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Dive into the research topics where Hugo Lagercrantz is active.

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Featured researches published by Hugo Lagercrantz.


JAMA | 2009

One-year survival of extremely preterm infants after active perinatal care in sweden

Mats Blennow; Uwe Ewald; Tomas Fritz; Per Åke Holmgren; Annika Jeppsson; Eva Lindberg; Anita Lundqvist; Solveig Nordén Lindeberg; Elisabeth Olhager; Ingrid Östlund; Marija Simic; Gunnar Sjoers; Lennart Stigson; Vineta Fellman; Lena Hellström-Westas; Mikael Norman; Magnus Westgren; Gerd Holmström; Ricardo Laurini; Karin Stjernqvist; Karin Källén; Hugo Lagercrantz; Karel Marsal; Fredrik Serenius; Margareta Wennergren; Tore Nilstun; Petra Otterblad Olausson; Bo Strömberg

CONTEXT Up-to-date information on infant survival after extremely preterm birth is needed for assessing perinatal care services, clinical guidelines, and parental counseling. OBJECTIVE To determine the 1-year survival in all infants born before 27 gestational weeks in Sweden during 2004-2007. DESIGN, SETTING, AND PATIENTS Population-based prospective observational study of extremely preterm infants (707 live-born and 304 stillbirths) born to 887 mothers in 904 deliveries (102 multiple births) in all obstetric and neonatal units in Sweden from April 1, 2004, to March 31, 2007. MAIN OUTCOME MEASURES Infant survival to 365 days and survival without major neonatal morbidity (intraventricular hemorrhage grade >2, retinopathy of prematurity stage >2, periventricular leukomalacia, necrotizing enterocolitis, severe bronchopulmonary dysplasia). Associations between perinatal interventions and survival. RESULTS The incidence of extreme prematurity was 3.3 per 1000 infants. Overall perinatal mortality was 45% (from 93% at 22 weeks to 24% at 26 weeks), with 30% stillbirths, including 6.5% intrapartum deaths. Of live-born infants, 91% were admitted to neonatal intensive care and 70% survived to 1 year of age (95% confidence interval [CI], 67%-73%). The Kaplan-Meier survival estimates for 22, 23, 24, 25, and 26 weeks were 9.8% (95% CI, 4%-23%), 53% (95% CI, 44%-63%), 67% (95% CI, 59%-75%), 82% (95% CI, 76%-87%), and 85% (95% CI, 81%-90%), respectively. Lower risk of infant death was associated with tocolytic treatment (adjusted for gestational age odds ratio [OR], 0.43; 95% CI, 0.36-0.52), antenatal corticosteroids (OR, 0.44; 95% CI, 0.24-0.81), surfactant treatment within 2 hours after birth (OR, 0.47; 95% CI, 0.32-0.71), and birth at a level III hospital (OR, 0.49; 95% CI, 0.32-0.75). Among 1-year survivors, 45% had no major neonatal morbidity. CONCLUSION During 2004 to 2007, 1-year survival of infants born alive at 22 to 26 weeks of gestation in Sweden was 70% and ranged from 9.8% at 22 weeks to 85% at 26 weeks.


Proceedings of the National Academy of Sciences of the United States of America | 2007

Resting-state networks in the infant brain

Peter Fransson; Béatrice Skiöld; Sandra Horsch; Anders Nordell; Mats Blennow; Hugo Lagercrantz; Ulrika Ådén

In the absence of any overt task performance, it has been shown that spontaneous, intrinsic brain activity is expressed as systemwide, resting-state networks in the adult brain. However, the route to adult patterns of resting-state activity through neuronal development in the human brain is currently unknown. Therefore, we used functional MRI to map patterns of resting-state activity in infants during sleep. We found five unique resting-states networks in the infant brain that encompassed the primary visual cortex, bilateral sensorimotor areas, bilateral auditory cortex, a network including the precuneus area, lateral parietal cortex, and the cerebellum as well as an anterior network that incorporated the medial and dorsolateral prefrontal cortex. These results suggest that resting-state networks driven by spontaneous signal fluctuations are present already in the infant brain. The potential link between the emergence of behavior and patterns of resting-state activity in the infant brain is discussed.


Pediatric Research | 1977

Catecholamine Release in the Newborn Infant at Birth

Hugo Lagercrantz; Peter Bistoletti

Summary: Catecholamines were determined by a fluorometric technique in umbilical blood which was collected from new born infants immediately alter birth. The mean catecholamine concentration was 62.1 nmol/liter in the umbilical artery and 29.3 nmol/liter in the umbilical vein of newborn full term infants delivered uneventfully. This value is considerably higher than in resting adults. Similar levels of catecholamines were seen alter elective cesarean sections, whereas considerably higher levels were found after breech deliveries. In the full term asphyxiated infants about a 4-fold increase of the catecholamine concentration was found in both the umbilical arterial and venous blood. The amine concentration level correlated inversely to the pH below 7.25 (10log catecholamine concentration versus pH, r = −0.71). Preterm infants had, in general, lower amine levels than full term infants both after uneventful deliveries and after intrauterine asphyxia. The catecholamine levels were considerably increased in the newborn infants who showed some kind of abnormal fetal heart rate variation during the last hour before birth; in particular baseline changes were associated with high levels whereas only a moderate increase was seen after loss of beat-to-beat variation.Speculation: The high catecholamine concentrations in umbilical blood, seen even after uneventful deliveries, indicate that the sympathoadrenal system might have a functional role in the fetus at delivery. The enormous levels at asphyxia might be of importance to sustain the circulatory homeostasis.


Experimental Neurology | 2004

Development of neurotransmitter systems during critical periods

Eric Herlenius; Hugo Lagercrantz

Neurotransmitters are released from neurons and mediate neuronal communication. Neuromodulators can also be released from other cells and influence the neuronal signaling. Both neurotransmitters and neuromodulators play an important role in the shaping and the wiring of the nervous system possibly during critical windows of the development. Monoamines are expressed in the very early embryo, at which stage the notochord already contains high noradrenaline levels. Purines and neuropeptides are probably also expressed at an early stage, in a similar way as they occur during early phylogenesis. The levels of most neurotransmitters and neuromodulators increase concomitantly with synapse formation. Some of them surge during the perinatal period (such as glutamate, catecholamines, and some neuropeptides) and then level off. The interesting question is to what extent the expression of neuroactive agents is related to the functional state of the fetus and the newborn. Monoamines are expressed in the very early embryo, at which stage the notochord already contains high noradrenaline levels. They may have an important role for neurotransmission in the fetus. In the adult mammal, the fast switching excitatory amino acids dominate. However, they also seem to be important for the wiring of the brain and the plasticity before birth. NMDA receptors that are supposed to mediate these effects dominate and are then substituted by AMPA receptors. The main inhibitory amino acids gamma-aminobutyric acid (GABA) and glycine are excitatory in the developing brain by depolarizing developing neurons that have high Cl- concentrations. This seems to be of major importance for the wiring of neuronal circuits. Prenatal or neonatal stress, for example, hypoxia, can affect the programming of neurotransmitter and receptor expression, which can lead to long-term behavioral effects.


Cerebral Cortex | 2011

The Functional Architecture of the Infant Brain as Revealed by Resting-State fMRI

Peter Fransson; Ulrika Ådén; Mats Blennow; Hugo Lagercrantz

The functional network topology of the adult human brain has recently begun to be noninvasively mapped using resting-state functional connectivity magnetic resonance imaging and described using mathematical tools originating from graph theory. Previous studies have revealed the existence of disproportionally connected brain regions, so called cortical hubs, which act as information convergence zones and supposedly capture key aspects of how the brains architecture supports human behavior and how it is affected by disease. In this study, we present results showing that cortical hubs and their associated cortical networks are largely confined to primary sensory and motor brain regions in the infant brain. Our findings in infants stand in stark contrast to the situation found in adults where the majority of cortical hubs and hub-related networks are located in heteromodal association cortex. Our findings suggest that the functional network architecture in infants is linked to support tasks that are of a perception-action nature.


Acta Paediatrica | 1992

Temperature, metabolic adaptation and crying in healthy full‐term newborns cared for skin‐to‐skin or in a cot

Kyllike Christensson; C Siles; L Moreno; A Belaustequi; P De La Fuente; Hugo Lagercrantz; P Puyol; Jan Winberg

The aim of the present study was to compare temperatures, metabolic adaptation and crying behavior in 50 healthy, full‐term, newborn infants who were randomized to be kept either skin‐to‐skin with the mother or next to the mother in a cot “separated”. The babies were studied during the first 90 min after birth. Axillary and skin temperatures were significantly higher in the skin‐to‐skin group; at 90 min after birth blood glucose was also significantly higher and the return towards zero of the negative base‐excess was more rapid as compared to the “separated” group. Babies kept in cots cried significantly more than those kept skin‐to‐skin with the mother. Keeping the baby skin‐to‐skin with the mother preserves energy and accelerates metabolic adaptation and may increase the well‐being of the newborn.


Early Human Development | 2001

Neurotransmitters and neuromodulators during early human development

Eric Herlenius; Hugo Lagercrantz

BACKGROUND Neurotransmitters such as monoamines appear in the embryo before the neurones are differentiated. They may have other functions than neurotransmission during embryogenesis such as differentiation and neuronal growth. For example, serotonin may act as a morphogen. A number of neuropeptides are expressed during ontogenesis, but their function has been difficult to establish. Maybe some of them remain as evolutionary residues. Fast-switching neurotransmitters like the excitatory amino acids and the more ionotropic receptors dominate in the human brain, but appear probably later during evolution as well as during ontogeny. METHODS The distribution of catecholamines during development has been analysed with a fluorescence method, while most of the other neurotransmitters have been mapped with immunohistochemical methods. The classical method to determine the physiological role of a neurotransmitter or modulator is to study the physiological effect of its antagonist, blocking the endogenous activity. By transgenic technique, the genes encoding for enzymes involved in the synthesis of neurotransmitters can be knocked-out. MAJOR FINDINGS Pharmacological blocking of endogenous activity has, for example, demonstrated that adenosine suppresses fetal respiration. Knocking out the dopamine beta-hydroxylase gene results in fetal death, suggesting that noradrenaline is essential for survival. Some neurotransmitters change their effect during embryogenesis, e.g. GABA which is excitatory in the embryo, but inhibitory after birth due to a switch from a high to low chloride content in the nerve cells. It is possible that this is of importance for the wiring of neuronal network in early life. NMDA receptors dominate in the foetus, while kainate and AMPA receptors appear later. At birth, there is a surge of neurotransmitters such as catecholamines, which may be of importance for the neonatal adaptation. CONCLUSIONS Neurotransmitters and modulators are not only important for the neural trafficking in the embryo, but also for the development of the neuronal circuits. Prenatal or neonatal stress (hypoxia), as well as various drugs, may disturb the wiring and cause long-term behavioural effects (fetal and neonatal programming).


Pediatric Research | 2003

Preterm Children Have Disturbances of White Matter at 11 Years of Age as Shown by Diffusion Tensor Imaging

Zoltan Nagy; Helena Westerberg; Stefan Skare; Jesper Andersson; Anders Lilja; Olof Flodmark; Elisabeth Fernell; Kirsten Holmberg; Birgitta Böhm; Hans Forssberg; Hugo Lagercrantz; Torkel Klingberg

Preterm birth frequently involves white matter injury and affects long-term neurologic and cognitive outcomes. Diffusion tensor imaging has been used to show that the white matter microstructure of newborn, preterm children is compromised in a regionally specific manner. However, until now it was not clear whether these lesions would persist and be detectible on long-term follow-up. Hence, we collected diffusion tensor imaging data on a 1.5-T scanner, and computed fractional anisotropy and coherence measures to compare the white matter integrity of children born preterm to that of control subjects. The subjects for the preterm group (10.9 ± 0.29 y; n = 9; birth weight ≤ 1500 g; mean gestational age, 28.6 ± 1.05 wk) possessed attention deficits, a common problem in preterms. They were compared with age- and sex-matched control children (10.8 ± 0.33 y; n = 10; birth weight ≥ 2500; gestational age, ≥ 37 wk). We found that the preterm group had lower fractional anisotropy values in the posterior corpus callosum and bilaterally in the internal capsules. In the posterior corpus callosum this difference in fractional anisotropy values may partially be related to a difference in white matter volume between the groups. An analysis of the coherence measure failed to indicate a group difference in the axonal organization. These results are in agreement with previous diffusion tensor imaging findings in newborn preterm children, and indicate that ex-preterm children with attention deficits have white matter disturbances that are not compensated for or repaired before 11 y of age.


Pediatric Research | 2003

Antimicrobial polypeptides of human vernix caseosa and amniotic fluid: implications for newborn innate defense.

Hiroyuki Yoshio; Maria Tollin; Gudmundur H. Gudmundsson; Hugo Lagercrantz; Hans Jörnvall; Giovanna Marchini; Birgitta Agerberth

Antimicrobial peptides/proteins are widespread in nature and play a critical role in host defense. To investigate whether these components contribute to surface protection of newborns at birth, we have characterized antimicrobial polypeptides in vernix caseosa (vernix) and amniotic fluid (AF). Concentrated peptide/protein extracts were obtained from 11 samples of vernix and six samples of AF and analyzed for antimicrobial activity using an inhibition zone assay. Proteins/peptides in all vernix extracts exhibited strong antibacterial activity against Bacillus megaterium (strain Bm11), in addition to antifungal activity against Candida albicans, whereas AF-derived proteins/peptides showed only the former activity. Fractions obtained after separation by reverse-phase HPLC exhibited antibacterial activity, with the most pronounced activity in a fraction containing α-defensins (HNP1-3). The presence of HNP1-3 was proved by dot blot analysis and confirmed by mass spectrometry. Lysozyme and ubiquitin were identified by sequence analysis in two fractions with antibacterial activity. Fractions of vernix and AF were also positive for LL-37 with dot blot and Western blot analyses, and one fraction apparently contained an extended form of LL-37. Interestingly, psoriasin, a calcium-binding protein that is upregulated in psoriatic skin and was found recently to exhibit antimicrobial activity, was characterized in the vernix extract. The presence of all of these antimicrobial polypeptides in vernix suggests that they are important for surface defense and may have an active biologic role against microbial invasion at birth.


Acta Paediatrica | 2010

Incidence of and risk factors for neonatal morbidity after active perinatal care : extremely preterm infants study in Sweden (EXPRESS)

Dordi Austeng; Mats Blennow; Uwe Ewald; Vineta Fellman; Thomas Fritz; Lena Hellström-Westas; Ann Hellström; Per Åke Holmgren; Gerd Holmström; Peter Jakobsson; Annika Jeppsson; Kent Johansson; Karin Källén; Hugo Lagercrantz; Ricardo Laurini; Eva Lindberg; Anita Lundqvist; Karel Marsal; Tore Nilstun; Solveig Nordén-Lindeberg; Mikael Norman; Elisabeth Olhager; Ingrid Oestlund; Fredrik Serenius; Marija Simic; Gunnar Sjörs; Lennart Stigson; Karin Stjernqvist; Bo Strömberg; Kristina Tornqvist

Aims:  The aim of this study was to determine the incidence of neonatal morbidity in extremely preterm infants and to identify associated risk factors.

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Jean-Marc Pequignot

Centre national de la recherche scientifique

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Marco Bartocci

Karolinska University Hospital

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