Evidence map›Paper›PMID 36442482›Full record

Trial reportThe Lancet. Child & adolescent health2023

Intensive compared with less intensive blood pressure control to prevent adverse cardiac remodelling in children with chronic kidney disease (HOT-KID): a parallel-group, open-label, multicentre, randomised, controlled trial.

Manish D Sinha, Haotian Gu, Abdel Douiri, Janette Cansick, Eric Finlay, Rodney Gilbert, Larissa Kerecuk, Andrew Lunn, Heather Maxwell, Henry Morgan and 9 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in The Lancet. Child & adolescent health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07768865 (Arterial Stiffness in Children and Young People With Hypertension and Chronic Kidney Disease), which is not on this map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% 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.

NCT07768865 recruitingnot on this mapstarted 2026, after this paper: background citation

Arterial Stiffness in Children and Young People With Hypertension and Chronic Kidney Disease

TypeobservationalSponsorKing's College LondonRan2026 to 2028Enrolled200ConditionsChronic Kidney Disease, Hypertension
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Impact of intensive blood pressure control on kidney outcomes.Current opinion in nephrology and hypertension · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Role of hypertension in progression of pediatric CKD.Pediatric nephrology (Berlin, Germany) · 2023
    Review
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 1 country.

Manish D SinhaBritish Heart Foundation Centre, King's College London, London, UK; Department of Paediatric Nephrology, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK. Electronic address: manish.sinha@nhs.net.
Haotian GuBritish Heart Foundation Centre, King's College London, London, UK.
Abdel DouiriDepartment of Medical Statistics, School of Population Health and Environmental Sciences, King's College London, London, UK.
Janette CansickDepartment of Paediatrics, Medway Maritime Hospital, Medway, UK.
Eric FinlayDepartment of Paediatric Nephrology, Leeds General Infirmary, Leeds, UK.
Rodney GilbertDepartment of Paediatric Nephrology, Southampton General Hospital, Southampton, UK.
Larissa KerecukDepartment of Paediatric Nephrology, Birmingham Children's Hospital, Birmingham, UK.
Andrew LunnDepartment of Paediatric Nephrology, Nottingham University Hospital NHS Trust, Nottingham, UK.
Heather MaxwellDepartment of Paediatric Nephrology, Glasgow Royal Infirmary, Glasgow, UK.
Henry MorganDepartment of Paediatric Nephrology, Alder Hey Children's Hospital, Liverpool, UK.
Mohan ShenoyDepartment of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester, UK.
Rukshana ShroffDepartment of Paediatric Nephrology, UCL Great Ormond Street Hospital and Institute of Child Health, London, UK.
Pushpa SubramaniamDepartment of Paediatrics, St Georges Hospital, London, UK.
Jane TizardDepartment of Paediatric Nephrology, Bristol Royal Hospital for Children, Bristol, UK.
Yincent TseDepartment of Paediatric Nephrology, Great North Children's Hospital, Newcastle upon Tyne, UK.
Reza RezaviDivision of Imaging Sciences, King's College London, London, UK.
John M SimpsonBritish Heart Foundation Centre, King's College London, London, UK; Department of Paediatric Cardiology, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Phil J ChowienczykBritish Heart Foundation Centre, King's College London, London, UK.
HOT-KID study
British Heart Foundation · GBBirmingham Children's Hospital · GBBristol Royal Hospital for Children · GBGreat North Children's Hospital · GBKing's College London · GBRoyal Manchester Children's Hospital · GBSouthampton General Hospital · GBUniversity of Liverpool · GB

Funding

British Heart Foundation PG/11/90/28994British Heart Foundation SP/14/8/31352Department of HealthMedical Research Council MR/M016560/1
6 · The paper itself

Abstract

backgroundOptimal target blood pressure to reduce adverse cardiac remodelling in children with chronic kidney disease is uncertain. We hypothesised that lower blood pressure would reduce adverse cardiac remodelling.

methodsHOT-KID, a parallel-group, open-label, multicentre, randomised, controlled trial, was done in 14 clinical centres across England and Scotland. We included children aged 2-15 years with stage 1-4 chronic kidney disease-ie, an estimated glomerular filtration rate (eGFR) higher than 15 mL/min per 1·73 m

findingsBetween Oct 30, 2012, and Jan 5, 2017, 64 participants were randomly assigned to the intensive treatment group and 60 to the standard treatment group (median age of participants was 10·0 years [IQR 6·8-12·6], 69 [56%] were male and 107 [86%] were of white ethnicity). Median follow-up was 38·7 months (IQR 28·1-52·2). Blood pressure was lower in the intensive treatment group compared with standard treatment group (mean systolic pressure lower by 4 mm Hg, p=0·0012) but in both groups was close to the 50th percentile. The mean annual reduction in LVMI was similar for intensive and standard treatments (-1·9 g/m

interpretationThese results suggest that cardiac remodelling in children with chronic kidney disease is related to blood pressure control and that a target office systolic blood pressure at the 50th percentile is close to the optimal target for preventing increased left ventricular mass.

fundingBritish Heart Foundation.

Indexed as

Angiotensin-Converting Enzyme InhibitorsRenal Insufficiency, ChronicAngiotensin Receptor AntagonistsBlood PressureChildFemaleHumansMaleVentricular RemodelingAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor Antagonists

Identifiers

PMID36442482
PMCPMC10202819
OpenAlexW4310081041

What OpenQuestion holds

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LicenceCC BY
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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.