Medication for severe acne alters skin microbiome

Authored by source.wustl.edu and submitted by mvea
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Isotretinoin, a form of vitamin A, has been prescribed to treat acne for decades. It reduces oil production in the skin, which helps prevent acne from forming.

But new research from Washington University School of Medicine in St. Louis has uncovered a previously unknown benefit of the medication. It shifts the skin microbiome of acne patients to more closely resemble that of people with normal skin. The new study is published Dec. 21 in the Journal of Investigative Dermatology.

The study sheds light on how isotretinoin works and provides information that could lead to developing microbiome-based acne treatments, according to the lead researchers, Makedonka Mitreva, associate professor of medicine; and William H. McCoy, MD, PhD, an instructor in medicine, and their colleagues. There is a need for such alternatives because isotretinoin — while effective — causes severe birth defects, so doctors must take added precautions for women of child-bearing age.

Doctors often prescribe antibiotics that target bacteria called Cutibacterium acnes — also called Propionibacterium acnes — which is associated with acne. But such antibiotics can contribute to the development of resistant strains of bacteria and can kill off potentially beneficial microbes as well. Isotretinoin is not an antibiotic. It is largely thought to treat acne by drying out the skin, making it a less inviting place for acne-causing and acne-promoting microbes to flourish. It is the only therapy that can reliably clear acne long term.

“There are greasy areas of the skin that support the growth of certain communities of bacteria, and we know that some of them appear to be associated with acne,” said McCoy, a dermatologist and the study’s first author. “We asked whether we would see fewer of those bad bacteria on the skin after isotretinoin treatment, and we did. But we also know that this drug doesn’t work on the bacteria themselves. It changes the patient’s skin. So if the microbes are changing, it’s in response to changes in the patient’s skin. The drug appears to make the skin less hospitable to acne-causing bacteria.”

The researchers studied bacteria sampled from facial skin swabs at four time points over the course of the 10-month study. The samples came from 17 patients whose acne was treated with isotretinoin and, as a comparison, eight untreated subjects. Of these eight, four had normal skin and four had acne. The researchers found that isotretinoin therapy increased the diversity of microbes found on the skin. Through DNA sequencing, the researchers also identified four types of bacteria that bloomed with isotretinoin treatment. None had previously been associated with improved acne.

Isotretinoin also reduced the overall number of Propionibacteriumbacteria, even as the treatment increased the diversity of the individual types of this bacteria. The 38 percent of isotretinoin-treated patients who did not show this beneficial pattern in the Propionibacterium communities is similar to the proportion of isotretinoin-treated patients in other studies who ended up needing additional rounds of therapy.

The study’s findings, according to the researchers, suggest that isotretinoin creates a “bottleneck” that selects for beneficial communities of Propionibacteria and other bacteria that appear to be healthy, creating a skin microbial community that reduces the chances of the acne returning, even when normal oil production returns to the skin after treatment stops.

“When you have a bottleneck, you create an opening for other microbes to move in and increase in abundance,” said Mitreva, the study’s senior author and an assistant director of the McDonnell Genome Institute at Washington University School of Medicine. “We see this happening here. After the treatment, the microbial communities shift to a mix of populations that appears to be healthier, and that shift persists months after the treatment.”

The researchers said it’s important to understand how isotretinoin works, in an effort to create new therapies that might be more effective or have fewer side effects. Since isotretinoin is known for causing birth defects, it should not be prescribed to women who are pregnant or trying to become pregnant. Women of reproductive age who take isotretinoin are prescribed birth control for the same reason.

“Women often will go without treatment for acne during their pregnancies because there just aren’t good therapies that are totally safe to use during that time,” McCoy said. “They need other options. Our study suggests there could be a way to provide some type of microbial ‘fertilizer’ or ‘weed killer’ on the skin to help promote the growth of healthy microbes. We’re conducting a larger study to look more closely at these questions.”

This work was supported by a 2015 American Acne and Rosacea Society Clinical Research Grant, the Oliver Langenberg Physician Scientist Training Pathway and the Washington University MA/MD Research Program. McCoy WH, Otchere E, Rosa BA, Martin, J, Mann CM, Mitreva M. Skin ecology during sebaceous drought — how skin microbes respond to isotretinoin. Journal of Investigative Dermatology. Dec. 21, 2018. Washington University School of Medicine’s 1,500 faculty physicians also are the medical staff of Barnes-Jewish and St. Louis Children’s hospitals. The School of Medicine is a leader in medical research, teaching and patient care, ranking among the top 10 medical schools in the nation by U.S. News & World Report. Through its affiliations with Barnes-Jewish and St. Louis Children’s hospitals, the School of Medicine is linked to BJC HealthCare.

Originally published by the School of Medicine

Viroplast on December 30th, 2018 at 19:00 UTC »

I take issue with the most popular understanding of the pathogenesis of acne (at least in the medical world), and I ran into problems with dermatologists who would simply tell me that acne is caused by bacteria on the skin or too much oil - take some antibiotics, wash your face, and wait to grow out of it.

First off, the idea that P. acnes causes acne makes zero sense. Acne is not a communicable disease, so right away we need to refine this simplistic model. Even pathogens that only infect some people due to immune susceptibilities or extreme environmental conditions (ex: the dermatophytes that cause athlete's foot) are still communicable on some level. We also know that healthy people have the same bacteria (P. acnes) implicated in acne, but at different levels. So P. acnes is a commensal, non-communicable (in terms of disease phenotype) bacteria that happens to be present at higher levels in inflammatory lesions. Somehow, we've translated this into 'P. acnes causes acne, and therefore if we kill it the acne will go away'. Incomplete science, bad medicine.

Next. Evidence has recently emerged that inflammatory events occur prior to colonization of the lesion with P. acnes. This bacteria therefore may serve to perpetuate an underlying inflammatory response, but doesn't seem to be the initial cause. There is also some evidence (which I can definitely confirm, at least for myself) that certain foods may lead to inflammatory skin responses such as acne. I find this to be the most interesting avenue of acne research because this suggests that there is a distal inflammatory response to digestive conditions, which is kind of cool mechanistically. But more importantly, it's a strike of evidence against the topical P. acnes hypothesis and in favor of a systemic condition.

Now, accutane/isotretinoin. No one's really known the mechanism of action for this drug - only that it's way more effective than topical retinoids even though, theoretically, you should be able to limit your treatment to the affected area with a topical retinoid and get the same effect as systemic isotretinoin (doesn't work in practice). Again, if acne was strictly a local disease, you wouldn't see such a disparity between local and systemic drugs, especially considering that local treatments allow for higher dosages because you don't have to worry so much about toxicity. In regards to the mechanism of isotretinoin, my dermatologist said it reduced skin oil and therefore prevented pores from clogging, reducing acne (even more outdated than the P. acnes hypothesis). Yeah, it definitely reduced skin oil, but after treatment the oil returns while the acne does not. Isotretinoin is systemic and has systemic effects. It changed my digestion and cured a secondary/unrelated skin condition that I had, after I withdrew the drug. It turns out that isotretinoin has immune modulating effects in addition to promoting apoptosis in all sorts of cells types throughout the body - the latter of which has been implicated (very recently) by some scientists in the appearance of side effects such has IBS, overall dryness, and depression.

Okay, back to the pathogenesis of acne. My point is that it's not caused by P. acnes or oily skin, and these myths need to stop being propagated by dermatologists who may not be informed or who may be informed, but seek to simplify for their patients. Beyond the front of what is known that I mentioned above, my experiences with acne (and as a biologist) suggest that acne is a multifactorial disease (like cancer) that has a variety of causes that manifest in similar ways; we've confused those manifestations as a singular cause, since disparate causes tend to get lost as noise during experimentation. I've experimented with myself (I know, N=1) and I can cause a delayed (2-3 days) inflammatory skin response that looks exactly like acne by eating certain foods. I've repeated this experiment many times. This response can be inhibited by taking specific combinations of probiotics at sufficiently high doses, or by extremely low dose isotretinoin. None of these environmental conditions are anywhere close to my face or chest, the sites of the condition. It's clear to me that immunity is at the core of acne pathogenesis, and everything else is tangential. The solution is to manipulate your immune system using bacteria (maybe promoting tolerance/Treg induction?) or retinoids (doing similar things?) or even antibiotics, and avoid eating things that initiate an inflammatory cascade (probably somewhat unique to the individual).

Finally, I want to say that it is not normal/healthy for almost 100% of teens (and a growing number of adults) in Western nations to be afflicted with this disease. Acne is a warning signal, like smallpox, to keep people away. I see it as an evolutionary adaptation; a general marker of stress or sickness. It does not happen in completely healthy individuals with balanced immune systems and low levels of spurious inflammation - by definition. And there should be more of an effort on everyone's part to solve the root of this problem instead of just covering up the spots.

Sethjustseth on December 30th, 2018 at 13:49 UTC »

Formerly known as Accutane. It helped my severe acne when nothing else would, but the side effects were also brutal.

mvea on December 30th, 2018 at 13:23 UTC »

The title of the post is a copy and paste from the first two paragraphs of the linked academic press release here:

Isotretinoin, a form of vitamin A, has been prescribed to treat acne for decades. It reduces oil production in the skin, which helps prevent acne from forming.

But new research from Washington University School of Medicine in St. Louis has uncovered a previously unknown benefit of the medication. It shifts the skin microbiome of acne patients to more closely resemble that of people with normal skin.

Journal Reference:

Skin Ecology During Sebaceous Drought—How Skin Microbes Respond to Isotretinoin

Martin, Caroline M. Mann, Makedonka Mitrev

Journal of Investigative Dermatology. 2018

Published Online: December 19, 2018

Doi: https://doi.org/10.1016/j.jid.2018.09.023

Link: https://www.jidonline.org/article/S0022-202X(18)32693-9/fulltext