Evidence map›Paper›PMID 32641324›Full record

ArticleBMJ open2020

Individualised risk prediction model for new-onset, progression and regression of chronic kidney disease in a retrospective cohort of patients with type 2 diabetes under primary care in Hong Kong.

Lin Yang, Tsun Kit Chu, Jinxiao Lian, Cheuk Wai Lo, Shi Zhao, Daihai He, Jing Qin, Jun Liang

Abstract read
In one paragraph

Article in BMJ open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Trajectories of kidney function and risk of mortality.International journal of epidemiology · 2023
    Article
  6. Article
  7. Interpretable Stratification for Chronic Kidney Disease Progression Based on Time to Event Analysis.AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science · 2023
    Article
  8. Article
  9. Article
  10. Modeling Chronic Kidney Disease in Type 2 Diabetes Mellitus: A Systematic Literature Review of Models, Data Sources, and Derivation Cohorts.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2022
    Review
  11. 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

8 authors.

Lin YangSchool of Nursing, Hong Kong Polytechnic University, Hong Kong, Hong Kong l.yang@polyu.edu.hk.ORCID 0000-0002-5964-3233
Tsun Kit ChuDepartment of Family Medicine and Primary Healthcare, New Territory West Cluster, Hospital Authority, Hong Kong, Hong Kong.
Jinxiao LianSchool of Optometry, Hong Kong Polytechnic University, Hong Kong, Hong Kong.
Cheuk Wai LoDepartment of Family Medicine and Primary Healthcare, New Territory West Cluster, Hospital Authority, Hong Kong, Hong Kong.
Shi ZhaoSchool of Nursing, Hong Kong Polytechnic University, Hong Kong, Hong Kong.
Daihai HeDepartment of Applied Mathematics, Hong Kong Polytechnic University, Kowloon, Hong Kong.ORCID 0000-0003-3253-654X
Jing QinSchool of Nursing, Hong Kong Polytechnic University, Hong Kong, Hong Kong.
Jun LiangDepartment of Family Medicine and Primary Healthcare, New Territory West Cluster, Hospital Authority, Hong Kong, Hong Kong.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study is aimed to develop and validate a prediction model for multistate transitions across different stages of chronic kidney disease (CKD) in patients with type 2 diabetes mellitus under primary care.

settingWe retrieved the anonymised electronic health records of a population-based retrospective cohort in Hong Kong.

participantsA total of 26 197 patients were included in the analysis. PRIMARY AND SECONDARY OUTCOME MEASURES: The new-onset, progression and regression of CKD were defined by the transitions of four stages that were classified by combining glomerular filtration rate and urine albumin-to-creatinine ratio. We applied a multiscale multistate Poisson regression model to estimate the rates of the stage transitions by integrating the baseline demographic characteristics, routine laboratory test results and clinical data from electronic health records.

resultsDuring the mean follow-up time of 1.8 years, there were 2632 patients newly diagnosed with CKD, 1746 progressed to the next stage and 1971 regressed into an earlier stage. The models achieved the best performance in predicting the new-onset and progression with the predictors of sex, age, body mass index, systolic blood pressure, diastolic blood pressure, serum creatinine, haemoglobin A1c, total cholesterol, low-density lipoprotein, high-density lipoprotein, triglycerides and drug prescriptions.

conclusionsThis study demonstrated that individual risks of new-onset and progression of CKD can be predicted from the routine physical and laboratory test results. The individualised prediction curves developed from this study could potentially be applied to routine clinical practices, to facilitate clinical decision making, risk communications with patients and early interventions.

Indexed as

Disease ProgressionAgedAlbuminuriaCohort StudiesDiabetes Mellitus, Type 2Diabetic NephropathiesFemaleGlomerular Filtration RateHong KongHumansMaleMiddle AgedModels, StatisticalRenal Insufficiency, ChronicRetrospective Studiesdiabetic nephropathy & vascular diseaseepidemiologyprimary carestatistics & research methods

Identifiers

PMID32641324
PMCPMC7348646

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.