Citations

Showing 10 of 107966 citations.

Substrate-Guided Proteomics Enhances Degradome Resolution
Arrell, D. Kent , Terzic, André

Mayo Clinic

Circulation: Cardiovascular Genetics | February 19, 2013 | Volume: 6 | Issue: 1 | Pages: 7-9

10.1161/circgenetics.111.000031 | PMID 23424255 Get It

Adapting Lymphedema Treatment to the Palliative Setting
Andrews, Karen L., Kollasch, Jenny, Schmidt, Kenley D., Basford, Jeffrey, Cheville, Andrea

Mayo Clinic

American Journal of Hospice and Palliative Medicine® | February 19, 2013 | Volume: 31 | Issue: 1 | Pages: 38-44

10.1177/1049909112475297 | PMID 23423772 Get It

Objective: To review the benefits of adapting the complex techniques of formal lymphedema therapy to the more generalized forms of edema often seen in the chronic disease and palliative care settings. Data Sources: Peer-reviewed literature and clinical practice. Conclusion: Lymphedema treatment modalities have much to offer beyond their well-characterized benefit in classical lymphedema. In modified forms, they may improve and lessen the burden of refractory edema originating from a diverse range of causes. Thoughtful planning and practice, however, are essential as an inadequate adaptation may result in unnecessary effort, injury for the patient, or an unsatisfactory outcome.
Rebuttal: Aortic regurgitation and device closure of ASD or PFO
Loar, Robert W. , Johnson, Jonathan N. , Taggart, Nathaniel W.

Mayo Clinic

Catheterization and Cardiovascular Interventions | February 19, 2013 | Volume: 85 | Issue: 1 | Pages: 179-179

10.1002/ccd.24876 | PMID 23420681 Get It

Bleeding disorders in adolescents with menorrhagia: an institutional experience
Rodriguez, Vilmarie , Alme, Charlotte, Killian, Jill M. , Weaver, A., Khan, Shakila P. , Simmons, Patricia S.

Mayo Clinic

Haemophilia | February 19, 2013 | Volume: 19 | Issue: 2 | Pages: No page available

10.1111/hae.12091 | PMID 23419108 Get It

Cation-chloride cotransporters in the nervous system
Benarroch, Eduardo E.

Mayo Clinic

Neurology | February 19, 2013 | Volume: 80 | Issue: 8 | Pages: 756-763

10.1212/wnl.0b013e318283bb1c | PMID 23420893 Get It

Free fatty acid flux in African‐American and caucasian adults—effect of sex and race
Nielsen, Søren , Sumner, Anne E. , Miller, Bernard V., Turková, Hana, Jensen, Michael D. , Klein, Samuel

Mayo Clinic

Obesity | February 18, 2013 | Volume: 21 | Issue: 9 | Pages: 1836-1842

10.1002/oby.20322 | PMID 23418014 Get It

ObjectiveObesity, insulin resistance, and diabetes disproportionately affect African‐American (AA) women. Abnormal adipose tissue free fatty acid (FFA) release is associated with these conditions. Resting energy expenditure (REE) and sex predict FFA release in Caucasians, but whether this is true in AA is unknown. The sex‐specific relationships between FFA release, REE, and race was compared.Design and Methods100 adults (47% AA, 50% male, age 32 ± 8 years [mean ± SD]) from three different centers underwent duplicate measures of FFA release ([U‐13C] palmitate) and REE (indirect calorimetry). Body composition was determined by DXA and abdominal imaging.ResultsAA participants had lower REE, but similar FFA concentrations and flux compared with Caucasian participants. The significant predictors of palmitate release were REE, sex, and race. REE and FFA flux were correlated in both sexes and both races. In a multiple linear regression analysis with palmitate flux as the dependent variable and REE, sex, race, total fat mass, fat‐free mass, and insulin as independent variables, REE was the only independent predictor of FFA release in men. Both REE and race predicted palmitate flux in women.ConclusionsFFA flux is related to REE, but the relationship differs in AA and Caucasian women.
Interactions of allelic variance of PNPLA3 with nongenetic factors in predicting nonalcoholic steatohepatitis and nonhepatic complications of severe obesity
Guichelaar, Maureen M. J., Viker, Kimberly, Sanderson, Schuyler O., Malinchoc, Michael, Watt, K.D.S., Swain, J., Sarr, Michael G. , Gawrieh, Samer , Olivier, Michael , Krishnan, Arunkumar , Charlton, Michael

Mayo Clinic

Obesity | February 18, 2013 | Volume: 21 | Issue: 9 | Pages: 1935-1941

10.1002/oby.20327 | PMID 23418085 Get It

Objective: Allelic variation (rs738409C→G) in adiponutrin (patatin‐like phospholipase domain‐containing protein 3, PNPLA3) has been associated with hepatic steatosis and liver fibrosis. The physiologic impact of the PNPLA3 G allele may be exacerbated in patients with severe obesity. In this study, we investigated the interactions of PNPLA3 rs738409 with a broad panel of metabolic and histologic characteristics of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis (NASH) in patients with medically complicated obesity.Design and Methods: Consecutive patients undergoing bariatric surgery were selected for a prospective study. They underwent extensive laboratory and histologic (liver biopsy) assessment, as well as evaluation of rs738409 polymorphism by TaqMan assay.Results: Only 12 (8.3%) of the 144 patients had normal liver histology, with 72 (50%) NASH, of whom 15 (10.4% of total patients) had fibrosis stage 2‐3. PNPLA3 GG genotype correlated positively (P < 0.05) with serum levels of alanine aminotransferase (ALT), asparate aminotransferase (AST), glucose, fibrinogen, and insulin‐dependent diabetes mellitus, homeostasis model assessment—insulin resistance, and presence of NASH. Multivariate analysis indicated that PNPLA3 rs738409 G versus C allele remained an (independent) risk factor for NASH, in addition to CK‐18 >145 IU/l, glucose >100 mg/dl, and C‐reactive protein (CRP) >0.8 mg/dl. The probability of NASH increased from 9% (no risk factor) to 82% if all four risk factors were present.Conclusions: In this cohort of patients with medically complicated obesity, PNPLA3 rs738409 G allelic expression is associated with hepatic (NASH) and nonhepatic complications of obesity, such as insulin resistance. These novel findings may be related to a greater impact of PNPLA3 variant in magnitude and scope in patients with severe obesity than in less obese populations. Further studies are needed to characterize the nature of these associations.
Simplifying the measurement of gastric accommodation using SPECT
Vijayvargiya, Prakhar , Camilleri, Michael , Shin, Andrea , Burton, Duane D. , Breen, Micheál A.

Mayo Clinic

Neurogastroenterology & Motility | February 18, 2013 | Volume: 25 | Issue: 6 | Pages: 542-546

10.1111/nmo.12099 | PMID 23413813 Get It

AbstractBackgroundNon‐invasive single photon emission computed tomography (SPECT) has been validated as a test for postprandial gastric volume accommodation, with volumes measured twice over 30 min and averaged. The purpose of this study is to simplify the SPECT measurement of gastric accommodation.MethodsThe primary aim of this study was to compare two postprandial gastric volume measurements with data collected retrospectively from 443 patients and healthy volunteers who had undergone SPECT in the last decade. The differences in the two gastric volumes were compared in the entire group and each subgroup, and the correlation between the two measurements and their differences across a wide range of gastric volumes were plotted.Key ResultsThere was a median difference of <2% (P = 0.041) between postprandial scan 1 (757 mL) and scan 2 (743 mL), with significant correlation (rs = 0.859, P < 0.01) and excellent agreement (SD 60 mL) between the two scans across the entire range of observed postprandial gastric volumes.Conclusions & InferencesA single postprandial scan can detect gastric accommodation with the same accuracy as averaging two postprandial scans. These data support simplifying SPECT measurement of postprandial gastric volume with a scan in the first 15 min after a meal.
Factors related to abdominal pain in gastroparesis: contrast to patients with predominant nausea and vomiting
Wilson, Laura , Koch, Kenneth L. , Pasricha, Pankaj J. , Snape, William J., McCallum, Richard W. , Sarosiek, Irene , Farrugia, Gianrico , Calles, J. , Lee, L., Tonascia, James , Ünalp–Arida, Aynur , Hamilton, Frank A., Hasler, William L. , Parkman, Henry P. , Abell, Thomas L. , Nguyen, Linda Anh B.

Mayo Clinic

Neurogastroenterology & Motility | February 18, 2013 | Volume: 25 | Issue: 5 | Pages: 427

10.1111/nmo.12091 | PMID 23414452 Get It

AbstractBackgroundFactors associated with abdominal pain in gastroparesis are incompletely evaluated and comparisons of pain vs other symptoms are limited. This study related pain to clinical factors in gastroparesis and contrasted pain/discomfort‐ with nausea/vomiting‐predominant disease.MethodsClinical and scintigraphy data were compared in 393 patients from seven centers of the NIDDK Gastroparesis Clinical Research Consortium with moderate‐severe (Patient Assessment of Upper Gastrointestinal Disorders Symptoms [PAGI‐SYM] score ≥3) vs none‐mild (PAGI‐SYM < 3) upper abdominal pain and predominant pain/discomfort vs nausea/vomiting.Key ResultsUpper abdominal pain was moderate‐severe in 261 (66%). Pain/discomfort was predominant in 81 (21%); nausea/vomiting was predominant in 172 (44%). Moderate‐severe pain was more prevalent with idiopathic gastroparesis and with lack of infectious prodrome (P ≤ 0.05) and correlated with scores for nausea/vomiting, bloating, lower abdominal pain/discomfort, bowel disturbances, and opiate and antiemetic use (P < 0.05), but not gastric emptying or diabetic neuropathy or control. Gastroparesis severity, quality of life, and depression and anxiety were worse with moderate‐severe pain (P ≤ 0.008). Factors associated with moderate‐severe pain were similar in diabetic and idiopathic gastroparesis. Compared to predominant nausea/vomiting, predominant pain/discomfort was associated with impaired quality of life, greater opiate, and less antiemetic use (P < 0.01), but similar severity and gastric retention.Conclusions & InferencesModerate‐severe abdominal pain is prevalent in gastroparesis, impairs quality of life, and is associated with idiopathic etiology, lack of infectious prodrome, and opiate use. Pain is predominant in one fifth of gastroparetics. Predominant pain has at least as great an impact on disease severity and quality of life as predominant nausea/vomiting.
Spinal stenosis frequent in children with multiple hereditary exostoses
Ashraf, Ali , Larson, A. Noelle , Ferski, Gabriela J., Mielke, Cary H., Wetjen, Nicholas M. , Guidera, Kenneth J., Larson, A Noelle

Mayo Clinic

Journal of Children's Orthopaedics | February 18, 2013 | Volume: 7 | Issue: 3 | Pages: 183-194

10.1007/s11832-013-0484-9 | PMID 24432077 Get It

Purpose Children with multiple hereditary exostoses (MHE) have numerous osteochondromas, with the most prominent lesions typically over the appendicular skeleton. A recent report noted a high rate of intracanal lesions in this patient population and recommended preventative spinal screening with magnetic resonance imaging (MRI) or computed tomography (CT). We sought to evaluate the prevalence of spinal stenosis from intracanal osteochondromas at our pediatric orthopedic center in order to evaluate if routine screening is warranted. Methods All pediatric patients treated for MHE were retrospectively identified. Records were reviewed to determine demographics, previous orthopedic surgery, and indication and results of axial spine imaging (CT or MRI). Imaging studies were reviewed to evaluate the presence of intracanal and compressive spinal lesions. Results Between 1990 and 2011, axial imaging was performed in nine patients with MHE due to concerns of pain, weakness, and/or dizziness. These patients had moderate disease involvement, with a mean of 4.9 previous orthopedic surgeries to address skeletal osteochondromas. Two patients with MHE had cervical spinal stenosis secondary to intracanal osteochondromas. Both children successfully underwent spinal decompression. Thus, of our MHE population undergoing axial imaging, 22 % were noted to have intracanal lesions. Conclusions Our experience reveals a >20 % rate of compressive intracanal osteochondromas in MHE patients undergoing spinal imaging. These two patients represent 5 % of the MHE patients treated at our center. These lesions may be slow growing, and significant consequences can occur if not identified promptly. Thus, we confer that routine axial screening of the spinal canal may be warranted in these children.