Pharmacological management of youth with type 2 diabetes and diabetic kidney disease: a comprehensive review of current treatments and future directions

被引:2
|
作者
Tommerdahl, Kalie L. [1 ,2 ,3 ,4 ]
Kula, Alexander J. [5 ,6 ]
Bjornstad, Petter [1 ,2 ,4 ,7 ,8 ]
机构
[1] Childrens Hosp Colorado, Dept Pediat, Sect Pediat Endocrinol, Aurora, CO USA
[2] Univ Colorado Anschutz Med Campus, Aurora, CO USA
[3] Univ Colorado, Barbara Davis Ctr Diabet, Sch Med, Aurora, CO USA
[4] Univ Colorado, Ludeman Family Ctr Womens Hlth Res, Div Gen Internal Med, Sch Med, Aurora, CO USA
[5] Lurie Childrens Hosp, Dept Pediat, Sect Pediat Nephrol, Chicago, IL USA
[6] Northwestern Univ, Feinberg Sch Med, Chicago, IL USA
[7] Univ Colorado Anschutz Med Campus, Dept Med, Div Renal Dis & Hypertens, Aurora, CO USA
[8] 13123 E 16th Ave, Box B265, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
Diabetic kidney disease; youth-onset type 2 diabetes; therapies; treatments; pediatrics; GLUCAGON-LIKE PEPTIDE-1; DOUBLE-BLIND; CARDIOVASCULAR OUTCOMES; INSULIN SENSITIVITY; PEDIATRIC-PATIENTS; GLUCOSE CONTROL; HEART-FAILURE; SINGLE-BLIND; METFORMIN; PLACEBO;
D O I
10.1080/14656566.2023.2203319
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionDiabetic kidney disease (DKD) is a leading cause of mortality in people with type 2 diabetes (T2D), and over 50% of individuals with youth-onset T2D will develop DKD as a young adult. Diagnosis of early-onset DKD remains a challenge in young persons with T2D secondary to a lack of available biomarkers for early DKD, while the injuries may still be reversible. Furthermore, multiple barriers exist to initiate timely prevention and treatment strategies for DKD, including a lack of Food and Drug Administration approval of medications in pediatrics; provider comfort with medication prescription, titration, and monitoring; and medication adherence.Areas coveredTherapies that have promise for slowing DKD progression in youth with T2D include metformin, renin-angiotensin-aldosterone system inhibitors, glucagon-like peptide-1 receptor agonists, sodium glucose co-transporter 2 inhibitors, thiazolidinediones, sulfonylureas, endothelin receptor agonists, and mineralocorticoid antagonists. Novel agents are also in development to act synergistically on the kidneys with the aforementioned medications. We comprehensively review the available pharmacologic strategies for DKD in youth-onset T2D including mechanisms of action, potential adverse effects, and kidney-specific effects, with an emphasis on published pediatric and adult trials.Expert opinionLarge clinical trials evaluating pharmacologic interventions targeting the treatment of DKD in youth-onset T2D are strongly needed.
引用
收藏
页码:913 / 924
页数:12
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