Lupus & antiphospholipid syndrome

Neutrophil gelatinase-associated lipocalin (NGAL) in lupus nephritis and beyond

Lupus Sci MedPublished Cross-sectional study

Authors' conclusion

Blood levels of NGAL are increased in patients with SLE with decreased kidney function, and in those with secondary APS.

Study context

Population
Two independent Swedish SLE cohorts, disease controls and healthy controlstwo SLE cohorts plus controls
Participants
124 / 308 / 38 / 77
Exposure
SLE vs disease controls and healthy controls
  • SLE exploratoryn = 124
  • SLE validationn = 308
  • Disease controlsn = 38
  • Healthy controlsn = 77reference
Outcome
NGAL levels in peripheral blood (ELISA)
Methodological detailsexploratory and validation cohorts, in vitro mechanistic experiments
  • Exploratory and validation cohorts
  • In vitro mechanistic experiments

Main finding

As reported in the abstract

Serum NGAL, SLE vs healthy controls (exploratory cohort)
  • SLE exploratory vs Healthy controls: P = 0.021

Observational data: associations, not effects.

Further findings

Serum NGAL, SLE vs healthy controls (exploratory cohort)

Serum NGAL increased in SLE vs healthy controls
P = 0.021

Serum NGAL and histologically proven membranoproliferative lupus nephritis (LN) (exploratory cohort)

Serum NGAL associated with membranoproliferative LN
P = 0.018

Plasma NGAL in history of LN and in secondary antiphospholipid syndrome (APS) (validation cohort)

Plasma NGAL elevated in history of LN
P = 0.0048
Plasma NGAL elevated in SLE with secondary APS vs without
P = 0.0022

NGAL discrimination of creatinine clearance <60 mL/min (CKD stage 3 or more)

AUC, exploratory and validation cohort, respectively
0.92 (p<0.0001) and 0.94 (p=0.0088)
  • High accuracy in both cohorts

NGAL secretion by immune complexes (IC)-stimulated neutrophils

Neutrophils stimulated with IC secrete more NGAL vs baseline; blocked by adding a TLR8i

Original publication

Neutrophil gelatinase-associated lipocalin (NGAL) in lupus nephritis and beyond. Lupus Sci Med. Published 14 January 2025. doi:10.1136/lupus-2024-001418

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.