2025年11月10日 / 最終更新日 : 2025年11月10日 ad_y ニュース

2025年 新着論文 50　バイオインフォマティクス分野から論文が発表されました

Familial fibrotic hypersensitivity pneumonitis: A distinct clinical phenotype with shorter leukocyte telomere length

Respir Investig. 2025 Nov 5;63(6):1338-1346. doi: 10.1016/j.resinv.2025.10.012. Online ahead of print.

Authors

Masashi Nishimura  1 , Hideya Kitamura  2 , Yoichi Tagami  3 , Kazushi Fujimoto  4 , Takashi Fukushima  4 , Ryota Otoshi  4 , Takashi Niwa  4 , Jun Aoki  5 , Taiki Fukuda  6 , Tomoe Sawazumi  7 , Tae Iwasawa  5 , Koji Okudela  8 , Tamiko Takemura  7 , Yayoi Natsume-Kitatani  9 , Yu Hara  10 , Takeshi Kaneko  10 , Takashi Ogura  4

Affiliations

  • 1 Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan; Department of Pulmonology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan; Division of Infectious Diseases and Respiratory Medicine, Department of Internal Medicine, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan.
  • 2 Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan. Electronic address: hideyaksf3924@gmail.com.
  • 3 Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan; Department of Pulmonology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.
  • 4 Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan.
  • 5 Department of Radiology, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan.
  • 6 Department of Radiology, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan; Department of Radiology, The Jikei University School of Medicine, 3-25-8 Nishi-Shimbashi, Minato-ku, Tokyo, 105-8461, Japan.
  • 7 Department of Pathology, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan.
  • 8 Department of Pathology, Kanagawa Cardiovascular and Respiratory Center, 6-16-1 Tomioka-higashi, Kanazawa-ku, Yokohama, Kanagawa, 236-0051, Japan; Department of Pathology, Saitama Medical University, 38 Morohongo, Moroyama-machi, Iruma-gun, Saitama, 350-0495, Japan.
  • 9 Artificial Intelligence Center for Health and Biomedical Research, National Institutes of Biomedical Innovation, Health and Nutrition, 7-6-8 Saito-Asagi, Ibaraki, Osaka, 567-0085, Japan; Institute of Advanced Medical Sciences, Tokushima University, 3-18-15 Kuramoto, Tokushima, Tokushima, 770-8503, Japan; Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
  • 10 Department of Pulmonology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.

Abstract

Background: Family history is an important factor in recognizing the prognosis of interstitial lung disease (ILD), however, its significance in fibrotic hypersensitivity pneumonitis (HP), as based on the latest international guidelines, remains unclear. This study aimed to investigate the distinct clinical profile and leukocyte telomere length (LTL) of familial fibrotic HP.

Methods: We retrospectively reviewed 490 patients who underwent leukocyte telomere length (LTL) measurement, and identified 131 patients with fibrotic HP, including 19 familial cases. Chest HRCT images were reviewed using automatic deep learning-based lung analysis.

Results: Familial fibrotic HP patients were younger (age ≥60: 68.4 % vs. 91.9 %, p = 0.02) and had lower diffusing capacity for carbon monoxide (DLco) (mean [SD]: 70.9 [23.6] vs. 82.9 [23.2], p = 0.031) compared to non-familial cases. Despite similar imaging patterns and AI-based CT analysis, pathological features of usual interstitial pneumonia (UIP) were more frequent in familial cases. Age-adjusted LTL was significantly shorter in the familial group (mean [SD]: -0.26 [0.26] vs. -0.06 [0.28], p = 0.004). Furthermore, LTL correlated with serum KL-6 (r = -0.603, p = 0.006), %DLco(r = 0.629, p = 0.007), and fibrotic features according to deep learning-based CT analysis; the consolidation with traction bronchiectasis ratio (r = -0.48, p = 0.038) and the traction bronchiectasis ratio (r = -0.489, p = 0.034).

Conclusion: Familial fibrotic HP may represent a distinct clinical phenotype characterized by shorter telomeres, with LTL emerging as a potential biomarker for disease severity.

Keywords: Family history; Fibrotic hypersensitivity pneumonitis; Interstitial lung disease; Telomere length.

Conflict of interest statement

Declaration of competing interest Y.N.K. received research funding from the Ministry of Health, Labour and Welfare of Japan (JPMH20AC5001) during the past three years. The other authors have no conflicts of interest.

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