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血清IL-6、CysC、T3水平和影像学总负荷评分与脑小血管病患者认知障碍的相关性分析 Correlation Analysis of Serum IL-6, CysC, T3 Levels, and Total Imaging Burden Score with Cognitive Impairment in Patients with Cerebral Small Vessel Disease

2025· article· zh· W6891651941 on OpenAlexaboutno aff

Bibliographic record

VenueDOAJ (DOAJ: Directory of Open Access Journals) · 2025
Typearticle
Languagezh
FieldNeuroscience
TopicNeurological Disease Mechanisms and Treatments
Canadian institutionsnot available
Fundersnot available
KeywordsCognitive impairmentLogistic regressionCognitionDiseaseCorrelationCystatin CMultivariate analysisMontreal Cognitive Assessment

Abstract

fetched live from OpenAlex

目的 探讨血清IL-6、胱抑素C(cystatin C,CysC)、三碘甲状腺原氨酸(triiodothyronine,T3)水平以及影像学总负荷评分与脑小血管病(cerebral small vessel disease,CSVD)患者认知障碍的相关性。 方法 回顾性连续纳入2021年1月—2023年1月就诊的CSVD患者,根据住院期间MoCA评分分为认知障碍组和认知功能正常组。收集患者的人口学信息、既往病史、实验室及影像学检查等数据。分析血清IL-6、CysC、T3水平以及影像学总负荷评分对CSVD患者认知障碍的预测价值。 结果 共纳入CSVD患者142例,其中认知障碍组61例(43.0%),认知功能正常组81例(57.0%)。与认知功能正常组相比,认知障碍组IL-6、Hcy、CysC水平较高,T3水平较低,影像学总负荷中度和重度的比例较高,差异有统计学意义。多因素logistic回归分析显示,血清IL-6水平升高(OR 1.070,95%CI 1.039~1.103,P<0.001)、CysC水平升高(OR 2.117,95%CI 1.027~5.500,P=0.004)、T3水平降低(OR 2.314,95%CI 1.361~3.935,P=0.003)以及影像学总负荷中度(OR 1.017,95%CI 1.002~1.032,P=0.029)和重度(OR 9.032,95%CI 6.076~18.012,P<0.001)是CSVD患者发生认知障碍的独立相关因素。血清IL-6、CysC、T3水平和重度影像学总负荷预测认知障碍的AUC分别为0.888、0.812、0.918、0.889,最佳截断值分别为2.010 pg/mL、0.982 ng/L、1.302 nmol/L和3.6分。 结论 血清IL-6和CysC水平升高、T3水平降低以及中、重度影像学总负荷与CSVD患者发生认知障碍有相关性,可作为识别CSVD患者认知障碍的依据。 Abstract: Objective To investigate the correlation between serum IL-6, cystatin C (CysC), triiodothyronine (T3) levels, and total imaging burden score with cognitive impairment in patients with cerebral small vessel disease (CSVD). Methods CSVD patients treated from January 2021 to January 2023 were retrospectively included and subsequently divided into the cognitive impairment group and the normal cognitive function group based on their MoCA scores during hospitalization. The demographic information, past medical history, and laboratory and imaging data of the patients were collected. The predictive value of serum IL-6, CysC, T3, and total imaging burden score for cognitive impairment in CSVD patients was analyzed. Results A total of 142 patients with CSVD were included, with 61 cases (43.0%) in the cognitive impairment group and 81 cases (57.0%) in the normal cognitive function group. The levels of IL-6, Hcy, and CysC were higher, the level of T3 was lower, and the proportion of moderate to severe total imaging burden was higher in the cognitive impairment group, with statistically significant differences. Multivariate logistic regression analysis showed that elevated serum IL-6 levels (OR 1.070, 95%CI 1.039-1.103, P<0.001), elevated CysC levels (OR 2.117, 95%CI 1.027-5.500, P=0.004), decreased T3 levels (OR 2.314, 95%CI 1.361-3.935, P=0.003), and moderate (OR 1.017, 95%CI 1.002-1.032, P=0.029) and severe (OR 9.032, 95%CI 6.076-18.012, P<0.001) total imaging burden were risk factors for cognitive impairment in patients with CSVD. The AUC values for predicting cognitive impairment of serum IL-6, CysC, T3, and severe total imaging burden were 0.888, 0.812, 0.918, and 0.889, respectively, with the optimal cutoff values of 2.010 pg/mL, 0.982 ng/L, 1.302 nmol/L, and 3.6 points. Conclusions Elevated serum IL-6 and CysC levels, decreased T3 levels, and severe total imaging burden are correlated with cognitive impairment in patients with CSVD and can serve as a basis for identifying cognitive impairment in CSVD patients.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.099
GPT teacher head0.431
Teacher spread0.332 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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