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1.
Neuroimage Clin ; 11: 139-148, 2016.
Article in English | MEDLINE | ID: mdl-26937382

ABSTRACT

Ventriculomegaly (VM) is the most common central nervous system abnormality diagnosed antenatally, and is associated with developmental delay in childhood. We tested the hypothesis that antenatally diagnosed isolated VM represents a biological marker for altered white matter (WM) and cortical grey matter (GM) development in neonates. 25 controls and 21 neonates with antenatally diagnosed isolated VM had magnetic resonance imaging at 41.97(± 2.94) and 45.34(± 2.14) weeks respectively. T2-weighted scans were segmented for volumetric analyses of the lateral ventricles, WM and cortical GM. Diffusion tensor imaging (DTI) measures were assessed using voxel-wise methods in WM and cortical GM; comparisons were made between cohorts. Ventricular and cortical GM volumes were increased, and WM relative volume was reduced in the VM group. Regional decreases in fractional anisotropy (FA) and increases in mean diffusivity (MD) were demonstrated in WM of the VM group compared to controls. No differences in cortical DTI metrics were observed. At 2 years, neurodevelopmental delays, especially in language, were observed in 6/12 cases in the VM cohort. WM alterations in isolated VM cases may be consistent with abnormal development of WM tracts involved in language and cognition. Alterations in WM FA and MD may represent neural correlates for later neurodevelopmental deficits.


Subject(s)
Cognition/physiology , Hydrocephalus/diagnostic imaging , White Matter/diagnostic imaging , Adult , Anisotropy , Diffusion Tensor Imaging/methods , Female , Gray Matter/diagnostic imaging , Gray Matter/physiopathology , Humans , Hydrocephalus/physiopathology , Infant , Infant, Newborn , Magnetic Resonance Imaging/methods , Male , White Matter/physiopathology
2.
Soft Matter ; 10(40): 8083-94, 2014 Oct 28.
Article in English | MEDLINE | ID: mdl-25171774

ABSTRACT

Polymer nanocomposites are an important and growing class of materials where nanoparticles are mixed in a polymer matrix. Much of the interest in polymer nanocomposites is derived from the nanoparticles' ability to impart properties to the polymer not commonly found in polymer materials, such as tunable optical, electrical, and mechanical properties. Grafting polymer chains to the surface of a nanoparticle is one of the most common routes towards promoting dispersion of nanoparticles in a polymer matrix. However, we only understand the thermodynamics of grafted nanoparticles in a polymer matrix in the simplest of cases, and this problem is exacerbated by the lack of theoretical and computational tools capable of efficiently predicting the structure of phase separated grafted nanoparticle/polymer blends. In this work, we extend a recently developed field theoretic framework to study the distribution of homogeneously grafted nanoparticles in homopolymer thin films and blends. We demonstrate that our method reproduces trends observed experimentally in homopolymer thin films, and then we examine how the nanoparticle size, grafting density, and the length of the grafted chains relative to the matrix chains affects the distribution of the grafted nanoparticles in phase separated polymer blends. We find that position of the nanoparticles relative to the interface in the blends is sensitive to the brush conformation, even when the nanoparticles are miscible in one of the two homopolymer phases.

3.
Aging Ment Health ; 9(6): 571-5, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16214705

ABSTRACT

This study is based on a total cohort (N = 192) of people born in 1902 and 1903 and living in southern Sweden. Subjects were assessed at baseline when 67 years of age and on eight further occasions over 34 years or until death. The participation rate in the nine examinations ranged from 78-100%. Interviews, psychological tests, and medical examinations were used as well as information on medical diagnoses from primary health care records and hospital records. The cumulative probability for the development of clinical depression during the follow-up was 8% and for anxiety 6%. The incidence rate for depression and for anxiety was highest during the period 67-81 years. Persons with poor financial status were more likely to be diagnosed with depression but no significant risk factor for anxiety was found. Only 14% developed depression and anxiety during the follow-up period, females more often than men. The strongest risk factors for the development of depression were perceived economic problems.


Subject(s)
Anxiety Disorders/epidemiology , Depressive Disorder/epidemiology , Aged , Aged, 80 and over , Anxiety Disorders/diagnosis , Anxiety Disorders/psychology , Cohort Studies , Cross-Sectional Studies , Depressive Disorder/diagnosis , Depressive Disorder/psychology , Female , Geriatric Assessment , Health Status , Humans , Incidence , Longitudinal Studies , Male , Outcome Assessment, Health Care , Prospective Studies , Risk Factors , Socioeconomic Factors , Sweden
4.
Science ; 310(5745): 96-100, 2005 Oct 07.
Article in English | MEDLINE | ID: mdl-16210536

ABSTRACT

Most people hold beliefs about personality characteristics typical of members of their own and others' cultures. These perceptions of national character may be generalizations from personal experience, stereotypes with a "kernel of truth," or inaccurate stereotypes. We obtained national character ratings of 3989 people from 49 cultures and compared them with the average personality scores of culture members assessed by observer ratings and self-reports. National character ratings were reliable but did not converge with assessed traits. Perceptions of national character thus appear to be unfounded stereotypes that may serve the function of maintaining a national identity.


Subject(s)
Character , Culture , Ethnicity , Personality , Adolescent , Adult , Cross-Cultural Comparison , Female , Humans , Male , Personality Assessment , Reproducibility of Results , Social Perception , Stereotyping , Surveys and Questionnaires
5.
Acta Paediatr ; 94(3): 287-94, 2005 Mar.
Article in English | MEDLINE | ID: mdl-16028646

ABSTRACT

AIM: This is the ninth report from the western-Swedish study of the prevalence and origin of cerebral palsy. METHODS: A population-based study covering the 88 371 live births in the area in 1995-1998. Birth characteristics, neuroimaging findings and risk factors in children with cerebral palsy were recorded, prevalence was calculated, and aetiology was analysed. RESULTS: The study comprised 170 children with cerebral palsy, i.e. a prevalence of 1.92 per 1000 live births. Excluding eight post-neonatally derived cases, the gestational age-specific prevalences were 77 per 1000 for children born before 28 wk of gestation, 40 for children born at 28-31 wk, 7 for children born at 32-36 wk and 1.1 for children born after 36 wk of gestation. Spastic hemiplegia, diplegia and tetraplegia accounted for 38%, 35% and 6%, respectively, dyskinetic cerebral palsy for 15%, and ataxia for 6%. For the first time, hemiplegia was now most common, due to the decline in preterm diplegia. There was a further increase in full-term dyskinetic cerebral palsy. The origin of cerebral palsy in children born at term was considered to be prenatal in 38%, peri/neonatal in 35% and unclassifiable in 27%, while in children born preterm it was 17%, 49% and 33%, respectively. CONCLUSION: The decreasing trend from the period 1991-1994 continued, both in children born at term and especially in those born preterm. However, the increase in dyskinetic cerebral palsy in children born at term was a matter of concern. In this group, a perinatal hypoxic ischaemic encephalopathy had been present in 71%.


Subject(s)
Cerebral Palsy/epidemiology , Apgar Score , Female , Gestational Age , Humans , Infant, Newborn , Infant, Premature , Magnetic Resonance Imaging , Male , Prevalence , Risk Factors , Sweden/epidemiology , Tomography, X-Ray Computed
6.
Pediatrics ; 115(3): e283-9, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15741353

ABSTRACT

OBJECTIVE: To date, very few studies have been conducted on the neurodevelopmental well-being of children conceived through intracytoplasmic sperm injection (ICSI). The limitations of these studies often include a lack of comparison with a demographically matched, naturally conceived (NC) group and the investigation of only very young children, with relatively small samples sizes. One study showed that there were no differences in IQ scores among ICSI-conceived, in vitro fertilization (IVF)-conceived, and NC children at 5 years of age. Unfortunately, psychomotor development was not assessed in that study. Because findings regarding these children's cognitive and motor development are inconclusive, the aim of this study was to shed more light on the cognitive and motor development of 5-year-old ICSI-conceived children. METHODS: A total of 511 ICSI-conceived children were compared with 424 IVF-conceived children and 488 NC controls. Children were recruited in 5 European countries, ie, Belgium, Denmark, Greece, Sweden, and the United Kingdom. Participation rates ranged from 45% to 96% in the ICSI and IVF groups and from 34% to 78% in the NC group. Cognitive and motor development was assessed with the Wechsler Preschool and Primary Scale of Intelligence-Revised (WPPSI-R) and McCarthy Scales of Children's Abilities (MSCA) Motor Scale, respectively. The WPPSI-R consists of 2 major scales, ie, Verbal and Performance, each including 6 subtests. The 6 Performance Scale subtests are object assembly, geometric design, block design, mazes, picture completion, and animal pegs. The 6 Verbal Scale subtests are information, comprehension, arithmetic, vocabulary, similarities, and sentences. Scores on the Performance and Verbal Scale subtests are summed to yield the performance IQ (PIQ) and verbal IQ (VIQ), respectively. Scores on both the Performance Scale and the Verbal Scale yield the full-scale IQ (FSIQ). IQ scales have a mean score of 100 and a SD of 15. Each subtest has a mean score of 10 and a SD of 3. The MSCA consists of 6 scales, ie, Verbal, Perceptual-Performance, Quantitative, General Cognitive, Memory, and Motor Scale. In this study, only the Motor Scale was administered. This scale assesses the child's coordination during performance of a variety of gross- and fine-motor tasks. Leg coordination, arm coordination, and imitative action tests provide measures of gross-motor ability. Draw-a-design and draw-a-child assess fine-motor coordination, as revealed by the levels of hand coordination and finger dexterity. The mean score for this test is 50, with a SD of . RESULTS: No differences were identified among ICSI, IVF, and NC children with respect to VIQ, PIQ, or FSIQ scores of the WPPSI-R. Furthermore, there were no differences between groups regarding the discrepancy between VIQ and PIQ scores. These results were not influenced by gender, country, or maternal educational level. However, in the subgroup of firstborn children with mothers who gave birth at an older age (33-45 years), NC children obtained significantly better VIQ and FSIQ scores than did children conceived through assisted reproductive technologies. These differences in VIQ and FSIQ scores between ICSI/IVF and NC children were relative, because NC children scored <1 IQ point higher than ICSI/IVF children. Therefore, these scores show no clinical relevance. For Verbal Scale subtests, variables such as age of the mother at the time of the birth, educational level of the mother, and gender and nationality of the child interacted with mode of conception, resulting in clinically irrelevant differences between scores for the ICSI/IVF and NC groups on the arithmetic, vocabulary, and comprehension subtests. For Performance Scale subtests, these same demographic factors interacted with mode of conception for the block design, object assembly, and animal pegs subtests, again resulting in clinically irrelevant differences among groups. In the 3 groups (ICSI, IVF, and NC), we observed equal numbers of children scoring below 1 SD from the mean on the WPPSI-R and the MSCA. CONCLUSIONS: This study includes a substantial number of children from several European countries. Apart from a few interaction effects between mode of conception and demographic variables, no differences were found when ICSI, IVF, and NC scores on the WPPSI-R and MSCA Motor Scale were compared. Nevertheless, the aforementioned interaction effects could indicate that demographic variables such as maternal age at the time of the birth and maternal educational level play different roles in the cognitive development of IVF and ICSI children, compared with NC children. Additional research is needed to explore and verify this finding. Previous studies revealed that ICSI children, in comparison with NC children, more frequently obtained scores below 1 SD from the mean on 3 subtests of the Performance Scale (object assembly, block design, and mazes) or showed a trend of 5.2% of ICSI children, compared with 2.5% of IVF children and 0.9% of NC children, obtaining a score below 1 SD from the mean, but those findings were not confirmed in this study. Here no differences were found among the 3 groups in the numbers of children scoring below 1 SD from the mean on the VIQ, PIQ, and FSIQ tests and the Verbal and Performance Scale subtests. Motor development results were somewhat more conclusive. There were no differences between the scores of ICSI, IVF, and NC children on the MCSA Motor Scale. No interaction effects were found between mode of conception and demographic variables, indicating that these results are not influenced by gender, nationality, maternal educational level, or maternal age at the time of the birth. Furthermore, equal proportions of children in all 3 groups scored below 1 SD from the mean. The results of this study are reassuring for parents who conceived through ICSI (or IVF). The findings indicate that the motor and cognitive development of their offspring is very similar to that of NC children. However, demographic factors such as maternal educational level and maternal age at the time of the birth might play different roles in the cognitive development of ICSI and IVF children, compared with NC children.


Subject(s)
Child Development , Fertilization in Vitro , Intelligence , Motor Skills , Sperm Injections, Intracytoplasmic , Case-Control Studies , Child, Preschool , Europe , Female , Fertilization , Humans , Male , Psychological Tests , Reference Values , Selection Bias
7.
Hum Reprod ; 19(6): 1480-7, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15105405

ABSTRACT

BACKGROUND: ICSI is used with increasing frequency, but there is less information about the children born following this method of assisted reproduction than other forms of IVF. Some authors have suggested that it may contribute to more family stress than IVF. METHODS: ICSI conceived children were compared with IVF conceived children and naturally conceived (NC) controls. They were selected in five European countries: Belgium, Denmark, Greece, Sweden and the UK, and seen for psychological testing and a paediatric examination when they were 5 years old. In all countries, except Greece, mothers and fathers were asked to complete questionnaires about parental well-being, family relationships, parenting and child behaviour. RESULTS: Very few differences were found between the ICSI and NC group or the ICSI and IVF group. The only significant differences were that mothers in the ICSI conceived group reported fewer hostile or aggressive feelings towards the child and higher levels of commitment to parenting than the mothers of NC children. CONCLUSIONS: The study confirms the results of previous work with IVF families. This should be encouraging for families using these techniques in the future.


Subject(s)
Child Development , Emotions , Family Relations , Fertilization in Vitro , Social Behavior , Sperm Injections, Intracytoplasmic , Adult , Aggression , Case-Control Studies , Child, Preschool , Europe , Female , Hostility , Humans , Male , Mothers/psychology , Parent-Child Relations , Parenting/psychology , Physical Examination , Psychological Tests
8.
Health Soc Care Community ; 11(2): 95-102, 2003 Mar.
Article in English | MEDLINE | ID: mdl-14629211

ABSTRACT

The present study was designed to describe the pattern of long-term formal support received by people with mental disorders, and to investigate the relationship between the medical, psychological and social characteristics of the participants and types of formal support. This study is based on a cohort (n = 192) of people born in 1902 and 1903 in a community in Southern Sweden. The research participants were assessed using interviews, psychological tests and medical examinations. Information was collected about the use of primary healthcare and social services. The first assessment took place when the cohort was aged 67 years, and then on eight further occasions until they were 92. The participation rate ranged from 72% to 100%. During the observation period of 25 years, 53% of people with dementia eventually received both home help and institutional care compared to 34% of people with other psychiatric diagnoses and 12% of people with good mental health. The last group had all physical health problems and/or problems with activities of daily living. However, 35% of the dementia group, 46% with other psychiatric diagnoses and 52% of people with good mental health did not receive any formal support. Males and self-employed people were significantly less likely to use formal support. The institutionalised group reported loneliness significantly more often than the other two groups. In a logistic regression analysis, loneliness, low social class, high blood pressure and low problem-solving ability were predictors of formal support use. People with a mental disorder, including dementia, were significantly more likely to use formal support compared to people with good mental health. Social factors were the main factors predicting formal support.


Subject(s)
Community Mental Health Services/organization & administration , Health Services for the Aged/organization & administration , Mental Disorders/therapy , Needs Assessment/standards , Quality of Life , Social Support , Activities of Daily Living , Aged , Aged, 80 and over , Dementia/therapy , Female , Follow-Up Studies , Health Status , Humans , Male , Stress, Psychological , Sweden
9.
Clin Endocrinol (Oxf) ; 59(4): 482-6, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14510911

ABSTRACT

OBJECTIVE: Leptin and growth hormone-binding protein (GHBP) both show gender differences that might be explained by sex hormones. To study the potential relevance of oestradiol and testosterone, we have examined 80-year-old subjects in whom oestradiol is higher in men than in women. The interrelationships between leptin, insulin, GHBP and fat mass in this age group were also investigated. DESIGN AND SUBJECTS: Ninety-four subjects (55 females and 39 males), all 80 years old, were investigated in a community-based study. None of the investigated subjects was being treated for diabetes mellitus and none of the women had oestrogen replacement. METHODS: Levels of testosterone, oestradiol, SHBG, IGF-I, GHBP, glucose, insulin and leptin were analysed. Body composition was measured with bioimpedance analysis (BIA). RESULTS: As in younger age groups, serum leptin, the ratio leptin/kilogram fat mass and serum GHBP were higher in the women (all, P< or =0.007), although serum oestradiol was higher in the men (P<0.001). There were no significant associations between sex hormones and leptin or GHBP either in women or in men (all, r<0.13, P>0.1). Leptin correlated to kilogram fat mass in both women (r=0.55, P<0.001) and men (r=0.47, P=0.003), but in contrast, there were no significant correlations between GHBP and fat mass and GHBP and IGF-I, either in women or in men (all, r<0.24, P>0.2). Insulin and leptin were significantly associated with GHBP, both in women (r=0.48, P<0.001 and r=0.43, P=0.001, respectively) and in men (r=0.40, P=0.01 and r=0.34, P=0.03, respectively). CONCLUSIONS: Although the 80-year-old men had higher oestradiol levels than the women, the women had higher levels of leptin and GHBP. There were no correlations between sex hormones and leptin and GHBP, which indicates that the gender differences are not caused by sex hormones in old age. In contrast to studies in younger subjects, GHBP did not correlate to fat mass in the investigated 80-year-old men and women. In the older subjects investigated, as in younger subjects, GHBP was significantly correlated with leptin and insulin.


Subject(s)
Carrier Proteins/blood , Gonadal Steroid Hormones/blood , Leptin/blood , Aged , Aged, 80 and over , Cohort Studies , Estradiol/blood , Female , Humans , Male , Sex Factors , Sex Hormone-Binding Globulin/analysis , Testosterone/blood
10.
Aging Ment Health ; 7(1): 61-72, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12554316

ABSTRACT

One hundred and sixty-eight men who were participants in the study "Men born in 1914" had their blood pressure and cognitive function examined when they were 68 years old. They were then re-examined at the age of 81. Decline on five standardized cognitive tests at the age of 81 years was studied in relation to four levels of baseline blood pressure at the age of 68. Results from multivariate analyses suggested that blood pressure, when studied in conjunction with other factors related to cognitive function, contribute to a rather modest extent and not unambiguously to the variability in cognitive decline. When decline on each separate test had been combined into a composite measure, where equal weight had been given to memory, crystallized and fluid abilities, it was shown that hypertension stage 2 (SBP 160-179 mmHg or DBP 100-109 mmHg) was associated with greater levels of overall decline. Hypertension stage 3 (SBP > or =180 mmHg or DBP > or =110 mmHg), on the other hand, was associated with lower levels of overall decline. Depressive symptoms at follow-up had a negative effect on cognitive levels and were discussed as potential confounders of hypertension-related cerebral lesions.


Subject(s)
Cognition Disorders/epidemiology , Hypertension/epidemiology , Aged , Aged, 80 and over , Cognition Disorders/diagnosis , Cohort Studies , Depression/diagnosis , Depression/psychology , Follow-Up Studies , Humans , Hypertension/diagnosis , Male , Neuropsychological Tests , Predictive Value of Tests , Prospective Studies , Severity of Illness Index , Surveys and Questionnaires
11.
Acta Paediatr ; 91(8): 946-51, 2002.
Article in English | MEDLINE | ID: mdl-12222720

ABSTRACT

UNLABELLED: Previous studies have indicated that foetomaternal infection increases the risk of spastic cerebral palsy (CP) in term infants, whereas this association appears to be less evident in preterm infants. The aim of this study was to analyse infection-related risk factors for spastic CP in preterm infants. A population-based series of preterm infants with spastic CP, 91 very preterm (<32 wk) and 57 moderately preterm (32-36 wk), born in 1983-90, were included and matched with a control group (n = 296). In total, 154 maternal, antenatal and intrapartal variables were retrieved from obstetric records. In the entire group, histological chorioamnionitis/pyelonephritis, long interval between rupture of membranes and birth, admission-delivery interval <4 h and Apgar scores of <7 at 1 min just significantly increased the risk of CP, and Apgar scores of <7 at 5 and 10 min were strongly associated with an increased risk. Abruptio placentae, Apgar scores <7 at 1 min and pathological non-stress test (reason for delivery) were significant risk factors of CP only in the moderately preterm and hemiplegic groups, whereas fever before delivery was a significant risk factor in the very preterm and spastic diplegic groups. Antibiotics during pregnancy was associated with CP only in the spastic diplegic CP group. CONCLUSION: Antenatal infections marginally increased the risk of CP. Low Apgar score and abruptio placentae were associated with CP, especially in moderately preterm infants with hemiplegic CP.


Subject(s)
Cerebral Palsy/etiology , Infant, Premature , Obstetric Labor Complications , Pregnancy Complications, Infectious , Apgar Score , Birth Weight , Case-Control Studies , Cohort Studies , Female , Gestational Age , Humans , Infant, Newborn , Male , Pregnancy , Risk Factors
12.
Aging Ment Health ; 6(2): 178-85, 2002 May.
Article in English | MEDLINE | ID: mdl-12028888

ABSTRACT

Quality of life has various dimensions with multiple meanings for people. One vital issue is whether a person's subjective experienced quality of life correlates with his or her personality. Several studies show a correlation between personality and quality of life, life satisfaction or well-being. The aim of this study was to examine the relationship between personality and life quality, in particular the way in which multi-dimensional conceptualization of personality relates to a multi-dimensional definition of life quality. Seventy-eight elderly individuals completed a quality of life questionnaire, the Lund Gerontology Centre's Life Quality Questionnaire (LGC), and a personality questionnaire, the Gordon Personal Profile Inventory (GP:A). Discriminant analysis showed that various personality characteristics relate to different aspects of life quality. Vigour alone predicted current quality of life, while emotional stability was related to psychological well-being and satisfaction with significant relationships. Ascendancy and ability to maintain personal relations were related to an optimistic outlook on life and absence of psychosomatic symptoms. Original thinking and sociability related to increased psychosomatic symptoms and sociability also correlated negatively with satisfaction with significant relationships. The results support the idea that various personality characteristics are related to various life quality dimensions in the investigated group, increasing the understanding of unique experience of life quality for each individual.


Subject(s)
Aging/psychology , Personality , Quality of Life , Social Behavior , Aged , Aged, 80 and over , Cross-Sectional Studies , Female , Humans , Interpersonal Relations , Male , Middle Aged , Psychometrics , Surveys and Questionnaires
13.
Neuropediatrics ; 33(6): 324-6, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12571789

ABSTRACT

From a follow-up series of 24 classical Rett syndrome females (13-59 years of age), side asymmetries of neuroimpairments were systematically investigated. A characteristic right-sided dominance in terms of dysfunction and neurology was revealed. Differences in the perinatal/early postnatal development of finer brain net structures between brain halves are suggested as a possible explanation.


Subject(s)
Functional Laterality/genetics , Neurologic Examination , Rett Syndrome/genetics , Adolescent , Adult , Female , Follow-Up Studies , Functional Laterality/physiology , Humans , Middle Aged , Rett Syndrome/diagnosis
14.
Brain Dev ; 23 Suppl 1: S28-31, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11738838

ABSTRACT

Rett syndrome, today known as a worldwide important cause behind severe mental retardation in females, has been seen in Sweden since the 1960s (the senior author). This study gives population representative clinical and sociomedical follow-up data from West Sweden (1/4 of the population in Sweden). The series comprises 54 females diagnosed in 1971-1998, 5-60 years old, median age 20. Mortality in 1971-2000 was 18% (10/54), median age at death 20. Death usually had been sudden and unexpected. The sociomedical follow-up emphasized the adult group. The large majority had usually moved to small group homes, a good and well-accepted environment once the staff had learned the particularities of these so uniquely neurodevelopmentally disabled women.


Subject(s)
National Health Programs/statistics & numerical data , Rett Syndrome/therapy , Social Support , Adolescent , Adult , Age Factors , Child , Child, Preschool , Female , Follow-Up Studies , Group Homes , Humans , Middle Aged , National Health Programs/organization & administration , Quality of Health Care , Rett Syndrome/mortality , Rett Syndrome/psychology , Sweden
15.
Brain Dev ; 23 Suppl 1: S224-6, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11738877

ABSTRACT

Through 1998-1999 the Swedish research team have systematically mapped 45 of 54 females with Rett syndrome (RS) aged 5-57 years (Berg M. Uppföljning av flickor med Rett syndrom i Västsverige. Socialmedicinsk kartläggning, Stencilerad rapport, Sahlgrenska universitetssjukhuset, Göteborg, 1999; Läkartidningen (Swedish Medical Journal) 96 (1999) 5488). The emphasis is on the RS females' adjustment to grown-up living. At an adult age the large majority moved over to a Swedish type of small group home. We visited these girls in their group homes and got information about their adaptation to this special home situation. We noted their behaviour and contact with the staff and interviewed their parents. The results showed that the young women usually had adjusted well. The adjustment seemed to depend on the degree of planning before the girls moved from their parents to special group homes. These seem to provide a good environment for the RS females, in respect of both physical and social aspects. Although neuropaediatrics in Sweden today has advanced in RS knowledge, the result from this research shows that in Swedish society there is still a great ignorance of RS, even among medical professionals. In particular there is a gap of knowledge when the medical responsibility had to be transferred over to adult medicine. Many of the parents emphasized the great importance of how they were listened to by professionals in public medical and social services. It is essential that professionals always listen to information from parents and personal assistants.


Subject(s)
Rett Syndrome/psychology , Social Support , Adaptation, Psychological , Adolescent , Adult , Child , Child, Preschool , Female , Follow-Up Studies , Group Homes , Humans , Middle Aged , Patient Care Team , Quality of Health Care , Rett Syndrome/mortality , Rett Syndrome/therapy , Sweden , Time Factors
16.
Exp Aging Res ; 27(4): 319-40, 2001.
Article in English | MEDLINE | ID: mdl-11681196

ABSTRACT

Hypertension and its consequences on cognition was analyzed using data from the study "Men born in 1914" in Malmö, Sweden, a prospective cohort study of cardiovascular disease. The baseline examinations took place in 1982/83 where 500 men participated in extensive medical and social examinations. A neuropsychological investigation was completed including five standardized cognitive tests. The specific purpose of the study was to investigate whether hypertension was associated with cognitive performance. By the use of multiple regression analyses, normal blood pressure and three stages of hypertension were analyzed in relation to test performance. Hypertension Stage 3 was associated with lower performance on tests measuring psychomotor speed and visuospatial memory, whereas hypertension Stage 1 was associated with higher performance on tests measuring verbal ability and constructional ability. The associations were unconfounded by clinical manifestations of atherosclerosis, history of stroke, depressive mood, and antihypertensive drug treatment.


Subject(s)
Cognition , Geriatric Psychiatry , Hypertension/psychology , Aged , Humans , Male , Multivariate Analysis , Population Surveillance , Sweden
17.
Neuropediatrics ; 32(4): 217-8, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11571704

ABSTRACT

Mutations in the MECP2 gene are known to be associated with Rett Syndrome (RTT) in the large majority of sporadic cases. Four Swedish families with a total of eight RTT patients (two in each family), were screened and found negative for MECP2 mutations. The series included females with both classical and forme fruste phenotypes. Rett syndrome thus might still be complex and genetically multifactorial.


Subject(s)
Chromosomal Proteins, Non-Histone , DNA-Binding Proteins/genetics , Repressor Proteins , Rett Syndrome/genetics , Adult , Aged , Child , DNA Mutational Analysis , Female , Humans , Methyl-CpG-Binding Protein 2 , Middle Aged , Mutation , Phenotype , Polymerase Chain Reaction , Sweden
18.
Stroke ; 32(8): 1712-20, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11486095

ABSTRACT

BACKGROUND AND PURPOSE: Although hypertension is a major risk factor for stroke, many hypertensive persons remain healthy. The aim of the present study was to analyze whether adaptation in a stressful situation was associated with the incidence of stroke in hypertensive men. METHODS: Two hundred thirty-eight hypertensive men were followed from baseline in 1982/1983 until first stroke, death, or December 31, 1996. Adaptation to stress was studied with the serial Color-Word Test. In the Regression dimension, 4 patterns of adaptation could be distinguished according to mastering of the test. Successful mastering of the test was shown in stabilized patterns, increasing difficulty in cumulative patterns, fluctuating difficulty in dissociative patterns, and fluctuating difficulty that increased during testing in cumulative-dissociative patterns. The patterns were compared regarding stroke incidence. RESULTS: Forty-three men experienced a stroke during follow-up. Stroke rates per 1000 person-years were 12.6 for men with stabilized patterns, 14.3 for men with cumulative patterns, 16.2 for men with dissociative patterns, and 31.2 for men with cumulative-dissociative patterns. Multivariate analysis, adjusted for relevant cerebrovascular risk factors, showed that the cumulative-dissociative pattern of the Regression dimension was associated with an increased risk of stroke during follow-up (relative risk 3.00, 95% CI 1.32 to 6.81). CONCLUSIONS: The specific behavior pattern, characterized by the greatest difficulties in managing the test, was associated with incidence of stroke in hypertensive men. One interpretation is that hypertensive men who chronically fail to find successful strategies in stressful situations are vulnerable to the damaging effects of stress and thereby at an increased risk of a future stroke.


Subject(s)
Adaptation, Psychological , Hypertension/epidemiology , Stress, Psychological/epidemiology , Stress, Psychological/psychology , Stroke/epidemiology , Adaptation, Psychological/classification , Cohort Studies , Comorbidity , Disease-Free Survival , Follow-Up Studies , Humans , Incidence , Male , Multivariate Analysis , Neuropsychological Tests , Prospective Studies , Risk Factors , Sweden/epidemiology
19.
Lakartidningen ; 98(20): 2457-62, 2001 May 16.
Article in Swedish | MEDLINE | ID: mdl-11433977

ABSTRACT

A number of models of aging have identified predictors of longevity, well-being and life quality among the elderly. The predictive patterns are multifactorial, and in all models psychological aspects are important. Most of all it is a matter of personality, intellectual functioning, adaptive capacity and coping, as well as making use of one's life-spain experiences. Personality, by consensus deemed to be essentially stable all through life, exerts a constant influence on the individual for better or for worse, steering the individual toward excessive wear and tear or constructive development and maturity. Some aspects of intellectual functioning are more important than others in this context, e.g. crystallized and fluid intelligence and episodic short term memory. Crystallized intelligence usually remains unchanged throughout life and even improves with age, while fluid intelligence and episodic memory decline. In very old age as for instance in centenarians, fluid intelligence is found to be a very strong predictor of future survival. Among the elderly in general, terminal decline is evident shortly before death. Coping strategies and capacity combined with type of incidents, change or threat are found to be strong predictors of both life satisfaction and survival after 80 years of age. Identifying the importance of coping in old age has brought about a change in perspective in caring for the elderly in which the psychological aspects become more important as a complement to the medical model. Increasingly, autobiographical reflections or life-story telling, also when used in group sessions, is shown to be one way of increasing well-being and life satisfaction among the elderly.


Subject(s)
Aging/psychology , Longevity , Adaptation, Psychological , Aged , Aged, 80 and over/psychology , Humans , Intelligence , Personal Satisfaction , Personality , Quality of Life
20.
Eur Child Adolesc Psychiatry ; 10(2): 117-21, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11469283

ABSTRACT

Rett syndrome (RS) is a neurodevelopmental disorder almost exclusively affecting females. We have studied the mutation spectrum of the responsible gene MECP2, encoding methyl-CpG-binding protein 2 (MeCP2), in 16 sporadic classical RS females from Sweden. In 13 of 16 patients (81%) we detected nonsense or missense mutations in the coding parts of MECP2. This mutation rate is in agreement with other reports (65-80%). In all, 12 different mutations and one polymorphism were found; three of the mutations have not been reported previously. The missense mutations were restricted to highly conserved regions of the gene. None of the mutations was detected in parents; thus, they had probably arisen de novo. In contrast, two normal variants, one intron deletion and one silent mutation, were seen singly only in two patients' mothers; neither has been reported previously. One patient showed two different mutations closely located, i.e. 802C > T (R268W) together with 808C > T (R270X). Another patient had a mutation in the stop codon 1459T > C (X487R), leading to a gene product prolonged with 27 amino acids. In conclusion, our results indicate that the majority of Swedish RS patients (81%) have mutations in MECP2 that are sporadic cases with de novo mutations. Moreover, both missense and nonsense mutations occur, but in different parts of the gene, probably reflecting the function of the domains in MeCP2. This study has improved our ability to offer these families an early confirmation of Rett diagnoses.


Subject(s)
Chromosomal Proteins, Non-Histone , DNA-Binding Proteins/genetics , Genetic Testing , Mutation, Missense/genetics , Repressor Proteins , Rett Syndrome/genetics , Child , Exons , Female , Genetic Carrier Screening , Humans , Methyl-CpG-Binding Protein 2 , Polymorphism, Genetic/genetics , Rett Syndrome/diagnosis , Sweden , Trinucleotide Repeats
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