Effect of immune responses on breath methane dynamics.

Abstract

Methane (CH₄) which can be detected in human breath has long been exclusively associated with anaerobic microbial activity (methanogenesis) in the gastrointestinal tract. However, recent studies challenge this understanding by revealing that CH₄might also be produced endogenously in cells through oxidative-reductive stress reactions. Consequently, variations in breath CH₄levels compared to an individual's baseline level might indicate enhanced oxidative stress levels, and, therefore, monitoring breath CH₄levels might offer great potential for 'in vivo' diagnostics such as disease diagnosis, monitoring the efficacy of treatments, or during the application of personalized medicine. To evaluate the effects from immune responses triggered by infections, inflammations, and induced perturbation by vaccination on CH₄dynamics in breath, two subjects were monitored over a period of almost 2 years. Breath CH₄levels were measured by gas chromatography equipped with a flame-ionization detector. Both subjects exhibited significant deviations (positive and negative, respectively) from their normal CH₄breath levels during periods of potential enhanced immune activity. Deviations from the 'healthy state' were indicated by the exceeding of individual CH₄ranges. Moreover, for the first time we could clearly prove CH₄degradation induced through vaccination by measuring stable carbon isotopes of CH₄using gas chromatograph-combustion-isotope ratio mass spectrometry. Hence, breath CH₄concentration and isotopic analyses may be used as a biomarker to evaluate specific immune responses and individual immune states.