Tsoukalas Dimitris, Sarandi Evangelia, Fragoulakis Vassilleios, Xenidis Symeon, Mhliopoulou Maria, Charta Maria, Paramera Efstathia, Papakonstantinou Evangelos, Tsatsakis Aristidis
European Institute of Molecular Medicine, Rome, Italy.
Metabolomic Medicine, Athens, Greece.
BMJ Nutr Prev Health. 2024 Dec 7;7(2):e000883. doi: 10.1136/bmjnph-2024-000883. eCollection 2024.
Non-communicable diseases (NCDs), known as chronic diseases, significantly impact patients' quality of life (QoL) and increase medical expenses. The majority of risk factors are modifiable, and metabolomics has been suggested as a promising strategy for their evaluation, though real-world data are scarce. This study evaluated the QoL improvement and cost-effectiveness of a metabolomics-based treatment for NCDs, aiming to restore metabolic dysfunctions and nutritional deficiencies.
We performed a pre-post intervention analysis using clinical, metabolomics, QoL and economic data obtained from the electronic health records of 765 patients visiting a private practice. The intervention consisted of personalised treatment to restore metabolic dysfunctions and nutritional deficiencies identified by metabolomics alongside the standard treatment for their condition. The mean intervention duration was 401 days.
Significant improvement was identified in energy levels, sleep quality, gastrointestinal function and physical activity (p<0.001). 67.9% of participants reported significant improvement in the overall QoL, and the average quality-adjusted life-years (QALYs) increased by 0.064 (95% uncertainty interval 0.050 to 0.078) post-treatment. The incremental cost-effectiveness ratio was estimated at €49.774/QALY (95% CI €40.110 to €61.433). Metabolic profiling demonstrated that 16/35 organic acids and 11/24 total fatty acids were significantly changed post-treatment (p<0.001), participating in key pathways such as energy metabolism, microbiome and neurotransmitter turnover. Vitamin D and 5-methyltetrahydrofolate insufficiency was significantly restored (p=0.036).
This is the first study providing evidence that the integration of metabolomics in clinical practice can have a clinical benefit for patients' QoL and may be a cost-effective method.
非传染性疾病(NCDs),即慢性病,对患者的生活质量(QoL)有重大影响,并增加医疗费用。大多数风险因素是可改变的,代谢组学已被认为是评估这些因素的一种有前景的策略,尽管实际数据很少。本研究评估了基于代谢组学的非传染性疾病治疗对生活质量的改善和成本效益,旨在恢复代谢功能障碍和营养缺乏。
我们使用从765名就诊于私人诊所的患者的电子健康记录中获取的临床、代谢组学、生活质量和经济数据进行了干预前后分析。干预措施包括个性化治疗,以恢复代谢组学确定的代谢功能障碍和营养缺乏,同时结合针对其病情的标准治疗。平均干预持续时间为401天。
在能量水平、睡眠质量、胃肠功能和身体活动方面发现了显著改善(p<0.001)。67.9%的参与者报告总体生活质量有显著改善,治疗后平均质量调整生命年(QALYs)增加了0.064(95%不确定区间0.050至0.078)。增量成本效益比估计为49.774欧元/QALY(95%CI 40.110欧元至61.433欧元)。代谢谱分析表明,16/35种有机酸和11/24种总脂肪酸在治疗后有显著变化(p<0.001),参与能量代谢、微生物群和神经递质周转等关键途径。维生素D和5-甲基四氢叶酸缺乏症得到显著恢复(p=0.036)。
这是第一项提供证据表明将代谢组学整合到临床实践中对患者生活质量有临床益处且可能是一种具有成本效益的方法的研究。