Obesogenic Medication Use in End-Stage Kidney Disease and Association With Transplant Listing

IF 1.9 4区 医学 Q2 SURGERY
Babak J. Orandi, Yiting Li, Timur Seckin, Sunjae Bae, Bonnie E. Lonze, Christine J. Ren-Fielding, Holly Lofton, Akash Gujral, Dorry L. Segev, Mara McAdams-DeMarco
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Abstract

Objectives

Obesogenic medications are a putative contributor to the obesity epidemic. While 20% of adults take ≥1 obesogenic medication, the proportion in the end-stage kidney disease (ESKD) population—a group enriched for cardiometabolic complications—is unknown. Obesogenic medications may contribute to obesity and hamper weight loss efforts to achieve transplant listing.

Methods

Using 2017–2020 USRDS and Medicare claims, patients were identified as taking obesogenic medications if prescribed anticonvulsants, antidepressants, antidiabetics, anti-inflammatories, antipsychotics, and/or antihypertensives known to cause weight gain for ≥30 days in their first hemodialysis year. Ordinal logistic and Cox regression with inverse probability of treatment weighting were used to quantify obesogenic medications’ association with body mass index (BMI) and listing, respectively.

Results

Among 271 401 hemodialysis initiates, 63.5% took ≥1 obesogenic medication. For those in underweight, normal weight, overweight, and class I, II, and III categories, 54.3%, 58.4%, 63.1%, 66.5%, 68.6%, and 68.8% took ≥1, respectively. Number of obesogenic medications was associated with increased BMI; use of one was associated with 13% increased odds of higher BMI (aOR [adjusted odds ratio] 1.14; 95%CI: 1.13–1.16; p < 0.001), use of three was associated with a 55% increase (aOR 1.55; 95%CI: 1.53–1.57; p < 0.001). Any use was associated with 6% lower odds of transplant listing (aHR [adjusted hazard ratio] 0.94; 95%CI: 0.92–0.96; p < 0.001). Within each BMI category, obesogenic medication use was associated with lower listing likelihood.

Conclusions

Obesogenic medication use is common in ESKD patients—particularly those with obesity—and is associated with lower listing likelihood. Whenever possible, non-obesogenic alternatives should be chosen for ESKD patients attempting weight loss to achieve transplant listing.

终末期肾病患者的致肥药物使用及与移植手术列表的关系
目标 致肥药物可能是导致肥胖流行的原因之一。虽然 20% 的成年人服用≥1 种致肥药物,但在终末期肾病(ESKD)人群--一个富含心脏代谢并发症的群体--中的比例尚不清楚。致胖药物可能会导致肥胖,并阻碍为实现移植上市而进行的减肥努力。 方法 使用 2017-2020 年 USRDS 和医疗保险报销单,如果患者在血液透析第一年内服用抗惊厥药、抗抑郁药、抗糖尿病药、抗炎药、抗精神病药和/或已知会导致体重增加的抗高血压药≥30 天,则确定其服用了致肥胖药物。采用逆概率治疗加权的顺序逻辑回归和 Cox 回归分别量化致肥药物与体重指数(BMI)和上市的关系。 结果 在 271401 名血液透析患者中,63.5% 的人服用了≥1 种致肥药物。在体重不足、体重正常、超重和 I 级、II 级和 III 级人群中,分别有 54.3%、58.4%、63.1%、66.5%、68.6% 和 68.8% 的人服用≥1 种致肥药物。致胖药物的数量与体重指数(BMI)的升高有关;使用一种致胖药物会使 BMI 升高的几率增加 13%(aOR [调整后的几率比] 1.14;95%CI:1.13-1.16;p <;0.001),使用三种致胖药物会使 BMI 升高的几率增加 55%(aOR 1.55;95%CI:1.53-1.57;p <;0.001)。使用任何一种药物都会导致移植列表几率降低 6%(aHR [调整后危险比] 0.94;95%CI:0.92-0.96;p <;0.001)。在每个体重指数类别中,肥胖药物的使用都与较低的上市几率相关。 结论 在 ESKD 患者中,尤其是肥胖患者中,使用致肥药物很常见,而且与较低的上市可能性有关。在可能的情况下,ESKD 患者应选择不致肥的替代药物来减轻体重,以达到移植上市的目的。
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来源期刊
Clinical Transplantation
Clinical Transplantation 医学-外科
CiteScore
3.70
自引率
4.80%
发文量
286
审稿时长
2 months
期刊介绍: Clinical Transplantation: The Journal of Clinical and Translational Research aims to serve as a channel of rapid communication for all those involved in the care of patients who require, or have had, organ or tissue transplants, including: kidney, intestine, liver, pancreas, islets, heart, heart valves, lung, bone marrow, cornea, skin, bone, and cartilage, viable or stored. Published monthly, Clinical Transplantation’s scope is focused on the complete spectrum of present transplant therapies, as well as also those that are experimental or may become possible in future. Topics include: Immunology and immunosuppression; Patient preparation; Social, ethical, and psychological issues; Complications, short- and long-term results; Artificial organs; Donation and preservation of organ and tissue; Translational studies; Advances in tissue typing; Updates on transplant pathology;. Clinical and translational studies are particularly welcome, as well as focused reviews. Full-length papers and short communications are invited. Clinical reviews are encouraged, as well as seminal papers in basic science which might lead to immediate clinical application. Prominence is regularly given to the results of cooperative surveys conducted by the organ and tissue transplant registries. Clinical Transplantation: The Journal of Clinical and Translational Research is essential reading for clinicians and researchers in the diverse field of transplantation: surgeons; clinical immunologists; cryobiologists; hematologists; gastroenterologists; hepatologists; pulmonologists; nephrologists; cardiologists; and endocrinologists. It will also be of interest to sociologists, psychologists, research workers, and to all health professionals whose combined efforts will improve the prognosis of transplant recipients.
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