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

18 de junio de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Aún no reclutando

Descripción detallada

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 de estudio

De observación

Inscripción (Estimado)

120

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Utku Gurhan, MD
  • Número de teléfono: +90 539 112 6898
  • Correo electrónico: utkugrhn@gmail.com

Ubicaciones de estudio

      • Kyrenia, Chipre
        • University of Kyrenia, Dr. Suat Gunsel Hospital - Department of Orthopaedics and Traumatology
        • Contacto:
        • Investigador principal:
          • Utku Gurhan, MD
        • Sub-Investigador:
          • Fazli Levent Umur, MD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

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.

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in WOMAC total score at 6 months
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Treatment response at 6 months (responder versus non-responder)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Platelet-rich plasma product characterization
Periodo de tiempo: 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)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

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

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • 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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de julio de 2027

Finalización del estudio (Estimado)

1 de julio de 2027

Fechas de registro del estudio

Enviado por primera vez

20 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

20 de mayo de 2026

Publicado por primera vez (Actual)

1 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

23 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

18 de junio de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan 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.

Marco de tiempo para compartir IPD

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

Criterios de acceso compartido de IPD

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

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • CIF
  • CÓDIGO_ANALÍTICO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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