Krzysztof Batko, Anna Sączek, Małgorzata Banaszkiewicz, Jolanta Małyszko, Ewa Koc-Żórawska, Marcin Żórawski, Karolina Niezabitowska, Katarzyna Siek, Andrzej Kraśniak, Marcin Krzanowski, Katarzyna Krzanowska
{"title":"揭示血清卡利司他汀对肾移植幸存者心肾预后的作用。","authors":"Krzysztof Batko, Anna Sączek, Małgorzata Banaszkiewicz, Jolanta Małyszko, Ewa Koc-Żórawska, Marcin Żórawski, Karolina Niezabitowska, Katarzyna Siek, Andrzej Kraśniak, Marcin Krzanowski, Katarzyna Krzanowska","doi":"10.1159/000543652","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Kallistatin, a serine protease inhibitor, has been implicated in cardiovascular and renal protection. This study investigates its association with clinical characteristics and outcomes in long-term kidney transplant recipients (KTRs).</p><p><strong>Methods: </strong>In this longitudinal observational cohort study, we enrolled 101 KTRs between September 2016 and October 2017. The median (interquartile range) time post-transplant was 52 (36-97) months, and the follow-up time was 83 (41-85) months. All patients had documented graft function of ≥24 months and no record of acute rejection or active or chronic infection at presentation. Serum kallistatin and high-sensitivity interleukin-6 were measured at baseline using commercially available enzyme-linked immunosorbent assays. A control group of 32 healthy volunteers was also recruited.</p><p><strong>Results: </strong>Higher serum kallistatin levels were observed in KTRs compared to healthy controls (15.9 vs. 13.8 µg/mL; p = 0.007). Concentrations were lower in diabetic versus non-diabetic KTR (14.8 vs. 16.4 µg/mL; p = 0.021). A significant interaction between diabetic status and body mass index indicated a positive association with kallistatin levels only in diabetic KTRs (p = 0.046). Linear mixed models assessing estimated glomerular filtration rate (eGFR) change over time showed improved fit after kallistatin was included in a base model with age, sex, and baseline eGFR (p = 0.024). Cox regression showed that higher kallistatin levels were associated with an increased risk of graft loss (HR: 1.120; p = 0.049), but also remained independent of time after transplantation (HR: 1.147; p = 0.030). No association was observed for all-cause mortality. The best performance was estimated for kallistatin models adjusting for time post-transplant (c-index 0.779) and diabetic status (c-index 0.707).</p><p><strong>Conclusion: </strong>This study highlights the complex interactions between kallistatin, renal function, and cardiometabolic status in stable, long-term KTRs. Higher kallistatin levels are associated with an increased risk of graft loss in non-diabetic patients while showing a protective effect in diabetic patients. 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A significant interaction between diabetic status and body mass index indicated a positive association with kallistatin levels only in diabetic KTRs (p = 0.046). Linear mixed models assessing estimated glomerular filtration rate (eGFR) change over time showed improved fit after kallistatin was included in a base model with age, sex, and baseline eGFR (p = 0.024). Cox regression showed that higher kallistatin levels were associated with an increased risk of graft loss (HR: 1.120; p = 0.049), but also remained independent of time after transplantation (HR: 1.147; p = 0.030). No association was observed for all-cause mortality. The best performance was estimated for kallistatin models adjusting for time post-transplant (c-index 0.779) and diabetic status (c-index 0.707).</p><p><strong>Conclusion: </strong>This study highlights the complex interactions between kallistatin, renal function, and cardiometabolic status in stable, long-term KTRs. 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引用次数: 0
摘要
卡利司他汀是一种丝氨酸蛋白酶抑制剂,具有心血管和肾脏保护作用。本研究探讨其与长期肾移植受者(KTRs)临床特征和预后的关系。方法:在这项纵向观察队列研究中,我们在2016年9月至2017年10月期间招募了101名ktr。移植后中位(IQR)时间52(36-97)个月,随访时间83(41-85)个月。所有患者的移植物功能≥24个月,就诊时无急性排斥反应或活动性或慢性感染记录。使用市售的酶联免疫吸附法在基线时测定血清卡利司他汀和高敏白介素-6 (hsIL-6)。另外还招募了32名健康志愿者作为对照组。结果:与健康对照组相比,KTRs血清中卡利司他汀水平较高(15.9 vs. 13.8µg/ml;P = 0.007)。糖尿病患者的KTR浓度低于非糖尿病患者(14.8 μ g/ml vs 16.4 μ g/ml;P = 0.021)。糖尿病状态和BMI之间的显著相互作用表明,仅在糖尿病ktr中,与卡利司他汀水平呈正相关(P=0.046)。评估eGFR随时间变化的线性混合模型显示,将卡利司他汀纳入具有年龄、性别和基线eGFR的基础模型后,拟合度得到改善(χ²=5.089,P=0.020)。Cox回归显示,糖尿病患者较高的卡利司他汀水平与移植物丢失的风险增加相关(HR 1.120;P=0.049),且与移植后时间无关(HR 1.147;P = 0.030)。未观察到与全因死亡率相关。经移植后时间(c-index 0.779)和糖尿病状态(c-index 0.707)调整后的卡利司他汀模型估计表现最佳。结论:本研究强调了稳定、长期KTRs中卡利司他汀、肾功能和心脏代谢状态之间复杂的相互作用。在非糖尿病患者中,较高的卡利司他汀水平与移植物丢失的风险增加相关,而在糖尿病患者中显示出保护作用。这些发现支持ktr患者心肾代谢健康的综合管理。
Unravelling the Role of Serum Kallistatin on Cardiorenal Outcomes in Kidney Transplant Survivors.
Introduction: Kallistatin, a serine protease inhibitor, has been implicated in cardiovascular and renal protection. This study investigates its association with clinical characteristics and outcomes in long-term kidney transplant recipients (KTRs).
Methods: In this longitudinal observational cohort study, we enrolled 101 KTRs between September 2016 and October 2017. The median (interquartile range) time post-transplant was 52 (36-97) months, and the follow-up time was 83 (41-85) months. All patients had documented graft function of ≥24 months and no record of acute rejection or active or chronic infection at presentation. Serum kallistatin and high-sensitivity interleukin-6 were measured at baseline using commercially available enzyme-linked immunosorbent assays. A control group of 32 healthy volunteers was also recruited.
Results: Higher serum kallistatin levels were observed in KTRs compared to healthy controls (15.9 vs. 13.8 µg/mL; p = 0.007). Concentrations were lower in diabetic versus non-diabetic KTR (14.8 vs. 16.4 µg/mL; p = 0.021). A significant interaction between diabetic status and body mass index indicated a positive association with kallistatin levels only in diabetic KTRs (p = 0.046). Linear mixed models assessing estimated glomerular filtration rate (eGFR) change over time showed improved fit after kallistatin was included in a base model with age, sex, and baseline eGFR (p = 0.024). Cox regression showed that higher kallistatin levels were associated with an increased risk of graft loss (HR: 1.120; p = 0.049), but also remained independent of time after transplantation (HR: 1.147; p = 0.030). No association was observed for all-cause mortality. The best performance was estimated for kallistatin models adjusting for time post-transplant (c-index 0.779) and diabetic status (c-index 0.707).
Conclusion: This study highlights the complex interactions between kallistatin, renal function, and cardiometabolic status in stable, long-term KTRs. Higher kallistatin levels are associated with an increased risk of graft loss in non-diabetic patients while showing a protective effect in diabetic patients. These findings support integrated management of cardio-reno-metabolic health in KTRs.
期刊介绍:
This journal comprises both clinical and basic studies at the interface of nephrology, hypertension and cardiovascular research. The topics to be covered include the structural organization and biochemistry of the normal and diseased kidney, the molecular biology of transporters, the physiology and pathophysiology of glomerular filtration and tubular transport, endothelial and vascular smooth muscle cell function and blood pressure control, as well as water, electrolyte and mineral metabolism. Also discussed are the (patho)physiology and (patho) biochemistry of renal hormones, the molecular biology, genetics and clinical course of renal disease and hypertension, the renal elimination, action and clinical use of drugs, as well as dialysis and transplantation. Featuring peer-reviewed original papers, editorials translating basic science into patient-oriented research and disease, in depth reviews, and regular special topic sections, ''Kidney & Blood Pressure Research'' is an important source of information for researchers in nephrology and cardiovascular medicine.