1 Centre for Rheumatology Research, University College London, London, United Kingdom.
2 The Arthritis Research UK Centre for Adolescent Rheumatology, University College London, London, United Kingdom.
Lupus. 2019 May;28(6):755-763. doi: 10.1177/0961203319845473. Epub 2019 Apr 26.
Cardiovascular disease is the leading cause of mortality in patients with systemic lupus erythematosus. Therefore, using diet to control blood lipid levels and modify cardiovascular disease risk could be a promising therapeutic strategy to control disease symptoms. The primary objective of this study was to learn about systemic lupus erythematosus patient experiences with diet, including their opinion on considering diet as a therapeutic option. The secondary objective was to obtain this information in a cost- and time-effective manner.
A lay summary and a 15-question diet-based online survey were publicly available for 3 weeks. Social media was used to promote the survey through relevant charities, hospitals and research groups.
A total of 300 responses were received, 284 from patients with systemic lupus erythematosus. Patients reported that there was a lack of clinical counselling regarding diet, with only 24% stating their doctor had spoken to them about diet. Despite this, 100% of patients stated they would change their diet if they knew it would help their symptoms and 83% would take part in a future diet-based clinical trial. Text analysis of patient research suggestions identified a particular interest in using diet to treat fatigue and manage disease flares.
This project successfully gathered patient information regarding diet and systemic lupus erythematosus over a short timeframe using an anonymous social media platform. The survey provided evidence that patients support further research and potential diet intervention studies investigating the effect of diet on the symptoms of systemic lupus erythematosus.
心血管疾病是系统性红斑狼疮患者死亡的主要原因。因此,通过饮食来控制血脂水平并改变心血管疾病风险可能是控制疾病症状的一种有前途的治疗策略。本研究的主要目的是了解系统性红斑狼疮患者的饮食体验,包括他们对将饮食视为治疗选择的看法。次要目的是以具有成本效益和时间效益的方式获得这些信息。
提供通俗易懂的摘要和基于饮食的 15 个问题的在线调查,为期 3 周。通过相关慈善机构、医院和研究小组利用社交媒体宣传调查。
共收到 300 份回复,其中 284 份来自系统性红斑狼疮患者。患者报告称,他们缺乏关于饮食的临床咨询,只有 24%的患者表示医生曾与他们讨论过饮食问题。尽管如此,100%的患者表示如果他们知道饮食有助于改善症状,他们会改变饮食,83%的患者会参加未来的基于饮食的临床试验。对患者研究建议的文本分析表明,他们特别有兴趣使用饮食来治疗疲劳和控制疾病发作。
本项目使用匿名社交媒体平台在短时间内成功收集了患者关于饮食和系统性红斑狼疮的信息。该调查提供的证据表明,患者支持进一步研究和潜在的饮食干预研究,以调查饮食对系统性红斑狼疮症状的影响。