Paradoxical relationship between body mass index and bone mineral density in patients with non-small cell lung cancer with brain metastasisopen access
- Authors
- Nam, Min Woo; Kim, Jae Min; Cheong, Jin Hwan; Ryu, Je Il; Han, Myun Hoon
- Issue Date
- Jun-2019
- Publisher
- PUBLIC LIBRARY SCIENCE
- Citation
- PLOS ONE, v.14, no.6, pp.1 - 16
- Indexed
- SCIE
SCOPUS
- Journal Title
- PLOS ONE
- Volume
- 14
- Number
- 6
- Start Page
- 1
- End Page
- 16
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/147736
- DOI
- 10.1371/journal.pone.0218825
- ISSN
- 1932-6203
- Abstract
- Background and purpose
Low body mass index (BMI) at presentation has been reported to be associated with higher incidence and mortality of lung cancer, but studies on the relationship between brain metastasis and BMI at presentation are lacking. This study aimed to evaluate the association between brain metastasis and BMI and bone mineral density (BMD) in NSCLC.
Methods
We retrospectively enrolled patients with non–small cell lung cancer who underwent brain magnetic resonance imaging with contrast within 3 months of diagnosis. The BMI was collected, and the BMD was measured in Hounsfield unit (HU) on initial staging computed tomography scans. The independent relationship between BMI and BMD was assessed using multivariable linear regression according to the presence of brain metastasis.
Results
A total of 356 consecutive NSCLC patients were enrolled in the study over a 8-year period in a single institution. Lower BMI with higher BMD was an independent predictive factor for brain metastasis in patients with NSCLC, relative to the other group (HR, 2.03; 95% CI, 1.21 to 3.40; P = 0.007). We also found a significant negative correlation between BMI and BMD among patients with NSCLC with brain metastases (B, -3.343; 95% confidence interval, -6.352 to -0.333; P = 0.030).
Conclusions
Brain metastasis may possibly be associated with lower BMI and higher BMD in NSCLC patients. We expect that these results may facilitate future predictions of brain metastases during the clinical course of NSCLC and enhance our understanding of the underlying mechanisms that link brain metastases and lung cancer.
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