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Blood Cell Ratios as Predictors of Response to Platelet-Rich Plasma in Knee Osteoarthritis (PRP-NLR)

20 maggio 2026 aggiornato da: Utku Gürhan

Baseline Neutrophil-to-Lymphocyte Ratio and Related Complete Blood Count-Derived Inflammatory Indices as Predictors of Clinical Response to Intra-Articular Platelet-Rich Plasma in Knee Osteoarthritis: A Prospective Single-Arm Cohort Study

Intra-articular platelet-rich plasma (PRP) injection is a widely used treatment for knee osteoarthritis, but patients respond to it very differently and there is currently no simple, inexpensive way to predict who will benefit. The neutrophil-to-lymphocyte ratio (NLR) and related indices derived from a routine complete blood count reflect a person's baseline inflammatory state. This prospective single-arm observational cohort study investigates whether the baseline NLR, together with the platelet-to-lymphocyte ratio (PLR), the systemic immune-inflammation index (SII), and the monocyte-to-lymphocyte ratio (MLR), predicts the clinical response to intra-articular PRP in patients with Kellgren-Lawrence grade 2 to 3 knee osteoarthritis. The investigators will enroll 120 patients aged 40 to 60 years, each of whom receives a standardized course of three leukocyte-poor PRP injections one week apart. Patients are followed for 6 months, and the primary clinical outcome is the change in the WOMAC osteoarthritis index at 6 months. Outcome assessors are blinded to patients' blood-count values. If a baseline blood ratio predicts response, it could become a low-cost tool to guide patient selection for PRP.

Panoramica dello studio

Stato

Non ancora reclutamento

Descrizione dettagliata

Background and Rationale: Intra-articular platelet-rich plasma (PRP) is increasingly used for symptomatic knee osteoarthritis, but the clinical response is highly variable and no inexpensive, routinely available biomarker currently guides patient selection. Recent work indicates that the peripheral-blood inflammatory phenotype is associated with PRP response (Tonutti et al., 2025) and that the absolute neutrophil count is an independent early-response predictor (De Luca et al., 2025). However, simple complete-blood-count-derived ratios such as the neutrophil-to-lymphocyte ratio (NLR) have not been tested prospectively for this purpose. This study addresses that gap with a pragmatic, low-cost translational biomarker design.

Design: Prospective, single-arm, observational cohort study. Outcome assessors are blinded to patients' blood-count values; patients are not informed of their NLR; statistical analysis is conducted blinded.

Population and Setting: 120 patients aged 40 to 60 years with symptomatic Kellgren-Lawrence grade 2 to 3 knee osteoarthritis and a body mass index below 40, recruited over a 4-month window (target 30 enrollments per month) from the Department of Orthopaedics and Traumatology, University of Kyrenia, Dr. Suat Gunsel Hospital. Approximately 180 patients are anticipated to be screened, with a target of 102 completed, analyzable participants after an estimated 15 percent attrition.

Intervention (uniform, per protocol): Each participant receives three leukocyte-poor PRP injections at one-week intervals. PRP is prepared by manual double-spin centrifugation (soft spin 1500 rpm for 5 minutes, then hard spin 3300 rpm for 10 minutes) from 20 mL of whole blood per session (total 60 mL per patient across the three sessions), anticoagulated with 8.5 percent ACD-A, without exogenous activation, targeting a 4 to 6 fold platelet concentration. Injections are delivered under ultrasound guidance via a superolateral approach with skin infiltration of 1 percent lidocaine. A 48-hour restriction on non-steroidal anti-inflammatory drugs is applied after each injection.

Biomarkers: The primary predictor is the baseline NLR. Secondary predictors are PLR, SII, and MLR; tertiary predictors are C-reactive protein and erythrocyte sedimentation rate. All are derived from a routine baseline complete blood count.

Outcomes: The primary clinical outcome is the change in WOMAC total score at 6 months. Treatment response is defined a priori as at least 30 percent improvement in WOMAC together with fulfilment of the OMERACT-OARSI responder criteria. Clinical assessments occur at baseline and at 1, 3, and 6 months.

PRP Product Characterization: Quality control is performed in two tiers. Tier 1 (all 120 patients, all 360 batches) records the final platelet concentration, the total leukocyte count, and the final volume. Tier 2, a pre-specified validation subset of approximately 40 patients (the first 20 consecutive patients plus every fifth subsequent patient, approximately 120 batches), additionally records the leukocyte differential and erythrocyte contamination.

Statistical Analysis and Sample Size: The primary analysis is a multivariable linear regression of 6-month WOMAC change on baseline NLR, adjusted for age, body mass index, Kellgren-Lawrence grade, and baseline WOMAC. A secondary analysis evaluates the discriminative performance of baseline NLR for responder status by receiver operating characteristic analysis. For the primary regression (alpha 0.05, power 0.80, one numerator degree of freedom, five predictors, effect size f-squared 0.10), 82 participants are required; the secondary analysis requires 95. To satisfy both, the enrollment target is 120, anticipating 102 completers.

Ethics and Reporting: Ethics approval is sought from the Girne University Clinical Research Ethics Committee. Reporting follows the STROBE and REMARK recommendations, and the protocol follows SPIRIT guidance.

Tipo di studio

Osservativo

Iscrizione (Stimato)

120

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

      • Kyrenia, Cipro
        • University of Kyrenia, Dr. Suat Gunsel Hospital - Department of Orthopaedics and Traumatology
        • Contatto:
        • Investigatore principale:
          • Utku Gurhan, MD
        • Sub-investigatore:
          • Fazli Levent Umur, MD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

No

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Adult patients aged 40 to 60 years presenting to the orthopedic clinic of the University of Kyrenia, Dr. Suat Gunsel Hospital, with symptomatic primary knee osteoarthritis of Kellgren-Lawrence grade 2 or 3, who are candidates for and scheduled to receive a course of intra-articular platelet-rich plasma for the index knee.

Descrizione

Inclusion Criteria:

  • Age 40 to 60 years
  • Symptomatic primary knee osteoarthritis, Kellgren-Lawrence grade 2 or 3 on weight-bearing radiographs
  • Body mass index below 40
  • Candidate for and scheduled to receive a course of intra-articular platelet-rich plasma for the index knee
  • Able and willing to provide written informed consent and to attend the 6-month follow-up schedule

Exclusion Criteria:

  • Systemic inflammatory or autoimmune disease
  • Active acute infection at the time of enrollment
  • Current anticoagulant or antiplatelet therapy, or current or recent chemotherapy
  • Any contraindication to platelet-rich plasma per the 2025 GRIIP recommendations
  • Intra-articular injection of the index knee within the previous 6 months
  • Inability to comply with the planned follow-up schedule

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in WOMAC total score at 6 months
Lasso di tempo: Baseline to 6 months
Change from baseline in the total score of the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) at 6 months after the first injection. The primary analysis is a multivariable linear regression testing the baseline neutrophil-to-lymphocyte ratio (NLR) as the predictor of interest, adjusted for age, body mass index, Kellgren-Lawrence grade, and baseline WOMAC score.
Baseline to 6 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Treatment response at 6 months (responder versus non-responder)
Lasso di tempo: Baseline to 6 months
Treatment response is defined a priori as at least 30 percent improvement in WOMAC total score together with fulfilment of the OMERACT-OARSI responder criteria. The discriminative performance of the baseline NLR for responder status is assessed by receiver operating characteristic analysis with the optimal threshold identified by the Youden index.
Baseline to 6 months
Predictive value of PLR, SII, and MLR for 6-month WOMAC change
Lasso di tempo: Baseline to 6 months
Association of the baseline platelet-to-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), and monocyte-to-lymphocyte ratio (MLR) with the change in WOMAC total score at 6 months, evaluated by multivariable regression.
Baseline to 6 months
Change in WOMAC total score at 1 and 3 months
Lasso di tempo: Baseline to 1 month and to 3 months
Change from baseline in WOMAC total score at the 1-month and 3-month assessments, describing the trajectory of clinical response.
Baseline to 1 month and to 3 months
Change in knee pain on a Visual Analogue Scale
Lasso di tempo: Baseline to 1, 3, and 6 months
Change from baseline in knee pain on a Visual Analogue Scale at the 1-month, 3-month, and 6-month assessments.
Baseline to 1, 3, and 6 months
Change in the Knee injury and Osteoarthritis Outcome Score (KOOS)
Lasso di tempo: Baseline to 6 months
Change from baseline in the Knee injury and Osteoarthritis Outcome Score (KOOS) subscale scores at 6 months.
Baseline to 6 months
Association of baseline CRP and ESR with treatment response
Lasso di tempo: Baseline to 6 months
Exploratory association of the baseline C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) with 6-month treatment response.
Baseline to 6 months

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Platelet-rich plasma product characterization
Lasso di tempo: At the three injection sessions (study weeks 1, 2, and 3)
Two-tier quality control of the PRP product. Tier 1 (all 120 patients, all 360 batches): final platelet concentration, total leukocyte count, and final volume. Tier 2 (a pre-specified validation subset of approximately 40 patients, approximately 120 batches): leukocyte differential and erythrocyte contamination.
At the three injection sessions (study weeks 1, 2, and 3)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Utku Gurhan, MD, University of Kyrenia
  • Sub-investigatore: Fazli Levent Umur, MD, University of Kyrenia
  • Sub-investigatore: Enes Sari, MD, Near East University
  • Sub-investigatore: Yakup Kahve, MD, Ankara City Hospital Bilkent

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

  • Tonutti et al. Biomed Pharmacother. 2025. doi:10.1016/j.biopha.2025.118674
  • De Luca et al. Nutrients. 2025. doi:10.3390/nu17193134
  • Lee et al. BMC Musculoskelet Disord. 2024. doi:10.1186/s12891-024-07475-1
  • Zhang et al. Front Med (Lausanne). 2026. doi:10.3389/fmed.2026.1787872
  • Louis et al. Arthroscopy. 2021. doi:10.1016/j.arthro.2021.03.074
  • GRIIP recommendations on intra-articular orthobiologics. Knee Surg Sports Traumatol Arthrosc. 2025. doi:10.1002/ksa.12682

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 settembre 2026

Completamento primario (Stimato)

1 luglio 2027

Completamento dello studio (Stimato)

1 luglio 2027

Date di iscrizione allo studio

Primo inviato

20 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

20 maggio 2026

Primo Inserito (Effettivo)

1 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

20 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano IPD

De-identified participant-level data will be made available upon reasonable request to the corresponding author after publication, subject to institutional and ethics-committee approval. Aggregated summary tables will accompany the published manuscript as supplementary material.

Periodo di condivisione IPD

Beginning 6 months after manuscript publication, with no specified end date.

Criteri di accesso alla condivisione IPD

Reasonable request for academic research purposes; a data use agreement to be signed.

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • ICF
  • CODICE_ANALITICO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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