1 型或 2 型糖尿病患者的心理健康障碍与慢性糖尿病并发症之间的双向关系。

Diabetes care Pub Date : 2024-09-01 DOI:10.2337/dc24-0818
Maya Watanabe, Evan L Reynolds, Mousumi Banerjee, Morten Charles, Kara Mizokami-Stout, Dana Albright, Lynn Ang, Joyce M Lee, Rodica Pop-Busui, Eva L Feldman, Brian C Callaghan
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引用次数: 0

摘要

研究目的确定1型或2型糖尿病患者的慢性糖尿病并发症(CDCs)发生时间与心理健康障碍(MHDs)之间的双向关系:我们利用一个具有全国代表性的医疗索赔数据库,采用倾向得分准随机化技术,按年龄(0-19 岁、20-39 岁、40-59 岁和 60 岁以上)分层,识别出匹配的 1 型或 2 型糖尿病患者或非糖尿病患者。CDC 和 MHD 使用 ICD-9/10 编码进行识别。我们分别拟合了CDC或MHD诊断随时间变化的Cox比例危险模型,以研究它们与MHD或CDC发病危险的关系:从 2001 年到 2018 年,共纳入了 553,552 人(44,735 人患有 1 型糖尿病,152,187 人患有 2 型糖尿病,356,630 人未患糖尿病)。我们发现,患有 CDC 会增加罹患 MHD 的风险(危险比 [HR] 1.9-2.9;P <0.05,年龄越大,HR 越高),而患有 MHD 会增加罹患 CDC 的风险(HR 1.4-2.5;P <0.05,0-19 岁年龄层的 HR 最高)。在这些年龄层中,交互效应为0.05):我们发现,在人的一生中,疾病预防控制中心与多发性硬化症之间存在一致的双向联系,这凸显了疾病预防控制中心与多发性硬化症之间的重要关系。预防和治疗其中一种合并症有助于降低另一种合并症的发病风险。
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Bidirectional Associations Between Mental Health Disorders and Chronic Diabetic Complications in Individuals With Type 1 or Type 2 Diabetes.

Objective: To determine bidirectional associations between the timing of chronic diabetes complications (CDCs) and mental health disorders (MHDs) in individuals with type 1 or type 2 diabetes.

Research design and methods: We used a nationally representative health care claims database to identify matched individuals with type 1 or 2 diabetes or without diabetes using a propensity score quasirandomization technique stratified by age (0-19, 20-39, 40-59, and ≥60 years). CDCs and MHDs were identified using ICD-9/10 codes. We fit Cox proportional hazards models with time-varying diagnoses of CDCs or MHDs to investigate their association with the hazard of developing MHDs or CDCs, respectively.

Results: From 2001 to 2018, a total of 553,552 individuals were included (44,735 with type 1 diabetes, 152,187 with type 2 diabetes, and 356,630 without diabetes). We found that having a CDC increased the hazard of developing an MHD (hazard ratio [HR] 1.9-2.9; P < 0.05, with higher HRs in older age strata), and having an MHD increased the hazard of developing a CDC (HR 1.4-2.5; P < 0.05, with the highest HR in age stratum 0-19 years). In those aged <60 years, individuals with type 1 diabetes were more likely to have CDCs, whereas individuals with type 2 diabetes were more likely to have MHDs. However, the relationship between CDCs and MHDs in either direction was not affected by diabetes type (P > 0.05 for interaction effects).

Conclusions: We found a consistent bidirectional association between CDCs and MHDs across the life span, highlighting the important relationship between CDCs and MHDs. Prevention and treatment of either comorbidity may help reduce the risk of developing the other.

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