Evidence map›Paper›PMID 32634148›Full record

Observational studyPloS one2020

Effect of kidney donation on bone mineral metabolism.

Thomas F Hiemstra, Jane C Smith, Kenneth Lim, Dihua Xu, Shreya Kulkarni, J Andrew Bradley, Kaido Paapstel, Inez Schoenmakers, John R Bradley, Laurie Tomlinson and 2 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

12 authors at 5 institutions in 3 countries.

Thomas F HiemstraCambridge Clinical Trials Unit, University of Cambridge, Cambridge, United Kingdom.
Jane C SmithDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
Kenneth LimDivision of Nephrology, Indiana University School of Medicine, Indianapolis, IN, United States of America.ORCID 0000-0001-7178-2183
Dihua XuDivision of Nephrology, Indiana University School of Medicine, Indianapolis, IN, United States of America.
Shreya KulkarniDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
J Andrew BradleyDepartment of Medicine and Surgery, University of Cambridge, Cambridge, United Kingdom.
Kaido PaapstelEndothelial Centre, University of Tartu, Tartu, Estonia.
Inez SchoenmakersSchool of Medicine, University of East Anglia, Norwich, United Kingdom.
John R BradleyDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
Laurie TomlinsonLondon School of Hygiene and Tropical Medicine, London, United Kingdom.
Carmel M McEnieryDepartment of Medicine, University of Cambridge, Cambridge, United Kingdom.
Ian B WilkinsonCambridge Clinical Trials Unit, University of Cambridge, Cambridge, United Kingdom.
University of Cambridge · GBIndiana University School of MedicineLondon School of Hygiene & Tropical Medicine · GBUniversity of East Anglia · GBUniversity of Tartu · EE

Funding

Dissecting the role of soluble α-Klotho in cardiovascular agingK23DK115683 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI LIM, KENNETH · 2018 to 2022
$912k
British Heart FoundationDepartment of Health 14/49/127Department of Health 16/167/120NIDDK NIH HHS K23 DK115683
6 · The paper itself

Abstract

Kidney donation results in reductions in kidney function and lasting perturbations in phosphate homeostasis, which may lead to adverse cardiovascular sequelae. However, the acute effects of kidney donation on bone mineral parameters including regulators of calcium and phosphate metabolism are unknown. We conducted a prospective observational controlled study to determine the acute effects of kidney donation on mineral metabolism and skeletal health. Biochemical endpoints were determined before and after donation on days 1, 2 and 3, 6 weeks and 12 months in donors and at baseline, 6 weeks and 12 months in controls. Baseline characteristic of donors (n = 34) and controls (n = 34) were similar: age (53±10 vs 50±14 years, p = 0.33), BMI (26.3±2.89 vs 25.9±3.65, p = 0.59), systolic BP (128±13 vs 130±6 mmHg, p = 0.59), diastolic BP (80±9 vs 81±9 mmHg, p = 0.68) and baseline GFR (84.4±20.2 vs 83.6±25.2 ml/min/1.73m2, p = 0.89). eGFR reduced from 84.4±20.2 to 52.3±17.5 ml/min/1.73m2 (p<0.001) by day 1 with incomplete recovery by 12 months (67.7±22.6; p = 0.002). Phosphate increased by day 1 (1.1(0.9-1.2) to 1.3(1.1-1.4) mmol/L, p <0.001) but declined to 0.8(0.8-1.0) mmol/L (p<0.001) before normalizing by 6 weeks. Calcium declined on day 1 (p = 0.003) but recovered at 6 weeks or 12 months. PTH and FGF-23 remained unchanged, but α-Klotho reduced by day 1 (p = 0.001) and remained low at 6 weeks (p = 0.02) and 1 year (p = 0.04). In this study, we conclude that kidney donation results in acute disturbances in mineral metabolism characterised by a reduced phosphate and circulating α-Klotho concentration without acute changes in the phosphaturic hormones FGF23 and PTH.

Indexed as

Bone DensityKidney TransplantationTissue DonorsAdultCase-Control StudiesFemaleFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseHumansKlotho ProteinsMaleMiddle AgedMineralsParathyroid HormonePhosphatesFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseKlotho ProteinsMineralsParathyroid HormonePhosphates

Identifiers

PMID32634148
PMCPMC7340316
OpenAlexW3040931645

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.