# Diagnostic Value of Mean Platelet Volume and Hematological Inflammatory Ratios in Brucellosis: A Case–Control Study

**Authors:** Enes Dalmanoğlu, Yeşim Çağlar, Gülce Eylül Aldemir

PMC · DOI: 10.3390/life16020352 · 2026-02-18

## TL;DR

This study shows that blood tests like mean platelet volume and inflammatory ratios can help diagnose brucellosis, especially in resource-limited areas.

## Contribution

The study introduces a combined model using MPV, ESR, and CRP for improved brucellosis diagnosis.

## Key findings

- Brucellosis patients had significantly lower MPV and altered inflammatory ratios compared to healthy controls.
- The combined model of MPV, ESR, and CRP achieved high diagnostic accuracy (AUC = 0.891).
- ESR alone showed the best individual diagnostic performance (AUC = 0.842).

## Abstract

Brucellosis diagnosis remains challenging in resource-limited endemic settings. This retrospective case–control study evaluated the diagnostic utility of mean platelet volume (MPV) and hematological inflammatory ratios in brucellosis. Fifty patients with confirmed brucellosis and 50 age-matched healthy controls were included at a university hospital in Turkey (2015–2018). Complete blood count parameters, hematological ratios (neutrophil-to-lymphocyte ratio [NLR], platelet-to-lymphocyte ratio [PLR], lymphocyte-to-monocyte ratio [LMR]), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) were measured at diagnosis. Receiver operating characteristic (ROC) curve analysis evaluated diagnostic performance; multivariate logistic regression developed a combined model. Brucellosis patients showed significantly lower MPV (8.04 ± 0.95 vs. 8.56 ± 0.69 fL, p = 0.002), higher platelet counts (305.0 ± 116.0 vs. 246.0 ± 55.2 × 103/μL, p = 0.002), lower NLR (median: 1.69 vs. 2.07, p = 0.013), and higher LMR (median: 5.28 vs. 4.12, p = 0.008). ESR demonstrated the best individual diagnostic performance (area under the curve [AUC] = 0.842). The combined model (MPV + ESR + CRP) achieved superior performance (AUC = 0.891, sensitivity 84%, specificity 86%). Limitations include the single-center retrospective design, lack of internal validation, and comparison with healthy controls only. Notably, healthy controls were deliberately selected to establish baseline hematological profiles associated with brucellosis rather than to differentiate it from other infections. Brucellosis presents a unique hematological profile with decreased MPV and altered inflammatory ratios. The combined model offers a potentially cost-effective screening approach for endemic settings, pending external validation.

## Linked entities

- **Diseases:** brucellosis (MONDO:0005683)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, THPO (thrombopoietin) [NCBI Gene 7066] {aka CAMT2, MGDF, MKCSF, ML, MPLLG, THC9}, SAT1 (spermidine/spermine N1-acetyltransferase 1) [NCBI Gene 6303] {aka DC21, KFSD, KFSDX, SAT, SSAT, SSAT-1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** orchitis (MESH:D009920), hepatitis B (MESH:D006509), anorexia (MESH:D000855), malignancies (MESH:D009369), alcohol abuse (MESH:D000437), injury to (MESH:D014947), liver disease (MESH:D008107), Inflammatory (MESH:D007249), NLR (MESH:D015467), lupus (MESH:D008180), periprosthetic joint infection (MESH:D057068), acute (MESH:D000208), febrile illnesses (MESH:D005334), acute pyelonephritis (MESH:D011704), ankylosing spondylitis (MESH:D013167), pneumonia (MESH:D011014), lymphadenopathy (MESH:D008206), familial Mediterranean fever (MESH:D010505), autoimmune diseases (MESH:D001327), febrile (MESH:D000071072), arthralgia (MESH:D018771), weight loss (MESH:D015431), acute hepatitis B (MESH:D017114), urinary tract infections (MESH:D014552), advanced (MESH:D020178), infected (MESH:D007239), thrombocytopenia (MESH:D013921), adult-onset Still's disease (MESH:D016706), hematological disorders (MESH:D006402), viral infections (MESH:D014777), neutrophilia (MESH:C563010), portal hypertension (MESH:D006975), bacterial meningitis (MESH:D016920), rheumatoid arthritis (MESH:D001172), thrombotic (MESH:D013927), sepsis (MESH:D018805), Brucella infection (MESH:D002006), chronic (MESH:D002908), Infectious Diseases (MESH:D003141), typhoid fever (MESH:D014435), septic (MESH:D001170), chronic hepatitis B (MESH:D019694), myalgia (MESH:D063806), zoonotic (MESH:D015047), tuberculosis (MESH:D014376), orthopedic infections (MESH:D009140), bacterial infection (MESH:D001424), reactive thrombocytosis (MESH:D013922), infective endocarditis (MESH:D004696), inflammatory bowel disease (MESH:D015212), kidney disease (MESH:D007674)
- **Chemicals:** ciprofloxacin (MESH:D002939), streptomycin (MESH:D013307), EDTA (MESH:D004492), doxycycline (MESH:D004318), rifampin (MESH:D012293), fatty acids (MESH:D005227), K2-EDTA (-), lipopolysaccharide (MESH:D008070)
- **Species:** Salmonella enterica subsp. enterica serovar Typhi (no rank) [taxon 90370], Meleagris gallopavo (common turkey, species) [taxon 9103], Brucella (genus) [taxon 234], Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773], Brucella melitensis (species) [taxon 29459], Coxiella burnetii (species) [taxon 777], Bos taurus (bovine, species) [taxon 9913]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12942087/full.md

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Source: https://tomesphere.com/paper/PMC12942087