Saturday, 22 October 2011

Life With Low Serotonin, Revisited

Last year I covered the case of a young man born with a genetic disorder which caused him to suffer low levels of the monoamine neurotransmitters - serotonin, dopamine, and noradrenaline.



These are the chemicals that are widely thought to be deficient in depression, and they're the target of antidepressant drugs (especially serotonin).

If low monoamines cause depression, you'd expect someone with low monoamines to be depressed, at least on the simplest view. But the case from last year had no reported mood problems, although he did show appetite, sleep and concentration problems that were cured by serotonin replacement therapy.

Now a new case report has just appeared that tells a different story. Gabriella Horvath and colleagues from British Columbia describe two sisters. Both had a normal birth and childhood, but at the ages of 11 and 15 respectively, began to suffer severe migraines and other symptoms. Sister 1:
started having hemiplegic migraine at age 11 years, initially occurring every 3–8 weeks, lasting 4–48 hours, presenting with right or left-sided numbness and paralysis, no visual disturbances, but slurred speech, associated with vomiting, headache, and confusion, followed by weakness lasting up to 7 days, and then complete recovery. The frequency of her migraine increased slowly with age up to twice a month...
Between 12 and 20 years she had developed progressive spastic paraparesis; sensory loss in stocking distribution... urinary and bowel incontinence; bladder instability... irritable bowel syndrome; sleep problems; depressed mood; and anxiety. She needed to use a wheelchair for most of the time by the age of 17.
Sister 2 had a rather different course:
The older sister originally presented at the age of 15 years with a history of hemiplegic migraine and seizures and myoclonic jerks. EEG showed generalized spike-and-wave activity, and polyspikes with photoconvulsive [light-induced seizures] response, in keeping with juvenile myoclonic epilepsy. Her seizures were brief and infrequent and not associated with the migraine episodes...

She subsequently developed progressive weakness, frequent falls, depression, and mild bladder instability...
Various blood and genetic tests failed to get to the bottom of it. MRI scans showed abnormalities in the spinal cord and parts of the brainstem in both cases, but why?

Spinal tap studies in Sister 1 revealed very low levels of 5HIAA, which is a by-product of brain serotonin (5HT). This suggested low 5HT levels. So doctors started her on 5HTP to try to boost it.

They report that 5HTP treatment caused "improvement" in all symptoms, including the migraines, slurred speech, depression, and movement, but not immediately. She gradually went from being in a wheelchair to being able to walk around the house on crutches, although she used a wheelchair outside. However, after 3 years of treatment, at age 20, she suddenly fell into a coma lasting 2 months. She is now recovering.

Sister 2 also had low 5HIAA, and was given 5HTP. She also reported symptomatic improvement.



Blood tests reported very low platelet serotonin levels. 5HTP treatment increased this but they were still below normal. Platelet 5HT reuptake rate was also low, suggesting a problem with the 5HT reuptake transporter protein 5HTT.

But the 5HTT gene (famously known as "The Happiness Gene" although that's questionable) seemed entirely normal in these patients. The authors say however that the symptoms are, in some ways, reminiscent of mice who lack the 5HT reuptake protein (5HTT knockout mice), who also show low serotonin. Also, if it were genetic, that wouldn't explain why there were no problems at all during childhood.

So this case is a mystery. The low serotonin has no known cause, and it might just be a side effect of a deeper underlying problem, but serotonin has long been linked to migraines so it might account for some of the symptoms. The fact that 5HTP helped supports this, though it wasn't a controlled trial so we can't know for sure.

As for the depression and anxiety, improved by 5HTP, this could have been a result of low serotonin, but it could also have been a psychological reaction to the severe medical problems. It's impossible to know.

ResearchBlogging.orgHorvath GA, Selby K, Poskitt K, Hyland K, Waters PJ, Coulter-Mackie M, & Stockler-Ipsiroglu SG (2011). Hemiplegic migraine, seizures, progressive spastic paraparesis, mood disorder, and coma in siblings with low systemic serotonin. Cephalalgia : an international journal of headache PMID: 22013141

10 comments:

Anonymous said...

I'm not so sure about the idea that if it was genetic, it would have shown up earlier; I get menstrual migraines, and there's probably (from what i've read - it's not my area of expertise at all) a link between estrogen levels and serotonin levels, and the drop in both triggers the migraine - and I think there may be a genetic factor there. Could it not be the case that some things with a genetic cause/factor don't show up until puberty?

Christian said...

Still toying with these upper level signals? When are you silly scientists gonna get it?

:^)

The root of these issues is disrupted glutamate homeostasis.

http://cat.inist.fr/?aModele=afficheN&cpsidt=23957362

http://jn.physiology.org/content/82/2/533.full

http://cep.sagepub.com/content/15/2/132.short

Altostrata said...

Oh, for God's sake, when are we going to give up on trying to link the three humours to depression? Serotonin, norepinephrine, and dopamine have multiple functions in the brain and body.

Christian has a good point. Antidepressant withdrawal syndrome probably also involves glutamatergic dysregulation, see http://tinyurl.com/67vpjtq You see, you jack up serotonin, brain conforms, take away the serotonin, glutamatergic system is dysregulated. QED.

WM said...

The serotonin/monoamine hypothesis is stupidly limited. I too find it amazing how resistant most scientists are to change. The monoamine hypothesis was mostly based on serendipitous findings that monoamine agents had antidepressant activity. Yet preclinical studies with NMDA antagonists show they have far superior antidepressant activity. Ketamine can alleviate depressive symptoms within hours, even in patients resistant to everything else (including ECT). Furthermore the antidepressant activity is maintained for over a week. Subunit studies show the NMDA receptor is massively under-expressed in the PFC and over-expressed in the amygdala in MDD. Brain studies show massive loss of glx (glutamate-glutamine) in MDD and increases in BP. The loss of glia in depression will also imply disturbed glutamate handling. The inflammatory and neuroplastic hypotheses of depression also corroborate with glutamate dysfunction in MDD. Finally serotonergic agents modulate NMDA receptor expression, and specifically decrease extrasynaptic NMDA receptor expression.

http://bb-cfs.blogspot.com/2011/08/depression-hypotheses.html?utm_source=BP_recent

It's also probably no coincidence that magnesium deficiency and depression are so prevalent today. Magnesium being vital for the voltage-dependant blocking of the NMDA receptor.

Christian said...

Altostrata, good to read you. Just for fun I thought I would let you know this fellow is a good friend of mine:
http://www.people.com/people/archive/article/0,,20140034,00.html

Scientific institutions have a hard time breaking out of institutionalized thought. It is a direct result of having to kiss that butts of bosses and professors. It takes some time but they are getting closer to leaving the "humorous" paradigm behind thanks to some brave individuals.

The fun thing about glutamate as a root cause is that it is very easy to bring back to homeostasis without the use of pharmaceuticals.

Christian said...

Wll:Power, well, you are a good read as well.

I want to tell you a short story f my life. I come from a long line of Bipolar's and was hospitalized twice, once from mania and once from depression.

By lowering my blood glutamate levels through diet I am able to be symptom free with only the occasional use of medications because of occasional stress induced glutamate release. Six years later, no relapses. I, and my mother as well, have suffered from ME which for me has subsided.

My hypothesis sprang from this study:
http://www.dana.org/news/cerebrum/detail.aspx?id=7376

orcasha said...

Moving away from the monoamine hypothesis as it stands will be an extremely difficult task, especially due to the large amount of financial interest already invested.

On the other side, completely discounting the effect monoamines have on aspects of depression is problematic. For example, the age old "5-HT decreases causes depression" seems to be morphing into "complications in 5-HT synthesis in the CNS coupled with peripheral factors leads to problems with inhibition in certain regions as well as disruption of neurotransmitter modulation, such as excitatory neurotransmitters (eg glutamate) in the PFC which is further compounded by moderate cell death in key structures due to hormonal and biochemical changes". This however doesn't have the same soundbite efficency...

WM said...
This comment has been removed by the author.
XLMIC said...

In agreement with Anonymous. Hormonal changes with the onset of puberty could very well have had something to do with the manifestation of symptoms.

All I want to know is: WHAT DO I DO?

I had no issues with any of this that I knew of until about 6 years ago. I now suffer from recurrent migraines that last 48 hours almost like clockwork. They now seem to show up randomly but I know better than to believe that. I now get them once a week. I've tried so many things. I just want to not feel like shit. There are too many conflicting opinions out there for someone who is so frequently in pain to sort through. I just want help. Help that WORKS.

I have 4 little kids and they deserve a much better mom than the one they're getting.

Low Serotonin said...

Always a pleasure to follow your articles and the debate comment area.