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1.
Int J Obes (Lond) ; 46(2): 441-443, 2022 02.
Article in English | MEDLINE | ID: mdl-34743177

ABSTRACT

Celiac disease (CD) is not commonly associated with obesity; however, many patients are overweight or obese at time of diagnosis. As the number of people in the United States with obesity continues to rise, it is not known if the prevalence of obesity among patients with CD has also increased. This study utilized an electronic health record database incorporating over 360 individual hospitals in the United States (Explorys Incorporated, Cleveland, OH). Adult patients who had an esophagogastroduodenoscopy at least 1 day prior to reporting of CD from the years 2014 to 2018 formed the study population. From 2014 to 2018, 13,410 patients had a diagnosis of CD. The prevalence of obesity was 45,000/100,000 persons in this CD population. Prevalence of class I (BMI 30-34.9), II (BMI 35-39.9), and III (BMI > 40) obesity in patients with CD continued to rise over the 5-year span. Class I obesity had the highest prevalence and Class II the highest prevalence increase when obesity classes were compared. Clinicians should be aware of obesity as a comorbidity of increasing prevalence when providing longitudinal care for patients with CD.


Subject(s)
Celiac Disease/diagnosis , Obesity/diagnosis , Adult , Body Mass Index , Celiac Disease/epidemiology , Female , Humans , Male , Middle Aged , Obesity/epidemiology , Prevalence , Risk Factors , United States/epidemiology
2.
Obes Surg ; 30(2): 407-415, 2020 02.
Article in English | MEDLINE | ID: mdl-31646474

ABSTRACT

BACKGROUND: Evolving epidemiological data, backed by mechanistic evidence, supports a paradoxical increase in the risk of colorectal cancer after Roux-en-Y gastric bypass surgery (RYGB). We examined the risk of colonic polyps after RYGB. METHODS: A single-center retrospective study included colonoscopies performed between the years 1994 and 2018. To focus on the long-term impact of RYGB on precancerous colonic polyps, we compared patients at average risk for CRC who underwent colonoscopy ≥ 5 years after RYGB (n = 86) versus pre-RYGB (n = 106). We analyzed our data using inverse probability of treatment weighting (IPTW) using propensity scores in order to account for multiple potential confounders. RESULTS: After IPTW, we found no statistical differences between pre- and post-RYGB patients for risk of any polyp (33.2% pre- vs. 32.7% post-RYGB). However, the percentage of serrated polyps was higher ≥ 5 years post-RYGB compared with pre-RYGB (8.7% vs. 2.1%, p = 0.04, relative risk = 4.22; 95% CI 0.97, 18.4). Body mass index ≥ 30 kg/m2 at time of colonoscopy was associated with a greater risk for any polyp after RYGB (OR 6.23; 95% CI 1.16, 33.41). There was also a trend towards increased risk of polyps in post-RYGB patients who were current smokers (OR = 4.97; 95% CI 0.82, 30) or with age > 55 years (OR = 2.49; 95% CI 0.88, 7.00). CONCLUSION: Our data suggest that RYGB is associated with an increased risk of serrated polyps after 5 years from surgery. Prospective studies defining this risk and examining mechanisms will be instrumental for application of CRC preventative strategies in this population.


Subject(s)
Colonic Polyps/epidemiology , Colonic Polyps/etiology , Gastric Bypass , Obesity, Morbid/epidemiology , Obesity, Morbid/surgery , Weight Loss/physiology , Aged , Body Mass Index , Colonic Polyps/diagnosis , Colonoscopy , Colorectal Neoplasms/diagnosis , Colorectal Neoplasms/epidemiology , Colorectal Neoplasms/etiology , Female , Follow-Up Studies , Gastric Bypass/adverse effects , Gastric Bypass/statistics & numerical data , Humans , Male , Middle Aged , Ohio/epidemiology , Precancerous Conditions/diagnosis , Precancerous Conditions/epidemiology , Precancerous Conditions/etiology , Retrospective Studies , Risk Factors , Time Factors , Treatment Outcome
3.
J Hum Genet ; 55(9): 613-20, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20574427

ABSTRACT

We attempted to refine the understanding of an association of Y-chromosomal haplogroup I (hg-I) with enhanced AIDS progression that had been previously reported. First, we compared the progression phenotype between hg-I and its phylogenetically closest haplogroup J. Then, we took a candidate gene approach resequencing DDX3Y, a crucial autoimmunity gene, in hg-I and other common European Y-chromosome haplogroups looking for functional variants. We extended the genetic analyses to CD24L4 and compared and contrasted the roles of disease-based selection, demographic history and population structure shaping the contemporary genetic landscape of hg-I chromosomes. Our results confirmed and refined the AIDS progression signal to hg-I, though no gene variant was identified that can explain the disease association. Molecular evolutionary and genetic analyses of the examined loci suggested a unique evolutionary history in hg-I, probably shaped by complex interactions of selection, demographic history and high geographical differentiation leading to the formation of distinct hg-I subhaplogroups that today are associated with HIV/AIDS onset. Clearly, further studies on Y-chromosome candidate loci sequencing to discover functional variants and discern the roles of evolutionary factors are warranted.


Subject(s)
Acquired Immunodeficiency Syndrome/genetics , Chromosomes, Human, Y , DEAD-box RNA Helicases/genetics , Haplotypes , Polymorphism, Single Nucleotide , Alleles , CD24 Antigen/genetics , Disease Progression , Genetic Variation , Genetics, Population , Humans , Male , Minor Histocompatibility Antigens , Phylogeny , White People/genetics
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