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Vascular endothelial growth factor D in the diagnosis of lymphangioleiomyomatosis

https://doi.org/10.18093/0869-0189-2025-35-5-753-757

Abstract

Morphological verification is not always required to make a definitive diagnosis of lymphangioleiomyomatosis (LAM) with a typical picture of cysts in the lungs using high-resolution computed tomography. Vascular endothelial growth factor D – VEGF-D (vascular endothelial growth factor D) is used worldwide as a laboratory marker of LAM with a diagnostic threshold of 800 pg/ml and higher in the blood [1]. There was no such possibility in the Russian Federation until April 2023. The aim of the study was to evaluate the diagnostic value of the serum levels of vascular endothelial growth factor D (VEGF-D) in patients with LAM in the Russian Federation. Methods. Blood serum samples were prospectively collected in the laboratory of the State Budgetary Institution of Healthcare of the city of Moscow “Moscow Clinical Scientific and Practical Center named after A.S.Loginov of the Department of Healthcare of the City of Moscow” from 71 patients with multiple air cavities in the lungs using high-resolution computed tomography of the chest organs. VEGF-D levels were measured using enzyme immunoassay, and diagnostic value was assessed using performance curve analysis (ROC-curve). Results. Patients with identified LAM accounted for 48 (68%) of all the included patients (n = 71) with cystic lung disease, with the average age of 48.2 ± 12.9 years. The group of patients with lung cysts not associated with LAM and the group of patients with LAM significantly differed in VEGF-D levels: 552 ± 276.5 pg/ml vs 1,425 ± 872.1 pg/ml, respectively (p < 0.0001). The level of VEFG-D was higher in women with LAM and extrapulmonary manifestations of the disease than in women without extrapulmonary changes: 1,510 ± 968.6 pg/ml vs 1,328.5 ± 761.0 pg/ml, respectively. However, the difference was not statistically significant (p < 0.06). The level of VEFG-D was higher than 800 pg/ml in 75% of patients with LAM. The area under the ROC curve for VEFG-D in LAM was 0.866 (95% CI – 0.783 – 0.950; p < 0.0001). The threshold value of VEFG-D of 738 pg/ml had a sensitivity of 81% and a specificity of 79% for the diagnosis of an identified LAM. Conclusion. Our data indicate that measurement of VEGF-D blood serum levels allows diagnosing LAM in 75% of cases with clinical and radiological suspicion of LAM without morphological examination of lung tissue.

About the Authors

M. A. Makarova
Federal State Autonomous Educational Institution of Higher Education “N.I.Pirogov Russian National Research Medical University” of the Ministry of Health of the Russian Federation ; Federal State Budgetary Institution “Pulmonology Scientific Research Institute” under Federal Medical and Biological Agency of Russian Federation ; Moscow State Budgetary Healthcare Institution “Moscow City Hospital named after S.S.Yudin, Moscow Healthcare Department”
Russian Federation

Marina A. Makarova, Candidate of Medicine, Associate Professor, Department of Pulmonology, Faculty of Additional Professional Education; Researcher, Laboratory of Intensive Care and Respiratory Failure; Pulmonologist, Department of Respiratory Medicine

Author ID: 766549 

ul. Ostrovityanova 1, Moscow, 117997, tel.: (499) 780-08-43 

Orekhovyy bul’var 28, build. 10, Moscow, 115682 

ul. Akademika Millionshchikova 1, Moscow, 115487 


Competing Interests:

There is no conflict of interest. 



G. E. Baimakanova
Federal State Autonomous Educational Institution of Higher Education “N.I.Pirogov Russian National Research Medical University” of the Ministry of Health of the Russian Federation ; State Budgetary Institution of Healthcare of the city of Moscow “Moscow Clinical Scientific and Practical Center named after A.S.Loginov of the Department of Healthcare of the City of Moscow”
Russian Federation

Gulsara E. Baymakanova, Doctor of Medicine, Professor of the Pulmonology Department, Institute of Continuing Education and Professional Development; Head of the Department of Pulmonology

AuthorID: 512881 

ul. Ostrovityanova 1, Moscow, 117997, tel.: (495) 304-30-39 

Shosse Entuziastov 86, Moscow, 111123 


Competing Interests:

There is no conflict of interest. 



A. S. Belevskiy
Federal State Autonomous Educational Institution of Higher Education “N.I.Pirogov Russian National Research Medical University” of the Ministry of Health of the Russian Federation
Russian Federation

Andrey S. Belevskiy, Doctor of Medicine, Professor; Head of the Pulmonology Department, Faculty of Additional Professional Education Institute of Continuing Education and Professional Development; President of the Russian Respiratory Society, Chief Pulmonologist of the Moscow Government Health Department

ul. Ostrovityanova 1, Moscow, 117997, tel.: (495) 963-24-67 


Competing Interests:

There is no conflict of interest. 



A. S. Chegodar
State Budgetary Institution of Healthcare of the city of Moscow “Moscow Clinical Scientific and Practical Center named after A.S.Loginov of the Department of Healthcare of the City of Moscow”
Russian Federation

Anzhelika S. Chegodar, Head of the Laboratory for Polymerase Chain Reaction Diagnostics, Clinical Laboratory Diagnostics Physician

AuthorID: 1108923 

Shosse Entuziastov 86, Moscow, 111123, tel.: (495) 304-30-35


Competing Interests:

There is no conflict of interest. 



N. A. Bodunova
State Budgetary Institution of Healthcare of the city of Moscow “Moscow Clinical Scientific and Practical Center named after A.S.Loginov of the Department of Healthcare of the City of Moscow”
Russian Federation

Natalia A. Bodunova, Candidate of Medicine, Gastroenterologist, Head of the City Medical Genetics Center, Head of the Center for Personalized Medicine

AuthorID: 790892 

Shosse Entuziastov 86, Moscow, 111123, tel.: (495) 304-30-35


Competing Interests:

There is no conflict of interest. 



References

1. McCormack F.X., Travis W.D., Colby T.V. et al. Lymphangioleiomyomatosis: calling it what it is: a low-grade, destructive, metastasizing neoplasm. Am. J. Respir. Crit. Care Med. 2012; 186: 1210–1212. DOI: 10.1164/rccm.201205-0848OE.

2. Bokhari S.M.Z., Hamar P. Vascular endothelial growth factor-D (VEGF-D): An angiogenesis bypass in malignant tumors. Int. J. Mol. Sci. 2023; 24 (17): 13317. DOI: 10.3390/ijms241713317.

3. Yamada Y., Nezu J.I., Shimane M., Hirata Y. Molecular cloning of a novel vascular endothelial growth factor, VEGF-D. Genomics. 1997; 42 (3): 483–488. DOI: 10.1006/geno.1997.4774.

4. Stacker S.A., Achen M.G. Emerging roles for VEGF-D in human disease. Biomolecules. 2018; 8 (1): 1. DOI: 10.3390/biom8010001.

5. Seyama K., Kumasaka T., Souma S. et al. Vascular endothelial growth factor-D is increased in serum of patients with lymphangioleiomyomatosis. Lymphat. Res. Biol. 2006; 4 (3): 143–152. DOI: 10.1089/lrb.2006.4.143.

6. Johnson S.R., Cordier J.F., Lazor R. et al. European Respiratory Society guidelines for the diagnosis and management of lymphangioleiomyomatosis. Eur. Respir. J. 2010; 35 (1): 14–26. DOI: 10.1183/09031936.00076209.

7. Li M., Zhu W.Y., Wang J. et al. Diagnostic performance of VEGF-D for lymphangioleiomyomatosis: a meta-analysis. J. Bras. Pneumol. 2022; 48 (1): e20210337. DOI: 10.36416/1806-3756/e20210337.


Supplementary files

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For citations:


Makarova M.A., Baimakanova G.E., Belevskiy A.S., Chegodar A.S., Bodunova N.A. Vascular endothelial growth factor D in the diagnosis of lymphangioleiomyomatosis. PULMONOLOGIYA. 2025;35(5):753-757. (In Russ.) https://doi.org/10.18093/0869-0189-2025-35-5-753-757

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ISSN 0869-0189 (Print)
ISSN 2541-9617 (Online)