Dear Editor,
We read with interest the Mirsadraee et al's article entitled “Prevalence of Asthma in Children of Chemical Warfare Victims” in the third issue of 2011 [1].
They skillfully reported an interesting investigation about the effect of Mustard Gas (MG) on the victim's offspring. They demonstrated that the asthma was more common amongst children of MG victims compared to the control group. Also they generalized their findings as “chemical agents may increase the prevalence of asthma in the offspring of chemical warfare victims”. But it seems that there are some remarks which should be considered before generalizing the results.
Asthma is one of the most common chronic immune based disorders identified with restrictive pattern in pulmonary function test. There are so many factors which promote asthma in children. Exposure to the cigarette smoke can predispose children for asthma or at least one episode of upper respiratory tract infection[2]. In the mentioned study, the prevalence of parental smoking in group with MG exposure was significantly higher than in the control group; therefore it can disturb the findings.
Also, the children with low socioeconomic situation are predisposed for asthma[3] and because of low physical ability to work and high medication cost, the chemical warfare veterans (CWVs) likely are in low socioeconomic situation. Therefore, the authors should have matched cases for the socioeconomic situation but there is no precise information about it.
On the other hand, PTSD and other psychiatric disorders are common in CWVs[4] and also previous reports demonstrated the association between parental psychiatry distress and offspring asthma[5]. It is needed to consider the CWV's psychological status before assessing their children for stress related disorders.
Although there are evidences about the relationship between chemical warfare contact and genomic mutation of multi-potential cells such as spermatogonia[6], report about the offspring's somatic anomaly in parental SM exposure is so limited[7].
Nevertheless, one conflicting evidence that may question the effects of MG on victims’ offspring is the different manifestation in victims and their children which in the mentioned study was considered as asthma. The clinical manifestation of MG lung injury in majority of exposed patients is Bronchiolitis obliterans (BO)[8]. The mechanism of BO is related to the chronic inflammation due to deficiency of antioxidants but the well defined mechanism for asthma is immune system imbalance[9].
Also, few studies have pointed to cellular/molecular similarities between these two disorders (MG lung injury and asthma)[10]. Recently, the role of glutathione as an antioxidant and therefore its related enzymes such as glutathione S-transferase was discussed in asthma similar to MG lung injury[9, 11]. On the other hand, the significant role of interleukin-5 and eosinophils (an effective cytokine and immune cell in asthma) in the long term complication of chemical lung injury was identified[12].
The pure impacts of MG regardless concomitant complication must be evaluated in further investigations to confirm its effect on the genome of offspring due to victim's genome mutation in reproductive germ cells. It seems that there are several queries to charge MG as a guilty of victims’ offspring sequels. Future investigation should be focused on the genomic evaluation of victim's reproductive germ cells and its relation with offspring disorders regarding the role of gender[13] and also duration of exposure[14] for adjusting these confounders.
References
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