Skip to main content

Table 1 Bioactive lipids and cytokines measured in sepsis and other critically ill patients correlated with prognosis

From: n-3 fatty acids, γ-linolenic acid, and antioxidants in sepsis

Source of body fluid/tissue

Bioactive lipids to be measured

Time when measured in sepsis/critical illness

Method of measurement

Probable change

Plasma

PUFAs: LA, GLA, DGLA, AA, ALA, EPA, DHA and their trans-fatty acids

On admission, every 24 hours until discharge or death

GC; LC-MS

GLA, AA, EPA and DHA ↓ at admission; restored to normal if appropriate external supplementation is given; trans-fatty acids ↑ at admission, will decrease if inflammation is contained and indicates relatively good prognosis

Plasma

Various PGs, LTs, TXs

On admission, every 24 hours until discharge or death

ELISA-HPLC

↑ in 2-series PGs and TXs, and 4-series LTs indicates inflammatory process is dominant; ↑ in 3-series PGs and TXs, and 5-series LTs indicates that the administered EPA is being converted to these products; to be correlated with levels of lipoxins, resolvins, protectins and maresins; ↓ in 2-series PGs and TXs, and 4-series LTs after GLA/EPA/DHA supplementation indicates decreasing tendency of inflammation

Plasma

Lipoxins, resolvins, protectins, maresins

On admission, every 24 hours until discharge or death

LC-MS

Lipoxins, resolvins, protectins, maresins ↓ at admission; restored to normal if patient is improving, remain low if prognosis is poor

Plasma

Nitrolipids

On admission, every 24 hours until discharge or death

LC-MS/MS-MS

Nitrolipids ↓ at admission; restored to normal if patient is improving, remain low if prognosis is poor

Plasma

Isoprostanes

On admission, every 24 hours until discharge or death

LC-MS/MS-MS

Isoprostanes ↑ at admission; restored to normal if patient is improving, remain high if prognosis is poor

Plasma

Cytokines

On admission, every 24 hours until discharge or death

ELISA and/or flow cytometric-based immunofluorescence assays

If proinflammatory cytokines ↑, inflammation is dominant; if anti-inflammatory cytokines ↑, recovery process is on the anvil; correlation needs to be made among cytokine profile, bioactive lipids and clinical picture

  1. Shown are bioactive lipids and cytokines that could be measured at various time points in patients with sepsis and other critical illnesses and correlated with prognosis. These bioactive lipids/cytokines and other compounds could also be measured in urine at different time points and correlated with their plasma levels and prognosis of the patient. Although not mentioned in the table, other measurements that could be performed include lipid peroxides, nitric oxide, antioxidants (such as superoxide dismutase, glutathione, catalase) and adipose-fatty acid binding protein. AA, arachidonic acid; ALA, α-linolenic acid; DGLA, dihomo-γ-linolenic acid; DHA, docosahexaenoic acid; ELISA, enzyme-linked immunosorbent assay; EPA, eicosapentaenoic acid; GC, gas chromatography; GLA, γ-linolenic acid; HPLC, high-performance liquid chromatography; LA, linoleic acid; LC-MS, liquid chromatography-mass spectrometry; LT, leukotriene; MS-MS, tandem mass spectrometry; PG, prostaglandin; PUFA, polyunsaturated fatty acid; TX, thromboxane.