Increased Plasma Levels of Triglyceride-Enriched Lipoproteins Associate with Systemic Inflammation, Lipopolysaccharides, and Gut Dysbiosis in Common Variable Immunodeficiency

被引:8
|
作者
Macpherson, Magnhild E. E. [1 ,2 ]
Skarpengland, Tonje [1 ,2 ]
Hov, Johannes R. R. [1 ,3 ,4 ,5 ]
Ranheim, Trine [1 ]
Vestad, Beate [1 ,4 ]
Dahl, Tuva B. B. [1 ,6 ]
Fraz, Mai S. A. [2 ]
Michelsen, Annika E. E. [1 ,3 ]
Holven, Kirsten B. B. [7 ,8 ]
Fevang, Borre [1 ,2 ,9 ]
Berge, Rolf K. K. [10 ,11 ]
Aukrust, Pal [1 ,2 ,3 ]
Halvorsen, Bente [1 ,3 ]
Jorgensen, Silje F. F. [1 ,2 ]
机构
[1] Oslo Univ Hosp, Res Inst Internal Med, Rikshospitalet, Oslo, Norway
[2] Oslo Univ Hosp, Sect Clin Immunol & Infect Dis, Rikshospitalet, Oslo, Norway
[3] Univ Oslo, Inst Clin Med, Oslo, Norway
[4] Oslo Univ Hosp, Norwegian PSC Res Ctr, Dept Transplantat Med, Div Surg Inflammatory Dis & Transplantat,Rikshospi, Oslo, Norway
[5] Oslo Univ Hosp, Dept Transplantat Med, Div Surg Inflammatory Dis & Transplantat, Sect Gastroenterol, Oslo, Norway
[6] Oslo Univ Hosp, Dept Acute Med, Oslo, Norway
[7] Univ Oslo, Inst Basic Med Sci, Dept Nutr, Oslo, Norway
[8] Oslo Univ Hosp, Norwegian Natl Advisory Unit Familial Hypercholest, Rikshospitalet, Oslo, Norway
[9] Oslo Univ Hosp, Ctr Rare Disorders, Oslo, Norway
[10] Univ Bergen, Dept Clin Sci, N-5020 Bergen, Norway
[11] Haukeland Hosp, Dept Heart Dis, N-5021 Bergen, Norway
关键词
Triglycerides; VLDL; Lipids; LPS; CVID; Gut microbiota; Metabolism; DENSITY-LIPOPROTEIN; RISK; MARKERS;
D O I
10.1007/s10875-023-01475-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
PurposeTriglycerides (TG) and their major transport lipoprotein in the circulation (VLDL) appear to be related to inflammation. Patients with common variable immunodeficiency (CVID) have inflammatory complications associated with gut microbial dysbiosis. We hypothesized that CVID patients have disturbed TG/VLDL profiles associated with these clinical characteristics.MethodsWe measured plasma concentrations of TGs, inflammatory markers, and lipopolysaccharide (LPS) in 95 CVID patients and 28 healthy controls. Additionally, in 40 CVID patients, we explored plasma lipoprotein profiling, fatty acid, gut microbial dysbiosis, and diet.ResultsTG levels were increased in CVID patients as compared to healthy controls (1.36 +/- 0.53 mmol/l versus 1.08 +/- 0.56 [mean, SD], respectively, P = 0.008), particularly in the clinical subgroup "Complications," characterized by autoimmunity and organ-specific inflammation, compared to "Infection only" (1.41 mmol/l, 0.71[median, IQR] versus [1.02 mmol/l, 0.50], P = 0.021). Lipoprotein profile analyses showed increased levels of all sizes of VLDL particles in CVID patients compared to controls. TG levels correlated positively with CRP (rho = 0.256, P = 0.015), IL-6 (rho = 0.237, P = 0.021), IL-12 (rho = 0.265, P = 0.009), LPS (r = 0.654, P = 6.59 x 10(-13)), CVID-specific gut dysbiosis index (r = 0.315, P = 0.048), and inversely with a favorable fatty acid profile (docosahexaenoic acid [rho = - 0.369, P = 0.021] and linoleic acid [rho = - 0.375, P = 0.019]). TGs and VLDL lipids did not appear to be associated with diet and there were no differences in body mass index (BMI) between CVID patients and controls.ConclusionWe found increased plasma levels of TGs and all sizes of VLDL particles, which were associated with systemic inflammation, LPS, and gut dysbiosis in CVID, but not diet or BMI.
引用
收藏
页码:1229 / 1240
页数:12
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