TY - JOUR
T1 - Comprehensive aptamer-based screening identifies a spectrum of urinary biomarkers of lupus nephritis across ethnicities
AU - Stanley, Samantha
AU - Vanarsa, Kamala
AU - Soliman, Samar
AU - Habazi, Deena
AU - Pedroza, Claudia
AU - Gidley, Gabriel
AU - Zhang, Ting
AU - Mohan, Shree
AU - Der, Evan
AU - Suryawanshi, Hemant
AU - Tuschl, Thomas
AU - Buyon, Jill
AU - Putterman, Chaim
AU - Mok, Chi Chiu
AU - Petri, Michelle
AU - Saxena, Ramesh
AU - Mohan, Chandra
N1 - Publisher Copyright: © 2020, The Author(s).
PY - 2020/5/4
Y1 - 2020/5/4
N2 - Emerging urinary biomarkers continue to show promise in evaluating lupus nephritis (LN). Here, we screen urine from active LN patients for 1129 proteins using an aptamer-based platform, followed by ELISA validation in two independent cohorts comprised of 127 inactive lupus, 107 active LN, 67 active non-renal lupus patients and 74 healthy controls, of three different ethnicities. Urine proteins that best distinguish active LN from inactive disease are ALCAM, PF-4, properdin, and VCAM-1 among African-Americans, sE-selectin, VCAM-1, BFL-1 and Hemopexin among Caucasians, and ALCAM, VCAM-1, TFPI and PF-4 among Asians. Most of these correlate significantly with disease activity indices in the respective ethnic groups, and surpass conventional metrics in identifying active LN, with better sensitivity, and negative/positive predictive values. Several elevated urinary molecules are also expressed within the kidneys in LN, based on single-cell RNAseq analysis. Longitudinal studies are warranted to assess the utility of these biomarkers in tracking lupus nephritis.
AB - Emerging urinary biomarkers continue to show promise in evaluating lupus nephritis (LN). Here, we screen urine from active LN patients for 1129 proteins using an aptamer-based platform, followed by ELISA validation in two independent cohorts comprised of 127 inactive lupus, 107 active LN, 67 active non-renal lupus patients and 74 healthy controls, of three different ethnicities. Urine proteins that best distinguish active LN from inactive disease are ALCAM, PF-4, properdin, and VCAM-1 among African-Americans, sE-selectin, VCAM-1, BFL-1 and Hemopexin among Caucasians, and ALCAM, VCAM-1, TFPI and PF-4 among Asians. Most of these correlate significantly with disease activity indices in the respective ethnic groups, and surpass conventional metrics in identifying active LN, with better sensitivity, and negative/positive predictive values. Several elevated urinary molecules are also expressed within the kidneys in LN, based on single-cell RNAseq analysis. Longitudinal studies are warranted to assess the utility of these biomarkers in tracking lupus nephritis.
UR - http://www.scopus.com/inward/record.url?scp=85084235042&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/s41467-020-15986-3
DO - https://doi.org/10.1038/s41467-020-15986-3
M3 - مقالة
C2 - 32366845
SN - 2041-1723
VL - 11
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 2197
ER -