Emir Tas , Amanda Flint , Ingrid Libman , Radhika Muzumdar , Xiawei Ou , David K. Williams , Elisabet Børsheim , Eva C. Diaz
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Participants were categorized into two groups based on vitamin D status at the end of the observation period: those whose vitamin D levels increased or remained sufficient (VDI, n = 22) and those whose levels decreased or remained insufficient/deficient (VDD, n = 22). Liver fat percentage was measured using magnetic resonance imaging (MRI) fat-fraction, and IR was assessed using the updated Homeostatic Model Assessment for Insulin Resistance (HOMA2-IR) and the triglyceride-to-high-density lipoprotein cholesterol ratio (TG/HDL).</div></div><div><h3>Results</h3><div>Across the cohort, liver fat was positively associated with HOMA2-IR (β = 0.08, p = 0.023). The association between changes in vitamin D status and HOMA2-IR trajectories was modified by liver fat but only in Hispanic adolescents (β = −0.18, p < 0.001). Among Hispanic adolescents in the VDD group, HOMA-IR worsened, particularly at higher levels of liver fat. In non-Hispanic adolescents, HOMA-IR increased in the VDD group (β = 0.65, p = 0.033) compared to the VDI group, independent of baseline liver fat. Across the cohort, changes in vitamin D status interacted with liver fat to influence TG/HDL trajectories (β = 0.20, p = 0.034).</div></div><div><h3>Conclusions</h3><div>The metabolic response to changes in vitamin D status in adolescents with IR may vary based on racial and ethnic differences and liver fat status. These findings underscore the importance of considering liver fat and racial/ethnic background in vitamin D and metabolic health studies. Future research with more extensive and diverse cohorts spanning the fatty liver disease spectrum is needed to clarify these relationships.</div></div>","PeriodicalId":100977,"journal":{"name":"Obesity Pillars","volume":"14 ","pages":"Article 100173"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The association between hepatic steatosis, vitamin D status, and insulin resistance in adolescents with obesity\",\"authors\":\"Emir Tas , Amanda Flint , Ingrid Libman , Radhika Muzumdar , Xiawei Ou , David K. Williams , Elisabet Børsheim , Eva C. Diaz\",\"doi\":\"10.1016/j.obpill.2025.100173\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Epidemiological studies suggest an inverse relationship between circulating 25-hydroxy-vitamin D [25(OH)D] levels and insulin resistance (IR), yet interventional studies have yielded inconsistent findings. This study examined the relationship between changes in vitamin D status and markers of IR in adolescents, with a focus on the modifying effect of liver fat.</div></div><div><h3>Methods</h3><div>A post-hoc analysis was performed using data from 44 adolescents participating in a 6-month observational study evaluating biomarkers of hepatosteatosis. Participants were categorized into two groups based on vitamin D status at the end of the observation period: those whose vitamin D levels increased or remained sufficient (VDI, n = 22) and those whose levels decreased or remained insufficient/deficient (VDD, n = 22). Liver fat percentage was measured using magnetic resonance imaging (MRI) fat-fraction, and IR was assessed using the updated Homeostatic Model Assessment for Insulin Resistance (HOMA2-IR) and the triglyceride-to-high-density lipoprotein cholesterol ratio (TG/HDL).</div></div><div><h3>Results</h3><div>Across the cohort, liver fat was positively associated with HOMA2-IR (β = 0.08, p = 0.023). The association between changes in vitamin D status and HOMA2-IR trajectories was modified by liver fat but only in Hispanic adolescents (β = −0.18, p < 0.001). Among Hispanic adolescents in the VDD group, HOMA-IR worsened, particularly at higher levels of liver fat. In non-Hispanic adolescents, HOMA-IR increased in the VDD group (β = 0.65, p = 0.033) compared to the VDI group, independent of baseline liver fat. Across the cohort, changes in vitamin D status interacted with liver fat to influence TG/HDL trajectories (β = 0.20, p = 0.034).</div></div><div><h3>Conclusions</h3><div>The metabolic response to changes in vitamin D status in adolescents with IR may vary based on racial and ethnic differences and liver fat status. These findings underscore the importance of considering liver fat and racial/ethnic background in vitamin D and metabolic health studies. 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引用次数: 0
摘要
流行病学研究表明,循环25-羟基维生素D [25(OH)D]水平与胰岛素抵抗(IR)呈负相关,但介入性研究的结果不一致。本研究考察了青少年维生素D状态变化与IR标志物之间的关系,重点关注肝脏脂肪的调节作用。方法对44名青少年参与的一项为期6个月的观察性研究的数据进行事后分析,该研究评估了肝成骨病的生物标志物。根据观察结束时的维生素D状况,参与者被分为两组:维生素D水平增加或保持充足的(VDI, n = 22)和维生素D水平下降或仍然不足/缺乏的(VDD, n = 22)。使用磁共振成像(MRI)脂肪分数测量肝脏脂肪百分比,使用更新的胰岛素抵抗稳态模型评估(HOMA2-IR)和甘油三酯与高密度脂蛋白胆固醇比率(TG/HDL)评估IR。结果在整个队列中,肝脏脂肪与HOMA2-IR呈正相关(β = 0.08, p = 0.023)。肝脏脂肪改变了维生素D状态和HOMA2-IR轨迹之间的关系,但仅限于西班牙裔青少年(β = - 0.18, p <;0.001)。在VDD组的西班牙裔青少年中,HOMA-IR恶化,特别是在肝脏脂肪水平较高的情况下。在非西班牙裔青少年中,与VDI组相比,VDD组HOMA-IR升高(β = 0.65, p = 0.033),与基线肝脂肪无关。在整个队列中,维生素D状态的变化与肝脏脂肪相互作用,影响TG/HDL轨迹(β = 0.20, p = 0.034)。结论IR青少年对维生素D水平变化的代谢反应可能因种族、民族差异和肝脏脂肪状况而异。这些发现强调了在维生素D和代谢健康研究中考虑肝脏脂肪和种族/民族背景的重要性。未来的研究需要更广泛和多样化的跨越脂肪肝疾病谱系的队列来澄清这些关系。
The association between hepatic steatosis, vitamin D status, and insulin resistance in adolescents with obesity
Introduction
Epidemiological studies suggest an inverse relationship between circulating 25-hydroxy-vitamin D [25(OH)D] levels and insulin resistance (IR), yet interventional studies have yielded inconsistent findings. This study examined the relationship between changes in vitamin D status and markers of IR in adolescents, with a focus on the modifying effect of liver fat.
Methods
A post-hoc analysis was performed using data from 44 adolescents participating in a 6-month observational study evaluating biomarkers of hepatosteatosis. Participants were categorized into two groups based on vitamin D status at the end of the observation period: those whose vitamin D levels increased or remained sufficient (VDI, n = 22) and those whose levels decreased or remained insufficient/deficient (VDD, n = 22). Liver fat percentage was measured using magnetic resonance imaging (MRI) fat-fraction, and IR was assessed using the updated Homeostatic Model Assessment for Insulin Resistance (HOMA2-IR) and the triglyceride-to-high-density lipoprotein cholesterol ratio (TG/HDL).
Results
Across the cohort, liver fat was positively associated with HOMA2-IR (β = 0.08, p = 0.023). The association between changes in vitamin D status and HOMA2-IR trajectories was modified by liver fat but only in Hispanic adolescents (β = −0.18, p < 0.001). Among Hispanic adolescents in the VDD group, HOMA-IR worsened, particularly at higher levels of liver fat. In non-Hispanic adolescents, HOMA-IR increased in the VDD group (β = 0.65, p = 0.033) compared to the VDI group, independent of baseline liver fat. Across the cohort, changes in vitamin D status interacted with liver fat to influence TG/HDL trajectories (β = 0.20, p = 0.034).
Conclusions
The metabolic response to changes in vitamin D status in adolescents with IR may vary based on racial and ethnic differences and liver fat status. These findings underscore the importance of considering liver fat and racial/ethnic background in vitamin D and metabolic health studies. Future research with more extensive and diverse cohorts spanning the fatty liver disease spectrum is needed to clarify these relationships.