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  1. Article ; Online: Differences in bacterial taxa between treatment-naive patients with major depressive disorder and non-affected controls may be related to a proinflammatory profile.

    Knudsen, Julie Kristine / Bundgaard-Nielsen, Caspar / Leutscher, Peter / Hjerrild, Simon / Nielsen, René Ernst / Sørensen, Suzette

    BMC psychiatry

    2024  Volume 24, Issue 1, Page(s) 84

    Abstract: ... microbiota was characterized by 16 S rRNA gene sequencing targeting the hypervariable V4 region. Plasma ...

    Abstract Background: Major depressive disorder (MDD) is characterized by sadness and anhedonia, but also physical symptoms such as changes in appetite and weight. Gut microbiota has been hypothesized to be involved in MDD through gut-brain axis signaling. Moreover, antidepressants display antibacterial properties in the gastrointestinal tract. The aim of this study was to compare the gut microbiota and systemic inflammatory profile of young patients with MDD before and after initiation of antidepressant treatment and/or psychotherapy in comparison with a non-depressed control group (nonMDD).
    Methods: Fecal and blood samples were collected at baseline and at follow-up after four and twelve weeks, respectively. Patients started treatment immediately after collection of the baseline samples. The gut microbiota was characterized by 16 S rRNA gene sequencing targeting the hypervariable V4 region. Plasma levels of 49 unique immune markers were assessed using Mesoscale.
    Results: In total, 27 MDD patients and 32 nonMDD controls were included in the study. The gut microbiota in the baseline samples of MDD versus nonMDD participants did not differ regarding α- or β-diversity. However, there was a higher relative abundance of the genera Ruminococcus gnavus group, and a lower relative abundance of the genera Desulfovibrio, Tyzzerella, Megamonas, Olsenella, Gordonibacter, Allisonella and Rothia in the MDD group compared to the nonMDD group. In the MDD group, there was an increase in the genera Rothia, Desulfovibrio, Gordinobacteer and Lactobacillus, while genera belonging to the Firmicutes phylum were found depleted at twelve weeks follow-up compared to baseline. In the MDD group, IL-7, IL-8 and IL-17b levels were elevated compared to the nonMDD group at baseline. Furthermore, MDI score in the MDD group was found to correlate with Bray-Curtis dissimilarity at baseline, and several inflammatory markers at both baseline and after initiation of antidepressant treatment.
    Conclusion: Several bacterial taxa differed between the MDD group and the nonMDD group at baseline and changed in relative abundance during antidepressant treatment and/or psychotherapy. The MDD group was furthermore found to have a pro-inflammatory profile compared to the nonMDD group at baseline. Further studies are required to investigate the gut microbiota and pro-inflammatory profile of patients with MDD.
    MeSH term(s) Humans ; Depressive Disorder, Major/drug therapy ; Gastrointestinal Microbiome ; Antidepressive Agents ; Cognition ; Psychotherapy
    Chemical Substances Antidepressive Agents
    Language English
    Publishing date 2024-01-31
    Publishing country England
    Document type Journal Article
    ZDB-ID 2050438-X
    ISSN 1471-244X ; 1471-244X
    ISSN (online) 1471-244X
    ISSN 1471-244X
    DOI 10.1186/s12888-024-05547-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Long-term follow-up on patient-reported outcomes after supervised exercise training in individuals at risk of complications to type 2 diabetes.

    Danielsen, Julie H / Nielsen, Susanne G / Varming, Annemarie R / Vilsbøll, Tina / Molsted, Stig

    Diabetes & metabolic syndrome

    2024  Volume 18, Issue 2, Page(s) 102953

    Abstract: ... s chair-stand test) and working capacity (Aastrand or Graded Cycling Test).: Results: 153 ...

    Abstract Aims: We investigated long-term changes of patient-reported outcomes after a supervised exercise intervention in individuals with type 2 diabetes (T2D).
    Methods: In an intervention study without a control group, follow-up assessments were performed 12 months after initiating 12 weeks of physical exercise in individuals with T2D at intermediate or high risk of complications. Primary outcomes were health-related quality of life assessed with EQ-5D-5L, empowerment with Diabetes Empowerment Scale-Short Form, and self-reported physical activity with the Physical Activity Scale. Secondary outcomes were physical function (30-s chair-stand test) and working capacity (Aastrand or Graded Cycling Test).
    Results: 153 participants completed follow-up (35% women, age (mean ± SD) 67 ± 11 years, body mass index 33.1 ± 5.9 kg/m
    Conclusions: Health-related quality of life, empowerment, and self-reported moderate intensity physical activity time remained elevated at the long-term follow-up after a supervised exercise intervention.
    MeSH term(s) Humans ; Female ; Middle Aged ; Aged ; Male ; Follow-Up Studies ; Quality of Life ; Diabetes Mellitus, Type 2/complications ; Exercise ; Patient Reported Outcome Measures
    Language English
    Publishing date 2024-02-03
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2273766-2
    ISSN 1878-0334 ; 1871-4021
    ISSN (online) 1878-0334
    ISSN 1871-4021
    DOI 10.1016/j.dsx.2024.102953
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Reply to Letter to the editor regarding "Posterior tilt in nondisplaced femoral neck fractures increases the risk of reoperations after osteosynthesis. A systematic review and meta-analysis".

    Nielsen, Line L / Smidt, Nanna S / Erichsen, Julie L / Palm, Henrik / Viberg, Bjarke

    Injury

    2023  

    Language English
    Publishing date 2023-02-23
    Publishing country Netherlands
    Document type Letter
    ZDB-ID 218778-4
    ISSN 1879-0267 ; 0020-1383
    ISSN (online) 1879-0267
    ISSN 0020-1383
    DOI 10.1016/j.injury.2023.02.044
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Mental Health Staff's Perspectives on Tapering of Antipsychotic Medication: A Focus Group Study.

    Roed, Kickan / Buus, Niels / Nielsen, Jimmi / Christensen, Puk S / Midtgaard, Julie

    Qualitative health research

    2023  Volume 33, Issue 13, Page(s) 1165–1176

    Abstract: Contemporary practices of long-term antipsychotic maintenance treatment for schizophrenia are being challenged, and clinicians must consider the possibilities of reducing long-term maintenance use. However, research indicates that people with ... ...

    Abstract Contemporary practices of long-term antipsychotic maintenance treatment for schizophrenia are being challenged, and clinicians must consider the possibilities of reducing long-term maintenance use. However, research indicates that people with schizophrenia receive little support from mental health staff to reduce antipsychotic medication. This article reports a study which aimed to investigate interdisciplinary mental health staff's accounts of tapering of antipsychotic medication and to explore different positions that mental health staff assign to themselves and others. Six focus groups were conducted with 39 mental health staff from outpatient clinics, inpatient units, forensic mental health units, and community mental health services. The data analysis combined analyses of the interactions during focus groups and the thematic content. Results were considered from a discourse analytic perspective considering the function and consequence of accounts applied by the mental health staff. The mental health staff accounted for their perspectives on tapering from the following three distinctive positions: 1) No, patients will eventually realize that they need the medication, 2) Yes, but tapering means running a big risk of relapse in symptoms, and 3) Yes, we need to welcome risks to support personal recovery. Our findings indicated that there was reluctance among interdisciplinary mental health staff to let service users make decisions and limited possibilities for people with schizophrenia to have their request for tapering of their antipsychotic medication met by mental health staff.
    MeSH term(s) Humans ; Mental Health ; Focus Groups ; Antipsychotic Agents/therapeutic use ; Schizophrenia/drug therapy ; Chronic Disease
    Chemical Substances Antipsychotic Agents
    Language English
    Publishing date 2023-09-14
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1275716-0
    ISSN 1552-7557 ; 1049-7323
    ISSN (online) 1552-7557
    ISSN 1049-7323
    DOI 10.1177/10497323231195821
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Expression of Secretin and its Receptor Along the Intestinal Tract in Type 2 Diabetes Patients and Healthy Controls.

    Gilliam-Vigh, Hannah / Jorsal, Tina / Nielsen, Sophie W / Forman, Julie L / Pedersen, Jens / Poulsen, Steen S / Vilsbøll, Tina / Knop, Filip K

    The Journal of clinical endocrinology and metabolism

    2023  Volume 108, Issue 12, Page(s) e1597–e1602

    Abstract: Context: The hormone secretin (SCT) is released from intestinal S cells and acts via the SCT ... the intestinal mucosal expression profile of SCT and SCTR and evaluated the density of S cells along ... a progressive and similar decrease in SCT and SCTR mRNA expression and S-cell density along the small intestine ...

    Abstract Context: The hormone secretin (SCT) is released from intestinal S cells and acts via the SCT receptor (SCTR). Circulating SCT levels increase after Roux-en-Y gastric bypass surgery and have been associated with massive weight loss and high remission rates of type 2 diabetes (T2D) linked to these operations. Exogenous SCT was recently shown to reduce ad libitum food intake in healthy volunteers.
    Objective: To understand SCT biology and its potential role in T2D pathophysiology, we examined the intestinal mucosal expression profile of SCT and SCTR and evaluated the density of S cells along the intestinal tract of individuals with T2D and healthy controls.
    Methods: Using immunohistochemistry and messenger RNA (mRNA) sequencing, we analyzed intestinal mucosa biopsies sampled along the small intestine at 30-cm intervals and from 7 well-defined anatomical sites along the large intestine (during 2 sessions of double-balloon enteroscopy) in 12 individuals with T2D and 12 healthy controls.
    Results: Both groups exhibited a progressive and similar decrease in SCT and SCTR mRNA expression and S-cell density along the small intestine, with reductions of 14, 100, and 50 times, respectively, in the ileum compared to the duodenum (used as reference). Negligible amounts of SCTR and SCT mRNA, as well as low S-cell density, were found in the large intestine. No significant differences were observed between the groups.
    Conclusion: SCT and SCTR mRNA expression and S-cell density were abundant in the duodenum and decreased along the small intestine. Very low SCT and SCTR mRNA levels and S-cell numbers were observed in the large intestine, without aberrations in individuals with T2D compared to healthy controls.
    MeSH term(s) Humans ; Carrier Proteins/metabolism ; Diabetes Mellitus, Type 2/genetics ; Diabetes Mellitus, Type 2/metabolism ; Gastrointestinal Hormones ; RNA, Messenger/metabolism ; Secretin/genetics ; Secretin/metabolism ; Signal Transduction/physiology
    Chemical Substances Carrier Proteins ; Gastrointestinal Hormones ; RNA, Messenger ; Secretin (1393-25-5) ; secretin receptor
    Language English
    Publishing date 2023-11-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3029-6
    ISSN 1945-7197 ; 0021-972X
    ISSN (online) 1945-7197
    ISSN 0021-972X
    DOI 10.1210/clinem/dgad372
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Effects of empagliflozin on right ventricular adaptation to pressure overload.

    Axelsen, Julie S / Nielsen-Kudsk, Anders H / Schwab, Janne / Ringgaard, Steffen / Nielsen-Kudsk, Jens Erik / de Man, Frances S / Andersen, Asger / Andersen, Stine

    Frontiers in cardiovascular medicine

    2023  Volume 10, Page(s) 1302265

    Abstract: Background: Right ventricular (RV) failure is the prime cause of death in patients with pulmonary arterial hypertension. Novel treatment strategies that protect the RV are needed. Empagliflozin, a sodium-glucose co-transporter-2 inhibitor, shows ... ...

    Abstract Background: Right ventricular (RV) failure is the prime cause of death in patients with pulmonary arterial hypertension. Novel treatment strategies that protect the RV are needed. Empagliflozin, a sodium-glucose co-transporter-2 inhibitor, shows cardioprotective effects on the left ventricle in clinical and preclinical studies, but its direct effects on RV remain elusive. We investigated the effects of empagliflozin on RV dysfunction induced by pulmonary trunk banding (PTB).
    Methods: Male Wistar rats (116 ± 10 g) were randomized to PTB or sham surgery. One week after surgery, PTB animals received empagliflozin mixed into the chow (300 mg empagliflozin/kg chow; PTB-empa,
    Results: PTB caused RV failure evident by decreased cardiac output compared with sham. PTB-empa rats had a 49% increase in water intake compared with PTB-control yet no differences in hematocrit or blood glucose. Treatment with empagliflozin decreased RV end-systolic pressures without any changes in RV cardiac output or ventricular-arterial coupling (Ees/Ea). The decrease in RV end-systolic pressure was complemented by a slight reduction in RV cross sectional area as a sign of reduced hypertrophy. Load-independent measures of RV systolic and diastolic function were not affected in PTB-empa rats compared with PTB-control.
    Conclusion: Empagliflozin treatment reduced RV end-systolic pressure in RV failure induced by pressure overload. Further studies are needed to elucidate whether this simply relates to a diuretic effect and/or additional independent beneficial RV effects.
    Language English
    Publishing date 2023-12-14
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2781496-8
    ISSN 2297-055X
    ISSN 2297-055X
    DOI 10.3389/fcvm.2023.1302265
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Response to "Letter to the editor concerning feasibility and acceptability of a six-month exercise and patient education intervention for patients with hip dysplasia: A mixed methods study".

    Jacobsen, Julie S / Thorborg, Kristian / Sørensen, Dorthe / Jakobsen, Stig S / Nielsen, Rasmus O / Oestergaard, Lisa G / Søballe, Kjeld / Mechlenburg, Inger

    Musculoskeletal science & practice

    2022  Volume 67, Page(s) 102686

    MeSH term(s) Humans ; Hip Dislocation ; Feasibility Studies ; Patient Education as Topic ; Exercise ; Exercise Therapy
    Language English
    Publishing date 2022-11-08
    Publishing country Netherlands
    Document type Letter
    ZDB-ID 2888772-4
    ISSN 2468-7812
    ISSN (online) 2468-7812
    DOI 10.1016/j.msksp.2022.102686
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Separate and combined effects of long-term GIP and GLP-1 receptor activation in patients with type 2 diabetes: a structured summary of a study protocol for a double-blind, randomised, placebo-controlled clinical trial.

    Helsted, Mads M / Gasbjerg, Lærke S / Vilsbøll, Tina / Nielsen, Casper K / Forman, Julie L / Christensen, Mikkel B / Knop, Filip K

    BMJ open

    2023  Volume 13, Issue 2, Page(s) e065736

    Abstract: ... in period with subcutaneous (s.c.) placebo or semaglutide injections once-weekly (0.5 mg). Participants ... will then be randomised to 6 weeks' add-on treatment with continuous s.c. placebo or GIP infusion (16 pmol/kg ...

    Abstract Introduction: Due to reports of severely reduced insulinotropic effect of the incretin hormone glucose-dependent insulinotropic polypeptide (GIP) in type 2 diabetes (T2D), GIP has not been considered therapeutically viable. Recently, however, tirzepatide, a novel dual incretin receptor agonist (activating the GIP receptor and the glucagon-like peptide 1 (GLP-1) receptor) has demonstrated greater glucose and body weight-lowering properties as compared to GLP-1 receptor agonist therapy. The contribution of GIP receptor activation to effects of tirzepatide remains unknown. We will evaluate the glucose-lowering effect of exogenous GIP in the context of pharmacological GLP-1 receptor activation in patients with T2D.
    Methods and analysis: In this randomised, double-blind, four-arm parallel, placebo-controlled trial, 60 patients with T2D will be included (18-74 of age; on diet and exercise and/or metformin therapy only; glycated haemoglobin 6.5-10.5% (48-91 mmol/mol)). Participants will be randomised to an 8-week run-in period with subcutaneous (s.c.) placebo or semaglutide injections once-weekly (0.5 mg). Participants will then be randomised to 6 weeks' add-on treatment with continuous s.c. placebo or GIP infusion (16 pmol/kg/min). The primary endpoint is change in mean glucose levels (assessed by 14-day continuous glucose monitoring) from the end of the run-in period to end of trial.
    Ethics and dissemination: The present study was approved by the Regional Committee on Health Research Ethics in the Capitol Region of Denmark (identification no. H-20070184) and by the Danish Medicines Agency (EudraCT no. 2020-004774-22). All results, positive, negative and inconclusive, will be disseminated at national and/or international scientific meetings and in peer-reviewed scientific journals.
    Trial registration numbers: NCT05078255 and U1111-1259-1491.
    MeSH term(s) Humans ; Incretins ; Diabetes Mellitus, Type 2/drug therapy ; Glucagon-Like Peptide-1 Receptor ; Blood Glucose Self-Monitoring ; Blood Glucose ; Glucose ; Randomized Controlled Trials as Topic
    Chemical Substances Incretins ; gastric inhibitory polypeptide receptor (D6H00MV7K8) ; Glucagon-Like Peptide-1 Receptor ; Blood Glucose ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2023-02-27
    Publishing country England
    Document type Clinical Trial Protocol ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2022-065736
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Expression of Neurotensin and Its Receptors Along the Intestinal Tract in Type 2 Diabetes Patients and Healthy Controls.

    Gilliam-Vigh, Hannah / Jorsal, Tina / Nielsen, Sophie W / Forman, Julie L / Pedersen, Jens / Poulsen, Steen S / Vilsbøll, Tina / Knop, Filip K

    The Journal of clinical endocrinology and metabolism

    2023  Volume 108, Issue 9, Page(s) 2211–2216

    Abstract: Context: Enteroendocrine N cells secrete neurotensin (NTS). NTS reduces food intake in rodents and may increase insulin release. In humans, postprandial NTS responses increase following Roux-en-Y gastric bypass, associating the hormone with the glucose- ...

    Abstract Context: Enteroendocrine N cells secrete neurotensin (NTS). NTS reduces food intake in rodents and may increase insulin release. In humans, postprandial NTS responses increase following Roux-en-Y gastric bypass, associating the hormone with the glucose- and body weight-lowering effects of these procedures.
    Objective: We looked at N cell density and mucosal messenger RNA (mRNA) expression profiles of NTS and NTS receptors in type 2 diabetes (T2D) patients and healthy controls.
    Methods: Using double-balloon enteroscopy, 12 patients with T2D and 12 sex-, age-, and body mass index-matched healthy controls had mucosa biopsies taken from the entire length of the small intestine (at 30-cm intervals) and from 7 anatomically well-defined locations in the large intestine. Biopsies were analyzed using immunohistochemistry and mRNA sequencing.
    Results: N cell density and NTS mRNA expression gradually increased from the duodenum to the ileum, while negligible NTS-positive cells and NTS mRNA expression were observed in the large intestine. NTS receptor 1 and 2 mRNA expression were not detected, but sortilin, a single-pass transmembrane neuropeptide receptor of which NTS also is a ligand, was uniformly expressed in the intestines. Patients with T2D exhibited lower levels of NTS-positive cells and mRNA expression than healthy controls, but this was not statistically significant after adjusting for multiple testing.
    Conclusion: This unique intestinal mapping of N cell density and NTS expression shows increasing levels from the small intestine's proximal to distal end (without differences between patients with T2D and healthy controls), while negligible N-cells and NTS mRNA expression were observed in the large intestine. Sortilin was expressed throughout the intestines in both groups; no NTS receptor 1 or 2 mRNA expression were detected.
    MeSH term(s) Humans ; Neurotensin/genetics ; Diabetes Mellitus, Type 2/metabolism ; Glucagon-Like Peptide 1/metabolism ; Intestines ; Proteins ; RNA, Messenger
    Chemical Substances Neurotensin (39379-15-2) ; Glucagon-Like Peptide 1 (89750-14-1) ; Proteins ; RNA, Messenger
    Language English
    Publishing date 2023-03-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3029-6
    ISSN 1945-7197 ; 0021-972X
    ISSN (online) 1945-7197
    ISSN 0021-972X
    DOI 10.1210/clinem/dgad146
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Response to the letter to the editor regarding "posterior tilt in nondisplaced femoral neck fractures increases the risk of reoperations after osteosynthesis. A systematic review and meta-analysis."

    Nielsen, Line L / Smidt, Nanna S / Erichsen, Julie L / Palm, Henrik / Viberg, Bjarke

    Injury

    2021  Volume 52, Issue 8, Page(s) 2488

    MeSH term(s) Femoral Neck Fractures/diagnostic imaging ; Femoral Neck Fractures/surgery ; Fracture Fixation, Internal ; Humans ; Postoperative Complications ; Reoperation
    Language English
    Publishing date 2021-04-17
    Publishing country Netherlands
    Document type Letter ; Comment
    ZDB-ID 218778-4
    ISSN 1879-0267 ; 0020-1383
    ISSN (online) 1879-0267
    ISSN 0020-1383
    DOI 10.1016/j.injury.2021.04.024
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