American Journal of Respiratory and Critical Care Medicine | 2019

Reply to Biswas: Acute and Chronic Effects of Cigarette Smoking on sRAGE

 
 
 
 
 
 
 
 
 

Abstract


In our recent research letter focusing on the acute effects of smoking on the serum levels of sRAGE (soluble receptor for advanced glycation end products), we showed that smoking three cigarettes within 1 hour significantly decreases serum sRAGE levels within 2 hours (1). In addition, we also determined the effect of chronic cigarette smoke exposure on serum sRAGE levels by comparing smokers with never smokers (originally reported as “data not shown”). Here, we did not find any difference in serum sRAGE levels, which is in line with previous studies (2). In contrast, as rightfully mentioned in the response to our research letter, Biswas and colleagues previously reported that serum sRAGE levels were increased in smokers compared with nonsmokers (3). Biswas explains the discrepancies between their study and other studies by noting that most of the studies were not specifically designed to explore the effect of smoking on sRAGE in healthy individuals, whereas their study was (4). Further, in his original paper, he states that the differences may also be explained by the fact that his study population was of overall younger age compared with those in the other studies (3). Indeed, characteristics of the study population may affect the outcomes of sRAGE measurements; however, other factors, including the method and timing of serum preparation, the method of sRAGE quantification, and, most importantly, the timing of the last smoked cigarette before blood sampling may also drive the observed differences in serum sRAGE levels. Although our initial research letter only showed data of serum sRAGE levels in healthy control subjects versus patients with chronic obstructive pulmonary disease (COPD) (1), our study was also designed to investigate the chronic effects of smoking in healthy individuals. Specifically, to investigate the effect of chronic smoke exposure on the serum levels of sRAGE, we used a well-controlled cohort (ClinicalTrials.gov Identifier: NCT00848406) of young (18–40 yr old) and old (.40 yr old) smokers and never smokers without airway obstruction (Figure 1A) (5). To adequately measure serum sRAGE levels, we used the highly sensitive and selective simplified immunoprecipitation in 96-well ELISA format–coupled liquid chromatography–mass spectrometry assay, which we recently demonstrated to be superior to the commonly used sRAGE ELISA (6). When we focused on the healthy control subjects, we found that there were no differences in serum sRAGE levels between smokers and never smokers, whether old or young (Figure 1B). Of note, the definition of “nonsmokers” in our study and the one used by Biswas are not exactly the same. Whereas our nonsmokers had never smoked, the nonsmokers in Biswas’s study included subjects who had not smoked during the last

Volume 199
Pages 806 - 807
DOI 10.1164/rccm.201812-2257LE
Language English
Journal American Journal of Respiratory and Critical Care Medicine

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