Zhiyu Gu , Rui Zhang , Weihong Chang , Hongxuan Fan , Zixuan Dou , Peng Liu , Aman Liu , Boda Zhou
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The exposures are eGFR<sub>Cystatin C</sub> & eGFR<sub>diff</sub>, outcome is self reported heart failure. Weighted multivariable-adjusted logistic regression and Kaplan-Meier survival analysis was used in corhort study. Inverse variance weighted (IVW) was applied in MR study.</div></div><div><h3>Results</h3><div>The cohort study included 2155 participants. Importantly, we simplified eGFR<sub>diff</sub> classification into ≥0 and < 0, and found that eGFR<sub>diff</sub>≥0 was associated with 52 % reduction of HF risk (OR 0.48, [95 % CI, 0.29–0.80], p = 0.005). We also found that 1 ml/min/1.73 m<sup>2</sup> of eGFR<sub>Cystatin C</sub> had a significant negative association with HF after adjusting for covariates. Interestingly, we showed a non-linear association between eGFR<sub>Cystatin C</sub> and HF, eGFR<sub>diff</sub> and HF. In participants without know HF, during a median follow-up of 17.3 years, those in the low eGFR<sub>Cystatin C</sub> or low eGFR<sub>diff</sub> groups showed significantly poorer survival. Moreover, MR analysis found genetic predisposition to cystatin C was significantly associated with an increased risk of HF.</div></div><div><h3>Conclusion</h3><div>Both decreased eGFR<sub>Cystatin C</sub> and eGFR<sub>diff</sub> levels were associated with heart failure and poor survival, but the latter seems more obvious.</div></div>","PeriodicalId":29726,"journal":{"name":"International Journal of Cardiology Cardiovascular Risk and Prevention","volume":"23 ","pages":"Article 200337"},"PeriodicalIF":1.9000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"eGFRCystatin C, difference between eGFRCystatin C and eGFRCre and heart failure: Insight from the NHANES 2001–2002 and Mendelian randomization analysis\",\"authors\":\"Zhiyu Gu , Rui Zhang , Weihong Chang , Hongxuan Fan , Zixuan Dou , Peng Liu , Aman Liu , Boda Zhou\",\"doi\":\"10.1016/j.ijcrp.2024.200337\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aim</h3><div>Estimated glomerular filtration rate (eGFR) derived from Cystatin C (eGFR<sub>Cystatin C</sub>), and the difference between Cystatin C and creatinine based eGFR (eGFR<sub>diff</sub>) has been suggested to be associated with cardiovascular disease. However, the association between eGFR<sub>Cystatin C</sub>,eGFR<sub>diff</sub> and heart failure (HF) risk has not been elucidated in a relatively healthy cohort.</div></div><div><h3>Methods</h3><div>We used cohort study data from the NHANES 2001–2002. Mendelian randomization (MR) study used GWAS data from 437,846 European participants. The exposures are eGFR<sub>Cystatin C</sub> & eGFR<sub>diff</sub>, outcome is self reported heart failure. Weighted multivariable-adjusted logistic regression and Kaplan-Meier survival analysis was used in corhort study. Inverse variance weighted (IVW) was applied in MR study.</div></div><div><h3>Results</h3><div>The cohort study included 2155 participants. Importantly, we simplified eGFR<sub>diff</sub> classification into ≥0 and < 0, and found that eGFR<sub>diff</sub>≥0 was associated with 52 % reduction of HF risk (OR 0.48, [95 % CI, 0.29–0.80], p = 0.005). We also found that 1 ml/min/1.73 m<sup>2</sup> of eGFR<sub>Cystatin C</sub> had a significant negative association with HF after adjusting for covariates. Interestingly, we showed a non-linear association between eGFR<sub>Cystatin C</sub> and HF, eGFR<sub>diff</sub> and HF. In participants without know HF, during a median follow-up of 17.3 years, those in the low eGFR<sub>Cystatin C</sub> or low eGFR<sub>diff</sub> groups showed significantly poorer survival. Moreover, MR analysis found genetic predisposition to cystatin C was significantly associated with an increased risk of HF.</div></div><div><h3>Conclusion</h3><div>Both decreased eGFR<sub>Cystatin C</sub> and eGFR<sub>diff</sub> levels were associated with heart failure and poor survival, but the latter seems more obvious.</div></div>\",\"PeriodicalId\":29726,\"journal\":{\"name\":\"International Journal of Cardiology Cardiovascular Risk and Prevention\",\"volume\":\"23 \",\"pages\":\"Article 200337\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-09-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Cardiology Cardiovascular Risk and Prevention\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772487524001028\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"PERIPHERAL VASCULAR DISEASE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Cardiology Cardiovascular Risk and Prevention","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772487524001028","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0
摘要
目的根据胱抑素 C 得出的估计肾小球滤过率(eGFR)(eGFRRCystatin C)以及胱抑素 C 和肌酐 eGFR 之间的差异(eGFRdiff)被认为与心血管疾病有关。然而,在一个相对健康的队列中,eGFRC胱抑素C、eGFRdiff与心力衰竭(HF)风险之间的关系尚未得到阐明。孟德尔随机化(MR)研究使用了 437 846 名欧洲参与者的 GWAS 数据。暴露因子为 eGFRC胱抑素 C & eGFRdiff,结果为自我报告的心力衰竭。在队列研究中使用了加权多变量调整逻辑回归和 Kaplan-Meier 生存分析。结果队列研究纳入了 2155 名参与者。重要的是,我们将 eGFRdiff 分类简化为≥0 和 <0,并发现 eGFRdiff≥0 与 52% 的 HF 风险降低相关(OR 0.48, [95 % CI, 0.29-0.80], p = 0.005)。我们还发现,在调整协变量后,1 ml/min/1.73 m2 的 eGFRCystatin C 与心房颤动有显著的负相关。有趣的是,我们发现 eGFRCystatin C 与 HF、eGFRdiff 与 HF 之间存在非线性关联。在中位随访 17.3 年的过程中,未发现患有高血压的参与者中,低 eGFRCystatin C 组或低 eGFRdiff 组的生存率明显较低。结论 eGFRCystatin C 和 eGFRdiff 水平的降低都与心衰和生存率低有关,但后者似乎更为明显。
eGFRCystatin C, difference between eGFRCystatin C and eGFRCre and heart failure: Insight from the NHANES 2001–2002 and Mendelian randomization analysis
Aim
Estimated glomerular filtration rate (eGFR) derived from Cystatin C (eGFRCystatin C), and the difference between Cystatin C and creatinine based eGFR (eGFRdiff) has been suggested to be associated with cardiovascular disease. However, the association between eGFRCystatin C,eGFRdiff and heart failure (HF) risk has not been elucidated in a relatively healthy cohort.
Methods
We used cohort study data from the NHANES 2001–2002. Mendelian randomization (MR) study used GWAS data from 437,846 European participants. The exposures are eGFRCystatin C & eGFRdiff, outcome is self reported heart failure. Weighted multivariable-adjusted logistic regression and Kaplan-Meier survival analysis was used in corhort study. Inverse variance weighted (IVW) was applied in MR study.
Results
The cohort study included 2155 participants. Importantly, we simplified eGFRdiff classification into ≥0 and < 0, and found that eGFRdiff≥0 was associated with 52 % reduction of HF risk (OR 0.48, [95 % CI, 0.29–0.80], p = 0.005). We also found that 1 ml/min/1.73 m2 of eGFRCystatin C had a significant negative association with HF after adjusting for covariates. Interestingly, we showed a non-linear association between eGFRCystatin C and HF, eGFRdiff and HF. In participants without know HF, during a median follow-up of 17.3 years, those in the low eGFRCystatin C or low eGFRdiff groups showed significantly poorer survival. Moreover, MR analysis found genetic predisposition to cystatin C was significantly associated with an increased risk of HF.
Conclusion
Both decreased eGFRCystatin C and eGFRdiff levels were associated with heart failure and poor survival, but the latter seems more obvious.