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Träfflista för sökning "WFRF:(Herlitz Agneta) srt2:(2010-2014)"

Sökning: WFRF:(Herlitz Agneta) > (2010-2014)

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1.
  • Herlitz, Agneta, et al. (författare)
  • A life-span approach to dementia
  • 2013
  • Ingår i: Dementia and Memory. - New York : Psychology Press. - 9781848722927 ; , s. 110-123
  • Bokkapitel (övrigt vetenskapligt/konstnärligt)
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2.
  • Herlitz, Agneta, et al. (författare)
  • Cognition
  • 2012
  • Ingår i: Handbook of clinical gender medicine. - Basel : S. Karger. - 9783805599290 ; , s. 504-507
  • Bokkapitel (refereegranskat)abstract
    • There are sex differences favoring men in visuospatial abilities and mathematical problem solving, whereas women outperform men on verbal production tasks, verbal episodic memory tasks, and face recognition. These differences are present in childhood, adolescence, and middle and old age, and the pattern is also seen in non-Western societies. Social and cultural factors affect the magnitude of these differences, but not the pattern. Prenatal levels of androgens affect play behavior, but have little influence on cognitive performance. For older adults, hormone treatment of estradiol and testosterone does not seem to affect cognitive sex differences or cognitive performance.
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3.
  • Herlitz, Agneta, et al. (författare)
  • Cognitive Sex Differences Are Not Magnified as a Function of Age, Sex Hormones, or Puberty Development During Early Adolescence
  • 2013
  • Ingår i: Developmental Neuropsychology. - : Informa UK Limited. - 8756-5641 .- 1532-6942. ; 38:3, s. 167-179
  • Tidskriftsartikel (refereegranskat)abstract
    • Are cognitive sex differences magnified by individual differences in age, sex hormones, or puberty development? Cross-sectional samples of 12- to 14-year-old boys (n = 85) and girls (n = 102) completed tasks assessing episodic memory, face recognition, verbal fluency, and mental rotations. Blood estradiol, free testosterone, and self-rated puberty scores were obtained. Sex differences were found on all cognitive measures. However, the magnitude was not larger for older children, hormones and cognitive performance were not associated, and early maturers did not perform better than late maturers. Thus, cognitive sex differences were not associated with age, levels of sex hormones, or puberty development.
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4.
  • Laukka, Erika J., et al. (författare)
  • Genetic Effects on Old-Age Cognitive Functioning : A Population-Based Study
  • 2013
  • Ingår i: Psychology and Aging. - : American Psychological Association (APA). - 0882-7974 .- 1939-1498. ; 28:1, s. 262-274
  • Tidskriftsartikel (refereegranskat)abstract
    • Associations between genotypes and cognitive outcomes may provide clues as to which mechanisms cause individual differences in old-age cognitive performance. We investigated the effects of five polymorphisms on cognitive functioning in a population-based sample of 2,694 persons without dementia (60-102 years). A structural equation model (SEM) was fit to the cognitive data, yielding five specific latent factors (perceptual speed, episodic memory, semantic memory, category fluency, and letter fluency), as well as a global cognitive factor. These factors showed the expected associations with chronological age. Genotyping was performed for five single-nucleotide polymorphisms that have been associated with cognitive performance: APOE (rs429358), COMT (rs4680), BDNF (rs6265), KIBRA (rs17070145), and CLSTN2 (rs6439886). After controlling for age, gender, and education, as well as correcting for multiple comparisons, we observed negative effects of being an APOE ε4 carrier on episodic memory and perceptual speed. Furthermore, being a CLSTN2 TT carrier was associated with poorer semantic memory. For the global factor, the same pattern of results was observed. In addition, being a BDNF any A carrier was associated with better cognitive performance. Also, older age was associated with stronger genetic effects of APOE on global cognition. However, this interaction effect was partly driven by the presence of preclinical dementia cases in our sample. Similarly, excluding future dementia cases attenuated the effects of APOE on episodic memory and global cognition, suggesting that part of the effects of APOE on old-age cognitive performance may be driven by dementia-related processes.
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5.
  • Libungan, Berglind, et al. (författare)
  • Secondary prevention in coronary artery disease. Achieved goals and possibilities for improvements.
  • 2012
  • Ingår i: International journal of cardiology. - : Elsevier BV. - 1874-1754 .- 0167-5273. ; 161:1, s. 18-24
  • Tidskriftsartikel (refereegranskat)abstract
    • AIM: To describe presence of risk indicators of recurrence 6months after hospitalisation due to coronary artery disease at a university clinic. METHODS: The presence of risk indicators, including tobacco use, lipid levels, blood pressure and glucometabolic status, including 24-hour blood pressure monitoring and an oral glucose-tolerance test, was analysed. RESULTS: Of 1465 patients who were screened, 402 took part in the survey (50% previous myocardial infarction and 50% angina pectoris). Mean age was 64years (range 40-85years) and 23% were women. Present medications were: lipid lowering drugs (statins; 94%), beta-blockers (85%), aspirin or warfarin (100%) and ACE-inhibitors or angiotensin II blockers (66%). Values above target levels recommended in guidelines were: a) low density lipoprotein (LDL) in 40%; b) mean blood pressure (day or night) in 38% and c) smoking in 13%. Of all patients, 66% had at least one risk factor (LDL or blood pressure above target levels or current smoking). An abnormal glucose-tolerance test was found in 59% of patients without known diabetes. If no history of diabetes, 85% had either LDL or blood pressure above target levels, current smoking or an abnormal glucose-tolerance test. However, with treatment intensification to patients with elevated risk factors 56% reached target levels for blood pressure and 79% reached target levels for LDL. CONCLUSION: Six months after hospitalisation due to coronary artery disease, despite the high use of medication aimed at prophylaxis against recurrence, the majority were either above target levels for LDL or blood pressure or continued to smoke.
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6.
  • Lovén, Johanna, et al. (författare)
  • Who are you looking at? : The influence of face gender on visual attention and memory for own- and other-race faces
  • 2012
  • Ingår i: Memory. - : Informa UK Limited. - 0965-8211 .- 1464-0686. ; 20:4, s. 321-331
  • Tidskriftsartikel (refereegranskat)abstract
    • Previous research suggests that the own-race bias (ORB) in memory for faces is a result of other-race faces receiving less visual attention at encoding. As women typically display an own-gender bias in memory for faces and men do not, we investigated whether face gender and sex of viewer influenced visual attention and memory for own- and other-race faces, and if preferential viewing of own-race faces contributed to the ORB in memory. Participants viewed pairs of female or male own- and other-race faces while their viewing time was recorded. Afterwards, they completed a surprise memory test. We found that (1) other-race males received the initial focus of attention, (2) own-race faces were viewed longer than other-race faces over time, although the difference was larger for female faces, and (3) even though longer viewing time increased the probability of remembering a face, it did not explain the magnified ORB in memory for female faces. Importantly, these findings highlight that face gender moderates attentional responses to and memory for own- and other-race faces.
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7.
  • Lovén, Johanna, et al. (författare)
  • Women's own-gender bias in face recognition memory : the role of attention at encoding
  • 2011
  • Ingår i: Experimental psychology (Göttingen). - Göttingen : Hogrefe & Huber Publishers. - 1618-3169 .- 2190-5142. ; 58:4, s. 333-340
  • Tidskriftsartikel (refereegranskat)abstract
    • Women remember more female than male faces, whereas men do not seem to display an own-gender bias in face recognition memory. Why women remember female faces to a greater extent than male faces is unclear; one proposition is that women attend more to and thereby process female faces more effortfully than male faces during encoding. A manipulation that distracts attention and reduces effortful processing may therefore decrease women's own-gender bias by reducing memory for female faces relative to male faces. In three separate experiments, women and men encoded female and male faces for later recognition in full attention and divided attention conditions. Results consistently showed that women, in contrast to men, displayed a reliable own-gender bias. Importantly, the magnitude of women's own-gender bias was not reduced in divided attention conditions, indicating that it is not a result of effortful processing of female faces. We suggest these results reflect that women have greater perceptual expertise for female faces, facilitating recognition memory.
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8.
  • Lövén, Johanna, et al. (författare)
  • Face gender modulates women’s brain activity during face encoding
  • 2014
  • Ingår i: Social Cognitive & Affective Neuroscience. - Oxford : Oxford University Press. - 1749-5016 .- 1749-5024. ; 9:7, s. 1000-1005
  • Tidskriftsartikel (refereegranskat)abstract
    • Women typically remember more female than male faces, whereas men do not show a reliable own-gender bias. However, little is known about the neural correlates of this own-gender bias in face recognition memory. Using functional magnetic resonance imaging (fMRI), we investigated whether face gender modulated brain activity in fusiform and inferior occipital gyri during incidental encoding of faces. Fifteen women and 14 men underwent fMRI while passively viewing female and male faces, followed by a surprise face recognition task. Women recognized more female than male faces and showed higher activity to female than male faces in individually defined regions of fusiform and inferior occipital gyri. In contrast, men's recognition memory and blood-oxygen-level-dependent response were not modulated by face gender. Importantly, higher activity in the left fusiform gyrus (FFG) to one gender was related to better memory performance for that gender. These findings suggest that the FFG is involved in the gender bias in memory for faces, which may be linked to differential experience with female and male faces.
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9.
  • Persson, Jonas, et al. (författare)
  • Remembering our origin : Gender differences in spatial memory are reflected in gender differences in hippocampal lateralization
  • 2013
  • Ingår i: Behavioural Brain Research. - : Elsevier. - 0166-4328 .- 1872-7549. ; 256, s. 219-228
  • Tidskriftsartikel (refereegranskat)abstract
    • Gender differences in spatial memory favoring men are frequently reported, and the involvement of the hippocampus in these functions is well-established. However, little is known of whether this behavioral gender difference is mirrored in a gender difference in hippocampal function. Here we assessed hippocampal activity, using functional MRI, while 24 men and women moved through three-dimensional virtual mazes (navigation phase) of varying length, and at the end-point estimated the direction of the starting-point (pointing phase). Men were indeed more accurate than women at estimating direction, and this was especially true in longer mazes. Both genders activated the posterior hippocampus throughout the whole task. During the navigation phase, men showed a larger activation in the right hippocampus than women, while in the pointing phase, women showed a larger activation in the left hippocampus than men. Right-lateralized activation during the navigation phase was associated with greater task performance, and may reflect a spatial strategy that is beneficial in this task. Left-sided activation during the pointing phase might reflect a less efficient post hoc verbal recapitulation of the route. This study is the first to identify neural correlates of the commonly observed male advantage in recalling one's original position, and points to hippocampal lateralization as a possible explanation for this behavioral gender difference. (C) 2013 Elsevier B.V. All rights reserved.
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10.
  • Persson, Jonas, et al. (författare)
  • Sex differences in volume and structural covariance of the anterior and posterior hippocampus
  • 2014
  • Ingår i: NeuroImage. - : Elsevier BV. - 1053-8119 .- 1095-9572. ; :99, s. 215-25
  • Tidskriftsartikel (refereegranskat)abstract
    • Sex differences in episodic and spatial memory are frequently observed, suggesting that there may be sex-related structural differences in the hippocampus (HC). Earlier findings are inconsistent, possibly due to a known variability along the hippocampal longitudinal axis. Here, we assessed potential sex differences in hippocampal volume and structural covariance with the rest of the brain in young men and women (N=76), considering the anterior (aHC) and posterior (pHC) hippocampus separately. Women exhibited a larger pHC than men adjusted for brain size. Using partial least squares, we identified two significant patterns of structural covariance of the aHC and pHC. The first included brain areas that covaried positively and negatively in volume with both the aHC and pHC in men, but showed greater covariance with the aHC than pHC in women. The second pattern revealed distinct structural covariance of the aHC and pHC that showed a clear difference between men and women: in men the pHC showed reliable structural covariance with the medial and lateral parietal lobes and the prefrontal cortex, whereas in women the aHC showed reliable structural covariance with the anterior temporal lobe bilaterally. This pattern converges with resting state functional connectivity of the aHC and pHC and suggests that these hippocampal sections interact with different brain regions, consistent with a division of labor with regards to episodic and spatial memory. Our findings lend support to a division of the HC into an anterior and posterior part and identify sex as a potential moderating factor when investigating hippocampal structure and connectivity.
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