Evidence map›Paper›PMID 41013586›Full record

ArticleLipids in health and disease2025

The association between dyslipidemia and intervertebral disc degeneration: a prospective cohort study based on the UK biobank.

Wangim Choi, Bo Gao, Jianan Chen, Tongzhou Liang, Wenjun Hu, Zaoqiang Zhang, Nianchun Liao, Huihong Shi, Song Liu, Yanbo Chen and 6 more

Abstract read
In one paragraph

Article in Lipids in health and disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Wangim Choi *Department of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Bo Gao *Department of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Jianan Chen *Department of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Tongzhou LiangThe Brain Cognition and Brain Disease Institute, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Wenjun HuDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Zaoqiang ZhangDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Nianchun LiaoDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Huihong ShiDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Song LiuDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Yanbo ChenDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Youxi LinDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Zhihuai DengDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Dongsheng HuangDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China.
Xianjian QiuDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China. qiuxj6@mail.sysu.edu.cn.
Peijie ShiDepartment of Endocrinology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. shipj5@mail.sysu.edu.cn.
Wenjie GaoDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Yingfeng Road No. 33, Guangzhou, 510130, China. gaowj7@mail.sysu.edu.cn.

Funding

Guangdong Basic and Applied Basic Research Foundation No.2022A1515012459, No.2023A1515012689Science and Technology Program of Guangzhou, China No. 2024A04J4684, No. 2025A03J41881The National Natural Science Foundation of China No.82072473, No.82202653The National Natural Science Foundation of China No.82103083The National Natural Science Foundation of China No.82302737The National Natural Science Foundation of China No.82372432
6 · The paper itself

Abstract

backgroundIntervertebral disc degeneration (IDD) is a progressive and debilitating condition associated with aging, inflammation, and metabolic disorders. Although dyslipidemia has been implicated in IDD pathogenesis, large-scale prospective evidence remains limited. This study aimed to investigate the observational association between serum lipid traits and IDD risk using data from the UK Biobank.

methodsA prospective cohort study was conducted among 298,226 participants (aged 37-73 years; 54.2% female, n = 161,770) without IDD at baseline. Serum lipid levels, including total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), apolipoprotein A (Apo A) and apolipoprotein B (Apo B), were measured at enrollment. IDD cases were identified via ICD-10 codes. Cox proportional hazards models, adjusted for demographic, lifestyle, and comorbid factors, were used to assess associations between lipid levels and IDD risk. Restricted cubic spline analyses explored potential nonlinear relationships, and subgroup analyses examined effect modifications.

resultsOver a median follow-up of 12 years, 8,745 participants developed IDD. Higher levels of TC (> 5.64 mmol/L) and TG (> 1.51 mmol/L) were significantly associated with increased IDD risk. Compared with the lowest quintile, the highest TC quintile was associated with a 10.2% increased risk (HR = 1.102; 95% CI: 1.029-1.181; P = 0.006), and the highest TG quintile with an 11.3% increased risk (HR = 1.113; 95% CI: 1.036-1.195; P = 0.003), after full adjustment. No significant associations were found for LDL-C, HDL-C, Apo A, or Apo B after multivariable adjustment (all P > 0.05). Subgroup analyses revealed significant interactions between age and TG (P for interaction < 0.05), with younger participants (≤ 60 years) showing a stronger association. Additionally, age modified the effects of HDL-C and Apo A. These findings provide observational evidence that lipid traits may be differentially associated with IDD risk across age groups.

conclusionsHigher TC and TG levels were associated with increased IDD risk. These findings provide observational evidence for the role of lipid levels in stratifying IDD risk. Routine lipid screening may help identify high-risk individuals and guide early prevention strategies.

Indexed as

DyslipidemiasIntervertebral Disc DegenerationAdultAgedBiological Specimen BanksCholesterol, HDLCholesterol, LDLFemaleHumansMaleMiddle AgedProportional Hazards ModelsProspective StudiesRisk FactorsTriglyceridesUK BiobankCholesterol, HDLCholesterol, LDLTriglyceridesDyslipidemiaIntervertebral disc degenerationSerum lipidsTotal cholesterolTriglyceridesUK biobank

Identifiers

PMID41013586
PMCPMC12465384

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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.