Division of Rheumatology, Inflammation and Immunity, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA, and Division of Rheumatology, Cumming School of Medicine, University of Calgary, Alberta, Canada.
Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA; Division of Cardiovascular Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA; and Center for Lipid Metabolomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Clin Exp Rheumatol. 2022 Nov;40(11):2196-2197. doi: 10.55563/clinexprheumatol/xxr27t. Epub 2022 Jul 21.
: Omega-3 fatty acid-derived “specialized pro-resolving mediators” are lipid mediators (LM) central to inflammation resolution. We investigated whether fish oil (FO) supplementation was associated with pro-inflammatory and pro-resolving LM levels in SLE patients compared to matched non-SLE controls.
: 16 SLE patients taking FO were matched (age, sex, race) to 16 non-SLE controls taking FO. Another 16 SLE patients not taking FO were matched to 16 non-SLE patients not taking FO. Demographic/clinical data were obtained by medical record review. Targeted liquid chromatography-tandem spectrometry was performed with plasma to quantify 27 LM. Multivariable linear analyses examined how SLE, FO, and their interaction were associated with LM levels, adjusting for potential confounders including inflammatory markers and SLE disease activity for SLE cases only.
: Higher levels of pro-inflammatory LMs were found in patients with SLE not on FO, compared to controls not on FO, particularly TXB (p=0.03). Lower levels of many SPMs were observed among patients with SLE taking FO compared to controls taking FO, including LXB (p<0.01) and 18-HEPE (p=0.04). In case-only analyses, taking FO was associated with higher 17-HDHA levels (p=0.05). There were no multiplicative interactions between FO effect and SLE status, and after adjustment for multiple comparisons, few of the associations persisted.
: In this cross-sectional exploratory study, higher levels of inflammatory LM and lower levels of SPMs were found in SLE patients than controls, among those taking and not taking FO. Further studies investigating the potentially beneficial biologic effects of FO preparations and doses in SLE are needed.
ω-3 脂肪酸衍生的“特殊的促解决介质”是炎症反应中脂质介质(LM)的关键。我们研究了与匹配的非 SLE 对照组相比,鱼油(FO)补充是否与 SLE 患者的促炎和促解决 LM 水平相关。
16 名服用 FO 的 SLE 患者与 16 名服用 FO 的非 SLE 对照者匹配(年龄、性别、种族)。另外 16 名未服用 FO 的 SLE 患者与 16 名未服用 FO 的非 SLE 患者相匹配。通过病历回顾获得人口统计学/临床数据。采用靶向液相色谱-串联质谱法对血浆进行分析,以定量 27 种 LM。多元线性分析检查 SLE、FO 及其相互作用如何与 LM 水平相关,仅在 SLE 病例中,调整潜在混杂因素,包括炎症标志物和 SLE 疾病活动度。
与未服用 FO 的非 SLE 对照组相比,未服用 FO 的 SLE 患者的促炎 LM 水平更高,特别是 TXB(p=0.03)。与服用 FO 的对照组相比,服用 FO 的 SLE 患者的许多 SPM 水平较低,包括 LXB(p<0.01)和 18-HEPE(p=0.04)。在仅病例分析中,服用 FO 与较高的 17-HDHA 水平相关(p=0.05)。FO 作用与 SLE 状态之间没有乘法相互作用,并且在进行多次比较调整后,很少有相关性仍然存在。
在这项横断面探索性研究中,与服用或未服用 FO 的对照组相比,服用 FO 的 SLE 患者的炎症 LM 水平更高,SPM 水平更低。需要进一步研究 FO 制剂和剂量在 SLE 中的潜在有益的生物学作用。