Plasma monocyte chemotactic protein-1 levels at 24 hours are a biomarker of primary graft dysfunction after lung transplantation.
Plasma monocyte chemotactic protein-1 levels at 24 hours are a biomarker of primary graft dysfunction after lung transplantation.
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DOI:
10.1016/j.trsl.2012.08.003
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发表时间:
2012-12
期刊:
影响因子:
--
通讯作者:
Ware LB
中科院分区:
文献类型:
--
作者:
Shah RJ;Diamond JM;Lederer DJ;Arcasoy SM;Cantu EM;Demissie EJ;Kawut SM;Kohl B;Lee JC;Sonett J;Christie JD;Ware LB
MCP-1, also known as CCL2, is a monocyte-attracting chemokine produced in lung epithelial cells. We previously reported an association of increased levels of plasma MCP-1 with primary graft dysfunction (PGD) after lung transplantation in a nested case control study of extreme phenotypes using a multiplex platform. In this study, we sought to evaluate the relationship between plasma MCP-1 levels as a biomarker across the full spectrum of PGD. We performed a prospective cohort study of 108 lung transplant recipients within the Lung Transplant Outcomes Group cohort. Plasma MCP-1 levels were measured pre-transplantation, 6 and 24 hours after transplantation. The primary outcome was development of grade 3 PGD within 72 hours of transplant, with secondary analyses at the 72- hour timepoint. Multivariable logistic regression was used to evaluate confounding. 30 subjects (28%) developed PGD. Median MCP-1 measured at 24 hours post transplant was elevated in subjects with PGD (167.95 vs. 103.5 pg/mL p=0.04). MCP-1 levels at 24 hours were associated with increased odds of grade 3 PGD after lung transplantation (OR for each 100 pg/mL 1.24, 95% CI 1.00, 1.53), and with grade 3 PGD present at the 72-hour timepoint (OR for each 100 pg/mL 1.57, 95% CI 1.18, 2.08), independent of confounding variables in multivariable analyses. MCP-1 levels measured pre-operatively and 6 hours after transplant were not significantly associated with PGD. Persistent elevations in MCP-1 levels at 24 hours are a biomarker of grade 3 PGD post-transplantation. Monocyte chemotaxis may play a role in the pathogenesis of PGD.
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影响因子:
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作者:
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通讯作者:
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DOI:
10.1164/rccm.200409-1243oc
发表时间:
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10.1164/rccm.200901-0118oc
发表时间:
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DOI:
10.1097/01.asn.0000059339.14780.e4
发表时间:
2003-04-01
影响因子:
13.6
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通讯作者:
Yokoyama, H
影响因子:
8.8
作者:
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通讯作者:
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