Soluble urine activated leukocyte cell adhesion molecule is a strong predictor of lupus nephritis
To evaluate urinary activated leucocyte cell adhesion molecule (ALCAM) and CD6 as predictors of LN progression or disease resolution across a 1-year study. Serum and urine samples from biopsy proven LN subjects (n = 122) were prospectively collected over the course of a year at 3- or 6-month interva...
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Published in | Rheumatology (Oxford, England) Vol. 64; no. 5; pp. 2676 - 2687 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
01.05.2025
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ISSN | 1462-0324 1462-0332 1462-0332 |
DOI | 10.1093/rheumatology/keae559 |
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Abstract | To evaluate urinary activated leucocyte cell adhesion molecule (ALCAM) and CD6 as predictors of LN progression or disease resolution across a 1-year study.
Serum and urine samples from biopsy proven LN subjects (n = 122) were prospectively collected over the course of a year at 3- or 6-month intervals (weeks 0, 12, 26 and 52) across multiple study sites and assessed for soluble ALCAM and CD6 levels. Urine creatinine from the same urine sample was used to normalize the levels of urinary ALCAM and urinary CD6. Measured levels of serum and urine ALCAM and CD6 were then analysed against disease metrics cross-sectionally and longitudinally.
Cross-sectional analysis at baseline revealed that urinary ALCAM significantly correlated with urine protein creatinine ratio, renal SLEDAI, and the Physician Global Assessment (PGA), and negatively correlated with serum C3 and C4. Receiver operating characteristic curve analysis demonstrated that urinary ALCAM is a predictor of LN with an area under the curve (AUC) of 0.97, compared with urinary CD6 with an AUC of 0.71. Importantly, the change in urinary ALCAM over a 3-month period distinguished between non-responders and responders at week 52.
Urinary ALCAM is reflective of changes in LN and may be predictive of response status. |
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AbstractList | To evaluate urinary activated leucocyte cell adhesion molecule (ALCAM) and CD6 as predictors of LN progression or disease resolution across a 1-year study.
Serum and urine samples from biopsy proven LN subjects (n = 122) were prospectively collected over the course of a year at 3- or 6-month intervals (weeks 0, 12, 26 and 52) across multiple study sites and assessed for soluble ALCAM and CD6 levels. Urine creatinine from the same urine sample was used to normalize the levels of urinary ALCAM and urinary CD6. Measured levels of serum and urine ALCAM and CD6 were then analysed against disease metrics cross-sectionally and longitudinally.
Cross-sectional analysis at baseline revealed that urinary ALCAM significantly correlated with urine protein creatinine ratio, renal SLEDAI, and the Physician Global Assessment (PGA), and negatively correlated with serum C3 and C4. Receiver operating characteristic curve analysis demonstrated that urinary ALCAM is a predictor of LN with an area under the curve (AUC) of 0.97, compared with urinary CD6 with an AUC of 0.71. Importantly, the change in urinary ALCAM over a 3-month period distinguished between non-responders and responders at week 52.
Urinary ALCAM is reflective of changes in LN and may be predictive of response status. To evaluate urinary activated leucocyte cell adhesion molecule (ALCAM) and CD6 as predictors of lupus nephritis (LN) progression or disease resolution across a 1-year study.OBJECTIVESTo evaluate urinary activated leucocyte cell adhesion molecule (ALCAM) and CD6 as predictors of lupus nephritis (LN) progression or disease resolution across a 1-year study.Serum and urine samples from biopsy proven LN subjects (n = 122) were prospectively collected over the course of a year at 3- or 6-month intervals (weeks 0, 12, 26, and 52) across multiple study sites and assessed for soluble ALCAM and CD6 levels. Urine creatinine from the same urine sample was used to normalize the levels of urinary ALCAM and urinary CD6. Measured levels of serum and urine ALCAM and CD6 were then analyzed against disease metrics cross-sectionally and longitudinally.METHODSSerum and urine samples from biopsy proven LN subjects (n = 122) were prospectively collected over the course of a year at 3- or 6-month intervals (weeks 0, 12, 26, and 52) across multiple study sites and assessed for soluble ALCAM and CD6 levels. Urine creatinine from the same urine sample was used to normalize the levels of urinary ALCAM and urinary CD6. Measured levels of serum and urine ALCAM and CD6 were then analyzed against disease metrics cross-sectionally and longitudinally.Cross-sectional analysis at baseline revealed that urinary ALCAM significantly correlated with urine protein creatinine ratio (UPCR), renal SLEDAI, and the Physician Global Assessment (PGA), and negatively correlated with serum C3 and C4. Receiver operating characteristic (ROC) curve analysis demonstrated that urinary ALCAM is a predictor of LN with an area under the curve (AUC) of 0.97, compared with urinary CD6 with an AUC of 0.71. Importantly, the change in urinary ALCAM over a 3-month period distinguished between non-responders and responders at week 52.RESULTSCross-sectional analysis at baseline revealed that urinary ALCAM significantly correlated with urine protein creatinine ratio (UPCR), renal SLEDAI, and the Physician Global Assessment (PGA), and negatively correlated with serum C3 and C4. Receiver operating characteristic (ROC) curve analysis demonstrated that urinary ALCAM is a predictor of LN with an area under the curve (AUC) of 0.97, compared with urinary CD6 with an AUC of 0.71. Importantly, the change in urinary ALCAM over a 3-month period distinguished between non-responders and responders at week 52.Urinary ALCAM is reflective of changes in LN and may be predictive of response status.CONCLUSIONUrinary ALCAM is reflective of changes in LN and may be predictive of response status. |
Author | Park, Meyeon Payan-Schober, Fernanda Suryawanshi, Hemant Chu, Dalena Utz, P J Connery, Sean Connelly, Stephen Goldman, Dan James, Judith Gupta, Rohit Kalunian, Ken Fava, Andrea Pichavant, Mina Raychaudhuri, Soumya Schwartz, Noa Arazi, Arnon Kretzler, Mattias Wofsy, David Maecker, Holden McMahon, Maureen Anolik, Jennifer Kamen, Diane Mohan, Chandra Brenner, Michael Kado, Ruba Rao, Deepak Zhang, Fan Fonseka, Chamith Waguespack, Dia Massarotti, Elena Guthridge, Joel Buyon, Jill P Davidson, Anne Hoover, Paul Hsu, Raymond Ampudia, Jeanette Putterman, Chaim Hildeman, David Slowikowski, Kamil Apruzzese, William Ng, Cherie T Tuschl, Thomas Pendergraft, William Clancy, Robert Cunningham, Melissa Der, Evan Petri, Michelle McCune, William Furie, Richard Hacohen, Nir Fung, Maple Dall’Era, Maria Berthier, Celine Buyon, Jill |
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ContentType | Journal Article |
Contributor | Park, Meyeon Payan-Schober, Fernanda Davidson, Anne Suryawanshi, Hemant Dall'Era, Maria Hoover, Paul Hsu, Raymond Utz, P J Connery, Sean Putterman, Chaim Goldman, Dan Hildeman, David James, Judith Slowikowski, Kamil Apruzzese, William Gupta, Rohit Kalunian, Ken Tuschl, Thomas Fava, Andrea Pichavant, Mina Raychaudhuri, Soumya Pendergraft, William Clancy, Robert Cunningham, Melissa Arazi, Arnon Kretzler, Mattias Wofsy, David Maecker, Holden Der, Evan McMahon, Maureen Petri, Michelle McCune, William Anolik, Jennifer Furie, Richard Hacohen, Nir Kamen, Diane Brenner, Michael Kado, Ruba Rao, Deepak Zhang, Fan Fonseka, Chamith Berthier, Celine Waguespack, Dia Buyon, Jill Massarotti, Elena Guthridge, Joel |
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Copyright | The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com. |
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Keywords | lupus nephritis ALCAM CD6 urine biomarkers |
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Snippet | To evaluate urinary activated leucocyte cell adhesion molecule (ALCAM) and CD6 as predictors of LN progression or disease resolution across a 1-year study.... To evaluate urinary activated leucocyte cell adhesion molecule (ALCAM) and CD6 as predictors of lupus nephritis (LN) progression or disease resolution across a... |
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SubjectTerms | Activated-Leukocyte Cell Adhesion Molecule - blood Activated-Leukocyte Cell Adhesion Molecule - urine Adult Antigens, CD - blood Antigens, CD - urine Antigens, Differentiation, T-Lymphocyte - urine Biomarkers - blood Biomarkers - urine Cell Adhesion Molecules, Neuronal - blood Cell Adhesion Molecules, Neuronal - urine Cross-Sectional Studies Disease Progression Female Humans Longitudinal Studies Lupus Nephritis - blood Lupus Nephritis - diagnosis Lupus Nephritis - urine Male Middle Aged Predictive Value of Tests Prospective Studies |
Title | Soluble urine activated leukocyte cell adhesion molecule is a strong predictor of lupus nephritis |
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