High Risk Of Coeliac Disease In Punjabis. Epidemiological Study In The South Asian And European Populations Of Leicestershire
The title of this post, is the same as that of this peer-reviewed paper on PubMed.gov.
This is the abstract of the paper.
The purpose of this study was to measure the incidence of coeliac disease in different ethnic communities and investigate the hypothesis that the incidence is decreasing in most European countries and the role incomplete retrieval of data may play. In a retrospective study of histologically confirmed cases of coeliac disease between 1975 and 1989 in the City of Leicester, 106 patients with coeliac disease were identified. Of these 86 were European and 20 Asian. The overall incidence of coeliac disease in Europeans was 2.5/10(5)/year (95% CI 2-3.2), in Gujaratis 0.9/10(5)/year (95% CI 0.4-1.8), and in Punjabis 6.9 (95% CI 3.2-12.3). These differences were independent of religious belief. The relative risk to Punjabis compared with Europeans is 2.9 (95% CI 1.5-5.3; chi 2 = 12.5, p < 0.01) and to Gujaratis 8.1 (95% CI 3-22.4; chi 2 = 25; p < 0.001). Gujaratis were at 0.4 risk of Europeans (90% CI 0.2-0.8; chi 2 = 6.7; p < 0.01). The incidence in the urban populations of Leicester was 6/10(5)/year (95% CI 1.3-1.9) which was significantly lower than the 3.2/10(5)/year (95% CI 2.7-3.8; chi 2 = 5.6; p < 0.001) in surrounding rural areas. This study shows that the incidence of coeliac disease in Punjabis (Sikhs, Hindus and Muslims) is 8 times higher than in Gujaratis (Hindus and Muslims) and 4 times higher than in Europeans in Leicester.
I find the last sentence in particular very significant.
I’m no medic, but I think it is reasonable to assume, that in a particular community for every diagnosed coeliac, there will be several undiagnosed coeliacs out there.
In this overview of coeliac disease on the NHS web site, this is said about the incidence of coeliac disease.
Coeliac disease is a condition that affects at least 1 in every 100 people in the UK.
But some experts think this may be underestimated because milder cases may go undiagnosed or be misdiagnosed as other digestive conditions, such as irritable bowel syndrome (IBS).
Reported cases of coeliac disease are around 3 times higher in women than men.
The one-in-100 figure is often used in web pages in European countries or Australia, Canada and the United States, so I’ll go along with that.
So does that mean that Punjabis living in Leicester, have a one-in-twenty-five likelihood of being coeliac?
Whether you have been diagnosed though, is a matter of pure luck.
I had been having gut problems for years and then one Autumn, I didn’t see my GP, but a very elderly locum, who as I had recently had my fiftieth birthday, gave me a present of my first blood test.
It turned out my B12 levels were very low and after several months of B12 injections, which made little difference to my B12, my GP decided to send me to a consultant at Addenbrooke’s Hospital in Cambridge.
My appointment was on a Monday morning and consultant took about ten minutes to ask a few questions, after which he said they would take a few bloods.
On the Wednesday morning, I received a letter that said, that I was probably suffering from coeliac disease and this would be confirmed by endoscopy.
Was I diagnosed solely by analysis of my blood? This was in 1997, which is after the date of the Leicester study.
Two endoscopies without sedative or anaesthetic were performed and I was confirmed as coeliac.
The first was performed by Dr. Richard Hardwick and the second by Dr. Rebecca Fitzgerald.
Both doctors feature in this story on the Cambridge University Hospitals web site, which is entitled Familial Gastric Cancer – Case Study.
My problems have been minor compared to the two sisters in the story.
My luck had been good and I recommend that everyone who feels they could be coeliac should get themselves tested.
Cases Of Covid-19 In Leicestershire
This article on the Leicester Mercury is entitled 11 Areas Of Leicestershire Have Among Worst Infection Rates in the UK.
In Coeliac Disease: Can We Avert The Impending Epidemic In India?, I started like this.
The title of this post, is the same as that of this article on the Indian Journal Of Research Medicine.
With the high levels of COVID-19 in Leicester and an Indian population who make up 28.3 % of the population of the city, I was searching the internet to see if there was any connection between those of Indian heritage and coeliac disease.
I know you should not try to prove a theory. But as a coeliac, I’m very interested to see how the millions of diagnosed coeliacs on a gluten-free diet like me, are faring in this pandemic.
I then talk about some extracts from the Indian research.
In a section entitled, which is entitled All Wheats Are Not Equal, I say this.
The other dimension to this problem is that not all wheat is alike when it comes to inducing celiac disease. The ancient or diploid wheats (e.g. Triticum monococcum) are poorly antigenic, while the modern hexaploid wheats e.g. Triticum aestivum) have highly antigenic glutens, more capable of inducing celiac disease in India, for centuries, grew diploid and later tetraploid wheat which is less antigenic, while hexaploid wheat used in making bread is recently introduced. Thus a change back to older varieties of wheat may have public health consequences.
So did all these factors come together to create the high levels of Covid-19 in Leicestershire?
Conclusion
I am getting bored with saying this. More research needs to be done!
Why A Lucky Few May Help The Rest Of Us Beat Disease
The title of this post, is the same as that of this article in The Times.
This is the sub-title.
A British biotech firm believes patients who defy odds could hold the key in their blood.
These three paragraphs introduce the article.
Patient 82 should be dead. At the age of 63 he was diagnosed with pancreatic cancer. In most cases, he would not have lasted a year. But seven years on, patient 82 is alive. Not merely alive — thriving.
He enjoys gardening. He likes seeing his grandchildren. He enjoys life.
How? The answer, a British biotech company believes, could lie in his blood. Now, with the help of dozens of other anonymous patients, all of whom have defied their cancer prognoses, they hope to find it.
Note, that the company is Alchemab Therapeutics.
The article got me thinking about myself.
I belong to a group of people, who are twenty-five percent less likely to suffer from cancer according to peer-reviewed research at Nottingham University.
I am coeliac and adhere to a strict gluten-free diet.
There may be other benefits too!
I have not had a serious dose of the covids, although I may have had a very mild case at the beginning of 2020 after I shared a train with a large number of exuberant Chinese students, who had recently arrived at Manchester Airport and were going to their new University across the Pennines.
I have also since found at least another seventy coeliacs, who have avoided serious doses of the covids.
Research From The University Of Padua
This paper on the US National Library of Medicine, which is from the University of Padua in Italy.
The University followed a group of 138 patients with coeliac disease, who had been on a gluten-free diet for at least six years, through the first wave of the Covid-19 pandemic in Padua.
This sentence, sums up the study.
In this analysis we report a real life “snapshot” of a cohort of CeD patients during the SARS-CoV-2 outbreak in Italy, all followed in one tertiary centre in a red area of Northern Italy. Our data show, in accordance with Emmi et al., the absolute absence of COVID-19 diagnosis in our population, although 18 subjects experienced flu-like symptoms with only one having undergone naso-pharyngeal swab.
It says that no test subject caught Covid-19, in an admittedly smallish number of patients.
But it reinforces my call for more research into whether if you are a diagnosed coeliac on a long-term gluten-free diet, you have an immune system, that gives you a degree of protection from the Covids.
The Times article mentions the immune system.
I believe my immune system to be strong after the reaction I had to the Astra Zeneca vaccine. I didn’t feel well to say the least after my Astra Zeneca vaccine and my GP and other doctors felt that it could be due to my immune system, thinking that the chimpanzee virus-based vaccine was a danger and attacking it.
Significantly, I had no reaction to the second dose. So had my immune system recognised the vaccine as a friend not a foe?
My son, who my late wife was sure was an undiagnosed coeliac, died of pancreatic cancer at just 37.
How did my late wife know? Don’t question her intuition and also she felt that my son and myself felt the same to her touch.
It should be noted that my son’s daughter was born with a Congenital hernia of the Diaphragm. Congenital defects can happen to people, who have a coeliac father.
At the age of 20, my granddaughter is fine now, after heroic surgery at the Royal London Hospital, at just a few days old.
Canary Wharf Boosts Its Science Ambitions
The title of this post, is the same as that of this article on The Times.
This are the introductory paragraphs.
Genomics England is to move its headquarters to Canary Wharf in east London this year as the financial quarter aims to become a life sciences hub.
The government-run DNA sequencing group will move in the autumn into One Canada Place, where its neighbours will include Brookfield, a Canadian property fund, and Reach, publisher of the Daily Express and OK! magazine.
Owned by the Department of Health and Social Care, Genomics England sequences the genomes of people with rare diseases and cancers to help doctors to treat them more effectively. With consent, some of that data is passed to researchers trying to develop new drugs and treatments.
If you type “Canary Wharf Science Hub into Google”, you find some serious articles.
This article in the FT is entitled Canary Wharf Proposes £500mn Lab Project To Reinvent Financial Hub.
This is a good idea, as scientist friends are always complaining about a lack of lab space in Cambridge and Oxford. Because of the Elizabeth Line, both these cities are not much more than an hour from Canary Wharf.
It should also fill the cafes and shops with scientists and engineers, who would replace some of those working from home because of the pandemic.
I wonder whether this model will work elsewhere?
Covid: Genes Hold Clues To Why Some People Get Severely Ill
The title of this post, is the same as that of this article on the BBC.
This is the opening paragraph.
Why some people with coronavirus have no symptoms and others get extremely ill is one of the pandemic’s biggest puzzles.
It is now less of a puzzle, thanks to research led by the University of Edinburgh.
These paragraphs explain the methodology.
Scientists looked at the DNA of patients in more than 200 intensive care units in UK hospitals.
They scanned each person’s genes, which contain the instructions for every biological process – including how to fight a virus.
Their genomes were then compared with the DNA of healthy people to pinpoint any genetic differences, and a number were found – the first in a gene called TYK2.
One of the other genes mentioned is IFNAR2, where this was said.
Variations in a gene called IFNAR2 were also identified in the intensive care patients.
IFNAR2 is linked to a potent anti-viral molecule called interferon, which helps to kick-start the immune system as soon as an infection is detected.
It’s thought that producing too little interferon can give the virus an early advantage, allowing it to quickly replicate, leading to more severe disease.
I know a bit about interferon and I must admit I’ve made a bit of profit on shares in Synairgen, which are linking interferon with an inhaler.
I then typed “coeliac disease and interferon” into Google and found this article on The Lancet, which is entitled Onset Of Coeliac Disease and Interferon Treatment.
My medical knowledge is very limited, but it does appear that if you are coeliac on a gluten-free diet, you don’t get any problems, with interferon.
The plot thickens!
Not for nothing, do some doctors coeliac disease, the Many-Headed Hydra.
Is Trump’s Recovery From The The Covids Down To His Mother?
Donald Trump’s mother was born Mary Anne MacLeod at Tong on the Isle of Lewis in Scotland.
This Google Map shows the position of Tong to the island’s capital of Stornoway.
This is Wikipedia’s introduction to the village.
Tong is a village on the Isle of Lewis, Scotland, 4 miles (6 kilometres) northeast of the main town of Stornoway on the B895 road to Back and Tolsta. The population of the village is 527 (2001 census). Fishing forms part of the local economy.
Families probably have to have granite in their genes to survive in places like that for decades.
By reputation, Highlanders are not wimps.
I have just looked up the rate of the covids in the Highlands.
The latest figure of lab-confirmed cases is 185.7 per 100,000 of the population, which compares to 617 for the whole of Scotland and 1952.4 for Manchester.
Is there something in Highland genes, that resists the covids?
Angelina Jolie Gene Testing For All?
The title of this post is the same as this article on the BBC.
This is said.
Testing all women for the “Angelina Jolie gene”, even if not considered at risk, would prevent cancers, save lives and is cost effective, say doctors.
Having lived for forty years with my wife, who suffered breast cancer and then a few years later died from a squamous cell carcinoma of the heart, I know a lot about the emotional problems of cancer.
Many cancers and other diseases, like my coeliac disease, can be found in our genes.
Our youngest son died of pancreatic cancer, which was probably not helped by his smoking and poor eating and health habits.
If he had been a coeliac, which could have been likely because of my genes, that wouldn’t have helped either! But he wouldn’t be tested!
Speaking for myself, my life might have been very different, if I had been genetically tested as a child!
In the future, genetic testing will become much more the norm, as doctors, researchers, scientists and engineers will reduce the cost of doing a full genetic test.
The BBC article also says this.
The study, published in the Journal of the National Cancer Institute, estimated the impact of screening all 27 million women over 30 in the UK.
They said it would:
- prevent 64,500 more breast cancers
- prevent 17,500 more ovarian cancers
- save 12,300 more lives
The study also said mass screening would be cost-effective for the health service.
But why stop at breast and ovarian cancer?
I feel strongly, that anybody likely to be a coeliac, should be tested at birth.
Keeping to a gluten-free diet, is getting easier every year and research at institutions like Nottingham University has shown, that coeliacs on a gluten-free diet are significantly less likely to get cancer, than the general population.
Sibling Wars
I agree with the princess in this story on the BBC, which is entitled Genetically-modified crops have benefits – Princess Anne.
But I doubt her elder brother does!
I Thought Dinosaurs Were Extinct
I watched a lot of the debate the so-called three parent babies and am very pleased that the House of Commons voted in favour. The debate is covered fully in this article on the BBC web site.
I saw several men and no women put up ridiculous arguments as to why they were voting against. Several of these dinosaurs are listed as Roman Catholic on Wikipedia.
But David Willetts, Liz McInnes and Jane Ellison amongst others put forward sane arguments that carried the day.
No MP has any business to use principles of his or her religion to legislate for others in the UK, who do not share their faith.
So if a Jewish or Muslim member, wants to bring in a bill banning the eating of pork in the UK, they should have no right.
I am old enough to remember the birth of Louise Brown; the world’s first IVF baby. We look at IVF as commonplace and Robert Edwards won a Nobel Prize for his work in the field, but at the time it was controversial.
I believe that in a few years time, this technique, which is being developed at Newcastle University, will also enter the mainstream too.
Three Parent Babies
MPs are set to debate the ethics of so-called three parent babies today.
I was reasonably lucky with my three children and there won’t be any more, as I’m had the snip.
But I’m certain, that C, would have been distraught, if she’d produced a string of handicapped babies. I certainly would have been and any technique that stopped problems is to be welcomed.
So let’s hope narrow-minded religious minorities don’t stop the adoption of this technique.
It is interesting to read this article in the Telegraph, which gives the view of Lord Winston, who is an Orthodox Jew
On a related point, I have a genetic disease, but sadly I only found out about my coeliac disease, when I was fifty. If I’d known earlier, it might have meant that my son, who died from cancer, had been found to carry the disease, so perhaps he would have led a better lifestyle.
If it had been known to earlier generations of my father’s family, I suspect that the family wouldn’t contain the large number of childless females and those who have suffered from serious cancer that it does.
Is There A Cardigan Gene?
My father liked to wear cardigans and so does my son. So is this in our genes?
I obviously don’t have that particular gene, as I’ve never worn a cardigan.
On the other hand, C had lots of them!