Evidence map›Paper›PMID 28416944›Full record

ArticleGenomics & informatics2017

Evaluation of Digital PCR as a Technique for Monitoring Acute Rejection in Kidney Transplantation.

Hyeseon Lee, Young-Mi Park, Yu-Mee We, Duck Jong Han, Jung-Woo Seo, Haena Moon, Yu-Ho Lee, Yang-Gyun Kim, Ju-Young Moon, Sang-Ho Lee and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Genomics & informatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Advances in Detection of Kidney Transplant Injury.Molecular diagnosis & therapy · 2019
    Review
  17. Article
  18. Article
  19. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Hyeseon LeeAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul 05505, Korea.
Young-Mi ParkAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul 05505, Korea.
Yu-Mee WeAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul 05505, Korea.
Duck Jong HanDepartment of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Jung-Woo SeoDepartment of Internal Medicine, Kyung Hee University Hospital at Gangdong, Seoul 05278, Korea.
Haena MoonDepartment of Internal Medicine, Kyung Hee University Hospital at Gangdong, Seoul 05278, Korea.
Yu-Ho LeeDepartment of Internal Medicine, Kyung Hee University Hospital at Gangdong, Seoul 05278, Korea.
Yang-Gyun KimDepartment of Internal Medicine, Kyung Hee University Hospital at Gangdong, Seoul 05278, Korea.
Ju-Young MoonDepartment of Internal Medicine, Kyung Hee University Hospital at Gangdong, Seoul 05278, Korea.
Sang-Ho LeeDepartment of Internal Medicine, Kyung Hee University Hospital at Gangdong, Seoul 05278, Korea.
Jong-Keuk LeeAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul 05505, Korea.
Ulsan College · KRUniversity of Ulsan · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early detection and proper management of kidney rejection are crucial for the long-term health of a transplant recipient. Recipients are normally monitored by serum creatinine measurement and sometimes with graft biopsies. Donor-derived cell-free deoxyribonucleic acid (cfDNA) in the recipient's plasma and/or urine may be a better indicator of acute rejection. We evaluated digital PCR (dPCR) as a system for monitoring graft status using single nucleotide polymorphism (SNP)-based detection of donor DNA in plasma or urine. We compared the detection abilities of the QX200, RainDrop, and QuantStudio 3D dPCR systems. The QX200 was the most accurate and sensitive. Plasma and/or urine samples were isolated from 34 kidney recipients at multiple time points after transplantation, and analyzed by dPCR using the QX200. We found that donor DNA was almost undetectable in plasma DNA samples, whereas a high percentage of donor DNA was measured in urine DNA samples, indicating that urine is a good source of cfDNA for patient monitoring. We found that at least 24% of the highly polymorphic SNPs used to identify individuals could also identify donor cfDNA in transplant patient samples. Our results further showed that autosomal, sex-specific, and mitochondrial SNPs were suitable markers for identifying donor cfDNA. Finally, we found that donor-derived cfDNA measurement by dPCR was not sufficient to predict a patient's clinical condition. Our results indicate that donor-derived cfDNA is not an accurate predictor of kidney status in kidney transplant patients.

Indexed as

acute rejectioncell-free DNAdigital PCRkidney transplantation

Identifiers

PMID28416944
PMCPMC5389945
OpenAlexW2607358843

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.