National Migraine Centre
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Families with autoimmune disease and migraines/useful blog by Professor Graham Hughes

Professor Graham Hughes August and September Blog 2015

I add this here due to the clear writing and understanding of family's with autoimmune diseases and migraines!

BLOG : August and September 2015

Almost the end of September! My apologies to those who follow the BLOG for the late arrival of the August blog. Unfortunately, at the end of August I had to go through abdominal surgery. I know it is something of a cliché, but it is often said that doctors make the worst patients – I certainly fall into that category – so impatient!

On a happier note, last week we had a small party at London Bridge Hospital to celebrate the 10th anniversary of the London Lupus Centre at this hospital. The party, hosted by John Reay, CEO at London Bridge Hospital, included the 9 doctors of the lupus team, the secretarial and nursing staff, and a number of medical colleagues from other specialities. Our 2 V.I.P. guests were Mrs Cheryl Marcus, the Founder of the national lupus charity, Lupus UK, and Lynn Faulds Wood, who did so much to put lupus on the map through her television and other work.

John Reay, in his speech, talked about the historic decisions 10 years ago to bring in highly specialist units such as the Liver Transplant Unit the London Lupus Centre into a private hospital. The Lupus Centre now sees some 400 lupus and Hughes Syndrome patients a month, from all corners of the world – from 57 countries to date.

For my part, working in such a positive and supportive environment has been pure joy. This is head and shoulders the best run hospital I have ever worked in.

Patient of the month

Mrs K.T., aged 46, was referred for a second opinion regarding a possible diagnosis of Hughes Syndrome.

For 6 – 8 years, she had suffered from a variety of symptoms, including fatigue, headaches, slight shortness of breath and some chest pains. She had been previously investigated and no firm diagnosis had been made (her current label was ‘fibromyalgia’! Her sister, aged 40, had lupus, and it was this sister who encouraged Mrs K.T. not to give up.

Finally, she was tested for lupus (negative) and with antiphospholipid tests (anticardiolipin and lupus anticoagulant) – also negative.

Mrs K.T. arrived at the London Lupus Centre armed with a printout of her history. And it was a very significant history : migraines since childhood, cold circulation, pregnancy loss – 1 miscarriage, 1 stillbirth at 8 months. No further pregnancies.

Her more recent history had included chest pains, an increase in intensity of her headaches, and, on questioning, worsening memory problems. Clinical examination revealed mild blotchy livedo (“corned beef skin”) on the arms and the knees. She also had dry eyes and a degree of tenderness in the small joints.

But it was her family history which was so significant – sisters and various aunts with thyroid disease, migraine, miscarriages, lupus, epilepsy and multiple sclerosis – all common enough in themselves, but in this family, pointing towards an ‘auto-immune’ tendency.

But our tests, again, were negative!

Her lupus sister (who came with the patient, also had Hughes Syndrome, including mini-strokes) was on anticoagulant treatment (warfarin) and now free of symptoms.

Negative tests. Brain and other scans normal. Should we treat?


Firstly, it is unusual to get so many clues in a patient – the clinical history, the physical findings, the powerful family history.

We made 2 decisions. Firstly, to treat, and , secondly to re-test the serum.

Mrs K.T. was started on low dose aspirin with little improvement. We then moved to our “3 week heparin trial” – a self-administered course of daily (low molecular weight)

heparin. An almost immediate amazing response. Disappearance of the headaches, the chest pains and the fatigue.

Two years later, the patient remains well and almost symptom-free on warfarin (Coumadin), with added Plaquenil (hydroxychloroquine) for her Sjogren’s aches and pains.

An guess what – a third (newer) test for Hughes Syndrome – the so called ‘Beta2’ test, came back strongly positive!

What is this patient teaching us?

As always, a number of lessons. The family history is so important. Hughes Syndrome is a major cause of ‘sticky blood’. There are other causes, but a major clue to the diagnosis of Hughes Syndrome is the “autoimmune connection” – patients and relatives often giving a history of autoimmune diseases, such as lupus, Sjogren’s or Hashimoto’s thyroid disease.

The second important lesson concerns the negative tests. As in other autoimmune diseases such as lupus and rheumatoid arthritis, the tests can be unhelpful. In Mrs K.T.’s case, only the ‘newer’ test – anti-Beta2 – was positive.

There are probably many patients out there who have all the features of Hughes Syndrome but who are ‘sero-negative’. Obviously, there is still a need for newer screening tests. For me, the concept of ‘sero-negative’ Hughes Syndrome is one of the most important in the whole of my clinical practice.

Which brings me to the “third lesson” – for doctors. Do not be afraid to treat. If the suspicion of the diagnosis is strong enough, consider treatment. The introduction of appropriate anti-clotting treatment in Hughes Syndrome can be life-changing.


7 Replies

If only doctors everywhere could hear and take on board that last paragraph.

Life for so many people with B12 absorption would be soooo much easier ... and that's a condition where it is well documented that you cannot rely upon the results of tests and need to look at the clinical position - but it seems that so many doctors just can't get their heads around the possibility ... or in the case of B12 the high probability ... that test results really don't tell you the whole story.

Thanks MaryF


Yes if iron is low it always drags B12 down, I don't trust the test, I very much enjoyed the lecture at Thyroid UK's Conference delivered by Martyn Hooper.



I don't have problems with anaemia or iron but I've had problems with B12 absorption for decades ... yet another one of the problems with B12 that so many GPs think that you have to be anaemic for B12 to be a factor. Never mind.


are you gluten free? MaryF


No, not glutten free - flirted with it a few times but doesn't really seem to make a difference so don't think it is a factor for me.

My B12 is now adequately controlled as I treat it myself - but do get very frustrated by the way so many others continue to have delayed diagnoses and are not being adequately treated.


Yes as said above I am a Martyn Hooper fan, and keep up with the petitions and groups. I am gluten free for a variety of reasons as I do think being intolerant does not help with absorption of things generally. I am guessing you have read Martyn's book? MaryF


Yes - both books - and he has a third out this month.

NCBI (US Gov Medical site) has quite a lot on coeliacs/gluten intolerance and effect on absorption of nutrients - including B12 and folate. Also quite a bit in relation to glycaemic index and how avoiding foods high in gluten also means avoiding many foods where sugars are quickly metabolised - so good for diabetics trying to control their blood sugars.

However, don't think I'm ever going to succeed in getting my mother to recognise that her blood sugars would be better controlled if she gave up bread (her diabetes is MODY and I don't have the gene ... though my brother does).


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