Fair Allocation of GLP-1 and Dual GLP-1-GIP Receptor Agonists Reply

被引：0

作者：

Mensah, Michael O. ^{[1
]}

Freitas, Daniel J. ^{[2
]}

Cartwright, Joseph R. ^{[3
]}

机构：

[1] Yale Univ, New Haven, CT 06520 USA

[2] San Francisco Dept Publ Hlth, San Francisco, CA USA

[3] Alameda Hlth Syst, Oakland, CA USA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 2024年 / 391卷 / 08期

关键词：

MORTALITY;

D O I：

10.1056/NEJMc2407932

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

To the Editor: The distribution framework for glucagon-like peptide-1 (GLP-1) receptor agonists proposed by Emanuel et al. in their Perspective article (May 30 issue)(1) considers potential years of life lost (PYLL) from obesity-related disease, but not race. How can clinicians and policymakers implement this framework "irrespective of factors such as race" (Table 1 in the article) when race and ethnic group are strongly associated with both PYLL and the risk of obesity-related disease? The PYLL metric - life expectancy minus the age at which a person dies - is seldom used in clinical medicine. But PYLL and life expectancy are . . .

引用

页码：775 / 776

页数：2

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