Could someone smarter than i am please address this?
The relevant sensationalism du jour:
[URL='http://www.11alive.com/story/news/health/2014/12/26/study-e-cigarettes-damage-healthy-cells/20907631/']Study: E-cigarettes damage healthy cells[/URL]
^Just an example, but most the news says the same thing copied and pasted.
The "source" that most said cut-and-paste jobs are citing:
[URL='http://multimedianewsroom.tv/story.php?id=899&enter=0']Study Links the Liquid Used in E-cigarettes to an Increased Risk of Viral Infections[/URL]
And the study itself:
[URL='http://www.plosone.org/article/info:doi/10.1371/journal.pone.0108342']PLOS ONE: Electronic Cigarette Liquid Increases Inflammation and Virus Infection in Primary Human Airway Epithelial Cells[/URL]
Briefly, they put an electronic cigarette on one end of an e-cigarette sucking machine, and human epithelial cells on the other end. The conclusion is that e-juice damages respiratory cells and compromises immune response. I can't make heads or tails of it, too much science in.
.
.
but,
you all ARE going to die,
,and that's the best excuse i can think of to live large.
Wishing all a healthy and prosperous 2015,
Carpe Annum!
This thread quite old but I decided to respond for general information. I looked at the original study ([URL]http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171526/[/URL][\plain]) published by Hong Wei Chu principal investigator and Wu Q. who, actually, is the guy who did the experiments (first author). In summary, the study aims to demonstrate that one flavored eliquid (we don't know which flavor) from InnoVapor LLC., Boise (I don’t know them either), with or without nicotine promotes inflammation and increased susceptibility to viral infection in primary human airway epithelial cells in vitro. They used cells that they call "normal cells” prepared from lung tissues “not suitable for transplantation”. They didn’t expose the cells to actual vapor as falsely reported, but they incubated the cells with the chosen eliquid diluted in cell culture media for 24 to 48 hrs. There is 5 figures in this paper:
- Fig 1: the cells don’t die upon ejuice exposure, which is a good thing.
- Fig 2: There is a nicotine independent modest increase of IL6 production (2 to 3 fold max, also note the size of the error bars) with the ejuice at the highest concentration, after 24 and 48hrs exposure. IL6 is a pro-inflammatory cytokine (small proteins) but has many other functions such as epithelial cell survival. Results not too compiling added to the fact that they only have 4 samples (n=4) without any indication of the number of times they did the experiment, certainly because they did it once… Also, there is plenty of other pro-inflammatory cytokines we usually look at to demonstrate inflammation. They didn’t look at them, or maybe they did but didn’t show the data…
- Fig 3: Indirectly, shows that the flavored ejuice [B]promotes human rhinovirus (HRV) infection. [/B]Indirectly, because they looked at virus acid nucleic (RNA) rather that viral titer. That’s ok though, except that n=5 and again without mention of the number of experiments. Also, I am not quite sure why the virus RNA quantities are lower after 24hrs compare to 6hrs.
- Fig 4: The chosen ejuice induces a further increase of IL6 production that the HRV virus alone. In other word they try to show that ejuice promotes more virus induced inflammation. This can be a good thing during an infection? Not compiling with a barely 2-fold effect… Note also, that the increase of IL6 without the virus is no even 2-fold increased which contrast with fig2.
- Fig 5: Attempt to identify the mechanism by which the flavored ejuice may enhances the virus infection…. Just a convenient guess in their partial demonstration, looking only at the RNA w/o analyzing the protein levels, with the same comment regarding the numbers.
This is just a quick summary of the results, with some of my criticisms, all for general information. Overall I think that this study has been quickly done and the results only applied to the flavored ejuice they have selected and therefore, cannot be generalized. Importantly, the ejuice without flavor or ejuices from other suppliers or different flavors have not be used in any experiments.
That said, I cannot claim yet that ejuice vapors don’t have any effects on lung inflammation or predisposition to viral infections but the poor quality of such studies is just frustrating knowing that no many are reading these papers before making public statements. It’s almost like they thought, let’s show that and it’ll work… “Publish or die” as they say in the field… They can add a new line in their publication record, justify the use of tax money provided by the NIH and ask for more, the politics and propagandists can use it in their anti-vaping or regulation agenda… and the firstauthor can move forward in his career[B]. [/B]Using the “risk of vaping” for the youth as a publishing topic seems to work even if the science behind is, in my view point, mediocre.
Flavors may be the main health hazards in ejuices, therefore this risk requires to be quantified in a systematic manner. Developing and validating a cost and timely effective functional assay to test the safety of ejuice flavors may become a requirement in the near future. Still, cigarettes are a known health hazard, but yet many still smoke. Thanks to vaping, we have a relatively safe way out of smoking, at least in my opinion.