Abstract

Many studies have found correlations between abnormal MPV and clinical reactivity in a variety of diseases. In the present paper, we sought MPV-related neurological diseases that are less frequently reported in the literature. The electronic medical records of 852 neurological patients with mean platelet volume (MPV) measurements (F = 45%, age = 55.7 ± 18.7, 8–104) were searched after the patients had received a diagnosis of a neurological disease (new and old episodes) according to the nine classes of the International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10). A set of consecutive statistical methods (i.e., cluster analysis, segmented regression, linear correlation, propensity score matching, and mixed effects Poisson regression) were used to establish a link between MPV and neurological disease. A statistically significant (p < 0.05) relationship with MPV was found only in pain syndrome patients, with seven out of eight clinically diagnosed migraine episodes. With all other ICD-10 classes of neurological diseases, the effect of MPV was found to be nonsignificant (p > 0.05). MPV may implicate a clinical relationship with pain syndrome and migraine episodes. More complex statistics could help analyse data and find new correlations.

Highlights

  • The mean platelet volume (MPV) is an measurable haematologic standard parameter

  • Large platelets are associated with prothrombotic states and cardiovascular disease, whereas small platelets are detected in chronic inflammatory diseases or rheumatoid arthritis [3]

  • In some studies, there was no statistically significant association between appendicitis and MPV [4,5,6], while in another, the MPV was significantly lower in acute gangrenous appendicitis than in control healthy subjects [7]

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Summary

Introduction

The mean platelet volume (MPV) is an measurable haematologic standard parameter. Many scientists have discussed its interpretation and have found correlations between abnormal MPV and clinical reactivity in a variety of diseases [1]. It is believed that several diseases are associated with MPV changes. Abnormal MPV is associated with poor prognosis in several diseases ( confirmed in our study [2]). The MPV is elevated in rheumatoid arthritis, and its cut-off level was estimated to be 10.4 fL [8]. The interpretation of the MPV is not as straightforward as it might appear [1]. One reason for this might be that there is currently no preanalytical standard when dealing with MPV measurements [9]. Some authors have even demonstrated the high technical

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