ArticleFrontiers in immunology2025
Construction and validation of a risk prediction model for hyperamylasemia after kidney transplantation.
Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Kidney transplantation (KT) is the preferred treatment for patients with end-stage renal disease (ESRD); however, postoperative hyperamylasemia (HA) remains common and has been associated with acute rejection (AR), infection, and impaired graft function. Early identification of HA risk factors is essential to improve outcomes of kidney transplant recipients (KTR). This study aimed to develop and internally validate a novel nomogram for predicting the risk of HA after KT, thereby supporting personalized monitoring, prevention and intervention strategies. Methods: We retrospectively analyzed KTR treated at the Transplant Medicine Institution of the Second Affiliated Hospital of Guangxi Medical University from July 2021 to June 2022. Based on admission dates, patients were assigned to a training cohort (n=243, July 2021 to March 2022) and a validation cohort (n=107, April 2022 to June 2022). In the training cohort, risk factors of HA were identified using logistic regression, Lasso regression and clinical consideration. Subsequently, a nomogram was developed to predict HA risk in patients who underwent KT based on the identified variables. Model performance was evaluated using receiver operating characteristic (ROC) curves, calibration plots, and decision curve analysis (DCA). Results: A total of 350 KTR and their corresponding 182 donors were enrolled in this study. The nomogram incorporated six predictive factors: recipient preoperative white blood cell (WBC) count, induction, tacrolimus (FK506) trough concentration, AR, donor age, and donor total bilirubin (TBIL) level according to results of logistic regression, Lasso regression and clinical consideration. The nomogram showed moderate predictive performance, with an area under the ROC curve (AUC) of 0.730 (Youden index = 0.683) in the training cohort and 0.731 (Youden index = 0.767) in the validation cohort. Furthermore, calibration plots indicated close agreement between predicted and actual outcomes, and DCA confirmed net clinical benefit across a range of threshold probabilities. Conclusions: A novel nomogram was established to predict HA after KT, which may support early risk stratification and personalized management of KTR. External multicenter validation is needed before clinical implementation.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.