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Prospective study on immune function in renal transplant patients during perioperative period: A prospective cohort study

Publication ,  Journal Article
Li, H; Xian, Y; Ma, M; Zhang, K; Hong, L
Published in: Medicine
October 18, 2024

Delayed graft function (DGF) is a type of acute renal failure that is closely linked to the immune system. The objective of this study is to investigate immune trends during the perioperative period of renal transplantation and compare the variations between patients with DGF and immediate graft function (IGF). A total of 48 kidney transplant patients were enrolled. Parameters including stimulated adenosine triphosphatase concentrations (sATP), nonstimulated ATP concentrations, white blood cells, and lymphocyte count were assessed. Patients were categorized into the DGF or IGF group. Clinical information and changes in immune markers were compared. Receiver operating characteristic analysis was performed to determine the sensitivity and specificity in predicting DGF. Additionally, separate immune function analyses were conducted for the 3 infection cases. Following induction immunosuppressive therapy, white blood cells, and neutrophil count showed a significant initial increase followed by a gradual decline. Lymphocyte count, nonstimulated ATP concentrations, and sATP exhibited an initial significant decrease followed by a slow recovery. Immune markers between the DGF and IGF groups were significantly different at day 4 after renal transplantation. Only sATP levels at day 4 after renal transplantation (area under the curve = 0.731, sensitivity = 0.864, specificity = 0.684) demonstrated predictive value for DGF occurrence. Among the 3 infection cases, 2 cases exhibited persistently decreased sATP levels and died within the first month and 6 months, while the remaining case showed a recovery of sATP levels at D9 and survived. These findings indicate that sATP level can potentially serve as a biomarker reflecting the impact of immunosuppressants. Poor recovery of sATP may be associated with DGF, infection, or even mortality.

Duke Scholars

Published In

Medicine

DOI

EISSN

1536-5964

Publication Date

October 18, 2024

Volume

103

Issue

42

Start / End Page

e40070 / e40070

Publisher

Ovid Technologies (Wolters Kluwer Health)

Related Subject Headings

  • Arthritis & Rheumatology
  • 3202 Clinical sciences
  • 32 Biomedical and clinical sciences
  • 1103 Clinical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Li, H., Xian, Y., Ma, M., Zhang, K., & Hong, L. (2024). Prospective study on immune function in renal transplant patients during perioperative period: A prospective cohort study. Medicine, 103(42), e40070–e40070. https://doi.org/10.1097/md.0000000000040070
Li, Heng, Ying Xian, Maolin Ma, Kouxing Zhang, and Liangqing Hong. “Prospective study on immune function in renal transplant patients during perioperative period: A prospective cohort study.” Medicine 103, no. 42 (October 18, 2024): e40070–e40070. https://doi.org/10.1097/md.0000000000040070.
Li H, Xian Y, Ma M, Zhang K, Hong L. Prospective study on immune function in renal transplant patients during perioperative period: A prospective cohort study. Medicine. 2024 Oct 18;103(42):e40070–e40070.
Li, Heng, et al. “Prospective study on immune function in renal transplant patients during perioperative period: A prospective cohort study.” Medicine, vol. 103, no. 42, Ovid Technologies (Wolters Kluwer Health), Oct. 2024, pp. e40070–e40070. Crossref, doi:10.1097/md.0000000000040070.
Li H, Xian Y, Ma M, Zhang K, Hong L. Prospective study on immune function in renal transplant patients during perioperative period: A prospective cohort study. Medicine. Ovid Technologies (Wolters Kluwer Health); 2024 Oct 18;103(42):e40070–e40070.

Published In

Medicine

DOI

EISSN

1536-5964

Publication Date

October 18, 2024

Volume

103

Issue

42

Start / End Page

e40070 / e40070

Publisher

Ovid Technologies (Wolters Kluwer Health)

Related Subject Headings

  • Arthritis & Rheumatology
  • 3202 Clinical sciences
  • 32 Biomedical and clinical sciences
  • 1103 Clinical Sciences