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2型糖尿病潜在增长模型方法的应用与报告存在巨大差异:一项文献综述。

Great diversity in the utilization and reporting of latent growth modeling approaches in type 2 diabetes: A literature review.

作者信息

O'Connor Sarah, Blais Claudia, Mésidor Miceline, Talbot Denis, Poirier Paul, Leclerc Jacinthe

机构信息

Research Centre, Institut universitaire de Cardiologie et Pneumologie de Québec-Université Laval (IUCPQ-UL), 2725 Ch. Ste-Foy, Quebec City, Quebec, G1V 4G5, Canada.

Faculty of Pharmacy, Université Laval, Ferdinand Vandry Pavillon, 1050 de La Médecine Avenue, Quebec City, Quebec, G1V 0A6, Canada.

出版信息

Heliyon. 2022 Sep 13;8(9):e10493. doi: 10.1016/j.heliyon.2022.e10493. eCollection 2022 Sep.

Abstract

INTRODUCTION

The progression of complications of type 2 diabetes (T2D) is unique to each patient and can be depicted through individual temporal trajectories. Latent growth modeling approaches (latent growth mixture models [LGMM] or latent class growth analysis [LCGA]) can be used to classify similar individual trajectories in non-observed groups (latent groups), sharing common characteristics. Although increasingly used in the field of T2D, many questions remain regarding the utilization of these methods.

OBJECTIVE

To review the literature of longitudinal studies using latent growth modeling approaches to study T2D.

METHODS

MEDLINE (Ovid), EMBASE, CINAHL and Wb of Science were searched through August 25, 2021. Data was collected on the type of latent growth modeling approaches (LGMM or LCGA), characteristics of studies and quality of reporting using the GRoLTS-Checklist and presented as frequencies.

RESULTS

From the 4,694 citations screened, a total of 38 studies were included. The studies were published beetween 2011 and 2021 and the length of follow-up ranged from 8 weeks to 14 years. Six studies used LGMM, while 32 studies used LCGA. The fields of research varied from clinical research, psychological science, healthcare utilization research and drug usage/pharmaco-epidemiology. Data sources included primary data (clinical trials, prospective/retrospective cohorts, surveys), or secondary data (health records/registries, medico-administrative). Fifty percent of studies evaluated trajectory groups as exposures for a subsequent clinical outcome, while 24% used predictive models of group membership and 5% used both. Regarding the quality of reporting, trajectory groups were adequately presented, however many studies failed to report important decisions made for the trajectory group identification.

CONCLUSION

Although LCGA were preferred, the contexts of utilization were diverse and unrelated to the type of methods. We recommend future authors to clearly report the decisions made regarding trajectory groups identification.

摘要

引言

2型糖尿病(T2D)并发症的进展因患者而异,可通过个体时间轨迹来描述。潜在增长建模方法(潜在增长混合模型[LGMM]或潜在类别增长分析[LCGA])可用于对未观察到的组(潜在组)中具有共同特征的相似个体轨迹进行分类。尽管这些方法在T2D领域的应用越来越广泛,但在其使用方面仍存在许多问题。

目的

回顾使用潜在增长建模方法研究T2D的纵向研究文献。

方法

检索截至2021年8月25日的MEDLINE(Ovid)、EMBASE、CINAHL和科学网数据库。使用GRoLTS清单收集有关潜在增长建模方法类型(LGMM或LCGA)、研究特征和报告质量的数据,并以频率形式呈现。

结果

在筛选的4694篇文献中,共纳入38项研究。这些研究发表于2011年至2021年之间,随访时间从8周至14年不等。6项研究使用LGMM,32项研究使用LCGA。研究领域包括临床研究、心理学、医疗保健利用研究和药物使用/药物流行病学。数据来源包括原始数据(临床试验、前瞻性/回顾性队列研究、调查)或二手数据(健康记录/登记处、医疗管理数据)。50%的研究将轨迹组评估为后续临床结局的暴露因素,24%的研究使用组成员预测模型,5%的研究同时使用这两种方法。关于报告质量,轨迹组得到了充分呈现,但许多研究未能报告在轨迹组识别过程中做出的重要决策。

结论

尽管LCGA更受青睐,但使用背景各不相同,且与方法类型无关。我们建议未来的作者明确报告在轨迹组识别方面做出的决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e5b/9508412/ad913234b5e2/gr1.jpg

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