Evidence map›Paper›PMID 41896831›Full record

ArticleBMC pulmonary medicine2026

Monocyte distribution width as an adjunctive biomarker for differentiating pulmonary tuberculosis from cavitary nontuberculous mycobacterial pulmonary disease.

Kentaro Wakamatsu, Zenzo Nagasawa, Kouta Katsuki, Hiroyuki Kumazoe, Tomoki Takeyama, Shigesato Inoue, Katuyuki Katahira, Mizuko Ose, Naotaka Noda, Kouta Miyamoto and 10 more

Abstract read
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Article in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

20 authors.

Kentaro WakamatsuDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan. wakamatsu.kentaro.fe@mail.hosp.go.jp.
Zenzo NagasawaDepartment of Medical Technology and Science, Faculty of Fukuoka Health Care, International University of Health and Welfare, Fukuoka City, Fukuoka, Japan.
Kouta KatsukiDepartment of Clinical Laboratory, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Hiroyuki KumazoeDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Tomoki TakeyamaDepartment of Clinical Laboratory, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Shigesato InoueDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Katuyuki KatahiraDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Mizuko OseDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Naotaka NodaDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Kouta MiyamotoDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Daigo KawanoDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Miyoko TatutaDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Satoru FukuyamaDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Miru IzumiDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Ruriko KiyotaniDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Izumi FukuiDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Satomi AsaiDepartment of Laboratory Medicine, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
Nobuhiko NagataDepartment of Respiratory Medicine, Fukuoka Sanno Hospital, Sawara Ward, Fukuoka, Japan.
Masayuki KawasakiDepartment of Respiratory Medicine, National Hospital Organization Omuta National Hospital, Omuta, Fukuoka, Japan.
Hozumi YamadaDepartment of Respiratory Medicine, Keitendo Koga Hospital, Kouhoku, Kisima, Saga, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRapid discrimination between pulmonary tuberculosis (PTB) and nontuberculous mycobacterial pulmonary disease (NTM-PD) remains clinically challenging, particularly in cavitary disease where radiological findings may overlap. Monocyte distribution width (MDW), automatically reported by contemporary hematology analyzers, has emerged as a potential biomarker of systemic immune activation; however, its role in differentiating PTB from cavitary NTM-PD remains unclear.

methodsWe retrospectively reviewed the records of consecutive patients diagnosed with PTB or NTM-PD at our institution between May 2021 and February 2025. All PTB cases were confirmed by culture and/or nucleic acid amplification testing (NAAT) identifying Mycobacterium tuberculosis; no cases were diagnosed solely on smear positivity. Clinical characteristics and laboratory data, including MDW, were compared between groups. Multivariable logistic regression analyses were performed using prespecified parsimonious models to minimize overfitting.

resultsOf the 115 patients, 73 had PTB and 42 had NTM-PD, including 18 with cavitary NTM-PD. Compared with patients with cavitary NTM-PD, patients with PTB had significantly lower lymphocyte counts and hemoglobin and albumin levels, and higher C-reactive protein levels and MDW. In multivariable analysis comparing all PTB cases with cavitary NTM-PD, MDW demonstrated a directional association with PTB after adjustment for radiological extent (adjusted OR 1.37, 95% CI 0.98–1.92, P = 0.066), whereas radiological grade remained independently associated (adjusted OR 0.15, 95% CI 0.04–0.52, P = 0.003). Receiver operating characteristic analysis of MDW yielded an area under the curve of 0.779, which should be interpreted as exploratory given the limited sample size and lack of independent significance.

conclusionIn this single-center retrospective study, MDW demonstrated a directional association with PTB and may provide adjunctive information during early clinical assessment of cavitary mycobacterial disease while awaiting microbiological confirmation. However, MDW was not independently predictive after multivariable adjustment, and its discriminatory performance should be interpreted cautiously. Larger prospective, multicenter studies are required to validate these findings.

Indexed as

MonocytesMycobacterium Infections, NontuberculousTuberculosis, PulmonaryAgedBiomarkersC-Reactive ProteinDiagnosis, DifferentialFemaleHumansLogistic ModelsMaleMiddle AgedMultivariate AnalysisRetrospective StudiesROC CurveBiomarkersC-Reactive ProteinCavitary lesionMycobacterium tuberculosisNontuberculous mycobacteriaPulmonary tuberculosis

Identifiers

PMID41896831
PMCPMC13151151

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