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Catching ME/CFS in the Act: The Collaborative on Fatigue Following Infection (COFFI)

It sounds like a great idea – combine all the post-infectious fatigue studies together into one database in order to find answers to one of the biggest questions in ME/CFS – why do some people stay ill after an infection while others recover?

infection - chronic fatigue

Every major infection has provoked a similar response – a significant number of people become chronically ill.

COFFI (Collaborative on Fatigue Following Infection) incorporates no less than 9 studies that have examined post-infective fatigue or illness. The Dubbo study – pioneered by Andrew Lloyd and funded by Australian Health Agencies and the Centers for Disease Control (CDC) in the U.S., still in some ways the best study – started it all off.

The most dramatic conclusion of the first Dubbo study was that somewhere around 10% of people exposed to a serious infection remained ill six months later. Remarkably, the kind of infection – viral or bacterial – didn’t matter. It seemed that being exposed to any serious infection left one at risk for a prolonged fatiguing illness.

Since the Dubbo studies began, eight other post-infectious cohort studies have finished up or are underway. The largest of these are the four Chicago cohort studies (about 1000 participants) under the direction of Ben Katz and Lenny Jason, which have been examining infectious mononucleosis college students for almost ten years. There’s also campylobacter gastroenteritis (n=600), Legionnaires disease (n=190), and Ross River Virus (n=60) cohorts. All told, about 3000 people have participated in 9 studies which have examined people who failed to recover from an infection.

COFFI believes that susceptible individuals develop prolonged fatigue after infection because of biological (immune system, autonomic nervous system, etc.), behavioral and/or environmental effects, which produce alterations in neurobehavioural, cardiovascular and/or immunological systems. The goal of the collaborative is to elucidate what went wrong in those with post-viral (and bacterial) illnesses.

On the face of it, the collaboration holds great promise. How better, after all, to learn about how an illness develops than to capture it in its earliest stages?

The Post-Infectious Illness Group

Different flavors of post-infectious illness exist. One set involving diseases like acute disseminated encephalomyelitis and Guillain-Barre Syndrome produces very dramatic symptoms (paralysis, coma) and is studied. The other produces less dramatic symptoms (fatigue, cognitive problems, PEM) etc., but despite the tremendous functional hits seen, has mostly skated under the scientific establishment’s radar.

The studies that have emerged in the second group look like the kind of studies you would expect from a niche topic. They tend to be underfunded, focus on more easily and cheaply assessed factors, are often light on biological analyses, and sometimes focus on behavioral factors.

Nevertheless, some foundational findings have emerged. First – any serious infection is going to incapacitate a significant subset of those afflicted. The results have been remarkably consistent across types of infectious onset, with most showing from 9-13% of those encountering a serious infection of any type are still ill at six months and 7-9% remain ill a year later.

That’s obviously not a small number of people.

Lloyd, the senior author of the collaborative, has enrolled a mishmash of partners. They include biologically oriented members (Ben Katz, Renee Taylor, Ute Vollmer-Conna, Knut-Arne Wensaas, Jeannine L.A. Hautvast), some in-betweener’s (Brun Wyller, Dedra Buchwald, Renee Taylor) and some behaviorists (Peter White, Esther Crawley, Gabrielle Murphy, Rona Moss-Morris).

The Epidemiological Efforts

Giardia

The Bergen Giardia studies demonstrate the funding woes present in this field. They’ve succeeded in documenting high rates of ME/CFS, chronic fatigue and/or irritable bowel syndrome (IBS) years after an extended Giardia outbreak in Norway.  The studies have established that the outbreak has had a significant health impact on a substantial number of people – an important finding for sure – but it’s been unable, until recently, to delve into any biological factors. (A genetic study is underway.)

The Biopsychosocial Efforts

Moss-Morris’s work shows that cognitive behavioral therapy (CBT) has moved into clearly defined biological illnesses such as MS and renal disease. She’s managed to study the behavioral aspects of fatigue and/or conducted CBT trials in no less than five diseases – ME/CFS, IBS, multiple sclerosis, renal disease and cancer. (The MS CBT trial was deemed successful.)

Moss-Morris assessed epidemiological and biopsychosocial factors in people who became ill following a campylobacter infection (food poisoning). Ironically, that study suggested that those who tried hardest to ignore or push past their illness (e.g. who felt “I must not let this get the better of me” and who engaged in all-or-nothing behavior) were most likely to get ill. (So much for the malingering hypothesis).

chaos

The biopsychological studies have failed to provide consistent theme

Psychologist Peter White must have been chagrined to find that his Bart cohort failed to indicate that mood disorders or negative life events contributed to a “fatigue syndrome” after an infection.

The results of Buchwald’s 2000 infectious mononucleosis study must have flummoxed everyone.

It suggested that a greater number of life events more than six months before the illness began and increased family support were predictive of those who remained ill.

The Q fever studies ended up with a similarly hard to understand mix of factors. Female gender, being younger, having a pre-existing health condition, and being hospitalized in the previous 3 months might make some sense, but why would consuming no alcohol and using medication contribute to a prolonged illness?

The Qure study found that long-term doxycycline treatment utterly failed to move the needle on the illness; i.e. a persistent bug is not responsible.  CBT, on the other hand, improved fatigue and symptoms somewhat but completely failed in the most important measure – improving functionality. (By reducing stress, behavioral therapies should provide some symptom reduction…)

The lack of a recognizable theme suggests that the biopsychosocial results are not getting at the root of anything.  If the goal is illness eradication, researchers need to dig into the biology, and biological efforts have indeed achieved better results.

Biological Efforts

The studies that have dug deeper into biology appear to have been more successful.  Blood tests in the Dubbo studies suggested that pathogen persistence was not the issue: in every case the pathogen appeared, at least, to have been vanquished.

The results of the Qure study on the effectiveness of long-term doxycycline treatment in those with prolonged Q fever suggested the same: it found that the standard treatment for the disease had no effect at all on those who remained ill.

Nor did immune activation over time – as measured by cytokine levels – appear to cause disease persistence in the Dubbo group.

The only risk factors identified occurred early in the illness. Higher levels of cytokines and symptom severity early in the illness appeared to set the stage for a prolonged illness. This suggested that the bug – whichever bug it was – did its damage early and then disappeared.

Genetic studies then suggested a reason why. Immune gene polymorphisms were found in this group which predisposed them to a heightened immune response when confronted with a pathogen.  With three studies confirming and extending that finding, it seems solid. It appears that people with polymorphisms in specific immune genes that heighten the inflammatory response are more likely to become and stay ill.

consistency

The biological studies have provided a more consistent theme of immune activation and autonomic nervous system activation.

The ongoing Chicago infectious mononucleosis studies have dug a bit deeper biologically and uncovered some interesting findings.  Autonomic symptoms and early illness severity were predictive of a prolonged illness (while perceived stress, stressful life events, family stress, difficulty functioning and attending school, and psychiatric disorders were not).

Six months of illness resulted in lower oxygen consumption and reduced peak oxygen pulse; i.e. problems utilizing oxygen – something that Hanson’s latest metabolomic study and others suggested may be happening. (The authors called this “reduced fitness” and “efficiency of exercise.”).  Plus, a network analysis was able to diagnose 80% of ill patients using immune factors, and at six months autonomic nervous symptoms stood out. The analysis suggested a powerful pro-inflammatory immune state persisted for as long as 24 months after the initial onset.

The new “Dubbo studies” (“The Sydney Infectious Outcomes Study (SIOS)) have found an early reduction in heart rate variability, suggesting autonomic nervous system involvement.

In contrast to the biopsychosocial-oriented studies, a theme may be emerging in the biological studies: immune activation and autonomic nervous system problems early, resulting possibly in problems with oxygen utilization, with autonomic nervous system problems persisting.

Wyller’s Weird Results Or Why a Poor Study is Worse Than No Study at All

Many of the post-infective studies have been confined to charting epidemiological factors. Only the initial Dubbo study and the Katz/Taylor Chicago studies have tried to dig deeply at all into biological factors. Even then the scope of the studies has been limited.

Brun Wyller’s CEBA studies (Chronic Fatigue Following Acute Epstein-Barr Virus Infection in Adolescents) appeared at first glance, to fix that. The three studies analyzed 149 factors including early illness severity, immune factors, neuroendocrine stress response, cognitive functioning, emotional disturbances, genetics/ epigenetics of candidate genes, personality traits, and critical life events during and after infectious mononucleosis (IM).

Steps Per Day

The first CEBA study (Lifestyle factors during acute Epstein Barr virus infection in adolescents predict physical activity six months later) assessed the effects of the 149 factors on the number of steps taken per day at six months in 200 individuals. None of the markers of infection or immune response studied affected activity levels.  (Nor did any psychological factors).

Instead, three factors – none of which showed up previously in the post-infectious studies – did. Baseline physical activity (steps per day), substance use (alcohol and illicit drugs), and human growth hormone were associated with reduced steps per day after six months. (Notice the opposing substance use results: low alcohol use was a risk factor for post-Q fever illness, while increased alcohol/substance use was a risk factor for post-infectious mononucleosis illness).

The results suggested that sedentary individuals with low HGH levels who were abusing alcohol/drugs and who became ill with IM are predisposed to be, guess what, more sedentary than usual six months after coming down with infectious mononucleosis.

That’s among the most underwhelming and just weird results I’ve ever seen, and one wonders why Wyller bothered to publish it.

Predictors of Chronic Fatigue

Predictors of chronic fatigue in adolescents six months after acute Epstein-Barr virus infection: A prospective cohort study.

Another study of Wyller’s cohort charted biological factors against fatigue at six months. The main finding that a bunch of symptoms (sensory sensitivity, pain severity, functional impairment, negative emotions) were associated with increased fatigue simply stated the obvious. The more fatigued a person was, the more negative emotions they had (what a surprise!), the more functionally limited they were (!!!!), and the more pain they were in (stunning!), etc.

The fact that viral load had no predictive value was in line with past studies. The slightly increased plasma C-reactive protein found (Wyller suggested it was caused by negative life events) and reduced plasma vitamin B12 levels were the only two biological factors that stood out.  Neither will move this field forward significantly.

Predictable Results?

So how did Wyller get such pitiful results?

It turned out the study was not as comprehensive as the 149 factors made it appear to be, and was rudimentary to boot.  Included in that 149 factor set were standard blood tests, demographic results, psychological testing, etc.

Wyller testing ME/CFS

Wyller’s testing regimen made a biological result unlikely.

Wyller used a Fatigue Scale – the Chalder Fatigue Scale – believed be problematic in ME/CFS.  His immune tests mostly consisted of immune cell counts which have historically not been particularly effective.  Natural killer cell cytotoxicity – which has consistently been found to be low in ME/CFS – was not done.

The one stressor used – during the autonomic nervous system testing (deep breathing while supine and during 3 minutes of standing) – was too mild (at least a 10 minute tilt table test is needed to diagnose POTS).

While changes in heart rate and blood pressure have been found in ME/CFS, heart rate variability is a more discerning factor and has been more commonly assessed and found altered in ME/CFS – but was not used in Wyller’s study. The cortisol blood test Wyller used has not been found effective in ME/CFS. (Blood cortisol awakening response and morning saliva cortisol tests (not done) have been more effective).

All in all, the study – with its lack of a significant stressor, its limited testing protocol and the use of measures which have not proved useful in ME/CFS – appears to have been almost doomed to failure.  One wonders why Wyller expected to find anything at all, and the results probably could have been predicted.

They also, not surprisingly, opened the door wide open to a biopsychosocial interpretation of ME/CFS that Wyller walked right through.  Wyller reported that,

“Taken together, the results seem to support a biopsychosocial rather than a biomedical perspective on the development of chronic fatigue and CFS.”

Lenny Jason’s Chicago Studies

The next Chicago studies, led by Lenny Jason, will examine many more biological factors in its next iteration. Unlike the Dubbo, Giardia, Wyller’s studies and others, Jason’s samples predate the illness onset, giving him the potential to uncover biological risk factors present before a person became ill.

He has blood samples from over 4,000 students, 4-5% of whom contracted infectious mononucleosis, which they are following. Papers should start appearing this spring/summer. As of October 2018, Jason was still in the process of applying for grants to study blood and saliva factors. They hope to study autonomic functioning, cytokine, metabolomic and saliva biological risk factors.

Jason’s preservation of his samples in a deep freeze means they’ll be able to be assessed as we learn more about ME/CFS over time.  They provide the potential for uncovering perhaps the greatest mystery of all in ME/CFS – what was going on before ME/CFS actually hit that put one at risk for it?

Conclusion

Time will tell if the The Collaborative on Fatigue Following Infection (COFFI) will help, hurt or do anything at all. If the embarrassingly rudimentary website with its weird ads is any indication, the group may not amount to much.

Wyller’s efforts indicate that rudimentary, poorly targeted efforts can do more harm than good if the authors decide to default to a historical norm: if you can’t find something biological, a biopsychosocial explanation must apply.  His results and other biopsychosocial study results are so bizarre, though, that one wonders if anyone will take them seriously.

trigger - post-infectious fatigue

The post-infectious studies have the possibility of catching the disease in the act.

The biological efforts are another story. These cohorts offer the enticing possibility of catching the disease in the act as it first manifests itself. The first post-infectious fatigue studies – the Dubbo studies – are still some of the best, and outlined some findings that have continued to stand: illness severity is a major risk factor and the bugs that triggered the illness in the first place don’t appear to play a role in prolonging it. The early cytokine and genetic results fit that picture: they suggest a stronger than usual early immune response may set the stage for ME/CFS.

Incorporating more sophisticated tests, the Chicago infectious immune studies add the possibility of long-term autonomic nervous system problems, further suggest immune issues play a role and, intriguingly, provide the first signs of impaired energy production during exercise.

Jason, if he can get the money to test his samples, has the opportunity, with his metabolomic, autonomic nervous system and immune testing, to provide more insights into how this illness got started in the first place and why it remains. Plus, his frozen samples provide the opportunity for future researchers to dig even deeper into these questions. They should prove invaluable.

 

 

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10 Comments

  • dejurgen

    February 23, 2019 at 10:33 pm - Reply

    Thanks once again for the excellent blog Cort!

    “but why would consuming no alcohol and using medication contribute to a prolonged illness?”
    -> The question about alcohol may be a simple one: a low amount of alcohol consumption protects the bowel. See http://www.naturalmedicinejournal.com/journal/2011-12/alcohol-consumption-and-risk-colorectal-cancer-0 for the easy to read version and http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111915/ for the research paper version titled “Inverse relationship between moderate alcohol intake and rectal cancer: Analysis of the North Carolina Colon Cancer Study”. It also discusses colon cancer with similar results.

    In order of colorectal cancer occurrence moderate alcohol consumption is better then no alcohol consumption but heavy alcohol consumption is the worst.

    Note that these results are “snowed under” by studies done that do not make the difference between moderate and heavy alcohol consumption. In the UK for example a government ordered study did find this beneficial effect of moderate alcohol consumption but the scientist had been pressured to “rephrase” the findings so that all alcohol consumption appeared bad for health. When the “alteration” in the paper later was exposed by other scientist it created some scandal. The UK government is the same one that ordered the PACE study and they have been caught red faced pressuring the scientist who did the study to the effect of alcohol consumption on health to “alter” the scientific outcome to “what was in line with what government officials desired: a more strict alcohol guideline”.

    This effect of alcohol on the bowel may not be that surprising. Bacteria are very competitive creatures often trying to kill of competing species. They produce chemicals that reduce the growth of bacteria including those of their own species but their own species is less affected. Such chemicals, among others are: acetic acid (vinegar), lactic acid, buteric acid and alcohol.

    -> All these chemicals, even in moderate amount, can help decrease growth of undesired and or desired bacteria in the gastro internal tract.

    Moderate alcohol consumption also is correlated with less infection with Helicobacter Pylori (and other bad ones). That is a bacteria often named in the same sentence as CFS and there is a correlation between this bacteria and colon cancer http://www.cghjournal.org/article/S1542-3565(16)30704-2/fulltext. It’s a bit hard to quote from this text as it only show the first page as an image. But it says that for moderate alcohol intake H. Pylori infection rates were less. Wine was better then beer. Drinking lots of brandy however made H. Pylori infections worse. Maybe that was enough to destroy the gut?

    The bowel has a huge impact on inflammatory response. And plenty of bad bacteria flourishing in it can cause quite an inflammatory up-flare, especially if they manage to cross over into the blood stream.

    How that translates to vulnerability to chronic disease is another issue. But I can quite well imagine that people with an increased pre-existing “inflammatory bowel” condition are likely getting their immune system more overwhelmed when a strong infection like EBV is added on top of it compared to people only having to deal with EBV alone.

    Well, the strong immune response that EBV must cause draws plenty and plenty of resources from the body. And the gut is the first to be cut off in case of emergency as being “non-urgent”. If it has to fight a “moderate” chronic gut inflammation/infection then it gets into deeper trouble when resources and blood flow are diverted away from it to help fight the EBV infection. That may well allow to entrench the gut condition a lot deeper into the body. If that would cause a sort of reinforced bad gut bacteria uptake in the bloodstream in combination with poor gut health then it would get a person pretty close to a bad vicious circle. This would resemble a lot “some form of chronic sepsis”, a condition CFS is sometimes told by doctors to resemble the most.

    As to why medicine consumption could be an indicator for having increased risk of chronic disease? Many of them have side effects on the stomach and gut. Having to deal with a combination of for example EBV, pre-existing gut inflammation/infection and a drug throwing the stomach and or gut out of balance (when blood flow to it is decreased due to the infection) may be quite a hard challenge for the body to cope with.

  • Richard Windsor

    February 24, 2019 at 12:03 am - Reply

    Isaac Newton’s comment “If I have seen further it is by standing on the shoulders of Giants.” seems not to have resonated with many researchers by your account. I find it interesting that your collection of studies is broad with one significant omission, that of “Post Treatment Lyme Syndrome” Many of us old farts who were diagnosed with CFS/FM in the 80s subsequently went on to discover that the real culprit was Lyme 🙁 .
    At this stage of investigation into the complexities of Borrelioses and co-infections, the “establishment” has its collective heads firmly up “in that place where the sun doesn’t shine”. That the overlap between post-infectious fatigue and late-stage Lyme suggests common pathways. However, the Lyme literature is more akin to Grimm’s Fairy Tales than to scientific discourse.
    Lyme stands isolated for several reasons:
    That the two-tier testing used for surveillance by the CDC has assumed canonical status despite its poor reliability.
    That a short course of Doxycycline will fix it despite the published evidence that all it does is suppress antibody production.
    That Borrelia are absent from the body in post-treatment patients despite landmark studies showing the presence of “persister cells”
    Is Lyme the outlier or in the case of persisting “post-infection Fatiguing illness” do we have the possibility of occult persister infectious agents which, after serious insult, are able to maintain the body in a continuous debilitated state?
    I’ve lost count of the number of candidate infectious agents that have, at various times, had their “heads above the parapet” but for various reasons (both good and bad) been eliminated as causal factors.
    Please keep up the good work 🙂

  • Ian stirling

    February 24, 2019 at 11:06 am - Reply

    Another interesting study found diagnosed rates of CFS amongst the whole population for Norway (?) And compared time periods when flu pandemic vaccine was delivered to flu infections.
    Flu infections caused CFS at an elevated rate, but not vaccination.
    (Far less than 1/8)

  • Ron P

    February 25, 2019 at 12:37 am - Reply

    Theory: Stress, physical and or mental weakens Adrenals.
    Something new to the environment impedes recovery.
    Incline Village was in the 80’s Many of us became ill in the 80’s
    Cell Phone Towers: 1983.

    It takes energy to remove toxins.

  • Sten Helmfrid

    February 25, 2019 at 7:55 am - Reply

    Thank you for an interesting blog post. In the Dubbo study, it didn’t matter which bug that triggered the fatigue syndrome. However, it must be pointed out that only three bugs were studied: Epstein–Barr virus, Ross River virus, and Coxiella burnetii. Professor Anthony Komaroff has pointed out that ME/CFS seems to be triggered predominantly by pathogens that can infect the central nervous system and/or are difficult for the immune system to erase. All three bugs in the Dubbo study belong to that category. A review paper by Kondo in 2006 points out that post-infectious fatigue syndromes only have been reported for a limited number of pathogens [Kondo K. Japan Med Assoc J. 2006;49(1):27–33].

    I think that the specificity of ME/CFS trigger pathogens is one of the factors that disagrees with the cognitive behavioral model. If the illness is perpetuated by false illness beliefs and psychosocial causal factors, the risk of developing a post-infectious fatigue syndrome should not depend on the type of trigger pathogen. Do you have any thoughts on this, Cort?

  • Cort Johnson

    February 25, 2019 at 5:25 pm - Reply

    Interesting! My understanding is that it generally takes a pretty strong pathogen to bring on ME/CFS (not usually the common cold) and the flu certainly fits that category. That itself is a clue; ie it a strong immune activation to start the process. I guess the question is – which hopefully the Jason study will help address – is what exactly happens with the immune system or alternately, or probably in conjunction with that – the HPA axis. Cortene believes it begins in the HPA axis.

  • Cort Johnson

    February 25, 2019 at 5:31 pm - Reply

    Great insight Sten! I had never thought of that. We can add Giardia to the list – a potentially difficult bug to eliminate as well. GIven that it effects the gut I imagine it may be able to effect the nervous system in some way as well.

  • Cort Johnson

    February 25, 2019 at 5:33 pm - Reply

    Interesting! Who knew? It makes sense when you lay it out that way.

  • Cort Johnson

    February 25, 2019 at 5:36 pm - Reply

    My guess is that understanding what’s going with post-treatment Lyme disease is going to be quite helpful for ME/CFS. I think they are slowly getting there. Check out this blog: http://simmaronresearch.com/2018/09/post-treatment-lyme-disease-unmasked-immune-holes/

  • Lora

    March 1, 2019 at 4:05 am - Reply

    Cort and Sten, Absolutely agree with both of you ..