-1
Language English
License 2022. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).
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0000-0002-2638-9590
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0000-0002-5099-0079
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PublicationSubtitle Journal of the International League of Associations for Rheumatology
PublicationTitle Clinical rheumatology
PublicationTitleAbbrev Clin Rheumatol
PublicationTitleAlternate Clin Rheumatol
PublicationYear 2023
Publisher Springer International Publishing
Springer Nature B.V
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Snippet Objectives To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and...
To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels...
ObjectivesTo evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and...
OBJECTIVES: To evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and...
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SubjectTerms adhesion
Arteriosclerosis
Arthritis, Rheumatoid - drug therapy
Atherosclerosis
blood
C-reactive protein
C-Reactive Protein - analysis
Cardiovascular diseases
cell adhesion
Cell adhesion & migration
Cell Adhesion Molecules
Cholesterol
Cross-Sectional Studies
Erythrocyte sedimentation rate
gender
High density lipoprotein
Humans
Intercellular Adhesion Molecule-1
Lipids
Lipoproteins (very low density)
Low density lipoprotein
Medicine
Medicine & Public Health
Original Article
Rheumatoid arthritis
Rheumatology
risk
Risk factors
Statins
therapeutics
ultrasonics
Vascular Cell Adhesion Molecule-1
vascular cell adhesion molecules
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Title Association of soluble cell adhesion molecules and lipid levels in rheumatoid arthritis patients
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