Evidence map›Paper›PMID 38835081›Full record

ArticleLipids in health and disease2024

High remnant-cholesterol levels increase the risk for end-stage renal disease: a nationwide, population-based, cohort study.

Han Na Jung, Ji Hye Huh, Eun Roh, Kyung-Do Han, Jun Goo Kang, Seong Jin Lee, Sung-Hee Ihm

Abstract read
In one paragraph

Article in Lipids in health and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
–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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  6. Observational
  7. Review
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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.

Han Na Jung *Department of Internal Medicine, Hallym University College of Medicine, 1, Hallymdaehak-Gil, Chuncheon-Si, Gangwon-Do, 24252, Republic of Korea.
Ji Hye Huh *Department of Internal Medicine, Hallym University College of Medicine, 1, Hallymdaehak-Gil, Chuncheon-Si, Gangwon-Do, 24252, Republic of Korea.
Eun RohDepartment of Internal Medicine, Hallym University College of Medicine, 1, Hallymdaehak-Gil, Chuncheon-Si, Gangwon-Do, 24252, Republic of Korea.
Kyung-Do HanDepartment of Statistics and Actuarial Science, College of Natural Sciences, Soongsil University, 369, Sangdo-Ro, Dongjak-Gu, Seoul, 06978, Republic of Korea. hkd917@naver.com.
Jun Goo KangDepartment of Internal Medicine, Hallym University College of Medicine, 1, Hallymdaehak-Gil, Chuncheon-Si, Gangwon-Do, 24252, Republic of Korea. kjg0804@empas.com.
Seong Jin LeeDepartment of Internal Medicine, Hallym University College of Medicine, 1, Hallymdaehak-Gil, Chuncheon-Si, Gangwon-Do, 24252, Republic of Korea.
Sung-Hee IhmDepartment of Internal Medicine, Hallym University College of Medicine, 1, Hallymdaehak-Gil, Chuncheon-Si, Gangwon-Do, 24252, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe effect of remnant-cholesterol (remnant-C) on incident end-stage renal disease (ESRD) has not been studied longitudinally. This retrospective cohort study evaluated the association between remnant-C and the development of ESRD in a nationwide Korean cohort.

methodsParticipants in a National Health Insurance Service health examination (n = 3,856,985) were followed up until the onset of ESRD. The median duration of follow-up was 10.3 years. The Martin-Hopkins equation was used to determine low-density lipoprotein cholesterol (LDL-C) levels from directly measured triglyceride, high-density lipoprotein cholesterol (HDL-C), and total cholesterol levels. Remnant-C levels were determined by subtracting HDL-C and LDL-C from total cholesterol. The risk for incident ESRD was calculated for each quartile of remnant-C, adjusting for conventional risk factors such as baseline renal function, comorbidities, and total cholesterol levels.

resultsESRD developed in 11,073 (0.29%) participants. The risk for ESRD exhibited a gradual increase according to higher levels of remnant-C, with a 61% increased risk in the highest quartile than in the lowest (hazard ratio [HR] 1.61 [95% confidence interval (CI) 1.50-1.72]). The elevated risk for ESRD in the highest quartile versus the lowest quartile was more prominent in younger than in older subjects (20-29 years, HR 4.07 [95% CI 2.85-5.83]; 30-39 years, HR 2.39 [95% CI 1.83-3.13]; ≥ 70 years, HR 1.32 [95% CI 1.16-1.51]). In addition, the increased risk for ESRD related to higher remnant-C levels was greater in females than in males.

conclusionsIndependent of conventional risk factors, remnant-C levels were positively associated with incident ESRD, particularly in younger populations and adult females. Reducing remnant-C levels may be a novel preventive strategy against ESRD.

Indexed as

CholesterolKidney Failure, ChronicTriglyceridesAdultAgedCholesterol, HDLCholesterol, LDLFemaleHumansMaleMiddle AgedProportional Hazards ModelsRepublic of KoreaRetrospective StudiesRisk FactorsCholesterolCholesterol, HDLCholesterol, LDLTriglyceridesEnd-stage renal diseaseKorean national health insurance serviceLipoproteinRemnant-cholesterolTriglyceride

Identifiers

PMID38835081
PMCPMC11149355

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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.