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Créé le : 13 septembre 2025
Créé le : 13 septembre 2025
1.“HGI quantifies this residual component and is calculated as observed HbA1c minus glucose-predicted HbA1c.HGI provides a phenotypic index of glycation propensity and glycemic variability, especially relevant among ICU patients with AF.
The variation captured by HGI likely reflects factors beyond ambient glucose—including erythrocyte redox status, intrinsic glycation activity, genetic susceptibility of red cells, and hemoglobin oxygenation—which may underlie interindividual differences in the HbA1c–fasting glucose relationship.
Accumulating evidence indicates that higher HGI is associated with greater prevalence and incidence of microvascular complications—such as diabetic retinopathy and chronic kidney disease—independent of conventional glycemic measures.
In cardiovascular cohorts, elevated HGI is associated with increased risk of atherosclerotic events and may delineate subgroups that experience differential benefit or harm from intensive glucose-lowering strategies.
Beyond diabetes, higher HGI is associated with insulin resistance, carotid atherosclerosis, and nonalcoholic fatty liver disease in general-population and nondiabetic cohorts, suggesting that HGI captures broader metabolic risk.
Across acute-care settings—including stroke, heart failure, and critical illness—both high and low HGI have been associated with mortality or poor functional recovery, supporting a nonlinear relationship between glycation phenotype and prognosis.
In AF, HGI can be viewed as a composite phenotypic index that integrates glycation propensity and glycemic variability and is influenced by red cell turnover .
A coherent mechanistic framework implicates the advanced glycation end products (AGE)–receptor for AGE (RAGE) axis, together with RAAS activation and autonomic–metabolic stress, in driving oxidative injury and profibrotic TGF-β/Smad signaling.Epigenetically mediated metabolic memory sustains hyperglycemia induced signaling beyond episodes of transient hyperglycemia.
”中“In AF, HGI can be viewed as a composite phenotypic index that integrates glycation propensity and glycemic variability and is influenced by red cell turnover .”不允许提及“influenced by red cell turnover”,给我一个修改“In AF, HGI can be viewed as a composite phenotypic index that integrates glycation propensity and glycemic variability and is influenced by red cell turnover .”之后还能自然流畅的版本,其他部位不需要你修改;
2.在这个对话中的段落中,你觉得如果删除掉“In AF, HGI can be viewed as a composite phenotypic index that integrates glycation propensity and glycemic variability and is influenced by red cell turnover .”可以吗?
下面按你的两点要求给出答案——
1)修改后的句子(去掉“influenced by red cell turnover”且读起来自然):
In AF, HGI can be viewed as a composite phenotypic index that integrates glycation propensity and glycemic variability.
(其余内容不变即可顺畅承接后文关于 AGE–RAGE 轴、RAAS 激活及代谢应激的机制段落。)
2)是否可以直接删除这一句?
可以删,段落在语法与逻辑上仍能连贯(前一句谈急性期结局、下一句转入机制)。不过,这一句在段落中起到把“AF”情境与“HGI”的概念性定位明确连接的“桥梁”作用:
“In AF, HGI can be viewed as a composite phenotypic index that integrates glycation propensity and glycemic variability.”可以改成“This phenotype is especially relevant among ICU patients with AF.”吗?从语言风格和逻辑结构上可以这么说吗?;
第二个问题,这个说法是否正确?是否有理论依据?
下面分别回答你的两个问题,并给出可直接替换/嵌入的写法。
“In AF, HGI can be viewed as a composite phenotypic index that integrates glycation propensity and glycemic variability.”
改成
“This phenotype is especially relevant among ICU patients with AF.”?
语言风格与逻辑结构:
更稳妥的两种写法(任选其一):
上面两种都避免了“red cell turnover”的表述,同时保持叙述自然顺畅。
结论(给写作用的短评):
机制与理论支撑(为何在 ICU‑AF 场景“特别相关”):
小提示:你原段前面已经出现“especially relevant among ICU patients with AF”的表述;为避免赘述,建议二选一:要么保留上面的“合并句”,要么保留前文那处“especially relevant …”,而把此处用于定义(或反之)。