Research Tracker›Biomarker Atlas›Gulf War Illness›C-Reactive Protein (CRP)

C-Reactive Protein (CRP) in Gulf War Illness

In Gulf War Illness (GWI, Gulf War Syndrome), published studies report higher levels of C-Reactive Protein (CRP), also described as Acute phase protein, than in healthy Gulf War veteran controls. Clinically, it has been associated with chronic low-grade inflammation. The finding is drawn from Johnson et al. 2016; it describes group-level differences, not a threshold that classifies an individual.

↑ ElevatedInflammatoryLOINC 1988-5

Summary

Direction in Gulf War Illness↑ Elevated — higher than in the comparison group
CategoryInflammatory
Also described asAcute phase protein
Compared againstHGV (healthy Gulf War veteran controls)
Associated symptomsChronic low-grade inflammation
Test typeBlood test (serum / plasma / whole blood)
LOINC code1988-5
SourceJohnson et al. 2016 — doi:10.1371/journal.pone.0157855
Condition atlasGulf War Illness Biomarker Atlas

Other conditions where CRP is reported

See the cross-condition hub: CRP across conditions.

Trials, interventions and tests

In clinical-trial registrations this marker maps to the outcome term C-Reactive Protein (21 registered trials use a matching outcome measure).

Clinical trials using C-Reactive Protein (CRP) as an outcome

13 more trials reference this marker.

Interventions studied alongside this marker

Hypothesis-generating links from trial outcome usage and literature co-occurrence. Not treatment recommendations.

Commercial test availability

C-Reactive Protein (CRP) — commercial laboratory test.

Links are for reference only; availability, specimen requirements and coverage vary by location.

Related Inflammatory markers in Gulf War Illness

Full list: Gulf War Illness Biomarker Atlas.

Frequently asked questions

Is C-Reactive Protein (CRP) high or low in Gulf War Illness?

Elevated. Studies summarised in the OSMF atlas report higher C-Reactive Protein (CRP) in Gulf War Illness than in healthy Gulf War veteran controls. Source: Johnson et al. 2016.

What symptoms is C-Reactive Protein (CRP) associated with in Gulf War Illness?

The cited literature associates this marker with Chronic low-grade inflammation. These are population-level associations and do not mean the marker causes the symptoms.

Which test measures C-Reactive Protein (CRP)?

It is measured as a blood test (serum / plasma / whole blood). The standard laboratory code is LOINC 1988-5. Commercial laboratories such as Quest Diagnostics, LabCorp, Ulta Lab Tests list an orderable assay.

Is one abnormal C-Reactive Protein (CRP) result diagnostic of Gulf War Illness?

No. No single biomarker is diagnostic of Gulf War Illness. C-Reactive Protein (CRP) findings come from group comparisons, overlap considerably between patients and controls, and vary with study design, timing and comparison group. A result should be interpreted by a clinician alongside symptoms, history and other tests.

Is C-Reactive Protein (CRP) specific to Gulf War Illness?

No. The same marker is also reported in Atrial Fibrillation, COPD, Inflammatory Bowel Disease (Crohn's/UC), Long COVID, Low Back Pain, Lyme Disease, ME/CFS, Major Depressive Disorder, Osteoarthritis, Rheumatoid Arthritis in this atlas, so it reflects shared biology (for example inflammation or vascular stress) rather than a condition-specific signature.

Cite this page

Open Source Medicine Foundation. (2026). C-Reactive Protein (CRP) in Gulf War Illness: direction, evidence and what it means. OSMF Research Tracker. Retrieved October 7, 2026, from https://research.opensourcemed.info/biomarkers/gulf-war-illness/c-reactive-protein-crp.html
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Last reviewed: 2026-06-29 · Page generated from gulf-war-illness.json · Browse: Gulf War Illness atlas · Biomarker Index · All marker pages

Disclaimer: This page is an educational synthesis of published, peer-reviewed research and is not medical advice. Biomarker findings vary across studies with case definitions, comparison groups, timing and assay methods. Direction of change reflects the predominant finding in the cited source and does not establish a diagnostic threshold. Discuss any test result with a qualified clinician.