Abstract
Background
Cigarette smoking is a risk factor for interstitial lung abnormalities (ILAs) and interstitial lung diseases (ILDs). Investigation defining the relationships between ILAs/ILDs and clinical, radiographic, and pathologic findings in smokers have been incomplete. Employing a cohort undergoing surgical resection for lung nodules/masses, we (1) define the prevalence of ILAs/ILDs, (2) delineate their clinical, radiographic and pathologic predictors, and (3) determine their associations with mortality.
Methods
Patients undergoing resection of lung nodules/masses between 2017 and 2020 at a rural Appalachian, tertiary medical center were retrospectively investigated. Predictors for ILAs/ILDs and mortality were assessed using multivariate logistic regression analysis.
Results
In the total study cohort of 352 patients, radiographic ILAs and ILDs were observed in 35.2% and 17.6%, respectively. Among ILA patterns, subpleural reticular changes (14.8%), non-emphysematous cysts, centrilobular (CL) ground glass opacities (GGOs) (8% each), and mixed CL-GGO and subpleural reticular changes (7.4%) were common. ILD patterns included combined pulmonary fibrosis emphysema (CPFE) (3.1%), respiratory bronchiolitis (RB)-ILD (3.1%), organizing pneumonitis (2.8%) and unclassifiable (4.8%). The group with radiographic ILAs/ILDs had a significantly higher proportion of ever smokers (49% vs. 39.9%), pack years of smoking (44.57 ± 36.21 vs. 34.96 ± 26.22), clinical comorbidities of COPD (35% vs. 26.5%) and mildly reduced diffusion capacity (% predicated 66.29 ± 20.55 vs. 71.84 ± 23). Radiographic centrilobular and paraseptal emphysema (40% vs. 22.2% and 17.6% vs. 9.6%, respectively) and isolated traction bronchiectasis (10.2% vs. 4.2%) were associated with ILAs/ILDs. Pathological variables of emphysema (34.9% vs. 18.5%), any fibrosis (15.9% vs. 4.6%), peribronchiolar metaplasia (PBM, 8% vs. 1.1%), RB (10.3% vs. 2.5%), and anthracosis (21.6% vs. 14.5%) were associated with ILAs/ILDs. Histologic emphysema showed positive correlations with any fibrosis, RB, anthracosis and ≥ 30 pack year of smoking. The group with ILAs/ILDs had significantly higher mortality (9.1% vs. 2.2%, OR 4.13, [95% CI of 1.84–9.25]).
Conclusions
In a rural cohort undergoing surgical resection, radiographic subclinical ILAs/ILDs patterns were highly prevalent and associated with ever smoking and intensity of smoking. The presence of radiographic ILA/ILD patterns and isolated honeycomb changes were associated with increased mortality. Subclinical ILAs/ILDs and histologic fibrosis correlated with clinical COPD as well as radiographic and pathologic emphysema emphasizing the co-existence of these pulmonary injuries in a heavily smoking population.
Similar content being viewed by others
Explore related subjects
Find the latest articles, discoveries, and news in related topics.Introduction
Cigarette smoking has been associated with the precursor lesions of interstitial lung abnormalities (ILAs) and a diversity of interstitial lung diseases (ILDs) including respiratory bronchiolitis–interstitial lung disease (RB-ILD), desquamative interstitial pneumonia (DIP), pulmonary Langerhans cell histiocytosis (PLCH), idiopathic pulmonary fibrosis (IPF), and combined pulmonary fibrosis and emphysema (CPFE) [1]. Penetration of smoking-related pulmonary injuries is variable with a prevalence of 3 to 17% (mean of 8%) for ILAs, < 1% for CPFE and 0.0005–0.002% for IPF [2]. Except for subclinical ILAs, these diseases often present with progressive dyspnea and some combination of other symptoms (cough, sputum and wheezing). Attempts to identify an individual lung disease overlooks co-existing pathology and disease following exposure to the shared risk factor of cigarette smoking [3, 4]. Investigation of the associations between subclinical ILAs and other cigarette smoking-related lung diseases have sometimes provided discrepant results. While identifying the potential role of current smoking in ILAs, Washko et al. demonstrated an inverse relationship with emphysema, with prevalence of 8% in COPD gene cohort [5]. These findings may have been confounded by the exclusion of radiographic emphysematous regions which may include smoking-related interstitial fibrosis, lack of histologic confirmation, and approximately one-third of patients meeting criteria for “indeterminate” ILA [6, 7]. Although comparison of quantitative methods of ILA evaluation to visual ILA showed potential modification from coexisting emphysema (5% or more) [8], a significant positive association was demonstrated between paraseptal emphysema and ILAs [9]. Recent studies have suggested that ILAs can show a higher prevalence (23.1 to 40.7%) and are associated with both a worse clinical course and higher mortality rates in COPD patients [10,11,12,13].
The Appalachian region is challenged with the highest rates of smoking (25.2%) in the United States [14]. Subsequently, there is an excessive burden of lung disease associated with smoking in this region [15, 16]. Employing a cohort diagnosed with lung nodule/mass and undergoing surgical resection, we (1) define the prevalence of ILAs/ILDs, (2) delineate clinical, radiographic and pathologic predictors of ILAs/ILDs, and (3) determine their associations with mortality.
Materials and methods
Study design
A single-center, retrospective, cohort study was conducted at West Virginia University Hospital (WVUH). The study protocol was reviewed and approved by the institutional review board (ID# 2010131995). During the study period (January 1, 2017 to December 31, 2020), patients who underwent surgical resection for suspicious lung nodules/masses coordinated through the thoracic oncology clinic of WVUH were identified. Groups with or without radiographic ILA and ILD patterns were defined (Fig. 1). Aims of this retrospective review were to define (1) the prevalence of subclinical radiographic ILA and ILD in the cohort, (2) clinical, radiographic and pathologic predictors of ILA/ILD, and (3) the impact of ILA/ILD on mortality with its predictors. Additionally, we explored the specific histologic associations for ILA/ILD patterns, and the relationship between cigarette smoking and histologic findings including emphysema. Patients were excluded from the study cohort if (1) a good quality CT scan of the chest was not obtained six months (or less) prior to surgery, (2) adequate lung tissue was not available to allow independent review, and (3) surgery performed for non-pulmonary malignancy/metastatic disease.
Data collection
Electronic medical charts were reviewed, and data collected including demographics, smoking status, pack-years of smoking, comorbidities, baseline supplemental oxygen use, and pulmonary function tests (PFTs).
Radiographic evaluation
Pre-operative CT scans (1 mm slice thickness for lung windows) were analyzed by three investigators to detect ILA/ILD patterns. Consensus of radiographic findings were recorded in accordance with the case definitions [5, 17] (Additional file 1). ILAs included diffuse centrilobular (CL) GGO, subpleural reticular changes, architectural distortion, traction bronchiectasis, honeycombing, and non-emphysematous cysts involving at least 5% of a lung zone. Imaging findings were excluded if they were restricted to dependent lung zones, focal paraspinal fibrosis, focal or unilateral abnormality, interstitial pulmonary edema or aspiration related findings of tree-in-bud or patchy ground glass and definite ILD patterns. Radiographic ILD patterns were reported including usual interstitial pneumonia (UIP), probable UIP, non-specific interstitial pneumonia (NSIP), RB-ILD, PLCH, DIP, CPFE, organizing pneumonia and unclassifiable patterns [18,19,20].
Pathologic evaluation
At least one tissue section, and typically 3–6 sections, were examined for interstitial lung changes. Areas distant from the tumor were evaluated. Microscopic analysis focused on identifying a variety of histopathologic patterns and features indicative of ILD [21]. Retrospective histopathologic review of 352 lung specimens was performed independently by two pathologists. Consensus of pathologic findings was obtained for all specimens.
Statistical analysis
Descriptive statistics included means, medians, and standard deviations to summarize continuous variables and frequency distributions to describe categorical variables. Chi-square or Fisher exact tests were used to detect differences in categorical variables between the groups, while means of continuous variables were compared using two-sided independent-samples t-tests. The Mann–Whitney U test was used when normality could not be assumed. Logistic regression analysis was used to determine significant predictors of ILAs/ILDs including histological features, association of smoking and various pathologic finding and to predict mortality at the end of the study. Level of significance, α = 0.05 was used for all analyses. All analyses were conducted using statistical software SPSS version 26.0.
Results
There was a total of 392 patients who underwent surgical resection for lung nodules/masses (Fig. 1). After exclusion of those patients without a good quality CT scan of the chest or lung tissue (n = 40, 10.2%), the final number of patients was 352 patients (89.8%) (Fig. 1). This cohort was almost entirely Caucasian (96.3%) with approximately equal numbers among the genders (57.1% female). The mean age was 66.15 ± 10.19 years and the mean body mass index (BMI) was 28.35 ± 6.88 kg/m2 reflecting an overweight cohort.
The group with radiographic ILA and ILD patterns (n = 186, 52.8%) included 124 (35.2%) and 62 (17.6%) patients, respectively. Findings of ILA included subpleural reticular changes (14.8%), CL-GGO, non-emphysematous cysts (8% each) and mixed CL-GGO with subpleural reticular changes (7.4%) (Table 1). ILD patterns recognized on the CT scan of the chest included UIP (0.6%), probable UIP (0.6%), NSIP (0.9%), RB-ILD (3.1%), LCH (0.6%), DIP (1.1%), CPFE (3.1%), OP (2.8%) and unclassifiable (4.8%) (Table 1). There were no significant differences between the two groups in mean age, gender, and BMI (Table 2). The group with ILA/ILD had a greater proportion of ever smokers (49% vs. 39.9%, p = 0.010), and pack years of exposure (44.57 ± 36.21 vs. 34.96 ± 26.22, p = 0.005). The total study cohort showed a high burden of comorbidities with hypertension (69.9%), hyperlipidemia (59.3%), gastro-esophageal reflux disease (GERD, 40.6%), coronary artery disease (37.2%), anxiety (32.7%), diabetes (24.4%), and hypothyroidism (18.1%) with no differences between the groups. Those patients with ILA/ILD had an increased prevalence of diagnosed COPD (35% vs. 26.4%, p = 0.044). Supplemental oxygen was used by 14.5% of patients in the cohort and there were no differences between the groups in this. This use of supplemental O2 was predominantly for COPD with only a small minority of patients in the total cohort diagnosed to have an ILD prior to surgery (1.5%).
A majority of the study cohort (95.4%) had pre-surgical PFTs performed. Mean ratio of FEV1/FVC for the cohort was obstructive (67.74 ± 12.17) with evidence of air trapping (mean % predicted residual volume (RV) of 141.13 ± 51.41) and mildly reduced % predicted diffusion capacity for carbon monoxide (DLCO, 69.06 ± 21.95), correlating with predominant clinical diagnosis of COPD in two-third of patients. There was no significant difference between the groups with and without ILA/ILD for percent predicted forced expiratory volume in one second (FEV1), forced vital capacity (FVC), ratio FEV1/FVC, total lung capacity (TLC) and RV values. The group with ILA/ILD had a significantly reduced percent predicted DLCO (66.29 ± 20.55 vs. 71.84 ± 23. p = 0.023) (Table 2).
Additional CT chest findings of any emphysema (44.6% vs. 25.8%, p < 0.001), CL emphysema (40.0% vs. 22.2%, p < 0.001), paraseptal emphysema (17.6% vs. 9.6%, p = 0.006), combination patterns of emphysema (18.2% vs. 10.2%, p = 0.007) and isolated traction bronchiectasis (10.2% vs. 4.3%, p = 0.005) were more frequent in the group with ILA/ILD patterns compared to group without. Only a minority of patients showed isolated honeycomb changes (2.2%) and there was no significant difference between the groups (Table 3).
Histologically, 92% of resected nodules/masses demonstrated malignancy and the group with ILA/ILD trended towards a greater prevalence of lung cancer (49.8% vs. 42.2%, p = 0.06). Adenocarcinoma was the most common subtype (50.0%), followed by squamous cell (27.3%) and small cell/neuroendocrine malignancy (9.4%), without significant difference between the groups. Concurrent pathological findings in the ILA/ILD group included emphysema (34.9% vs. 18.5%, p < 0.001), any pulmonary fibrosis (15.9% vs. 4.6%, p < 0.001), peribronchiolar metaplasia (PBM, 8.0% vs. 1.1%, p < 0.001), RB (10.3% vs. 2.5%, p < 0.001) and anthracosis (21.9% vs. 14.4%, p = 0.043) (Table 3). While pathological evidence of DIP trended towards significance in the ILA/ILD group (2.8% vs. 0.9%, p = 0.074), necrotizing granulomatous inflammation trended towards group without ILA/ILD (0.9% vs. 2.5%, p = 0.063).
Univariate analysis of clinical, radiographic and pathologic variables for ILA/ILD patterns are provided (Fig. 2). Ever smoking status and ≥ 30 pack years of smoking predicted ILA/ILD patterns by two-fold (OR 2.46, 95% CI [1.22–4.96] and OR 2.21, 95% CI [1.44–3.39], respectively). Clinical evidence of COPD as well as pathologic and radiographic findings of emphysema were also associated with presence of ILA/ILD (OR 1.56, 95% CI [1.01–2.40], p = 0.044; OR 4.62, 95% CI [2.79–7.66], p < 0.001 and OR 3.16, 95% CI [2.04–4.90], p < 0.001, respectively). Additionally, radiographic findings of paraseptal emphysema and isolated traction bronchiectasis predicted ILA/ILD. Pathologically, presence of PBM (OR 6.92, 95% CI [2.37–20.23], p < 0.001), any pulmonary fibrosis (OR 4.51, 95% CI [2.11–9.65], p < 0.001), RB (OR 4.21, 95% CI [1.96–9.05], p < 0.001) and anthracosis (OR 1.57, 95% CI [1.01–4.48], p = 0.043) were associated with ILA/ILD. Figure 3 provides representative CT chest images of patients with ILA and ILD in the cohort. Figure 4 shows corresponding non-malignant histological features identified on the surgical specimen of an ILD patient.
Pre-operative CT chest images of 71-year-old active smoker (55 pack years) who underwent right upper lobectomy for suspicious lung nodule showing: a subpleural reticular changes (arrow) and centrilobular ground glass opacities (arrowhead) consistent with interstitial lung abnormality and b traction bronchiectasis (arrow) and centrilobular emphysema (asterisk). Non-malignant histologic findings for this patient included emphysema, histologic fibrosis, respiratory bronchiolitis and peribronchiolar metaplasia (not shown). Additionally, pre-surgical CT chest images of a 58-year-old active smoker (30 pack years) who underwent right lower lobe lobectomy for suspicious lung nodule showing a CT pattern of combined pulmonary fibrosis emphysema (CPFE): c centrilobular and paraseptal emphysema (arrows) in upper lobes, and d reticular changes with honeycombing (arrow) in the right lower lobe. Corresponding histologic findings of this patient are shown in Fig. 4
Photomicrographs from 58-year-old active smoker (30 pack years) who had radiographic ILD pattern of combined pulmonary fibrosis emphysema (CPFE) and underwent right lower lobectomy for suspicious nodule showing: a peribronchiolar metaplasia (PBM, black arrow), interstitial fibrosis (arrow head), anthracotic pigment deposition (green arrow), and [100×] (b) emphysema (asterisk) and PBM (arrow) [100×] (c) pattern of desquamative interstitial pneumonitis (DIP) where alveoli were diffusely and extensively filled by macrophages (asterisk) [40×] (d) DIP with pigmented macrophages filling the alveoli (arrow) [200×]
The associations between specific radiographic ILA and ILD findings with the pathological features were explored using multivariate logistic model (Table 4). Of ILA findings, CL-GGO showed an association with PBM (OR 3.98, 95% CI [1.08–14.60], p = 0.037) whereas mixed CL-GGO and subpleural reticular changes were associated with histologic evidence of any pulmonary fibrosis (OR 2.98, 95% CI [1.16–7.63], p = 0.022). Subpleural reticular changes did not independently identify pathological predictors. Radiographic ILD patterns demonstrated a strong association with histologic evidence of any pulmonary fibrosis (OR 2.48, 95% CI [1.24–4.98], p = 0.010), PBM (OR 2.56, 95% CI 1.05–6.22], p = 0.038) and RB (OR 2.14, 95% CI [1.01–4.54], p = 0.046).
Since emphysema was a strong predictor of ILA/ILD, logistic regression analysis evaluating the relationship of histologic emphysema, other path features and smoking was performed (Table 5). These analyses suggested associations of histologic emphysema to any fibrosis (OR 2.24, 95% CI [1.15–4.37], p < 0.017), RB (OR 4.11, 95% CI [1.86–9.10], p < 0.001), anthracosis (OR 2.93, 95% CI [1.81–4.75], p < 0.001) and ≥ 30 pack years of smoking (OR 1.68, 95% CI [1.05–2.68], p = 0.038).
Patients with radiographic ILA/ILD were at increased risk for mortality (odds ratio 4.13, [95% CI of 1.84–9.25]). After adjusting for age, gender, BMI, and primary lung cancer status, multivariate logistic regression showed GERD (OR 2.53, [95% CI 1.25–5.15], p = 0.010), ≥ 30 pack year smoking (OR 2.32, [95% CI 1.01 -5.30], p = 0.046), radiographic ILA/ILD patterns (OR 4.04, [95% CI 1.74–9.40], p = 0.001) and radiographic isolated honeycomb changes (OR 7.32, [95% CI 1.35–39.84], p = 0.021) as predictors of mortality in the study cohort (Table 6).
Discussion
The study cohort revealed a high prevalence (52.8%) of subclinical ILA and ILD patterns which were significantly associated with ever smoking and intensity of smoking (≥ 30 pack years). While smoking status and smoking intensity have been significantly associated with ILA, our prevalence is greater than previously reported [5, 22]. There’s a lack of standardization of ILAs which makes strict comparisons of this prevalence between investigations difficult. Our study assessed ILA/ILD patterns on visual inspection of pre-surgical resection CT chest while others have relied on quantitative high attenuation areas (HAAs) to define ILAs [22, 23]. Pathological investigation which utilized tissue resected for lung cancer reported a similarly high prevalence of radiographic interstitial changes [13]. Applying different methodology, a comparable rate of interstitial fibrosis (60%) was pathologically identified in smokers [24, 25].
To better explain the paradox of variable clinical and pathophysiologic responses to an identical risk factor (i.e. smoking), the need for studies characterizing interactions between emphysema, pulmonary fibrosis and ILAs have been acknowledged [2]. A clinical diagnosis of COPD, radiographic and histologic emphysema predicted a presence of ILA/ILD in our smoking cohort. Histologically, the observation of any pulmonary fibrosis predicted ILAs (mixed ground glass opacities and subpleural changes) and ILDs in our cohort. Moreover, patients with pathologic evidence of emphysema in the resected lungs were more likely to have associated pulmonary fibrosis, RB, anthracosis and to have smoked for ≥ 30 pack years. Clinically, considerable overlap in physiological and radiographic features in smokers have led to increasing recognition of CPFE [26, 27]. In lung tissue resected with nodules, fibrosis could be detected in 50 to 70% while emphysema was observed in 20% or more [28]. One-third of patients undergoing lung volume reduction surgery for severe emphysema were noted to have unsuspected histologic findings including interstitial and subpleural fibrosis in approximately 20% of patients [29]. Pathological and radiological evidence of a relationship between lung fibrosis and emphysema has previously revealed two patterns [4]. The first pattern reflects a fibrosis which is initially localized and frequently clinically occult (respiratory bronchiolitis (RB), RB with interstitial lung disease (RB-ILD), RB-ILD with fibrosis, airspace enlargement with fibrosis, and smoking-related interstitial fibrosis (SRIF)). Such fibrosis can be an integral part of the emphysematous process and is characterized by increased collagen in the respiratory bronchiole accompanied by CL emphysema [30, 31]. The fibrosis can extend into adjacent alveolar walls (in subpleural and CL regions) in approximately half of current and ex-smokers [32, 33]. The second pattern includes fibrosis of a diffuse interstitial pneumonitis, most commonly UIP, mixed with CL or PS emphysema. These cases are included in CPFE [24, 34,35,36,37]. On pathological examination, there can be areas of (1) pure fibrotic interstitial pneumonia, (2) pure emphysema, and (3) fibrosis wrapped around emphysematous spaces with fibrotic changes, most frequently consistent with UIP [26].
Of various histologic features reported in this cohort, PBM was almost seven times more likely to predict radiographic ILA/ILD patterns. More specifically, PBM strongly associated with CL-GGO of ILA patterns and with ILD only pattern on CT chest. PBM is a non-specific reaction to bronchiolar injury, characterized by fibrosis and proliferation of bronchiolar epithelium along peribronchiolar alveolar walls. PBM is a common finding in ILDs ranging from 11% in RB-ILD to 50% in DIP, NSIP, and HP and 59% in UIP cases [38]. PBM identification in known airway centered lung injuries of RB, DIP and chronic HP suggest that PBM could be included in the response to particles including cigarette smoke. Such airway centered parenchymal fibrosis is frequently seen with the respiratory bronchiole of asymptomatic current or ex-smokers [32]. Pathologic-CT correlative investigation which evaluated cigarette smoking-induced parenchymal changes revealed that GGO on HRCT was associated with an accumulation of pigmented macrophages in alveolar spaces associated with fibrosis [39]. In addition, poorly defined parenchymal micronodules demonstrated pathological findings of bronchiolectasis with peribronchiolar fibrosis. Thus, the HRCT abnormalities of respiratory bronchiole (i.e. CL-GGO) and PBM appreciated in our cohort could correspond to some combination of the inflammation and fibrosis around the terminal bronchioles [40, 41]. Non-emphysematous cysts ILA pattern was observed in 8% of cohort and it showed a possible association with histologic DIP. Small (< 2 cm) thin-walled cysts admixed with GGO can be a unique feature in about one-third of DIP patients [42]. Cysts in DIP typically characterize the dilated bronchioles and alveolar ducts secondary to bronchiolar stenosis [43]. Non-emphysematous cysts of ILAs in our cohort may represent as an early response to smoking-related injury with a predilection towards development into DIP.
With availability of pre-surgical PFTs for majority of patients (> 95%), our findings provide comprehensive physiological evaluation and its interaction with diverse clinical, radiographic and pathologic variables recorded in the cohort. Decreased DLCO (< 70% predicted) was 1.5 times likely to predict ILAs/ILD in our cohort with lower mean DLCO values associated with ILA/ILD. As reported among patients with CPFE, the presence of interstitial abnormalities can augment percent predicted FEV1 with no difference in % predicted FVC, resulting into the pseudo-normalization of FEV1/FVC ratio [44, 45]. Moderate to severely reduced DLCO is a consistent and characteristic finding mentioned in CPFE patients reflecting the additive effects of emphysema and fibrosis on the reduction in surface area available for gas exchange [46]. A greater exposure to cigarette smoke and reduced DLCO were predictors for CPFE in a cohort of IPF patients [16]. Similar deleterious effect of emphysema in patients with interstitial features were reported by Ash SY et al. based on limited availability of DLCO findings in their study participants (< 5%) [10]. Therefore, an isolated reduction in DLCO can be a diagnostic clue for ILAs, particularly in a cohort with a high prevalence of emphysema.
In addition to GERD and ≥ 30 pack years of smoking, radiographic ILA/ILD and isolated honeycombing were the greatest predictors of mortality (OR 4.04 and 7.32, respectively) in our cohort. This was independent of age, BMI, lung cancer finding on resected nodule, and radiographic or histologic emphysema. The presence of ILA with the definite fibrosis pattern (pulmonary parenchymal architectural distortion with traction bronchiectasis and honeycombing) was previously associated with the highest risk of progression and increased mortality on 5-year follow up [47]. Traction bronchiectasis was similarly associated with shorter survival among subjects with ILA [48]. ILAs in a lung cancer screening population of relatively healthy smokers (> 20 py) were also associated with mortality but this was regardless of the interstitial morphological phenotype [49]. Analysis of a large research cohort showed an association of increased all-cause mortality with ILAs with the higher median pack years of smoking seen in subjects with ILAs [50].
We report several limitations for our study. It was a retrospective study at a single tertiary medical center which poses inherent limitations. Assertion of cigarette smoking behavior was obtained retrospectively introducing recall bias. A majority of participants were white. Our qualitative determination of ILAs instead of quantitative assessment may affect the repeatability of our findings; however, others have reported poor positive predictive value of quantitative high attenuation area (HAA) [8]. Moreover, considerable interobserver variability has been known to exist for fibrotic pattern recognition on a CT scan, even among thoracic experts [51, 52]. We did not quantify the extent of pulmonary emphysema, which could have assisted in defining its interplay with lung fibrosis and its impact on important clinical outcomes. Surgical resection was performed for suspected pulmonary nodules/masses but not designed to provide information about non-malignant path findings including ILA. Recent reporting guidelines recommend that pathologists should record and categorize the presence of non-neoplastic lung parenchymal changes including emphysema, RB, and interstitial fibrosis with any discernible patterns [53]. In contrast, strengths of the study include relatively large cohort with consecutively included patients undergoing surgical resection, detailed description of radiologic findings and their correlation with histological features.
Conclusion
With the highest national smoking rates observed in the Appalachian region, radiographic subclinical ILA/ILD patterns were highly prevalent. Correlating clinical, radiographic and pathologic characteristics, our analysis provided evidence of co-existence of emphysema and ILA/ILD either radiologically or histologically in association with smoking. In addition, the study finds a unique association of PBM to CL-GGO in ILA patterns which may be indicative of smoking associated small-airways injury. While confirming the role of ILA/ILD and honeycombing for increased mortality, GERD and cigarette smoking intensity showed a significant impact on mortality in our cohort. Analogous to CPFE, preserved spirometry and isolated reduction in DLCO might be a key physiological consequence of early interstitial changes with smoking. Additionally, the study participants showed the presence of diverse non-malignant lung pathologies from cigarette smoke exposure which could represent a continuum of injury process at a tissue level. Considering self-limiting nature of some of these inflammatory changes, greater emphasis should be placed on earlier identification of subclinical ILAs in emphysema patients to allow implementation of effective smoking cessation strategy.
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
Abbreviations
- CPFE:
-
Combined pulmonary fibrosis and emphysema
- CL:
-
Centrilobular
- DLCO :
-
Diffusion capacity for carbon monoxide
- DIP:
-
Desquamative interstitial pneumonia
- FEV1 :
-
Forced expiratory volume in one second
- FVC:
-
Forced vital
- GERD:
-
Gastro-esophageal acid reflex
- GGO:
-
Ground glass opacity
- ILAs:
-
Interstitial lung abnormalities
- ILDs:
-
Interstitial lung diseases
- IPF:
-
Idiopathic pulmonary fibrosis
- NSIP:
-
Non-specific interstitial pneumonia
- OR:
-
Odds ratio
- PBM:
-
Peribronchiolar metaplasia
- PFT:
-
Pulmonary function test
- PLCH:
-
Pulmonary Langerhans cell histiocytosis
- RB-ILD:
-
Respiratory bronchiolitis–interstitial lung disease
- RV:
-
Residual volume
- SRIF:
-
Smoking-related interstitial fibrosis
- TLC:
-
Total lung capacity
- UIP:
-
Usual interstitial pneumonia
References
Margaritopoulos GA, Vasarmidi E, Jacob J, Wells AU, Antoniou KM. Smoking and interstitial lung diseases. Eur Respir Rev. 2015;24(137):428–35. https://doi.org/10.1183/16000617.0050-2015.
Beghe B, Cerri S, Fabbri LM, Marchioni A. COPD, pulmonary fibrosis and ILAs in aging smokers: the paradox of striking different responses to the major risk factors. Int J Mol Sci. 2021;22(17):9292. https://doi.org/10.3390/ijms22179292.
Jankowich MD, Rounds S. Combined pulmonary fibrosis and emphysema alters physiology but has similar mortality to pulmonary fibrosis without emphysema. Lung. 2010;188(5):365–73. https://doi.org/10.1007/s00408-010-9251-6.
Wright JL, Tazelaar HD, Churg A. Fibrosis with emphysema. Histopathology. 2011;58(4):517–24. https://doi.org/10.1111/j.1365-2559.2010.03648.x.
Washko GR, Hunninghake GM, Fernandez IE, et al. Lung volumes and emphysema in smokers with interstitial lung abnormalities. N Engl J Med. 2011;364(10):897–906. https://doi.org/10.1056/NEJMoa1007285.
Butler MW, Fabre A, Dodd JD. Smokers with interstitial lung abnormalities. N Engl J Med. 2011;364(25):2465. https://doi.org/10.1056/NEJMc1104014 (author reply 2466).
King TE Jr. Smoking and subclinical interstitial lung disease. N Engl J Med. 2011;364(10):968–70. https://doi.org/10.1056/NEJMe1013966.
Kliment CR, Araki T, Doyle TJ, et al. A comparison of visual and quantitative methods to identify interstitial lung abnormalities. BMC Pulm Med. 2015;15:134. https://doi.org/10.1186/s12890-015-0124-x.
Araki T, Nishino M, Zazueta OE, et al. Paraseptal emphysema: Prevalence and distribution on CT and association with interstitial lung abnormalities. Eur J Radiol. 2015;84(7):1413–8. https://doi.org/10.1016/j.ejrad.2015.03.010.
Ash SY, Harmouche R, Ross JC, et al. Interstitial features at chest CT enhance the deleterious effects of emphysema in the COPDGene cohort. Radiology. 2018;288(2):600–9. https://doi.org/10.1148/radiol.2018172688.
Lee TS, Jin KN, Lee HW, et al. Interstitial lung abnormalities and the clinical course in patients With COPD. Chest. 2021;159(1):128–37. https://doi.org/10.1016/j.chest.2020.08.017.
Ohgiya M, Matsui H, Tamura A, Kato T, Akagawa S, Ohta K. The Evaluation of Interstitial Abnormalities in Group B of the 2011 Global Initiative for Chronic Obstructive Lung Disease (GOLD) Classification of Chronic Obstructive Pulmonary Disease (COPD). Intern Med. 2017;56(20):2711–7. https://doi.org/10.2169/internalmedicine.8406-16.
Otani H, Tanaka T, Murata K, et al. Smoking-related interstitial fibrosis combined with pulmonary emphysema: computed tomography-pathologic correlative study using lobectomy specimens. Int J Chron Obstruct Pulmon Dis. 2016;11:1521–32. https://doi.org/10.2147/COPD.S107938.
Prevention WDoT. West Virginia Department of Health and Human Resorces (WVDHHR). https://dhhr.wv.gov/wvdtp/cessation/pages/default.aspx. Accessed 25 Oct 2021.
DeBolt CL, Brizendine C, Tomann MM, Harris DA. Lung disease in Central Appalachia: it’s more than coal dust that drives disparities. Yale J Biol Med. 2021;94(3):477–86.
Sangani R, Ghio A, Culp S, Patel Z, Sharma S. Combined pulmonary fibrosis emphysema: role of cigarette smoking and pulmonary hypertension in a rural cohort. Int J Chron Obstruct Pulmon Dis. 2021;16:1873–85. https://doi.org/10.2147/COPD.S307192.
Hatabu H, Hunninghake GM, Richeldi L, et al. Interstitial lung abnormalities detected incidentally on CT: a Position Paper from the Fleischner Society. Lancet Respir Med. 2020;8(7):726–37. https://doi.org/10.1016/S2213-2600(20)30168-5.
American Thoracic S, European Respiratory S. American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001. Am J Respir Crit Care Med. 2002;165(2):277–304. https://doi.org/10.1164/ajrccm.165.2.ats01.
Travis WD, Costabel U, Hansell DM, et al. An official American Thoracic Society/European Respiratory Society statement: update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med. 2013;188(6):733–48. https://doi.org/10.1164/rccm.201308-1483ST.
Mueller-Mang C, Grosse C, Schmid K, Stiebellehner L, Bankier AA. What every radiologist should know about idiopathic interstitial pneumonias. Radiographics. 2007;27(3):595–615. https://doi.org/10.1148/rg.273065130.
Berg K, Wright JL. The pathology of chronic obstructive pulmonary disease: progress in the 20th and 21st centuries. Arch Pathol Lab Med. 2016;140(12):1423–8. https://doi.org/10.5858/arpa.2015-0455-RS.
Lederer DJ, Enright PL, Kawut SM, et al. Cigarette smoking is associated with subclinical parenchymal lung disease: the Multi-Ethnic Study of Atherosclerosis (MESA)-lung study. Am J Respir Crit Care Med. 2009;180(5):407–14. https://doi.org/10.1164/rccm.200812-1966OC.
Podolanczuk AJ, Oelsner EC, Barr RG, et al. High attenuation areas on chest computed tomography in community-dwelling adults: the MESA study. Eur Respir J. 2016;48(5):1442–52. https://doi.org/10.1183/13993003.00129-2016.
Katzenstein AL, Mukhopadhyay S, Zanardi C, Dexter E. Clinically occult interstitial fibrosis in smokers: classification and significance of a surprisingly common finding in lobectomy specimens. Hum Pathol. 2010;41(3):316–25. https://doi.org/10.1016/j.humpath.2009.09.003.
Kawabata Y, Hoshi E, Murai K, et al. Smoking-related changes in the background lung of specimens resected for lung cancer: a semiquantitative study with correlation to postoperative course. Histopathology. 2008;53(6):707–14. https://doi.org/10.1111/j.1365-2559.2008.03183.x.
Cottin V, Nunes H, Brillet PY, et al. Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity. Eur Respir J. 2005;26(4):586–93. https://doi.org/10.1183/09031936.05.00021005.
Wiggins J, Strickland B, Turner-Warwick M. Combined cryptogenic fibrosing alveolitis and emphysema: the value of high resolution computed tomography in assessment. Respir Med. 1990;84(5):365–9. https://doi.org/10.1016/s0954-6111(08)80070-4.
Miller ER, Putman RK, Vivero M, et al. Histopathology of interstitial lung abnormalities in the context of lung nodule resections. Am J Respir Crit Care Med. 2018;197(7):955–8. https://doi.org/10.1164/rccm.201708-1679LE.
Keller CA, Naunheim KS, Osterloh J, Espiritu J, McDonald JW, Ramos RR. Histopathologic diagnosis made in lung tissue resected from patients with severe emphysema undergoing lung volume reduction surgery. Chest. 1997;111(4):941–7. https://doi.org/10.1378/chest.111.4.941.
Thurlbeck WMWJ. Thurlbeck’s chronic airflow obstruction. 2nd ed. Hamilton: B.C. Decker Inc.; 1999.
Wick MR. Pathologic features of smoking-related lung diseases, with emphasis on smoking-related interstitial fibrosis and a consideration of differential diagnoses. Semin Diagn Pathol. 2018;35(5):315–23. https://doi.org/10.1053/j.semdp.2018.08.002.
Fraig M, Shreesha U, Savici D, Katzenstein AL. Respiratory bronchiolitis: a clinicopathologic study in current smokers, ex-smokers, and never-smokers. Am J Surg Pathol. 2002;26(5):647–53. https://doi.org/10.1097/00000478-200205000-00011.
Yousem SA. Respiratory bronchiolitis-associated interstitial lung disease with fibrosis is a lesion distinct from fibrotic nonspecific interstitial pneumonia: a proposal. Mod Pathol. 2006;19(11):1474–9. https://doi.org/10.1038/modpathol.3800671.
Auerbach O, Garfinkel L, Hammond EC. Relation of smoking and age to findings in lung parenchyma: a microscopic study. Chest. 1974;65(1):29–35. https://doi.org/10.1378/chest.65.1.29.
Cottin V, Cordier JF. Combined pulmonary fibrosis and emphysema in connective tissue disease. Curr Opin Pulm Med. 2012;18(5):418–27. https://doi.org/10.1097/MCP.0b013e328356803b.
Cottin V, Nunes H, Mouthon L, et al. Combined pulmonary fibrosis and emphysema syndrome in connective tissue disease. Arthritis Rheum. 2011;63(1):295–304. https://doi.org/10.1002/art.30077.
Kligerman S, Franks TJ, Galvin JR. Clinical–radiologic–pathologic correlation of smoking-related diffuse parenchymal lung disease. Radiol Clin North Am. 2016;54(6):1047–63. https://doi.org/10.1016/j.rcl.2016.05.010.
Fukuoka J, Franks TJ, Colby TV, et al. Peribronchiolar metaplasia: a common histologic lesion in diffuse lung disease and a rare cause of interstitial lung disease: clinicopathologic features of 15 cases. Am J Surg Pathol. 2005;29(7):948–54. https://doi.org/10.1097/01.pas.0000168177.71405.ac.
Remy-Jardin M, Remy J, Gosselin B, Becette V, Edme JL. Lung parenchymal changes secondary to cigarette smoking: pathologic-CT correlations. Radiology. 1993;186(3):643–51. https://doi.org/10.1148/radiology.186.3.8430168.
Muller NL, Miller RR. Diseases of the bronchioles: CT and histopathologic findings. Radiology. 1995;196(1):3–12. https://doi.org/10.1148/radiology.196.1.7784583.
Wells AU, Nicholson AG, Hansell DM. Challenges in pulmonary fibrosis. 4: smoking-induced diffuse interstitial lung diseases. Thorax. 2007;62(10):904–10. https://doi.org/10.1136/thx.2004.031021.
Godbert B, Wissler MP, Vignaud JM. Desquamative interstitial pneumonia: an analytic review with an emphasis on aetiology. Eur Respir Rev. 2013;22(128):117–23. https://doi.org/10.1183/09059180.00005812.
Boddu P, Parimi V, Taddonio M, Kane JR, Yeldandi A. Pathologic and radiologic correlation of adult cystic lung disease: a comprehensive review. Pathol Res Int. 2017;2017:3502438. https://doi.org/10.1155/2017/3502438.
Akagi T, Matsumoto T, Harada T, et al. Coexistent emphysema delays the decrease of vital capacity in idiopathic pulmonary fibrosis. Respir Med. 2009;103(8):1209–15. https://doi.org/10.1016/j.rmed.2009.02.001.
Cottin V. The impact of emphysema in pulmonary fibrosis. Eur Respir Rev. 2013;22(128):153–7. https://doi.org/10.1183/09059180.00000813.
Amariei DE, Dodia N, Deepak J, et al. Combined pulmonary fibrosis and emphysema: pulmonary function testing and a pathophysiology perspective. Medicina (Kaunas). 2019;55(9):580. https://doi.org/10.3390/medicina55090580.
Putman RK, Gudmundsson G, Axelsson GT, et al. Imaging patterns are associated with interstitial lung abnormality progression and mortality. Am J Respir Crit Care Med. 2019;200(2):175–83. https://doi.org/10.1164/rccm.201809-1652OC.
Hida T, Nishino M, Hino T, et al. Traction bronchiectasis/bronchiolectasis is associated with interstitial lung abnormality mortality. Eur J Radiol. 2020;129: 109073. https://doi.org/10.1016/j.ejrad.2020.109073.
Hoyer N, Wille MMW, Thomsen LH, et al. Interstitial lung abnormalities are associated with increased mortality in smokers. Respir Med. 2018;136:77–82. https://doi.org/10.1016/j.rmed.2018.02.001.
Putman RK, Hatabu H, Araki T, et al. Association between interstitial lung abnormalities and all-cause mortality. JAMA. 2016;315(7):672–81. https://doi.org/10.1001/jama.2016.0518.
Walsh SL, Calandriello L, Sverzellati N, Wells AU, Hansell DM, Consort UIPO. Interobserver agreement for the ATS/ERS/JRS/ALAT criteria for a UIP pattern on CT. Thorax. 2016;71(1):45–51. https://doi.org/10.1136/thoraxjnl-2015-207252.
Walsh SLF, Richeldi L. Subclinical interstitial lung abnormalities: lumping and splitting revisited. Am J Respir Crit Care Med. 2019;200(2):121–3. https://doi.org/10.1164/rccm.201901-0180ED.
Schneider F, Butnor K, Beasley MB, et al. Protocol for the examination of resection specimens from patients with primary non-small cell carcinoma, small cell carcinoma, or carcinoid tumor of the lung. College of American Pathologists (CAP); 2019. https://documents.cap.org/protocols/cp-gilower-colonrectum-resection-20-4100.pdf. Accessed 6 Jan 2022.
Acknowledgements
The authors sincerely thank Varun Badami, MD for the assistance with data-analysis.
Funding
Not applicable.
Author information
Authors and Affiliations
Contributions
Conception and design of the work: RGS, VD, AJG, GA. Data acquisition: RGS, VD, MJF, RZ, AK, ZP, EA, GA, JV. Data analysis: RGS, VD, AJG. Data interpretation: RGS, VD, AJG, JV. Manuscript drafting and revisions: RGS, AJG, VD, JV, MJF, RZ, ZP. All authors have read and approved the manuscript. RGS takes the responsibility of the content and accuracy of work presented in the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
The study protocol for retrospective review of electronic medical records was approved and “informed consent” was waived by the institutional review board of WVU (ID# 2010131995). As per the IRB questionaries: “Does the research qualify for Exempt Research Category 4—Secondary research for which consent is not required? Response: Yes. Explanation: Secondary research uses of identifiable private information or identifiable biospecimens, is recorded by the investigator in such a manner that the identity of the human subjects cannot readily be ascertained directly or through identifiers linked to the subjects, the investigator does not contact the subjects, and the investigator will not re-identify subjects.” All ethical standards were adhered in accordance with the Declaration of Helsinki.
Consent for publication
Not applicable.
Competing interests
The authors declare they have no financial or non-financial competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Additional file 1.
Radiographic and pathologic case definitions of emphysema, ILA and ILD.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Sangani, R.G., Deepak, V., Ghio, A.J. et al. Interstitial lung abnormalities and interstitial lung diseases associated with cigarette smoking in a rural cohort undergoing surgical resection. BMC Pulm Med 22, 172 (2022). https://doi.org/10.1186/s12890-022-01961-9
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12890-022-01961-9