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<rss version="2.0"><channel><title><![CDATA[Latest Celiac Disease News & Research:: Ground Breaking Celiac Disease Studies]]></title><link>https://www.celiac.com/celiac-disease/celiac-disease-gluten-intolerance-research/page/60/?d=2</link><description><![CDATA[Latest Celiac Disease News & Research:: Ground Breaking Celiac Disease Studies]]></description><language>en</language><item><title>Flattened Villi is Not Always Caused by Celiac Disease</title><link>https://www.celiac.com/celiac-disease/flattened-villi-is-not-always-caused-by-celiac-disease-r762/</link><description><![CDATA[
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<div>Am J Clin Pathol. 2004 Apr;121(4):546-50 </div> <p>Celiac.com 04/20/2004 – According to researchers  at the Department of Anatomic Pathology, William Beaumont Hospital, Royal  Oak, MI, the cause of flattened villi is not always celiac disease. The  researchers studied seven patients who experienced several weeks of gluten-sensitivity  and the same type of villi injury—"increased lymphoplasmacytic  lamina propria inflammation, moderate to complete villous flattening,  numerous crypt mitoses, and markedly increased villous intraepithelial  lymphocytes (IELs)." All patients were diagnosed with gluten sensitivity,  and all returned 9 to 38 weeks later questioning their diagnosis, as their  symptoms had substantially or completely disappeared, and clinical improvement  in these patients seemed unrelated to their ingestion of gluten. A follow  up endoscopy and colonoscopy was performed on these patients 4 to 16 months  later, and the results of each showed a normal mucosa. </p> <p>According to the researchers: </p> <div>  <p><div style="margin-left:25px">"Diseases other than GS can cause marked villous flattening  and increased villous IELs in adults. The cause of small bowel mucosal  injury is unknown. A similar non-GS-associated clinicopathologic complex,  assumed to be due to a protracted viral enteritis or slow regression  of a virus-induced immune reaction, occurs in children. The temporal  aspects of symptom improvement and mucosal restitution in these 7 patients  are similar to acute self-limited colitis. An overly exuberant  immune response to an infectious agent is possible."</div></p>
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]]></description><guid isPermaLink="false">762</guid><pubDate>Tue, 20 Apr 2004 00:00:00 +0000</pubDate></item><item><title>Study Finds Wheat-based Sourdough Bread Started with Selected Lactobacilli is Tolerated by Celiac Disease Patients</title><link>https://www.celiac.com/celiac-disease/study-finds-wheat-based-sourdough-bread-started-with-selected-lactobacilli-is-tolerated-by-celiac-disease-patients-r744/</link><description><![CDATA[
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<div>Appl Environ Microbiol. 2004 Feb;70(2):1088-1096</div> <p>Celiac.com 02/26/2004 - <em>Please note that the sourdough  bread used in this study is not your garden-variety sourdough bread, and  as far as I know it is not commercially available. Even though this study  had very promising results, it was conducted on a relatively small number  of people, and larger studies need to be carried out before reaching any  conclusions about the long-term safety of celiacs consuming this type  of sourdough bread. -Scott Adams</em></p> <p>Researchers in Europe conducted a novel study which utilized  a highly specialized sourdough lactobacilli containing peptidases that  have the ability to hydrolyze Pro-rich peptides, including the 33-mer  peptide, which is the main culprit in the immune response associated with  celiac disease. The sourdough bread in the study was made from a dough  mixture that contained 30% wheat flour and other nontoxic flours including  oat, millet, and buckwheat, which was then started with the specialized  lactobacilli. After 24 hours of fermentation all 33-mer peptides and low-molecular-mass,  alcohol-soluble polypeptides were almost totally hydrolyzed. </p> <p>For the next step in the study the researchers extracted  proteins fro the sourdough and used them to produce a "peptic-tryptic  digest" for in vitro agglutination tests on human K 562 subclone  cell. The agglutinating activity of the sourdough proteins was found to  be 250 times higher that that of normal bakers-yeast or lactobacilli  started breads. </p> <p>A double blind test was then conducted in which 17 celiac  disease patients were given 2 grams of gluten-containing bread started  with bakers yeast or lactobacilli. Thirteen of them showed distinct,  negative changes in their intestinal permeability after eating the bread,  and 4 of them did not show any negative effects. The specially prepared  sourdough bread was then given to all 17 patients and none of them had  intestinal permeability reactions that differed from their normal baseline  values. </p> <p>The researchers conclude: "These results showed  that a bread biotechnology that uses selected lactobacilli, nontoxic flours,  and a long fermentation time is a novel tool for decreasing the level  of gluten intolerance in humans."</p>
]]></description><guid isPermaLink="false">744</guid><pubDate>Thu, 26 Feb 2004 00:00:00 +0000</pubDate></item><item><title><![CDATA[UK Researchers find Celiac Disease in One Percent of Children and Conclude that it is a Largely Missed Children&#039;s Disease]]></title><link>https://www.celiac.com/celiac-disease/uk-researchers-find-celiac-disease-in-one-percent-of-children-and-conclude-that-it-is-a-largely-missed-children039s-disease-r741/</link><description><![CDATA[
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<div>BMJ 2004;328:322-323 (7 February)</div> <p>Celiac.com 02/18/2004 - A study conducted by researchers  in the UK has found that 1% of all seven year old children in the UK have  celiac disease, and most cases of celiac disease continue to remain undiagnosed.  The researchers tested 5,470 "normal" children using a two  stage screening that included an initial radioimmunoassay for antibodies  to tissue transglutaminase (endomysial antigen), and a further testing  of positive samples for IgA-EMA by indirect immunofluorescence. Children  with tTG antibodies under the 97.5th percentile were defined as antibody  negative. Out of those tested 54 were positive for IgA-EMA. Additionally:  "IgA-EMA positive children were shorter and weighed less than those  who tested negative for tTG antibody." </p> <p><strong>The Researchers Comment:</strong></p> <p><div style="margin-left:25px">"At age 7, 1% of children were IgA-EMA positive  and likely therefore to have sub clinical coeliac disease, though less  than 0.1% were reported to be on a gluten-free diet. The prevalence of  coeliac disease in these children is therefore comparable to that in UK  adults. The benefit of early diagnosis of sub clinical coeliac disease  remains unproven, but long term follow up of this cohort may help to resolve  this. If screening is worth while, it should be started in childhood."</div></p>
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<p><div style="margin-left:25px">"Since ALSPAC is an observational study based on  analysis of anonymous samples, confirmatory biopsy was not possible...®eported  clinical features were similar to those in adults with coeliac disease  identified by screening. Gastrointestinal symptoms were not prominent,  and the excess in girls mirrors that seen in affected adults. The most  striking observation was that children with IgA-EMA were shorter by more  than 0.76 standard deviation scores and lighter by 0.54 standard deviation  scores than antibody negative children matched for date and place of birth.  This equates to about 9 months growth and weight gain in an average child  around this age. These features were independent of gastrointestinal symptoms  and anemia and presumably unrelated to malabsorption."</div></p>
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<p><strong>Conclusion:</strong></p> <p>"Occult coeliac disease seems to start in childhood,  even in those who are subsequently diagnosed as adults. The search for  the trigger resulting in the breakdown of immune tolerance to gluten therefore  needs to focus on infancy and intrauterine life."</p>
]]></description><guid isPermaLink="false">741</guid><pubDate>Wed, 18 Feb 2004 00:00:00 +0000</pubDate></item><item><title>High Percentage of Celiacs Nonresponsive to Hepatitis B Vaccine</title><link>https://www.celiac.com/celiac-disease/high-percentage-of-celiacs-nonresponsive-to-hepatitis-b-vaccine-r717/</link><description><![CDATA[
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<div>  <p>Am J Gastroenterol. 2003 Oct;98(10):2289-92</p> <p>Celiac.com 11/26/2003 - The results of a study conducted by Dr. Joseph  Murray and colleagues at the Mayo Clinic in Rochester, Minnesota indicate  that an unusually high number of those with celiac disease do not develop  immunity from the hepatitis B vaccine. The team looked at 23 clinically  diagnosed celiacs who had been given a full series of hepatitis B vaccines.  Out of this group they identified 19 who had been tested for hepatitis  B Vaccine response, and of the 19 tested, 13 subjects did not develop  long-term immunity to the vaccine, which was determined by utilizing  the negative qualitative or quantitative anti-HBs antibody titer. </p> <p>The researchers note a strong association in celiac disease with a  particular HLA genotype of DQ2, which is also seen in nonresponders  to the hepatitis B vaccine. Each of the subjects in the study was either  homozygous or heterozygous for DQ2. The researchers postulate that a  majority of celiacs may be non-responsive to the vaccine because they  have "a failure of induction of humoral immune response needed  for development of long term immunity." The researchers are still  uncertain of the specific cause of the failed immune system response  in those with celiac disease.</p> </div> ]]></description><guid isPermaLink="false">717</guid><pubDate>Wed, 26 Nov 2003 00:00:00 +0000</pubDate></item><item><title>Dutch Research Team Identifies Specific Genes Responsible for Celiac Disease</title><link>https://www.celiac.com/celiac-disease/dutch-research-team-identifies-specific-genes-responsible-for-celiac-disease-r704/</link><description><![CDATA[
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<div>Gastroenterology, Oct 2003, Vol 125, No 4, p1032-41  </div> <p>Celiac.com 10/30/2003 – A Dutch research team has  identified the specific regions of chromosome 19 that contribute to celiac  disease. Despite its well-known association with human leukocyte antigen  (HLA)-DQ2 and DQ8, the pathogenesis of celiac disease has remained largely  unknown. The team studied 82 Dutch families who met strict diagnostic  criteria which included biopsies that presented Marsh III lesions. The  216 independent celiac disease patients were compared to 216 age and sex-matched  controls. </p> <p>As expected the study found significant linkage to the  suspected HLA region, but more importantly found additional, previously  unknown and significant linkages at 19p13.1 (with a peak at marker D19S899),  and at 6q21-22, which is ~70 cm downstream from the HLA region in question.  The researchers conclude: "Significant linkage of celiac disease  to chromosome region 19p13.1 was detected in our genome-wide screen. These  results were confirmed by the association of D19S899 to celiac disease  in an independent case-control cohort. Furthermore, we identified a possible  second celiac disease locus on chromosome region 6q21-22."</p> <p><em>The study was dedicated to the memory of Lodewijk  Sandkuijl (1953-2002), who died shortly after its completion. He was an  inspiration to the researchers and was a world expert on biostatistics.</em></p>
]]></description><guid isPermaLink="false">704</guid><pubDate>Thu, 30 Oct 2003 00:00:00 +0000</pubDate></item><item><title>Higher Rate of Gastrointestinal Symptoms in Women with Treated Celiac Disease</title><link>https://www.celiac.com/celiac-disease/higher-rate-of-gastrointestinal-symptoms-in-women-with-treated-celiac-disease-r696/</link><description><![CDATA[
<p>Celiac.com 09/29/2003 - <em>The results of a study  published in the September edition of American Journal of Gastroenterology  indicate that women with treated celiac disease suffer twice as many gastrointestinal  symptoms than do their male counterparts, and that men with treated celiac  disease suffered no more GI symptoms than did the normal population. More  studies need to be done, however, to determine why male celiacs seem to  respond better to treatment than females. Some <span class="ipsBadge ipsBadge_neutral" data-ipsDialog="" data-ipsDialog-size="narrow" data-ipsDialog-url="https://www.celiac.com/index.php?app=dp47badlinksfixer&amp;module=main&amp;controller=main&amp;do=retrieveUrl&amp;url=L2FydGljbGVzLzcwMC8xL1BlcmNlcHRpb25zLW9mLVF1YWxpdHktb2YtTGlmZS1pbi1NZW4tYW5kLVdvbWVuLXdpdGgtQ2VsaWFjLURpc2Vhc2UvUGFnZTEuaHRtbA==" rel="nofollow" style="cursor: pointer;">Open Original Shared Link</span> has already been done on this topic. -Scott</em></p> <p><em>Here is the abstract:</em></p> <p><div style="margin-left:25px">  </div></p>
<p><div style="margin-left:25px">Am J Gastroenterol. 2003 Sep;98(9):2023-6.</div><br><div style="margin-left:25px"> High rate of gastrointestinal symptoms in celiac patients living on  a gluten-free diet: controlled study.</div><br><div style="margin-left:25px"> Midhagen G, Hallert C.</div><br><div style="margin-left:25px"> Department of Internal Medicine, Skovde Hospital, Skovde, Sweden</div></p>
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<p><div style="margin-left:25px">The aim of this study was to determine the occurrence  of GI symptoms in adults with celiac disease (celiac disease) treated with a gluten-free  diet for several years. We studied a cohort of adults with celiac disease (n = 51;  59% women) aged 45-64 yr and proved to be in remission after 8-12 yr  of treatment. They were examined by the GI Symptom Rating Scale, which  comprises five syndromes: indigestion, diarrhea, constipation, abdominal  pain, and reflux. A general population sample (n = 182; 57% women) of  same age served as controls. Subjects with celiac disease reported significantly  more GI symptoms than the general population sample, as assessed by  the GI Symptom Rating Scale total score (p  </div></p>
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]]></description><guid isPermaLink="false">696</guid><pubDate>Mon, 29 Sep 2003 00:00:00 +0000</pubDate></item><item><title>Perceptions of Quality of Life in Men and Women with Celiac Disease</title><link>https://www.celiac.com/celiac-disease/perceptions-of-quality-of-life-in-men-and-women-with-celiac-disease-r692/</link><description><![CDATA[
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<p>Scand J Caring Sci. 2003 Sep;17(3):301-7</p> <p>Celiac.com 09/03/2003 - <em>A recent study published in  the Scandinavian Journal of Caring Sciences looked at the differences  in how men and women cope with celiac disease. The study concludes that  gender should be taken into account in the treatment of celiac disease  to improve its outcome. The biggest flaw in this study is with the number  of people in it—only 10. I think that it is difficult to draw such conclusions  using such a small sample of people, and that a larger study of this type  needs to be done to draw more solid conclusions. Additionally, the poorer  outcome for women in this study may be due to the fact that they experienced  more bowel-related symptoms than did the men, which may not be due at all to their "emotionally  oriented strategy" of coping. It could just be a fact that women with  celiac disease experience more real health problems than men, which is also in need of further study. - Scott Adams</em></p> <p>Here is the abstract:</p> <p><div style="margin-left:25px">"Perceptions of health-related quality of life of men and women  living with coeliac disease."</div><br><div style="margin-left:25px"> Hallert C, Sandlund O, Broqvist M.</div><br><div style="margin-left:25px"> Coeliac Centre, Faculty of Health Sciences, Linkoping University, Linkoping,  Sweden.</div></p>
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<p><div style="margin-left:25px">"Women with long-standing coeliac disease express  poorer health-related quality of life (HRQoL) than men do for unclear  reasons. This led us to explore differences in their understanding of  HRQoL using a phenomenographic approach. We interviewed 10 coeliac subjects  (mean age 57 years, range 35-73) who had been on a gluten-free diet  for 10 years and had scored either high or low in the Short Form 36  Health Survey (SF-36) General Health and Vitality scales. Three dimensions  were revealed that pertained to their perception of HRQoL: bodily sensations,  social consequences and coping strategies. Within these, the women experienced  more bowel symptoms than men did, despite keeping to a strict diet.  This item was the only one predicting the SF-36 scores. The women also  described more distress caused by the restrictions in daily life, closely  related to their controlling of food contents. The coeliac men took  advantage of using a problem-oriented coping approach while the women  seeking an emotionally oriented strategy showed less satisfaction with  the outcome. We conclude that the intriguing difference in HRQoL between  coeliac men and women may have some of its origin in the way living  with the disorder is conceptualized and coped with. The results imply  that in the management of coeliac patients, gender-related aspects need  to be taken into account to improve treatment outcome."</div></p>
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]]></description><guid isPermaLink="false">692</guid><pubDate>Wed, 03 Sep 2003 00:00:00 +0000</pubDate></item><item><title>44% of First-Degree Relatives of those with Celiac Disease also Affected</title><link>https://www.celiac.com/celiac-disease/44-of-first-degree-relatives-of-those-with-celiac-disease-also-affected-r684/</link><description><![CDATA[
<p>Scand J Gastroenterol. 2003 Jul;38(7):727-31. <br> Effectiveness of the sorbitol H2 breath test in detecting histological  damage among relatives of coeliacs.<br> Tursi A, Brandimarte G, Giorgetti GM, Inchingolo celiac disease.<br> Dept. of Emergency, L. Bonomo Hospital, Andria (BA), Italy. </p> <p>Celiac.com 08/07/2003 - An Italian study  conducted by Dr. L. Bonomo and colleagues and published in the July 2003  edition of Scandinavian Journal of Gastroenterology concludes that A  significant proportion of coeliacs may be missed if relatives are screened  by serology only, while the efficacy of sorbitol H2-BT in screening relatives  is confirmed. This study confirms that neither a breath test nor serology  can replace intestinal biopsy, which remains the gold standard for the  diagnosis of celiac disease, thus confirming the continued importance of performing  biopsies for diagnosing celiac disease. The studys goal was to determine  the diagnostic capabilities of serological tests (antigliadin (AGA), antiendomysium  (EMA) and anti-tissue transglutaminase (anti-tTG)) and sorbitol H2 breath  test (H2-BT) in the detection of celiac disease in first-degree relatives.  The study screened 111 first-degree relatives of 37 celiac families using  both test methods to determine candidates for small-bowel biopsy. First-degree  relatives with abnormal test results underwent a small-bowel biopsy, as  did those with negative serological and H2 breath test results who had  clinical complaints or suspected that they may have celiac disease. </p> <p>The biopsy results were expressed using the  Marsh classification system, and celiac disease was diagnosed in 49 of  the 111 screened relatives of celiacs, or in 44.14%. A breakdown of the  results is as follows: 5 showed Marsh IIIc, 8 Marsh IIIb, 16 Marsh IIIa,  13 Marsh II and 7 Marsh I lesions. 19 relatives showed the classical form  of celiac disease, 20 showed the sub-clinical form, and 10 showed the  silent form. The serological test results indicated an overall positivity  of only 36.73%, with strong positive results only in those with severe  intestinal damage and Marsh IIIb-c lesions. The sorbitol H2-BT breath  test results showed an overall positivity of 83.67%, and showed strong  positivity in patients with slight histological damage (Marsh I-IIIa).</p> ]]></description><guid isPermaLink="false">684</guid><pubDate>Thu, 07 Aug 2003 00:00:00 +0000</pubDate></item><item><title>17% of Celiac Disease Relatives also Affected</title><link>https://www.celiac.com/celiac-disease/17-of-celiac-disease-relatives-also-affected-r680/</link><description><![CDATA[
<p>Am J Gastroenterol. 2003 Feb;98(2):377-81</p> <p>Celiac.com 07/31/2003 -<em> The findings of this new  study are very significant for families of those with celiac disease.  The results indicate that 17% of those related to two celiac disease-diagnosed siblings will also have the  disease. Past studies have shown that around 10% of first-degree relatives of celiacs also have it, but this study is unique as it focuses on the increased risk for families where two siblings have the disease. This study further emphasizes the conclusions of past studies: <u>If you have a  relative with celiac disease--get tested, especially if it is a first-degree relative.</u> - Scott Adams</em></p> <p><div style="margin-left:25px">  </div></p>
<p><strong><div style="margin-left:25px">Abstract</div></strong><div style="margin-left:25px">:</div><br><div style="margin-left:25px"> "Prevalence of celiac disease among relatives of sib pairs with  celiac disease in U.S. families</div><br><div style="margin-left:25px"> Am J Gastroenterol. 2003 Feb;98(2):377-81 </div><br><div style="margin-left:25px"> Book L, Zone JJ, Neuhausen SL.</div><br><div style="margin-left:25px"> Division of Pediatric Gastroenterology and Nutrition, Department of  PediatricsUniversity of Utah, Salt Lake City, USA.</div></p>
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<p><div style="margin-left:25px">OBJECTIVE: Celiac disease is a familial malabsorptive disorder  with an estimated prevalence in first-degree relatives of 10-12%. The  prevalence for first-degree and more distant relatives has not been  determined in families where there are two affected first-degree relatives.  The aim of our investigation was to estimate the prevalence and relative  risk for celiac disease in relatives of two siblings diagnosed with  celiac disease.</div></p>
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<p><div style="margin-left:25px">METHODS: We ascertained sib pairs with celiac disease, and then  identified all living first-degree relatives and available second-degree  relatives to minimize ascertainment bias. We measured IgA endomysial  antibodies, a highly specific and sensitive assay for celiac disease,  in all subjects without a confirmed biopsy diagnosis. For those individuals  with positive serologic tests, IgA tissue transglutaminase antibody  tests and human leukocyte antigen DQA1 and DQB1 genotyping were performed  for additional confirmation. Individuals with positive biopsy and/or  serology were considered affected. We calculated the relative risk of  being affected with celiac disease using the lambda® statistic.</div></p>
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<p><div style="margin-left:25px">RESULTS: The prevalence of celiac disease in relatives of affected  sib pairs was as follows: 21.3% (13/61) of siblings (lambda(S) = 53);  14.7% (10/68) of offspring (lambda(O) = 37); 17.2% (28/163) of first-degree  relatives; 19.5% (16/82) of second-degree relatives; and 17.8% (52/292)  of all relatives (lambda® = 44.5).</div></p>
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<p><div style="margin-left:25px">CONCLUSIONS: In these families, we identified  a sibling risk approximately double that found in previous reports,  as well as significant risk for more distant relatives, probably because  of sharing of a common gene. In families where at least two siblings  have been diagnosed with celiac disease, relatives are at high risk  for celiac disease. Screening should be considered for all family members.  </div></p>
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]]></description><guid isPermaLink="false">680</guid><pubDate>Thu, 31 Jul 2003 00:00:00 +0000</pubDate></item><item><title>Swedish Study on the Causes of Death in Celiac Disease Patients</title><link>https://www.celiac.com/celiac-disease/swedish-study-on-the-causes-of-death-in-celiac-disease-patients-r679/</link><description><![CDATA[
<p>Arch Intern Med. 2003;163:1566-1572. <br> Ulrike Peters, PhD, MPH; Johan Askling, MD; Gloria Gridley, MS; Anders  Ekbom, MD, PhD; Martha Linet, MD </p> <p>Celiac.com 07/30/2003 -<em> The following abstract paints  a fairly bleak picture for those of us with celiac disease; however, after  taking a closer look at it I believe that it has some serious limitations  that should not be overlooked, and have likely produced skewed or irrelevant  results. For example, the study does not indicate whether or not the patients  in it followed a strict gluten-free diet. Other studies have shown that  the mortality risk for celiacs decreases to that of the normal population  when a gluten-free diet is followed for at least five years, and that it is also  affected by how soon the diagnosis is made and how soon treatment begins. It is well known that not  following a gluten-free diet will increase a celiacs risk of death  by many causes to many times that of the normal population, which is precisely  why it is so important to include such information in studies of this  type. In my opinion doing a study like this and not including such data  is like doing a study on diabetes where perhaps half or more people in  the study do not take insulin but ought to, and then publishing the ultra-high  mortality rate that would be its outcome: "Conclusion: Diabetics  have a 20-fold mortality rate over the normal population." The conclusion  would clearly not be true for those who took their insulin. </em></p> <p><em>Additionally the time period that is covered by this  study, 1964-1993, could be considered the dark ages of celiac disease,  even in Europe (we actually may be just entering the Renaissance age for  celiac disease here in the USA, but this could be argued!). Many doctors during this  time did not stress enough to their patients the importance of following  a strict gluten-free diet, just as many still do not even do this day. My doctor  didnt. He just diagnosed me and said I shouldnt eat gluten  (as opposed to telling me that it could kill me if I kept eating it),  and he didnt even explain to me HOW to avoid it! Is it possible  that some of the folks in this study, diagnosed as far back as 1964, might  have had similar experiences with their doctors? I would be willing  to bet that at least 50% of the people in this study (if not more) were  not following a strict gluten-free diet, or were not following the diet  at all. If this is true, it is kind of like studying a group of diabetics  whose only treatment was to be told by their doctors that they should avoid sugar, which seems absurd if you think about it.</em></p>
<p><em>Last, the study has considerable bias in that it recruited only hospitalized celiacs, presumably because they were already significantly ill, and those who never made it into a hospital were excluded. It reports findings of auto-immune diseases and small bowel/lymphomaexcesses--these are already well known--but what other researchers may disagree with is the scale of the excess--SMR is always a very crude method ofexpressing this in such studies. - Scott Adams (special thanks to Dr. Geoff Helliwell for his comments on this study)</em></p> <p><div style="margin-left:25px">  </div></p>
<p><strong><div style="margin-left:25px">Abstract</div></strong><div style="margin-left:25px">:</div><br><div style="margin-left:25px"> "Background: Patients with celiac disease have an increased risk  of death from gastrointestinal malignancies and lymphomas, but little  is known about mortality from other causes and few studies have assessed  long-term outcomes."</div></p>
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<p><div style="margin-left:25px">"Methods: Nationwide data on 10,032 Swedish patients hospitalized  from January 1, 1964, through December 31, 1993, with celiac disease and  surviving at least 12 months were linked with the national mortality register.  Mortality risks were computed as standardized mortality ratios (SMRs),  comparing mortality rates of patients with celiac disease with rates in  the general Swedish population."</div></p>
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<p><div style="margin-left:25px">"Results: A total of 828 patients with celiac disease died during  the follow-up period (1965-1994). For all causes of death combined, mortality  risks were significantly elevated: 2.0-fold (95% confidence interval [CI],  1.8-2.1) among all patients with celiac disease and 1.4-fold (95% CI,  1.2-1.6) among patients with celiac disease with no other discharge diagnoses  at initial hospitalization. The overall SMR did not differ by sex or calendar  year of initial hospitalization, whereas mortality risk in patients hospitalized  with celiac disease before the age of 2 years was significantly lower  by 60% (95% CI, 0.2-0.8) compared with the same age group of the general  population. Mortality risks were elevated for a wide array of diseases,  including non-Hodgkin lymphoma (SMR, 11.4), cancer of the small intestine  (SMR, 17.3), autoimmune diseases (including rheumatoid arthritis [sMR,  7.3] and diffuse diseases of connective tissue [sMR, 17.0]), allergic  disorders (such as asthma [sMR, 2.8]), inflammatory bowel diseases (including  ulcerative colitis and Crohns disease [sMR, 70.9]), diabetes mellitus  (SMR, 3.0), disorders of immune deficiency (SMR, 20.9), tuberculosis (SMR,  5.9), pneumonia (SMR, 2.9), and nephritis (SMR, 5.4)."</div></p>
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<p><div style="margin-left:25px">"Conclusion: The elevated mortality risk for all causes of death  combined reflected, for the most part, disorders characterized by immune  dysfunction."</div><br></p>
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]]></description><guid isPermaLink="false">679</guid><pubDate>Wed, 30 Jul 2003 00:00:00 +0000</pubDate></item><item><title>Celiac Disease and Mineralization Disturbances of Permanent Teeth</title><link>https://www.celiac.com/celiac-disease/celiac-disease-and-mineralization-disturbances-of-permanent-teeth-r664/</link><description><![CDATA[
<p>Rasmusson CG, Eriksson MA.<br> Department of Pedodontics, Uddevalla Hospital, Uddevalla, Sweden.<br> Int J Paediatr Dent 2001 May;11(3):179-83 </p> <p>Celiac.com 05/08/2003 - In a study from Finland in 1986 it was shown  that celiac disease was often associated with tooth enamel defects of  permanent teeth. This study also showed a strong association between the  time of gluten challenge in the diagnostic procedure and enamel defects.  In the current study, dental examinations were carried out for a group  of 40 children and adolescents suffering from celiac disease diagnosed  according to the criteria of The European Society of Pediatric Gastroenterology  and Nutrition (ESPGAN) at the Department of Pediatrics, Hospital of Uddevalla,  Sweden. A control group made of 40 healthy children of the same age, sex  and living area was examined in the same way. The results failed to show  disturbances of the same type, degree of severity or frequency as was  reported in Finland and no statistically significant differences concerning  enamel defects were found between the patients with celiac disease and  the controls.</p> <p>PMID: 11484467</p>
]]></description><guid isPermaLink="false">664</guid><pubDate>Thu, 08 May 2003 00:00:00 +0000</pubDate></item><item><title>Anti-tTG Serum Level Correlates to Degree of Intestinal Damage</title><link>https://www.celiac.com/celiac-disease/anti-ttg-serum-level-correlates-to-degree-of-intestinal-damage-r653/</link><description><![CDATA[
<p><em>Journal of Clinical Gastroenterology 2003; 36(3):219-221 </em>  </p>
<p>Celiac.com  03/28/2003 - A study by Antonio Tursi, M.D, et al, was recently conducted  to evaluate the correlation between the degree of histologic intestinal  damage in celiac patients and their level of positivity (serum value)  to anti-tissue transglutaminase antibodies (anti-tTG). The study looked  at 119 adult celiac patients who were diagnosed consecutively (47 men  and 72 women; mean age, 28 years; range, 22-51 years), and were stratified  for histologic damage according to Marsh classification. The final step  was to compare their Marsh histologic intestinal damage classification  with their anti-tTG serum values. Here are their results:</p> <p><div style="margin-left:25px"> </div></p>
<p><div style="margin-left:25px">Marsh I lesions were present in 13  patients (10.92%), Marsh II in 24 anti-tTG (20.16%), Marsh IIIa in 27  anti-tTG (22.68%), Marsh IIIb in 31 anti-tTG (26.05%) and Marsh IIIc  in 24 anti-tTG (20.16%). Anti-tTG positivity was ranging from 1 of 13  anti-tTG (7.69%) in Marsh I lesions to 23 of 24 anti-tTG (95.83%) in  Marsh IIIc lesions respectively (P  </div></p>
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<p>The researchers conclude that the mean serum  value in celiacs with severe enteropathy (Marsh IIIb-c lesions) was higher  than in those with only slight enteropathy (Marsh I-IIIa). Further, serologic  test results in the absence of histologic evaluation (biopsy) may "underestimate  the real prevalence of celiac disease," thus delaying a proper diagnosis  and putting patients at risk for a large variety of serious health problems.</p>
]]></description><guid isPermaLink="false">653</guid><pubDate>Fri, 28 Mar 2003 00:00:00 +0000</pubDate></item></channel></rss>
