Abstract
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Evaluation of Neutrophil-Related Parameters by Hematology Analyzer for Detection of Myelodysplastic Syndromes
by Yosuke Kato, Kiyoyuki Ogata, Yumi Yamamoto, Yuto Mochimaru, Daisuke Sakamoto, Koji Teruya, Tomohiko Taki, Satoko Yamasaki, Hiroaki Ohnishi
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Background: Myelodysplastic syndromes (MDS) are characterized by dysplasia, which is crucial for diagnosis. Dysplastic features in the WHO classification include granulocyte size abnormalities. However, the relationship between granulocyte size and automated hematology analyzer parameters has not been investigated.
In this study, we aimed to establish an objective marker for identifying dysplasia in MDS by evaluating the association between neutrophil-related parameters from an automated hematology analyzer and morphological dysplasia, including abnormalities in neutrophil size.
Methods: Samples were collected from 75 MDS and 149 non-MDS cases and analyzed using XR-1000. The non-MDS cases were classified into six disease groups. Neutrophil-related parameters, including forward scatter (NE-FSC), side scatter (NE-SSC), and side fluorescence (NE-SFL), were analyzed. Morphological dysplasia was assessed by light microscopy using Wright-Giemsa-stained smears. The neutrophil area was quantified with ImageJ software.
Results: Compared with the other groups, the NE-FSC values were significantly lower in the MDS group than in the four disease groups (p < 0.01). The NE-SFL values were significantly lower in the MDS group than in the two disease groups (p < 0.01). No significant differences in NE-SSC were observed between the MDS group and any of the six disease groups. Among the MDS cases, 47 cases showed ≥ 10% neutrophil dysplasia (MDS with dysplasia) and 28 cases showed < 10% (MDS without dysplasia). The control group consisted of 50 non-MDS cases with normal blood counts and smears. When comparing the three groups, NE-FSC was highest in controls, intermediate in MDS without dysplasia, and lowest in MDS with dysplasia (p < 0.01). NE-SFL and NE-SSC were significantly lower in MDS with dysplasia compared with both controls and MDS without dysplasia (p < 0.001), with no difference between controls and MDS without dysplasia. Neutrophil area was significantly smaller in both MDS groups than in controls (p < 0.001) but did not differ between MDS with and without dysplasia. ROC analysis was performed to evaluate the diagnostic accuracy between the MDS and non-MDS groups, and the AUCs were 0.756 for NE-FSC, 0.632 for NE-SSC, and 0.694 for NE-SFL.
Conclusions: NE-FSC is a useful parameter for detecting neutrophil dysplasia and may improve diagnostic accuracy in MDS.
DOI: 10.7754/Clin.Lab.2025.250830
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