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Dive into the research topics where Jakob Mortensen is active.

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Featured researches published by Jakob Mortensen.


Twin Research | 2003

Heritability of Adult Body Height: A Comparative Study of Twin Cohorts in Eight Countries

Karri Silventoinen; Sampo Sammalisto; Markus Perola; Dorret I. Boomsma; Belinda K. Cornes; Chayna J. Davis; Leo Dunkel; Marlies de Lange; Jennifer R. Harris; Jacob von Bornemann Hjelmborg; Michelle Luciano; Nicholas G. Martin; Jakob Mortensen; Lorenza Nisticò; Nancy L. Pedersen; Axel Skytthe; Tim D. Spector; Maria Antonietta Stazi; Gonneke Willemsen; Jaakko Kaprio

A major component of variation in body height is due to genetic differences, but environmental factors have a substantial contributory effect. In this study we aimed to analyse whether the genetic architecture of body height varies between affluent western societies. We analysed twin data from eight countries comprising 30,111 complete twin pairs by using the univariate genetic model of the Mx statistical package. Body height and zygosity were self-reported in seven populations and measured directly in one population. We found that there was substantial variation in mean body height between countries; body height was least in Italy (177 cm in men and 163 cm in women) and greatest in the Netherlands (184 cm and 171 cm, respectively). In men there was no corresponding variation in heritability of body height, heritability estimates ranging from 0.87 to 0.93 in populations under an additive genes/unique environment (AE) model. Among women the heritability estimates were generally lower than among men with greater variation between countries, ranging from 0.68 to 0.84 when an additive genes/shared environment/unique environment (ACE) model was used. In four populations where an AE model fit equally well or better, heritability ranged from 0.89 to 0.93. This difference between the sexes was mainly due to the effect of the shared environmental component of variance, which appears to be more important among women than among men in our study populations. Our results indicate that, in general, there are only minor differences in the genetic architecture of height between affluent Caucasian populations, especially among men.


Twin Research | 2003

Sex Differences in Heritability of BMI: A Comparative Study of Results from Twin Studies in Eight Countries

Karoline Schousboe; Gonneke Willemsen; Kirsten Ohm Kyvik; Jakob Mortensen; Dorret I. Boomsma; Belinda K. Cornes; Chayna J. Davis; Corrado Fagnani; Jacob von Bornemann Hjelmborg; Jaakko Kaprio; Marlies de Lange; Michelle Luciano; Nicholas G. Martin; Nancy L. Pedersen; Kirsi H. Pietiläinen; Aila Rissanen; Suoma E. Saarni; Thorkild I. A. Sørensen; G. Caroline M. van Baal; Jennifer R. Harris

Body mass index (BMI), a simple anthropometric measure, is the most frequently used measure of adiposity and has been instrumental in documenting the worldwide increase in the prevalence of obesity witnessed during the last decades. Although this increase in overweight and obesity is thought to be mainly due to environmental changes, i.e., sedentary lifestyles and high caloric diets, consistent evidence from twin studies demonstrates high heritability and the importance of genetic differences for normal variation in BMI. We analysed self-reported data on BMI from approximately 37,000 complete twin pairs (including opposite sex pairs) aged 20-29 and 30-39 from eight different twin registries participating in the GenomEUtwin project. Quantitative genetic analyses were conducted and sex differences were explored. Variation in BMI was greater for women than for men, and in both sexes was primarily explained by additive genetic variance in all countries. Sex differences in the variance components were consistently significant. Results from analyses of opposite sex pairs also showed evidence of sex-specific genetic effects suggesting there may be some differences between men and women in the genetic factors that influence variation in BMI. These results encourage the continued search for genes of importance to the body composition and the development of obesity. Furthermore, they suggest that strategies to identify predisposing genes may benefit from taking into account potential sex specific effects.


Annals of Surgical Oncology | 2009

Joint Practice Guidelines for Radionuclide Lymphoscintigraphy for Sentinel Node Localization in Oral/Oropharyngeal Squamous Cell Carcinoma

Lee W. T. Alkureishi; Zeynep Burak; Julio Alvarez; James R. Ballinger; Anders Bilde; Alan J. Britten; Luca Calabrese; Carlo Chiesa; Arturo Chiti; R. de Bree; H. W. Gray; Keith D. Hunter; Adorján F. Kovács; Michael Lassmann; Charles R. Leemans; G. Mamelle; Mark McGurk; Jakob Mortensen; Tito Poli; Taimur Shoaib; Philip Sloan; Jens Ahm Sørensen; Sandro J. Stoeckli; Jørn Bo Thomsen; Giuseppe Trifirò; Jochen A. Werner; Gary L. Ross

Involvement of the cervical lymph nodes is the most important prognostic factor for patients with oral/oropharyngeal squamous cell carcinoma (OSCC), and the decision of whether to electively treat patients with clinically negative necks remains a controversial topic. Sentinel node biopsy (SNB) provides a minimally invasive method for determining the disease status of the cervical node basin, without the need for a formal neck dissection. This technique potentially improves the accuracy of histologic nodal staging and avoids overtreating three-quarters of this patient population, minimizing associated morbidity. The technique has been validated for patients with OSCC, and larger-scale studies are in progress to determine its exact role in the management of this patient population. This document is designed to outline the current best practice guidelines for the provision of SNB in patients with early-stage OSCC, and to provide a framework for the currently evolving recommendations for its use. Preparation of this guideline was carried out by a multidisciplinary surgical/nuclear medicine/pathology expert panel under the joint auspices of the European Association of Nuclear Medicine (EANM) Oncology Committee and the Sentinel European Node Trial (SENT) Committee.


Gastroenterology Research and Practice | 2009

Short Bowel Patients Treated for Two Years with Glucagon-Like Peptide 2: Effects on Intestinal Morphology and Absorption, Renal Function, Bone and Body Composition, and Muscle Function

Palle B. Jeppesen; P. Lund; Ida B. Gottschalck; H. B. Nielsen; Jens J. Holst; Jakob Mortensen; S. S. Poulsen; Bjørn Quistorff; P.B. Mortensen

Background and aims. In a short-term study, Glucagon-like peptide 2 (GLP-2) has been shown to improve intestinal absorption in short bowel syndrome (SBS) patients. This study describes longitudinal changes in relation to GLP-2 treatment for two years. Methods. GLP-2, 400 micrograms, s.c.,TID, were offered, to eleven SBS patients keeping parenteral support constant. 72-hour nutritional balance studies were performed at baseline, weeks 13, 26, 52 during two years intermitted by an 8-week washout period. In addition, mucosal morphometrics, renal function (by creatinine clearance), body composition and bone mineral density (by DEXA), biochemical markers of bone turnover (by s-CTX and osteocalcin, PTH and vitamin D), and muscle function (NMR, lungfunction, exercise test) were measured. Results. GLP-2 compliance was >93%. Three of eleven patients did not complete the study. In the remaining 8 patients, GLP-2 significantly reduced the fecal wet weight from approximately 3.0 to approximately 2.0 kg/day. This was accompanied by a decline in the oral wet weight intake, maintaining intestinal wet weight absorption and urinary weight constant. Renal function improved. No significant changes were demonstrated in energy intake or absorption, and GLP-2 did not significantly affect mucosal morphology, body composition, bone mineral density or muscle function. Conclusions. GLP-2 treatment reduces fecal weight by approximately 1000 g/d and enables SBS patients to maintain their intestinal fluid and electrolyte absorption at lower oral intakes. This was accompanied by a 28% improvement in creatinine clearance.


Gastroenterology | 2013

Heritability and Familial Aggregation of Diverticular Disease: A Population-Based Study of Twins and Siblings

Lisa L. Strate; Rune Erichsen; John A. Baron; Jakob Mortensen; Jacob Krabbe Pedersen; Anders Riis; Kaare Christensen; Henrik Toft Sørensen

BACKGROUND & AIMS Little is known about the role of heritable factors in diverticular disease. We evaluated the contribution of heritable factors to the development of diverticular disease diagnosed at a hospitalization or outpatient visit. METHODS Using nationwide patient registries, we identified 142,123 incident cases of diverticular disease diagnosed at a hospitalization (1977-2011) or an outpatient hospital visit (1995-2011) in Denmark, including cases in 10,420 index siblings and 923 twins. We calculated standardized incidence ratios for siblings versus the general population and concordance rates for monozygotic versus dizygotic twin pairs as measures of relative risk (RR). RESULTS The RR for diverticular disease in siblings of index cases was 2.92 (95% confidence interval [CI], 2.50-3.39) compared with the general population. The RRs were similar irrespective of the sex of the sibling or index case and were particularly strong in siblings of hospitalized cases and cases that underwent surgery. The proband-wise concordance rate for monozygotic twins was double that of dizygotic twins (0.16 [95% CI, 0.11-0.22] vs 0.07 [95% CI, 0.05-0.11], respectively). The RR of diverticular disease in one twin when the other had diverticular disease was 14.5 (95% CI, 8.9-23) for monozygotic twins compared with 5.5 (95% CI, 3.3-8.6) for dizygotic twins. Associations were stronger in female monozygotic twins compared with male twins (tetrachoric correlation, 0.60 [95% CI, 0.49-0.70] vs 0.33 [95% CI, 0.13-0.51]; P = .03 in an analysis stratified by sex and zygosity). We estimate that 53% (95% CI, 45%-61%) of susceptibility to diverticular disease results from genetic factors. CONCLUSIONS Based on a population-based study in Denmark, genetic factors appear to contribute to development of diverticular disease.


Gastroenterology Research and Practice | 2009

Short bowel patients treated for two years with glucagon-like peptide 2 (GLP-2): compliance, safety, and effects on quality of life.

Palle B. Jeppesen; P. Lund; Ida B. Gottschalck; H. B. Nielsen; Jens J. Holst; Jakob Mortensen; S. S. Poulsen; Bjørn Quistorff; P.B. Mortensen

Background and aims. Glucagon-like peptide 2 (GLP-2) has been shown to improve intestinal absorption in short bowel syndrome (SBS) patients in a short-term study. This study describes safety, compliance, and changes in quality of life in 11 SBS patients at baseline, week 13, 26, and 52 during two years of subcutaneous GLP-2 treatment, 400 microgram TID, intermitted by an 8-week washout period. Methods. Safety and compliance was evaluated during the admissions. The Sickness Impact Profile (SIP), Short Form 36 (SF 36), and Inflammatory Bowel Disease Questionnaire (IBDQ) evaluated quality of life. Results. The predominant adverse event was transient abdominal discomfort in 5 of 11 patients, but in 2, both suffering from Crohns disease, it progressed to abdominal pain and led to discontinuation of GLP-2 treatment. One had a fibrostenotic lesion electively resected at the jejuno-ascendo-anastomosis. The investigator excluded a patient due to unreliable feedback. Stoma nipple enlargement was seen in all 9 jejunostomy patients. Reported GLP-2 compliance was excellent (>93%). GLP-2 improved the overall quality of life VAS-score (4.1 ± 2.8 cm versus 6.0 ± 2.4 cm, P < .01), the overall SIP score (10.3 ± 8.9% versus 6.2 ± 9.5%, P < .001), the mental component of the SF-36 (45 ± 13% versus 53 ± 11%, P < .05), and the overall IBDQ score (5.1 ± 0.9 versus 5.4 ± 0.9, P < .007) in the 8 patients completing the study. Conclusions. Long-term treatment with GLP-2 is feasible in SBS patients, although caution must be exercised in patients with a history of abdominal pain. Although conclusions cannot be made in a noncontrolled trial, the high reported compliance might reflect a high treatment satisfaction, where the clinical benefits of GLP-2 may outweigh the discomforts of injections.


European Journal of Clinical Nutrition | 2012

Randomised controlled trial of colostrum to improve intestinal function in patients with short bowel syndrome.

Peter Enemark Lund; Per T. Sangild; Lise Aunsholt; B. Hartmann; Jens J. Holst; Jakob Mortensen; P.B. Mortensen; Palle B. Jeppesen

Background/Objectives:Colostrum is rich in immunoregulatory, antimicrobial and trophic components supporting intestinal development and function in newborns. We assessed whether bovine colostrum could enhance intestinal adaptation and function in adult short bowel syndrome (SBS) patients.Subjects/Methods:Twelve SBS patients in this randomised cross-over study received 4 weeks oral supplement of bovine colostrum or an iso-energetic and iso-proteinaceous control (2.4 MJ/d, 500 ml/day) separated by a 4-week washout period. Patients were admitted four times for 72-h periods of fluid, electrolyte and nutrient balance studies. Meals, faeces and urine were weighed, and energy, macronutrient and electrolyte contents were analysed to calculate net nutrient uptake. Body composition was measured by dual-energy X-ray absorptiometry scans, and functional tests of handgrip strength and lung functions were performed. Eight patients completed the study and were included in the analysis.Results:Both supplements (colostrum and control) not only increased protein (0.96±0.42 MJ/d, P=0.004 1.03±0.44 MJ/d, P=0.003) and energy (1.46±1.02 MJ/d, P=0.005, 1.76±1.46 MJ/d, P=0.01) absorption but also absolute faecal wet weight excretions (231±248 g/d, P=0.002, 319±299 g/d, P=0.03), compared with baseline measurements. Both supplements improved handgrip strength (P=0.03) while only the control supplement increased lean body mass (1.12±1.33 kg, P<0.049). Colostrum was not found to be superior to the control.Conclusion:Intake of high-protein milk supplements increased net nutrient absorption for adult SBS patients, but at the expense of increased diarrhoea. Despite high contents of bioactive factors, colostrum did not significantly improve intestinal absorption, body composition or functional tests compared with the control.


Ejso | 2009

Rigid sigmoidoscopy and MRI are not interchangeable in determining the position of rectal cancers.

Gunnar Baatrup; M. Bolstad; Jakob Mortensen

PURPOSE 1) To analyse for interchangeability of rigid sigmoidoscopy and MRI in determining the distance from anus to tumour, and to determine if anterior/posterior location influences this difference. 2) To analyse the effect of preoperative chemo-radiotherapy on the distance from anus to tumour. METHODS Retrospective investigation of endoscopy reports and MRI series of 144 consecutive patients operated for rectal cancer. RESULTS The mean distance from the anal verge to the tumour measured by sigmoidoscopy was 82mm and by MRI 61mm (p<0.01). For tumours in the anterior quadrant this difference was 30mm and for tumours located in the posterior quadrant only 12mm. The distributions of the cancers as low, middle and high differ by more than 10% between the two methods. The coefficient of correlation between measurements was 0.9 but the variation was not acceptable. The length of the tumours decreased by 16mm after neoadjuvant treatment, but the distance from tumour to anus increased by only 4mm. CONCLUSION 1) MRI and sigmoidoscopy are not interchangeable in determining the distance from anus to tumour simply by correcting for the length of the anal canal. It has not been determined if measurements from MRI or sigmoidoscopy are more accurate, but current evidence concerning the effect of neoadjuvant irradiation at different positions in the rectum is based upon rigid sigmoidoscopy. 2) The gain in tumour free distance above the anus induced by neoadjuvant treatment is small. Facilitation of sphincter-saving surgery should not be an argument for neoadjuvant treatment.


Annals of Epidemiology | 2006

Age trajectories of grip strength: cross-sectional and longitudinal data among 8,342 Danes aged 46 to 102

Henrik Frederiksen; Jacob von Bornemann Hjelmborg; Jakob Mortensen; Matt McGue; James W. Vaupel; Kaare Christensen


Journal of Investigative Dermatology | 2007

Heritability of Hand Eczema Is Not Explained by Comorbidity with Atopic Dermatitis

Anne Lerbaek; Kirsten Ohm Kyvik; Jakob Mortensen; Lars E. Bryld; Torkil Menné; Tove Agner

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Kaare Christensen

University of Southern Denmark

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P.B. Mortensen

Copenhagen University Hospital

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Palle B. Jeppesen

Copenhagen University Hospital

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Axel Skytthe

University of Southern Denmark

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James W. Vaupel

University of Southern Denmark

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Jens J. Holst

University of Copenhagen

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Kirsten Ohm Kyvik

University of Southern Denmark

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P. Lund

University of Copenhagen

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Matt McGue

University of Minnesota

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