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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="research-article"><?properties open_access?><front><journal-meta><journal-id journal-id-type="nlm-ta">Korean J Intern Med</journal-id><journal-id journal-id-type="publisher-id">KJIM</journal-id><journal-title-group><journal-title>The Korean Journal of Internal Medicine</journal-title></journal-title-group><issn pub-type="ppub">1226-3303</issn><issn pub-type="epub">2005-6648</issn><publisher><publisher-name>The Korean Association of Internal Medicine</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">22205843</article-id><article-id pub-id-type="pmc">3245391</article-id><article-id pub-id-type="doi">10.3904/kjim.2011.26.4.427</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Article</subject></subj-group></article-categories><title-group><article-title>Gender Differences in Susceptibility to Smoking among Patients with Lung Cancer</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Ryu</surname><given-names>Jeong-Seon</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Jeon</surname><given-names>Sang-Hoon</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Jung-Soo</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Lee</surname><given-names>Jung Hwan</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Seong Hyun</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Hong</surname><given-names>Ji Taek</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Jeong</surname><given-names>Ju Hong</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Jeong</surname><given-names>Ji Joong</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Lee</surname><given-names>Myung Dong</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Min</surname><given-names>Sang Joon</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Nam</surname><given-names>Hae-Seong</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Cho</surname><given-names>Jae-Hwa</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Kwak</surname><given-names>Seung-Min</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Lee</surname><given-names>Hong Lyeol</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib><contrib contrib-type="author"><name><surname>Kim</surname><given-names>Hyun-Jung</given-names></name><xref ref-type="aff" rid="A1-kjim-26-427"/></contrib></contrib-group><aff id="A1-kjim-26-427">Department of Internal Medicine, Inha University Hospital, Inha University College of Medicine, Incheon, Korea.</aff><author-notes><corresp>Correspondence to: Jeong-Seon Ryu, M.D. Department of Internal Medicine and Center for Lung Cancer, Inha University Hospital, Sinheung-dong 3-ga, Jung-gu, Incheon 400-711, Korea. Tel: 82-32-890-3738, Fax: 82-32-882-6578, <email>jsryu@inha.ac.kr</email></corresp></author-notes><pub-date pub-type="ppub"><month>12</month><year>2011</year></pub-date><pub-date pub-type="epub"><day>28</day><month>11</month><year>2011</year></pub-date><volume>26</volume><issue>4</issue><fpage>427</fpage><lpage>431</lpage><history><date date-type="received"><day>26</day><month>9</month><year>2011</year></date><date date-type="rev-recd"><day>12</day><month>10</month><year>2011</year></date><date date-type="accepted"><day>17</day><month>10</month><year>2011</year></date></history><permissions><copyright-statement>Copyright &#xA9; 2011 The Korean Association of Internal Medicine</copyright-statement><copyright-year>2011</copyright-year><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/3.0"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">http://creativecommons.org/licenses/by-nc/3.0/</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><abstract><sec><title>Background/Aims</title><p>To determine whether female smokers are more or less susceptible to the detrimental pulmonary-function effects of smoking when compared to male smokers among patients with lung cancer.</p></sec><sec><title>Methods</title><p>Pack-years and pulmonary function indices were compared between 1,594 men and women with lung cancer ifferences in individual susceptibility to smoking were estimated using a susceptibility index formula.</p></sec><sec><title>Results</title><p>Of the patients, 959 (92.8%) men and 74 (7.2%) women were current smokers. Common histological types of lung cancer were squamous cell carcinoma, adenocarcinoma, and small cell carcinoma, among others. Women had a lower number of pack-years, forced expiratory volume in 1 second (FEV<sub>1</sub>, liters), forced vital capacity (FVC, liters), and total lung capacity (TLC, liters) compared to those of men (25.0 &#xB1; 19.2 vs. 42.9 &#xB1; 21.7 for pack-years; 1.4 &#xB1; 0.5 vs. 2.0 &#xB1; 0.6 for FEV<sub>1</sub>; 3.0 &#xB1; 0.7 vs. 2.0 &#xB1; 0.6 for FVC; 4.5 &#xB1; 0.8 vs. 5.7 &#xB1; 1.0 for TLC; all <italic>p</italic> &lt; 0.001). The susceptibility index for women was significantly higher compared to that of men (1.1 &#xB1; 4.1 vs. 0.7 &#xB1; 1.1; <italic>p</italic> = 0.001). A significant inverse association was shown between the susceptibility index and TLC and FVC (<italic>r</italic> = -0.200 for TLC, -0.273 for FVC; all <italic>p</italic> &lt; 0.001).</p></sec><sec><title>Conclusions</title><p>The results suggest that the detrimental effects of smoking on pulmonary function are greater in women, as compared to those in men, among patients with lung cancer.</p></sec></abstract><kwd-group><kwd>Gender</kwd><kwd>Lung neoplasms</kwd><kwd>Smoking</kwd><kwd>Disease susceptibility</kwd><kwd>Pulmonary function</kwd></kwd-group></article-meta></front><body><sec><title>INTRODUCTION</title><p>Lung cancer and chronic obstructive pulmonary disease, which are two distinct phenotypes, are highly likely to be attributable to smoking. To date, these two diseases are understood as a single continuum or a different outcome from the same insult [<xref ref-type="bibr" rid="B1-kjim-26-427">1</xref>]. The potential interaction of gender with the effects of smoking on the development of these diseases is a major clinical issue but one that is not well established. Pulmonary function is one of the most useful indicators for estimating the hazardous effects of smoking on the lungs [<xref ref-type="bibr" rid="B2-kjim-26-427">2</xref>].</p><p>Many studies had been conducted to verify whether the harmful effects of smoking on pulmonary function differ according to gender [<xref ref-type="bibr" rid="B3-kjim-26-427">3</xref>-<xref ref-type="bibr" rid="B12-kjim-26-427">12</xref>]. These studies were conducted on healthy populations or patients with chronic obstructive pulmonary disease and showed inconsistent results. Although the effects of smoking on carcinogenesis between men and women have been reported with mixed results in cohort and case-control studies, the effect of smoking on pulmonary function in patients with lung cancer according to gender has not been examined [<xref ref-type="bibr" rid="B13-kjim-26-427">13</xref>-<xref ref-type="bibr" rid="B16-kjim-26-427">16</xref>].</p><p>Therefore, we conducted this study to investigate if susceptibility to smoking was different between men and women in a hospital-based lung cancer cohort.</p></sec><sec sec-type="methods"><title>METHODS</title><sec><title>Patients and pulmonary function testing</title><p>Of approximately 2,300 patients with lung cancer who were diagnosed between 2001 and 2009 at the Lung Cancer Cohort of Inha University Hospital (Incheon, Korea) [<xref ref-type="bibr" rid="B17-kjim-26-427">17</xref>], all consecutive patients who were smokers or had a history of smoking and who took a pulmonary function test at diagnosis were initially considered for this study (<xref ref-type="fig" rid="F1-kjim-26-427">Fig. 1</xref>). Information including body mass index, histological type, and smoking habits was obtained from a data system. Patients with obstruction of the trachea or a lobar bronchus and significant pleural effusion were excluded, because these factors can potentially affect the results of pulmonary function testing.</p><p>Pulmonary function testing was performed by a certified technician following the American Thoracic Society recommendations [<xref ref-type="bibr" rid="B18-kjim-26-427">18</xref>]. Forced expiratory volume in 1 second (FEV<sub>1</sub>, liters or percentage), forced vital capacity (FVC, liters or percentage), and total lung capacity (TLC, liters or percentage) were estimated. Data on smoking habits were prospectively collected by a well trained research nurse who interviewed patients and asked "Have you ever smoked?", and "Do you smoke now?" Pack-years smoked were calculated by asking, "How many cigarettes do you smoke per day on average?" and "How long did you smoke?"</p></sec><sec><title>Outcome</title><p>We evaluated the susceptibility index (SI) to quantify the decrease in individual pulmonary function with a susceptibility index formula: [100 - % FEV<sub>1</sub>] / pack-years [<xref ref-type="bibr" rid="B9-kjim-26-427">9</xref>]. This formula assumes that each patient's baseline FEV<sub>1</sub> would be normal (100% of predicted) without the hazardous effects of smoking. The SI was defined as the loss of pulmonary function (measured in % predicted FEV<sub>1</sub>) per pack-year smoked.</p></sec><sec><title>Statistical analysis</title><p>Differences in clinical variables between men and women were compared using the &#x3C7;<sup>2</sup> test for categorical variables and the independent <italic>t</italic> test for continuous variables. Correlations between the SI and pulmonary function were evaluated with Pearson's &#x3C7;<sup>2</sup> test. All statistical testing was performed at the two-sided 0.05 level. All analyses were performed using SAS version 9.1.3 (SAS Institute, Cary, NC, USA).</p></sec></sec><sec><title>RESULTS</title><sec><title>Patient characteristics</title><p><xref ref-type="table" rid="T1-kjim-26-427">Table 1</xref> shows the distribution of clinical characteristics by gender in the 1,594 patients. Patients consisted of 1,490 men (959 current-smokers, 526 former-smokers) and 104 women (74 current-smokers, 29 former-smokers). Ages ranged from 28 to 89 years (median, 67). Pack-years smoked in women were significantly lower than those of men (<italic>p</italic> &lt; 0.001). No differences in body mass index or distribution of histological types or stage were found between men and women.</p></sec><sec><title>Pulmonary function and the SI</title><p>Women had significantly lower estimates of FEV<sub>1</sub>, FVC, and TLC compared to those of men (2.0 vs. 1.4, 3.0 vs. 2.0, 5.7 vs. 4.5, respectively; all <italic>p</italic> &lt; 0.001). The SI estimates in women were significantly higher compared to those in men (1.1 vs. 0.7% per pack-years; <italic>p</italic> = 0.001) (<xref ref-type="fig" rid="F2-kjim-26-427">Fig. 2</xref>). The SI estimate showed a significant inverse relationship with liters of FVC or TLC (<italic>r</italic> = -0.273, <italic>p</italic> &lt; 0.001 for FVC; <italic>r</italic> = -0.200, <italic>p</italic> &lt; 0.001 for TLC) (<xref ref-type="fig" rid="F3-kjim-26-427">Fig. 3</xref>). The SI estimates also showed a significant relationship with FVC based on gender (<italic>r</italic> = -0.331, <italic>p</italic> &lt; 0.001 for men; <italic>r</italic> = -0.380, <italic>p</italic> &lt; 0.001 for women) and TLC (<italic>r</italic> = -0.143, <italic>p</italic> = 0.002 for men; <italic>r</italic> = - 0.277, <italic>p</italic> = 0.053 for women, data not shown).</p></sec></sec><sec><title>DISCUSSION</title><p>This study demonstrated, for the first time, that pulmonary function in female patients with lung cancer may be more susceptible to the hazardous effects of smoking than that of men. The higher susceptibility of women, who showed a significantly lower amount of smoking compared to men, originated from their lower lung volume.</p><p>It has been a controversial issue as to whether a gender difference is present regarding the detrimental effects of smoking on pulmonary function [<xref ref-type="bibr" rid="B3-kjim-26-427">3</xref>-<xref ref-type="bibr" rid="B12-kjim-26-427">12</xref>]. Our results were similar to some previous cross-sectional or longitudinally designed studies conducted in an otherwise healthy population or in patients with chronic obstructive pulmonary disease [<xref ref-type="bibr" rid="B3-kjim-26-427">3</xref>,<xref ref-type="bibr" rid="B7-kjim-26-427">7</xref>-<xref ref-type="bibr" rid="B9-kjim-26-427">9</xref>]. However, to directly compare results of studies with different designs or subjects is a matter for concern because of epidemiological biases, such as a healthy smoking effect or a different prevalence of smokers, originating from the heterogeneity of the population, and the existence of individual variation regarding the harmful effects of smoking on pulmonary function. Unlike previous series, this study was conducted among patients with lung cancer who came from a hospital-based cohort. All subjects in this study were expected to have lung cancer due to smoking and, thus, were likely to have homogenous characteristics in terms of the hazardous effects of smoking.</p><p>In this study, we used the SI to evaluate susceptibility. This index was originally designed to quantify a decrease in FEV<sub>1</sub> as a result of pack-years smoked in patients with chronic obstructive pulmonary disease. Although women presented with significantly fewer pack-years, compared to those of men, the SI was significantly higher in women, as compared to that in men (0.7 vs. 1.1; <italic>p</italic> = 0.001). Dransfield et al. [<xref ref-type="bibr" rid="B9-kjim-26-427">9</xref>] reported that the SIs of men and women are 0.9 and 1.1, respectively, for Caucasians and 1.2 and 1.4, respectively, for African-American patients with chronic obstructive pulmonary disease. Considering similar SI estimates and different amounts smoked between these Caucasian and African-American women (40-45 pack-years) and Korean female patients with lung cancer (25 pack-years) in this study, it could be postulated that an ethnic difference may have modulated the deleterious ef fects. Our results showed a signif icant inverse relationship between SI and FVC and TLC, indicating that higher susceptibility in women might be attributed to their lower lung volume. It could be postulated that the more harmful effects of smoking could be expected after a given amount smoked in patients with a smaller lung volume.</p><p>The present study had some limitations. First, we did not collect detailed information on smoking habits such as brand name or depth of inhalation, which could affect pulmonary function [<xref ref-type="bibr" rid="B5-kjim-26-427">5</xref>]. Second, the number of female smokers with lung cancer in this study could be too small to compare variables by gender, given that the incidence of female smokers in South Korea is approximately 2%, which is much lower than that of other countries. Third, a serial estimate of the annual decline in pulmonary function is the most valuable method to assess the harmful effects of smoking. 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FEV<sub>1</sub>, forced expiratory volume in 1 sec; FVC, forced vital capacity; TLC, total lung capacity.</p></caption><graphic xlink:href="kjim-26-427-g001"/></fig><fig id="F2-kjim-26-427" position="float"><label>Figure 2</label><caption><p>Susceptibility index for patients with lung cancer according to gender.</p></caption><graphic xlink:href="kjim-26-427-g002"/></fig><fig id="F3-kjim-26-427" position="float"><label>Figure 3</label><caption><p>Correlations between the susceptibility index and pulmonary function in patients with lung cancer.</p></caption><graphic xlink:href="kjim-26-427-g003"/></fig><table-wrap id="T1-kjim-26-427" position="float"><label>Table 1</label><caption><p>Characteristics of the 1,594 patients with lung cancer and their smoking habits</p></caption><graphic xlink:href="kjim-26-427-i001"/><table-wrap-foot><fn><p>Values are presented as number (%).</p><p>FEV<sub>1</sub>, forced expiratory volume in 1 sec; FVC, forced vital capacity; TLC, total lung capacity.</p></fn></table-wrap-foot></table-wrap></floats-group></article>
