Evidence map›Paper›PMID 34668028›Full record

ArticleCalcified tissue international2022

Clinical Prediction of High-Turnover Bone Disease After Kidney Transplantation.

Satu M Keronen, Leena A L Martola, Patrik Finne, Inari S Burton, Xiaoyu F Tong, Heikki P Kröger, Eero O Honkanen

Open access · hybridAbstract read
In one paragraph

Article in Calcified tissue international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

7 authors at 2 institutions in 1 country.

Satu M KeronenAbdominal Center, Department of Nephrology, University of Helsinki and Helsinki University Hospital, (Haartmaninkatu 4), P.O. Box 372, 00029, HUS, Finland. satu.keronen@hus.fi.ORCID http://orcid.org/0000-0002-7954-5729
Leena A L MartolaAbdominal Center, Department of Nephrology, University of Helsinki and Helsinki University Hospital, (Haartmaninkatu 4), P.O. Box 372, 00029, HUS, Finland.
Patrik FinneAbdominal Center, Department of Nephrology, University of Helsinki and Helsinki University Hospital, (Haartmaninkatu 4), P.O. Box 372, 00029, HUS, Finland.
Inari S BurtonKuopio Musculoskeletal Research Unit (KMRU), University of Eastern Finland, P.O.Box 1627, 70211, Kuopio, Finland.
Xiaoyu F TongKuopio Musculoskeletal Research Unit (KMRU), University of Eastern Finland, P.O.Box 1627, 70211, Kuopio, Finland.
Heikki P KrögerKuopio Musculoskeletal Research Unit (KMRU), University of Eastern Finland, P.O.Box 1627, 70211, Kuopio, Finland.
Eero O HonkanenAbdominal Center, Department of Nephrology, University of Helsinki and Helsinki University Hospital, (Haartmaninkatu 4), P.O. Box 372, 00029, HUS, Finland.
University of Helsinki · FIUniversity of Eastern Finland · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone histomorphometric analysis is the most accurate method for the evaluation of bone turnover, but non-invasive tools are also required. We studied whether bone biomarkers can predict high bone turnover determined by bone histomorphometry after kidney transplantation. We retrospectively evaluated the results of bone biopsy specimens obtained from kidney transplant recipients due to the clinical suspicion of high bone turnover between 2000 and 2015. Bone biomarkers were acquired concurrently. Of 813 kidney transplant recipients, 154 (19%) biopsies were taken at a median of 28 (interquartile range, 18-70) months after engraftment. Of 114 patients included in the statistical analysis, 80 (70%) presented with high bone turnover. Normal or low bone turnover was detected in 34 patients (30%). For discriminating high bone turnover from non-high, alkaline phosphatase, parathyroid hormone, and ionized calcium had the areas under the receiver operating characteristic curve (AUCs) of 0.704, 0.661, and 0.619, respectively. The combination of these markers performed better with an AUC of 0.775. The positive predictive value for high turnover at a predicted probability cutoff of 90% was 95% while the negative predictive value was 35%. This study concurs with previous observations that hyperparathyroidism with or without hypercalcemia does not necessarily imply high bone turnover in kidney transplant recipients. The prediction of high bone turnover can be improved by considering alkaline phosphatase levels, as presented in the logistic regression model. If bone biopsy is not readily available, this model may serve as clinically available tool in recognizing high turnover after engraftment.

Indexed as

Bone DiseasesChronic Kidney Disease-Mineral and Bone DisorderKidney TransplantationAlkaline PhosphataseBiomarkersBone RemodelingFemaleHumansMaleParathyroid HormoneRetrospective StudiesAlkaline PhosphataseBiomarkersParathyroid HormoneCKD-MBDHyperparathyroidismKidney transplantation

Identifiers

PMID34668028
PMCPMC8860959
OpenAlexW3206666684

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Registered trials

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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.