Andreas Vestergaard Jensen
University of Copenhagen
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Featured researches published by Andreas Vestergaard Jensen.
Transactions of The Royal Society of Tropical Medicine and Hygiene | 2011
George PrayGod; Nyagosya Range; Daniel Faurholt-Jepsen; Kidola Jeremiah; Maria Faurholt-Jepsen; Martine G. Aabye; Lotte Jensen; Andreas Vestergaard Jensen; Harleen M. S. Grewal; Pascal Magnussen; John Changalucha; Aase Bengaard Andersen; Henrik Friis
This study aimed to estimate deficits in weight, arm fat area (AFA), arm muscle area (AMA) and handgrip strength among smear-positive pulmonary TB (PTB+) patients starting treatment. We conducted a cross-sectional study among PTB+ patients and age- and sex-matched neighborhood controls. HIV status, anthropometric measurements and handgrip strength were determined. Deficits in weight, AFA, AMA and handgrip strength associated with PTB+ and HIV were estimated using multiple regression analysis. We recruited 355 pairs of PTB+ patients and controls. PTB+ was associated with deficits of 10.0kg (95% CI 7.3; 12.7) in weight and 6.8kg (95% CI 5.2; 8.3) in handgrip strength among females and 9.1kg (95% CI 7.3; 10.9) in weight and 6.8kg (95% CI 5.2; 8.4) in handgrip strength among males. In both sexes, PTB+ was associated with deficits in AFA and AMA. Among females, HIV was associated with deficits in AMA and handgrip strength, but the deficit in handgrip strength was larger among PTB+ patients (3.2kg 95% CI 1.3; 5.2) than controls (-1.6kg 95% CI -4.8; 1.5) (interaction, P=0.009). These findings suggest that deficits in weight and handgrip strength among patients starting TB treatment are severe. Thus, nutritional support may be necessary to ensure reversal of the deficits, and may improve treatment outcomes.
Journal of Nutrition | 2011
George PrayGod; Nyagosya Range; Daniel Faurholt-Jepsen; Kidola Jeremiah; Maria Faurholt-Jepsen; Martine G. Aabye; Lotte Jensen; Andreas Vestergaard Jensen; Harleen M. S. Grewal; Pascal Magnussen; John Changalucha; Åse Bengård Andersen; Henrik Friis
Undernutrition is common among tuberculosis (TB) patients. The objective of this study was to assess the effect of multi-micronutrient supplementation during TB treatment on weight, body composition, and handgrip strength. A total of 865 patients with smear-positive (PTB+) or -negative (PTB-) pulmonary TB were randomly allocated to receive a daily biscuit with or without multi-micronutrients for 60 d during the intensive phase of TB treatment. Weight, arm fat area, arm muscle area, and handgrip strength were assessed at baseline and after 2 and 5 mo. At 2 mo, the multi-micronutrient supplementation led to a higher handgrip gain (1.22 kg; 95% CI = 0.50, 1.94; P = 0.001) but had no effects on other outcomes. The effects of multi-micronutrient supplementation were modified by HIV infection (P-interaction = 0.002). Among HIV- patients, multi-micronutrient supplementation increased weight gain by 590 g (95% CI = -40, 1210; P = 0.07) and handgrip strength by 1.6 kg (95% CI = 0.78, 2.47; P < 0.001), whereas among HIV+ patients, it reduced weight gain by 1440 g (95% CI = 290, 2590; P = 0.002) and had no effect on handgrip strength (0.07 kg; 95% CI = -1.30, 1.46; P = 0.91). The reduced weight gain among HIV+ patients receiving multi-micronutrient supplementation seemed to be explained by a higher proportion of patients reporting fever. At 5 mo, the effects on weight were sustained, whereas there was no effect on handgrip strength. In conclusion, multi-micronutrient supplementation given as a biscuit is beneficial among HIV- PTB patients and may be recommended to TB programs. More research is needed to develop an effective supplement for HIV+ PTB patients.
Scandinavian Journal of Infectious Diseases | 2014
Daniel Faurholt-Jepsen; Martine G. Aabye; Andreas Vestergaard Jensen; Nyagosya Range; George PrayGod; Kidola Jeremiah; John Changalucha; Maria Faurholt-Jepsen; Lotte Jensen; Signe M. Jensen; Henrik Krarup; Pernille Ravn; Henrik Friis; Åse Bengård Andersen
Abstract Background: Diabetes is increasingly common in TB endemic regions and plays a role as a possible risk factor for increased progression from latent TB infection (LTBI) to active TB disease. Although the pathophysiological mechanisms are not fully understood, the immune system is weakened in diabetes patients and therefore the validity of interferon gamma release assays (IGRA) may be compromised. The aim of the present study was to assess the association between diabetes and Mycobacterium tuberculosis (Mtb) antigen-specific interferon gamma (IFN-γ) release in a TB endemic area among culture-confirmed TB patients and non-TB controls. Methods: Culture-confirmed pulmonary TB patients (n = 187) and healthy non-TB neighbourhood controls (n = 190) from Mwanza, Tanzania were tested for the presence of circulating T cells recognizing Mtb antigens using an IGRA. The diabetes status of all participants was assessed using a standard oral glucose tolerance test. The impact of diabetes on the performance of the IGRA was estimated using robust linear and logistic regression. Results: Compared to normal glucose tolerance, diabetes was associated with reduced levels of Mtb-specific IFN-γ. Increasing levels of fasting blood glucose (B − 0.3, 95% confidence interval − 0.6 to − 0.03, p = 0.033) was negatively associated with IFN-γ. Although TB patients had higher specific and lower unspecific mitogen IFN-γ responses compared to non-TB controls, the association between diabetes and IFN-γ did not depend on TB status. Conclusion: Diabetes is associated with lower levels of Mtb antigen-specific IFN-γ, and the validity of IFN- γ tests for LTBI may be questionable in individuals with diabetes.
Infectious diseases | 2017
Stine Bang Andersen; Gertrud Baunbæk Egelund; Andreas Vestergaard Jensen; Pelle Trier Petersen; Gernot Rohde; Pernille Ravn
Abstract Background: C-reactive protein (CRP) is a well-known acute phase protein used to monitor the patient’s response during treatment in infectious diseases. Mortality from Community-acquired Pneumonia (CAP) remains high, particularly in hospitalized patients. Better risk prediction during hospitalization could improve management and ultimately reduce mortality levels. The aim of this study was to evaluate CRP on the 3rd day (CRP3) of hospitalization as a predictor for 30 days mortality. Methods: A retrospective multicentre cohort study of adult patients admitted with CAP at three Danish hospitals. Predictive associations of CRP3 (absolute levels and relative decline) and 30 days mortality were analysed using receiver operating characteristics and logistic regression. Results: Eight hundred and fourteen patients were included and 90 (11%) died within 30 days. The area under the curve for CRP3 level and decline for predicting 30 days mortality were 0.64 (0.57–0.70) and 0.71 (0.65–0.76). Risk of death was increased in patients with CRP3 level >75 mg/l (OR 2.44; 95%CI 1.36–4.37) and in patients with a CRP3 decline <50% (OR 4.25; 95%CI 2.30–7.83). In the multivariate analysis, the highest mortality risk was seen in patients who failed to decline by 50%, irrespective of the actual level of CRP (OR 7.8; 95%CI 3.2–19.3). Mortality risk increased significantly according to CRP decline for all strata of CURB-65 score. Conclusions: CRP responses day 3 is a valuable predictor of 30 days mortality in hospitalized CAP patients. Failure to decline in CRP was associated with a poor prognosis irrespective of the actual level of CRP or CURB-65.
Medicine | 2017
Gertrud Baunbæk Egelund; Gideon Ertner; Kristina Langholz Kristensen; Andreas Vestergaard Jensen; Thomas Benfield; Christian T. Brandt
Abstract Cerebrospinal fluid (CSF) analysis is the most important tool for assessing central nervous system (CNS) disease. An elevated CSF leukocyte count rarely provides the final diagnosis, but is almost always an indicator of inflammation within the CNS. The present study investigated the variety of diseases associated with CSF pleocytosis. CSF analyses were identified through the biochemical database used in the capital region of Denmark in the period from 2003 to 2010. In patients >15 years, clinical diagnoses associated with the finding of a CSF leukocyte count >10 × 106 cells/L were obtained from discharge records and patient files. A total of 1058 CSF samples from 1054 patients were included in the analysis. The median age was 50 (interquartile range: 36–67) and 53% were male. Eighty-one different diagnoses were identified in 1058 cases with an elevated CSF leukocyte count, besides unknown causes. Infections were the most common cause of CSF pleocytosis (61.4%) followed by miscellaneous causes (12.7%), vascular (9.7%), neurodegenerative (7%), neoplastic (5%), and inflammatory conditions (4.2%). Only infections presented with leukocyte counts >10,000 × 106/L. Infections represented 82.6% of all cases with a leukocyte count >100 × 106/L whereas 56.3% of cases with at leukocyte counts <100 × 106/L were dominated by disease not related to infection. The present study may serve as a reminder to clinicians of what diseases and disease categories to suspect when patients present with CSF biochemistry indicating CNS inflammation.
ERJ Open Research | 2017
Andreas Vestergaard Jensen; Gertrud Baunbæk Egelund; Stine Bang Andersen; Pelle Trier Petersen; Thomas Benfield; Daniel Faurholt-Jepsen; Gernot Rohde; Pernille Ravn
Hyperglycaemia is common in patients with community-acquired pneumonia (CAP) and is a predictor of severe outcomes. Data are scarce regarding whether this association is affected by diabetes mellitus (DM) and also regarding its importance for severe outcomes in hospital. We determined the impact of blood glucose on severe outcomes of CAP in hospital. We studied 1318 adult CAP patients hospitalised at three Danish hospitals. The association between blood glucose and DM status and severe clinical outcome (admission to an intensive care unit (ICU) and/or in-hospital mortality) was assessed by logistic regression. Models were adjusted for CURB-65 score and comorbidities. 12% of patients had DM. In patients without DM an increase in admission blood glucose was associated with risk for ICU admittance (OR 1.25, 95% CI 1.13–1.39), but not significantly associated with in-hospital mortality (OR 1.10, 95% CI 0.99–1.23). In patients with DM an increase in admission blood glucose was not associated with ICU admittance (OR 1.05, 95% CI 1.00–1.12) or in-hospital mortality (OR 1.05, 95% CI 0.99–1.12). An increase in admission blood glucose (only in patients without DM) was associated with a higher risk for ICU admittance and a trend towards higher in-hospital mortality. DM was not associated with a more severe outcome of CAP. An increase in blood glucose marks severity of community-acquired pneumonia in patients without diabetes mellitus http://ow.ly/3omE30c0whm
British Journal of Nutrition | 2012
George PrayGod; Nyagosya Range; Daniel Faurholt-Jepsen; Kidola Jeremiah; Maria Faurholt-Jepsen; Martine G. Aabye; Lotte Jensen; Andreas Vestergaard Jensen; Harleen M. S. Grewal; Pascal Magnussen; John Changalucha; Åse Bengård Andersen; Henrik Friis
BMC Infectious Diseases | 2010
Lotte Jensen; Andreas Vestergaard Jensen; George PrayGod; Jeremiah Kidola; Daniel Faurholt-Jepsen; John Changalucha; Nyagosya Range; Henrik Friis; Jannik Helweg-Larsen; Jørgen Skov Jensen; Aase Bengaard Andersen
BMC Pulmonary Medicine | 2017
Gertrud Baunbæk Egelund; Andreas Vestergaard Jensen; Stine Bang Andersen; Pelle Trier Petersen; Bjarne Ørskov Lindhardt; Christian von Plessen; Gernot Rohde; Pernille Ravn
European Journal of Clinical Microbiology & Infectious Diseases | 2018
Pelle Trier Petersen; Gertrud Baunbæk Egelund; Andreas Vestergaard Jensen; Stine Bang Andersen; Merete Frejstrup Pedersen; Gernot Rohde; Pernille Ravn