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心脏-肾脏-糖尿病-肝脏-代谢综合征(CARDIAL-MS):一种综合多系统代谢疾病的新定义。

CARDIAL-MS (CArdio-Renal-DIAbetes-Liver-Metabolic Syndrome): a new proposition for an integrated multisystem metabolic disease.

作者信息

Godoy-Matos Amélio F, Valério Cynthia Melissa, Júnior Wellington S Silva, de Araujo-Neto João Marcello, Sposito Andrei C, Suassuna José Hermógenes Rocco

机构信息

Sociedade Brasileira de Diabetes (SBD), São Paulo, Brazil.

Instituto Estadual de Diabetes e Endocrinologia do Rio de Janeiro (IEDE), Rio de Janeiro, RJ, Brazil.

出版信息

Diabetol Metab Syndr. 2025 Jun 16;17(1):218. doi: 10.1186/s13098-025-01796-4.

Abstract

BACKGROUND

Metabolic Syndrome-a constellation of insulin resistance, cardiovascular risk factors as hyperglycemia, hypertension, and dyslipidemia, and systemic metabolic dysfunction-may be driven by dysregulation of adipose tissue, which manifests as adiposopathy (pathogenic adipose tissue expansion or maldistribution), ectopic fat deposition (in the liver, muscle, pancreas, and cardiorenal systems), and altered secretion of adipokines/hepatokines. Weight gain, obesity, and/or unfavorable fat distribution create a scenario wherein the type, size, location, secretions, or even scarcity of adipocytes drive pathophysiological mechanisms leading to hepatic steatosis and steatohepatitis, type 2 diabetes, and heart and kidney disease. While recent frameworks, such as cardiovascular-kidney-metabolic syndrome, emphasize holistic staging, the central role of metabolic dysfunction-associated steatotic liver disease (MASLD) in multisystem morbidity remains underrecognized.

MAIN TEXT

This narrative review synthesizes evidence linking MASLD and diabetes to cardiovascular and kidney diseases through shared pathways of adiposopathy, ectopic lipid accumulation, and dysregulated adipokine/hepatokine signaling. We propose CARDIAL-MS (CArdio-Renal-DIAbetes-Liver-Metabolic Syndrome), an expanded pathophysiological model that unifies these interactions into four progressive stages: (1) weight gain and dysfunctional adipose tissue; (2) metabolic risk factors and markers of risk; (3) cardiometabolic diseases and chronic kidney disease; and (4) advanced cardio-renal-liver-metabolic disease. By integrating MASLD as a pivotal component, CARDIAL-MS reframes metabolic syndrome as a continuum of interconnected organ injuries rather than isolated risk factors.

CONCLUSION

CARDIAL-MS provides a staging model to identify patients at critical transition points-from reversible metabolic disturbances to irreversible organ damage. This model emphasizes early interventions targeting adipose tissue health and ectopic fat deposition to mitigate the progression of metabolic cardiorenal diseases. By recognizing the syndromic nature of these conditions, CARDIAL-MS offers clinicians an actionable paradigm for risk stratification, timely diagnosis, and personalized prevention strategies.

摘要

背景

代谢综合征——一种由胰岛素抵抗、心血管危险因素(如高血糖、高血压和血脂异常)以及全身代谢功能障碍组成的症候群——可能是由脂肪组织失调驱动的,表现为脂肪病(致病性脂肪组织扩张或分布异常)、异位脂肪沉积(在肝脏、肌肉、胰腺和心肾系统中)以及脂肪因子/肝因子分泌改变。体重增加、肥胖和/或不良的脂肪分布造成了一种情况,即脂肪细胞的类型、大小、位置、分泌甚至稀缺性驱动导致肝脂肪变性和脂肪性肝炎、2型糖尿病以及心脏和肾脏疾病的病理生理机制。虽然最近的框架,如心血管-肾脏-代谢综合征,强调整体分期,但代谢功能障碍相关脂肪性肝病(MASLD)在多系统发病中的核心作用仍未得到充分认识。

正文

本叙述性综述综合了证据,这些证据通过脂肪病、异位脂质积累以及失调的脂肪因子/肝因子信号传导的共同途径,将MASLD和糖尿病与心血管和肾脏疾病联系起来。我们提出了CARDIAL-MS(心-肾-糖尿病-肝脏-代谢综合征),这是一个扩展的病理生理模型,将这些相互作用统一为四个渐进阶段:(1)体重增加和功能失调的脂肪组织;(2)代谢危险因素和风险标志物;(3)心脏代谢疾病和慢性肾脏病;以及(4)晚期心-肾-肝-代谢疾病。通过将MASLD整合为一个关键组成部分,CARDIAL-MS将代谢综合征重新定义为相互关联的器官损伤的连续体,而不是孤立的危险因素。

结论

CARDIAL-MS提供了一个分期模型,以识别处于关键过渡点的患者——从可逆的代谢紊乱到不可逆的器官损伤。该模型强调早期干预以针对脂肪组织健康和异位脂肪沉积,以减轻代谢性心肾疾病的进展。通过认识到这些病症的综合征性质,CARDIAL-MS为临床医生提供了一个可操作的范例,用于风险分层、及时诊断和个性化预防策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2dc/12168269/3575ebb19178/13098_2025_1796_Fig1_HTML.jpg

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