The effects of background white noise on memory performance in inattentive school children
© Söderlund et al; licensee BioMed Central Ltd. 2010
Received: 2 March 2010
Accepted: 29 September 2010
Published: 29 September 2010
Noise is typically conceived of as being detrimental for cognitive performance; however, a recent computational model based on the concepts of stochastic resonance and dopamine related internal noise postulates that a moderate amount of auditive noise benefit individuals in hypodopaminergic states. On the basis of this model we predicted that inattentive children would be enhanced by adding background white noise while attentive children's performance would deteriorate.
Fifty-one secondary school pupils carried out an episodic verbal free recall test in two noise conditions. In the high noise condition, verb-noun sentences were presented during auditory background noise (white noise, 78 dB), and in the low noise condition sentences were presented without noise.
Exposure to background noise improved performance for inattentive children and worsened performance for attentive children and eliminated episodic memory differences between attentive and inattentive school children.
Consistent with the model, our data show that cognitive performance can be moderated by external background white noise stimulation in a non-clinical group of inattentive participants. This finding needs replicating in a larger sample using more noise levels but if replicated has great practical applications by offering a non-invasive way to improve school results in children with attentional problems.
It has long been known that cognitive processing is easily disturbed by incompatible environmental stimulation which distracts attention from tasks . This effect is believed to stem from competition for attentional resources between the distracting and the target stimuli. Such negative distractor effects hold across a wide variety of tasks and stimuli as well as in different participant populations [2–6]. For some populations the effects are predicted to be especially strong. For instance, individuals with attentional problems such as attention deficit/hyperactivity disorder (ADHD) are generally acknowledged to be more vulnerable to distraction than normal control children [7, 8].
At the same time there are reports of contradictory findings where certain types of task irrelevant noise actually improve the performance of children. Surprisingly, this effect may also be most pronounced in children with attention deficits. Under certain circumstances children with attentional problems (including those with ADHD) benefit from, rather than being distracted by, background task-irrelevant noise presented concurrently with a target task. For instance, Stansfeld et al.  found that under certain conditions road traffic noise can improve performance on episodic memory tasks in children at risk for attentional problems and academic under-achievement. Research data from our group demonstrated that adding background white noise to the environment enhanced memory performance of children with ADHD ; although in every day situations optimal levels of white noise will vary from one individual to another.
Why these paradoxical effects should occur is not well understood. Most accounts in the past, for example the optimal stimulation theory by Zentall and Zentall  and later models of cognitive energetic and motivational processes , have focused on the role of background stimulation as a generator of increased arousal which counteracts boredom. A recent computational model has attempted to explain these positive effects of background noise on performance in a different way . This model combines two factors: It explains (i) how noise enhances attention and performance in general by the concept of stochastic resonance (SR) and (ii) why there are individual differences in the way noise affects the brain by a model of individual differences in dopamine.
Stochastic Resonance - how noise strengthens the signal
SR or noise-improved signaling is a well-established phenomenon across a range of experimental settings; SR exists in any threshold-based system with noise that requires a threshold to be passed before a signal is registered. SR can be observed in nature in any non-linear dynamic system, which is not working at its optimum level, in particular SR has been found in the nervous system. The simplest examples of an SR-related benefit can be seen in the detection of sensory signals. When a weak signal (e.g. a tone stimulus) is presented below the hearing threshold it becomes detectable when random or white noise is added to the signal. In essence, this account proposes that the additional variability provided by the noise interacts with the weak signal pushing it above the detection threshold, see review in . For instance, SR has been found in several modalities; audition , vision , and touch  where stochastic noise improves sensory discriminability. Recently SR has been shown to work across modalities, for example when auditory noise improves visual signal detection . Most SR studies have used perception tasks, requiring the detection of weak peripheral sensory inputs. Few studies have examined how noise influences cognitive performance. Recent empirical evidence suggests that SR can also improve central processing and cognitive performance. For example, SR has been found in cognitive tasks where auditory noise improved the speed of arithmetic computations  and recall on visual memory tasks . Thus, adding noise to the input of the information processing system can increase its signal-to-noise output. SR is usually quantified by plotting detection, or cognitive performance, as a function of noise intensity. This relationship follows an inverted U-curve function, where performance peaks at a moderate noise level. That is, moderate noise is beneficial for performance whereas too little, or too much, noise attenuates performance. For extensive reviews on the influence of noise on the nervous system the reader is referred to recent reviews [14, 21]. Also detrimental effects of noise on the nervous system and in particular on speech processing are reported in a recent review .
Individual differences in the SR effect
The novel aspect of the proposed framework is that the SR phenomena differs between individuals and these differences are linked to attention ability and neurotransmission in the brain in such way that inattentive persons need more external noise for a proper cognitive functioning. In the model dopamine is the crucial neurotransmitter. This is because it modulates the neural cell's responses to the environment and determines the probability that it will fire following the presentation of a stimulus . Alterations in dopamine function are related to individual differences in attention [24, 25], cognition  and motivated behavior [27, 28]. Dopamine release has both tonic (background levels) and phasic (response to specific environmental events) components regulated by different brain regions [29, 30]. Tonic dopamine levels are suggested to modulate the phasic reactivity; a low tonic level increases stimulus dependent phasic release, and the opposite, a high tonic level suppresses phasic release . Low tonic levels cause neural instability associated with cognitive symptoms such as failure to sustain attention . The hypodopaminergic state in ADHD is distinguished by low tonic dopamine levels leading to excessive reactivity to environmental stimulation [33, 34]. If the firing probability or gain parameter is low, neurons will fire at random yielding poor cognitive performance. If the gain parameter is high there will be cognitive stability and thus high performance. This responsiveness of neurons is modulated via dopamine that enhances the differentiation between efferent firing and afferent external stimulation. It has been shown recently that neural noise related to dopamine tone is an integral part of inter-neuronal communication and that a sufficient level of noise may be necessary for normal function in the nervous system [21, 35], through the process of SR. That is, there exists both external noise - outside of the nervous system - and neural noise (related to dopamine tone) inside the system.
In this paper we investigate, for the first time, how noise influences cognitive performance in a normal, non-clinical, group of children that differ from each other in their attentional abilities. Recent evidence suggests that dopamine plays a role in attention also in non-clinical groups. When a visual orienting task was used to study a normal group of children, it was found that those children who were homozygous for alleles influencing dopamine transportation displayed inattention on left-hand sided stimuli, whereas those who were heterozygotes did not . The response to amphetamine has also been found to be influenced by genetic factors; it depends on the functional polymorphisms of the Catechol O-methyltranserase (COMT) gene in a normal population of humans. Mattay et al.  found that amphetamine enhanced prefrontal efficiency measured by fMRI for the val/val (high DA metabolism) genotype, whereas met/met (low DA metabolism), had no such effect on low to medium workload, and decreased efficiency on high workload tasks. Furthermore, preservations errors were decreased by amphetamine in the val/val, but not the met/met groups, in a Wisconsin Card Sorting Test (WCST). In another study on healthy controls by Mattay et al.  dextroamphetamine was found to increase N-back working memory performance in group with low baseline working-memory capacity, whereas the performance worsened in a group with high baseline performance . Dextroamphetamine also had differential effects on the BOLD fMRI response on these groups. These findings have been corroborated in a study using a spatial working memory task where stimulant medication only improved memory performance in healthy individuals with low baseline working memory capacity . This was also mirrored by increased cerebral blood flow in dorsolateral prefrontal cortex and posterior parietal cortex. Taken together these studies indicate that dopamine function influences performance and brain activity differently also in groups consisting of healthy controls depending on tasks that are linked to attention and working memory (e.g., WCST, N-back, spatial working memory). This body of data is consistent with the view that ADHD and related attentional problems is best conceptualized as a continuum rather than a discrete category and that ADHD symptoms are distributed in populations . The syndrome of ADHD represents a transition of degree rather than of a kind and diagnostic thresholds are therefore somewhat arbitrary resting on general and cultural norms about behavior and development . In addition, a comparison of the extreme points in a normal distribution shows the same heritability patterns as a comparison between ADHD and control . This, in turn, suggests that non-clinical persons with low and high attention may show similar effect from noise as ADHD and control persons do.
In this paper, we study inattentive and normally attentive children's episodic memory in a verb-noun sentence recall task under two conditions varying in terms of the levels of background auditive white noise. Our prediction is that in the low noise condition the inattentive children will perform less well than attentive children while in the high noise condition these differences should diminish as the addition of white noise benefits the inattentive but not the normally attentive children.
Participant characteristics and cognitive test scores
Cognitive and behavioral measures
N = 41
(20 boys, 21 girls)
N = 10
(5 boys, 5 girls)
Attentive vs. Inattentive
(1 = low, 7 = high)
1 - 7
1 - 7
t(49) = 6.67***
(1 = low, 7 = high)
1 - 7
1 - 7
t(49) = 4.11***
(1 = below, 2 = average, 3 = above)
1 - 3
1 - 3
t(49) = 0.94
(1 = low, 7 = high)
1 - 7
1 - 7
t(49) = 2.38*
16 - 55
19 - 53
t(49) = 1.09
4 - 42
4 - 23
t(49) = 3.22**
2 - 34
7 - 18
t(49) = 0.97
We used a 2 × 2 design, where noise levels (low versus high) was the within participant manipulation and the between group variable was teacher rated classroom attention level (normal versus inattentive).
All participants undertook a verbal episodic recall test. The to-be-remembered (TBR) items consisted of 96 sentences divided into 8 separate lists with 12 verb-noun sentences in each list. Each sentence consisted of a unique verb and a unique noun (e.g., "roll the ball") in Norwegian. The sentences were placed in random order. List-order (1-8) and condition-order (no noise vs. noise) were counterbalanced and noise was present on every second list. All to-be-remembered sentences were recorded on a CD. A new item was read every 9th second. The sentences were read in both the low noise and the high noise condition. The equivalent continuous sound level of the white noise was 78 and the speech signal was 86 dB; thus the signal-to-noise ratio was 8 dB. The signal was sufficiently strong so that all participants could perceive the content of the words in both conditions without error (i.e., the tests were a cognitive memory test and not a perceptual test). The two noise levels were chosen to correspond to levels that have been found in earlier studies to affect cognition in an arithmetic's test for a normal population  and working memory performance in patients with Alzheimer's disease . Recordings were made in a sound studio.
The testing was conducted at the child's school, following permission from parents and children. The University College of Sogndal, Norway and the regional ethic board in Stockholm approved the study. The participants were tested individually in a room during the school day. The test lasted for about 45 minutes including the presentation of instructions. Before starting the experiment proper, two practice sentences were presented. The time taken to present each list was approximately 1 minute and 40 seconds. The to-be-remembered sentences were presented concurrent with continuous white noise during the encoding phase in the high noise condition and in silence in the low noise condition. Noise conditions changed after every sentence list in outbalanced order. No noise was presented during retrieval. Directly after presentation of the last item in a list, participants performed a free recall test in which they spoke out loud as many sentences as possible, in any order.
As reported above the two groups differed with respect to reading skills, as judged by teachers; with the inattentive group having inferior reading skills compared to the attentive group. However, when reading ability was added as a covariate to the main analysis the original interaction effect, although diminished, persisted (F(48,1) = 7.13, p = .010). Reading level was independently related to performance (F(6,1) = 1.46, p = .213). A Spearman's rank order correlation revealed negative correlation between reader skills and positive effect of noise (r = .335, N = 51, p = .016), a positive correlation between attention and reading ability (r = .498, N = 51, p < .001) and finally, a high positive correlation between teacher ratings of inattention and hyperactivity (r = .789, N = 51, p < .001). However, there was no correlation between hyperactivity and noise-effect (r = .141, N = 51, p = .323).
We have proposed a framework for understanding individual difference in the facilitative effects of auditive white noise on performance. As predicted the results show different effects of noise in attentive and inattentive children selected from the normal population. There was significant improvement in performance for the children rated as inattentive by their teachers, and a significant decline in performance for those rated as attentive as noise levels were increased. Furthermore these effects seem independent of other factors measured in the study - attentional ability seems to be a key marker of this effect. Even if inattention and hyperactivity are strongly correlated, no correlation between hyperactivity and a positive noise effect was found, this suggests that in this study inattention is the key factor to explain noise improvement. These results are similar to those previously reported with ADHD patients . Here we discuss theoretical and practical implications of these findings.
From a theoretical point of view the findings are consistent with the suggestion that the neural noise level associated with dopamine tone in inattentive children is sub-optimal, see also  and that noise may enhance performance through the phenomenon of stochastic resonance (SR). According to the model developed here, noise in the environment yields an input to the perceptual system, which can either compensate for low noise in the neural system leading to an output consisting of improved cognitive performance, or, depending on pre-existing levels of neural noise, can add too much to an already well functioning system. The specific neuro-biological and neuro-chemical mechanisms responsible for these effects need further research. For instance, auditive white noise may have its effects either at a perceptual or neuro-psychological level or may operate a neuro-chemical level directly altering levels of dopamine release [13, 51]. Animal models of dopamine function or pharmacological probes to manipulate tonic and phasic dopamine are called for to investigate these effects.
Stimulant medication (e.g. methylphenidate) also improves cognitive performance in children with ADHD [52, 53]. This medication increases dopamine levels by blocking the dopamine transporter . Low performing healthy controls also benefit from increased dopamine transmission, which is manifested in improved cognitive performance and increased prefrontal cortical activity . Our data show that auditory white noise may exert potentially similar effects on cognition as medication through the phenomenon of stochastic resonance (SR). White noise is characterized by randomness and so introduces variability in the nervous system . A poorly tuned neural system benefit from additional white noise. In fact, the stochastic resonance theory predicts that noise that is applied to the signal as an input to a neural cell, improves the signaling efficiency of the output of that cell, where the non-linearity in the firing threshold of the neural cells is the key to improvement of the signal to noise ratio [14, 55].
Despite the fact that it appears that noise and methylphenidate both improve cognitive performance, the underlying mechanism that is the basis of these phenomena are likely to be different. According to the model theoretically speaking the difference between these phenomena is clear. Methylphenidate changes the strength (but not the variability) of the input, which is typically modeled by the gain parameter in abstract neural networks . In contrast, noise changes the variability of the input (but per definition does not influence the strength) of the input. However, despite these clear differences in the underlying level, the behavioral outcome may be similar, and the two mechanisms interact in a complex way, making it difficult to distinguish the phenomena at the behavioral level . Furthermore, direct evidence of difference between these levels is emerging. Pålsson and Söderlund et al. (Noise benefit in pre-pulse inhibition of the acoustic startle reflex, submitted) studied the effect of methylphenidate, dopamine and noise on the startle response in a rat model of ADHD. They found that both control and ADHD strains (SHR) benefited from noise; however, this effect was also found in dopamine lesioned rats, suggesting that dopamine is not a necessary requirement for the stochastic resonance phenomenon to occur.
Another theoretical interpretation of the data is that noise in a general way increase arousal that makes the subject more alert, and less drowsy. The optimal stimulation model states that hyperactivity is as a homeostatic response to underarousal in order to achieve an optimal arousal level . However, this model does not make any explicit predictions about the selective effects of external stimulation whereas in the current study inattentive persons benefited from extra stimulation and attentive children did not. In the cognitive energetic model state factors like arousal, activation and effort are taken into account to explain shortcomings in ADHD patients . According to this model state factors can be moderated by event rate (inter-stimulus-intervals, ISI) and workload in cognitive tasks both under- and over arousal can be produced. Recent research has shown that stimulant medication (methylphenidate) and shortened event rate can produce the same effect in a Go-Nogo task . From our point of view the term arousal is poorly defined in the literature, and could be interpreted in terms of wakefulness or in term of neural arousal. To fully investigate the arousal-noise hypothesis an experiment would have to be designed where physiological arousal is explicitly manipulated and measured. We argue that that proposed framework, including the dopaminergic influence on stochastic resonance, provides a more elaborated view both at the neural and at the behavioral level. To account for the current data an arousal view would have to argue for a selective lower arousal for the inattentive children. Finally, our experience is that the subjects in our experiment are fully aroused, the testing conditions at hand are very stimulating, and subjects are very motivated to perform well.
By highlighting the role of individual differences in the facilitative effects of auditive noise the current study refines our understanding of SR. SR exhibits an inverted U-curve function, where performance peaks at a moderate noise level. However, this is an oversimplification, as there is no absolute sense in which a moderate noise level is optimal. An "optimal" noise level for one individual could be either too high, or too low amount of noise for another individual. These complex interactions between noise and performance may account for some of the contradictory findings in the previous literature. For example, earlier research on noise in normal populations has shown both enhancing and diminishing effects of auditory white noise on cognition in non-clinical groups (90 dB) on simpler, short-term memory tasks like anagrams, whereas speech noise was detrimental . These noise effects also interacted with other variables such as gender and time of the day , which makes these results equivocal. No effect of white noise was found in digit span recall in two experiments, whereas speech noise had a detrimental effect [4, 5]. However, noise improvement was found in a simple addition task in selected groups, elderly and young participants  and among elderly and Alzheimer patients . In Broadbent's early research negative effects of noise have been found using high (excessive) noise levels around 100 dB [62–64]. In later experiments by Broadbent and colleagues, (memory recall of unrelated words) lower noise levels (80-85 dB) were used; results showed no effects of noise on memory when exposed during the encoding phase but deteriorating results if exposed during the recall phase [65, 66]. More recently, episodic memory has been found to be particularly vulnerable to speech noise, whereas traffic noise showed no effect . Results from the present study would indicate that the effects of external noise would have look quite different in many of these studies if participants had been divided into attentive and inattentive or young and elderly, that is high and low gain participants (tentatively high/low dopamine groups). Selective effects of noise can easily get hidden in group-means if some participants improve and others are impaired. Our data may encourage noise researchers to reanalyze their experiments dividing participants by individual differences in attention and performance. Preliminary data from our lab, on an ADHD rat model provide further support for the benefits of adding white noise. The Spontaneous hypertensive rat (SHR) showed improved sensorimotor gating by showing more a pronounced pre-pulse inhibition of the startle reflex when exposed to white noise as compared to control strains, even though control rats also increased their inhibition in noise conditions (Pålsson, Söderlund et al., Noise benefit in pre-pulse inhibition of the acoustic startle reflex, submitted).
Reading disability is a common co-morbidity in ADHD. Consistent with these findings, our data show lower reading skill for the inattentive group. Reading disability is also linked with reduced short-term verbal memory that requires phonetic coding of material, but not necessarily with executive functions or long-term memory [67, 68]. This is also consistent with our data that show a lower performance in the digits forward task that measures short-term memory, but no deficits for digits backward task that is related to working memory capacity. The MBA model accounts for these findings because the digits backward task is a more demanding task leading to higher brain arousal and thus good performance for inattentive children, whereas the less demanding digit forwards task does not sufficiently arouse the brain for the low attention children . Additionally, the positive correlation between reading ability and noise enhancement suggests that white noise may enhance awareness. This is consistent with the idea that dyslexia is caused by phonological deficits , however, a further investigation of phonologic awareness is outside the scoop of the present study.
The current study has a number of limitations. First, ratings of academic attainment and reading were based on single item non-validated scales. Second, only two noise levels were investigated. It would be interesting to include different levels so that the entire stochastic resonance curve can be mapped out. One prediction from our model is that in attentive group, a subset of participants will benefit from noise when levels are individually adjusted. Furthermore, it would be of interest to investigate if the SR effect is dependent on task difficulty. Third, only one test of cognitive ability was tested. Future research may study whether the effects found here generalizes to other tasks such as executive and inhibitory functions. This is of particular importance while investigating the possibility of noise, as an intervention in ADHD. A final limitation of the present study is that the experiment was not designed to study differential effects of noise on study and recall. The experiment manipulates noise at encoding, but not at retrieval, so the effects of noise seen can only be attributed to the conditions at encoding. To what extent noise presented at recall influences performance cannot be determined by the experiment. However, the MBA predicts that the conditions where noise is beneficial during encoding should also be beneficial for performance during retrieval. At same time it may be difficult to directly compare encoding and retrieval conditions, because the task demand for encoding task may differ from the demands at retrieval.
In summary, the present study suggests that cognitive performance can be moderated by external stimulation in a non-clinical group of teacher-rated inattentive participants. If replicated this finding could have practical applications offering a non-invasive help to improve school results in children with attentional problems. In particular awareness should be raised regarding the possibility that the environment has be individually adjusted to the need of the children, where inattentive children in a normal population show noise benefit when performing cognitive tasks. In our data these effects eliminated the differences between high performing, attentive and low performing inattentive children. The possibility that attention can be improved by the addition of carefully controlled levels of white noise into ones environment is potentially of major practical significance. Currently ADHD children are treated successful with medication, where environmental stimulation could be seen as a complementary method to deal with inattentive problems. This could be of particular importance for the significant population of parents that are uneasy about the use of medication.
The study was supported by the Swedish Research Council, grant VR 421-2007-2479.
- Broadbent DE: The effects of noise on behaviour. 1958, Elmsford, NY, US: Pergamon Press, IncGoogle Scholar
- Boman E, Enmarker I, Hygge S: Strength of noise effects on memory as a function of noise source and age. Noise Health. 2005, 7: 11-26. 10.4103/1463-1741.31636.View ArticlePubMedGoogle Scholar
- Hygge S, Boman E, Enmarker I: The effects of road traffic noise and meaningful irrelevant speech on different memory systems. Scand J Psychol. 2003, 44: 13-21. 10.1111/1467-9450.00316.View ArticlePubMedGoogle Scholar
- Belleville S, Rouleau N, Van der Linden M, Collette F: Effect of manipulation and irrelevant noise on working memory capacity of patients with Alzheimer's dementia. Neuropsychol. 2003, 17: 69-81. 10.1037/0894-4220.127.116.11.View ArticleGoogle Scholar
- Rouleau N, Belleville S: Irrelevant speech effect in aging: an assessment of inhibitory processes in working memory. J Gerontol B Psychol Sci Soc Sci. 1996, 51: P356-363.View ArticlePubMedGoogle Scholar
- Shidara M, Richmond BJ: Effect of visual noise on pattern recognition. Exp Brain Res. 2005, 163: 239-241. 10.1007/s00221-005-2230-0.View ArticlePubMedGoogle Scholar
- Corbett B, Stanczak DE: Neuropsychological performance of adults evidencing Attention-Deficit Hyperactivity Disorder. Archives Clin Neuropsychol. 1999, 14: 373-387.View ArticleGoogle Scholar
- Geffner D, Lucker JR, Koch W: Evaluation of auditory discrimination in children with ADD and without ADD. Child Psychiatry Hum Dev. 1996, 26: 169-180. 10.1007/BF02353358.View ArticlePubMedGoogle Scholar
- Stansfeld SA, Berglund B, Clark C, Lopez-Barrio I, Fischer P, Ohrstrom E, Haines MM, Head J, Hygge S, van Kamp I, Berry BF: Aircraft and road traffic noise and children's cognition and health: a cross-national study. Lancet. 2005, 365: 1942-1949. 10.1016/S0140-6736(05)66660-3.View ArticlePubMedGoogle Scholar
- Söderlund GBW, Sikström S, Smart A: Listen to the noise: Noise is beneficial for cognitive performance in ADHD. J Child Psychol Psychiatry. 2007, 48: 840-847. 10.1111/j.1469-7610.2007.01749.x.View ArticlePubMedGoogle Scholar
- Zentall SS, Zentall TR: Optimal stimulation: A model of disordered activity and performance in normal and deviant children. Psychol Bull. 1983, 94: 446-471. 10.1037/0033-2909.94.3.446.View ArticlePubMedGoogle Scholar
- Sonuga-Barke EJ, Wiersema JR, van der Meere JJ, Roeyers H: Context-dependent Dynamic Processes in Attention Deficit/Hyperactivity Disorder: Differentiating Common and Unique Effects of State Regulation Deficits and Delay Aversion. Neuropsychol Rev. 2010, 20: 86-102. 10.1007/s11065-009-9115-0.View ArticlePubMedGoogle Scholar
- Sikström S, Söderlund GBW: Stimulus-dependent dopamine release in attention-deficit/hyperactivity disorder. Psychol Rev. 2007, 114: 1047-1075. 10.1037/0033-295X.114.4.1047.View ArticlePubMedGoogle Scholar
- Moss F, Ward LM, Sannita WG: Stochastic resonance and sensory information processing: a tutorial and review of application. Clin Neurophysiol. 2004, 115: 267-281. 10.1016/j.clinph.2003.09.014.View ArticlePubMedGoogle Scholar
- Zeng FG, Fu QJ, Morse R: Human hearing enhanced by noise. Brain Res. 2000, 869: 251-255. 10.1016/S0006-8993(00)02475-6.View ArticlePubMedGoogle Scholar
- Simonotto E, Spano F, Riani M, Ferrari A, Levero F, Pilot A, Renzetti P, Parodi RC, Sardanelli F, Vitali P: fMRI studies of visual cortical activity during noise stimulation. Neurocomputing: An International Journal Special double volume: Computational neuroscience: Trends in research 1999. 1999, 26-27: 511-516.Google Scholar
- Wells C, Ward LM, Chua R, Timothy Inglis J: Touch noise increases vibrotactile sensitivity in old and young. Psychol Sci. 2005, 16: 313-320. 10.1111/j.0956-7976.2005.01533.x.View ArticlePubMedGoogle Scholar
- Manjarrez E, Mendez I, Martinez L, Flores A, Mirasso CR: Effects of auditory noise on the psychophysical detection of visual signals: cross-modal stochastic resonance. Neurosci Lett. 2007, 415: 231-236. 10.1016/j.neulet.2007.01.030.View ArticlePubMedGoogle Scholar
- Usher M, Feingold M: Stochastic resonance in the speed of memory retrieval. Biol Cybern. 2000, 83: L11-16. 10.1007/PL00007974.View ArticlePubMedGoogle Scholar
- Wilkinson D, Nicholls S, Pattenden C, Kilduff P, Milberg W: Galvanic vestibular stimulation speeds visual memory recall. Exp Brain Res. 2008, 189: 243-248. 10.1007/s00221-008-1463-0.View ArticlePubMedGoogle Scholar
- McDonnell MD, Stocks NG, Abbott D: Optimal stimulus and noise distributions for information transmission via suprathreshold stochastic resonance. Phys Rev E Stat Nonlin Soft Matter Phys. 2007, 75: 061105-10.1103/PhysRevE.75.061105.View ArticlePubMedGoogle Scholar
- Kujala T, Brattico E: Detrimental noise effects on brain's speech functions. Biol Psychol. 2009, 81: 135-143. 10.1016/j.biopsycho.2009.03.010.View ArticlePubMedGoogle Scholar
- Servan-Schreiber D, Printz H, Cohen JD: A network model of catecholamine effects: gain, signal-to-noise ratio, and behavior. Science. 1990, 249: 892-895. 10.1126/science.2392679.View ArticlePubMedGoogle Scholar
- Servan-Schreiber D, Bruno RM, Carter CS, Cohen JD: Dopamine and the mechanisms of cognition: Part I. A neural network model predicting dopamine effects on selective attention. Biol Psychiatry. 1998, 43: 713-722. 10.1016/S0006-3223(97)00448-4.View ArticlePubMedGoogle Scholar
- Prince J: Catecholamine dysfunction in attention-deficit/hyperactivity disorder: an update. J Clin Psychopharmacol. 2008, 28: S39-45. 10.1097/JCP.0b013e318174f92a.View ArticlePubMedGoogle Scholar
- Braver TS, Barch DM: A theory of cognitive control, aging cognition, and neuromodulation. Neurosci Biobehav Rev. 2002, 26: 809-817. 10.1016/S0149-7634(02)00067-2.View ArticlePubMedGoogle Scholar
- Wise RA: Dopamine, learning and motivation. Nat Rev Neurosci. 2004, 5: 483-494. 10.1038/nrn1406.View ArticlePubMedGoogle Scholar
- Grace AA, Floresco SB, Goto Y, Lodge DJ: Regulation of firing of dopaminergic neurons and control of goal-directed behaviors. Trends Neurosci. 2007, 30: 220-227. 10.1016/j.tins.2007.03.003.View ArticlePubMedGoogle Scholar
- Goto Y, Otani S, Grace AA: The Yin and Yang of dopamine release: a new perspective. Neuropharmacology. 2007, 53: 583-587. 10.1016/j.neuropharm.2007.07.007.PubMed CentralView ArticlePubMedGoogle Scholar
- Floresco SB, West AR, Ash B, Moore H, Grace AA: Afferent modulation of dopamine neuron firing differentially regulates tonic and phasic dopamine transmission. Nat Neurosci. 2003, 6: 968-973. 10.1038/nn1103.View ArticlePubMedGoogle Scholar
- Grace AA: Phasic versus tonic dopamine release and the modulation of dopamine system responsivity: a hypothesis for the etiology of schizophrenia. Neurosci. 1991, 41: 1-24. 10.1016/0306-4522(91)90196-U.View ArticleGoogle Scholar
- Bilder RM, Volavka J, Lachman HM, Grace AA: The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes. Neuropsychopharmacology. 2004, 29: 1943-1961. 10.1038/sj.npp.1300542.View ArticlePubMedGoogle Scholar
- Volkow ND, Wang GJ, Fowler JS, Ding YS: Imaging the effects of methylphenidate on brain dopamine: new model on its therapeutic actions for attention-deficit/hyperactivity disorder. Biol Psychiatry. 2005, 57: 1410-1415. 10.1016/j.biopsych.2004.11.006.View ArticlePubMedGoogle Scholar
- Seamans JK, Yang CR: The principal features and mechanisms of dopamine modulation in the prefrontal cortex. Prog Neurobiol. 2004, 74: 1-58. 10.1016/j.pneurobio.2004.05.006.View ArticlePubMedGoogle Scholar
- Ghosh A, Rho Y, McIntosh AR, Kotter R, Jirsa VK: Noise during rest enables the exploration of the brain's dynamic repertoire. PLoS Comput Biol. 2008, 4: e1000196-10.1371/journal.pcbi.1000196.PubMed CentralView ArticlePubMedGoogle Scholar
- Pan W, Soma R, Kwak S, Yamamoto Y: Improvement of motor functions by noisy vestibular stimulation in central neurodegenerative disorders. J Neurol. 2008, 255: 1657-1661. 10.1007/s00415-008-0950-3.View ArticlePubMedGoogle Scholar
- Yamamoto Y, Struzik ZR, Soma R, Ohashi K, Kwak S: Noisy vestibular stimulation improves autonomic and motor responsiveness in central neurodegenerative disorders. Ann Neurol. 2005, 58: 175-181. 10.1002/ana.20574.View ArticlePubMedGoogle Scholar
- Priplata AA, Niemi JB, Harry JD, Lipsitz LA, Collins JJ: Vibrating insoles and balance control in elderly people. Lancet. 2003, 362: 1123-1124. 10.1016/S0140-6736(03)14470-4.View ArticlePubMedGoogle Scholar
- Li SC, von Oertzen T, Lindenberger U: A neurocomputational model of stochastic resonance and aging. Neurocomputing. 2006, 69: 1553-1560. 10.1016/j.neucom.2005.06.015.View ArticleGoogle Scholar
- Bellgrove MA, Chambers CD, Johnson KA, Daibhis A, Daly M, Hawi Z, Lambert D, Gill M, Robertson IH: Dopaminergic genotype biases spatial attention in healthy children. Mol Psychiatry. 2007, 12: 786-792. 10.1038/sj.mp.4002022.View ArticlePubMedGoogle Scholar
- Mattay VS, Goldberg TE, Fera F, Hariri AR, Tessitore A, Egan MF, Kolachana B, Callicott JH, Weinberger DR: Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine. PNAS USA. 2003, 100: 6186-6191. 10.1073/pnas.0931309100.PubMed CentralView ArticlePubMedGoogle Scholar
- Mattay VS, Callicott JH, Bertolino A, Heaton I, Frank JA, Coppola R, Berman KF, Goldberg TE, Weinberger DR: Effects of dextroamphetamine on cognitive performance and cortical activation. Neuroimage. 2000, 12: 268-275. 10.1006/nimg.2000.0610.View ArticlePubMedGoogle Scholar
- Mehta MA, Owen AM, Sahakian BJ, Mavaddat N, Pickard JD, Robbins TW: Methylphenidate enhances working memory by modulating discrete frontal and parietal lobe regions in the human brain. J Neurosci. 2000, 20: RC65-PubMedGoogle Scholar
- Sonuga-Barke EJ, Halperin JM: Developmental phenotypes and causal pathways in attention deficit/hyperactivity disorder: towards the identificationof putative targets and potential treatments for early intervention. J Child Psychol & Psychiatry. 2010, 51: 368-389.View ArticleGoogle Scholar
- Timimi S, Taylor E: ADHD is best understood as a cultural construct. Br J Psychiatry. 2004, 184: 8-9. 10.1192/bjp.184.1.8.View ArticlePubMedGoogle Scholar
- Gjone H, Stevenson J, Sundet JM: Genetic influence on parent-reported attention-related problems in a Norwegian general population twin sample. J Am Acad Child Adolesc Psychiatry. 1996, 35: 588-596. 10.1097/00004583-199605000-00013. discussion 596-588View ArticlePubMedGoogle Scholar
- Bergman LR, Andershed AK: Predictors and outcomes of persistent or age-limited registered criminal behavior: a 30-year longitudinal study of a Swedish urban population. Aggress Behav. 2009, 35: 164-178. 10.1002/ab.20298.View ArticlePubMedGoogle Scholar
- Raven JC: Coloured Progressive Matrices. 1995, Oxford: Oxford Psychological PressGoogle Scholar
- Nilsson LG: Remembering actions and words. The Oxford handbook of memory. Edited by: Tulving E, Craik FIM. 2000, 137-148.Google Scholar
- Engelkamp J: Modality-specific encoding and word class in verbal learning. Practical aspects of memory: Current research and issues, Memory in everyday life. Edited by: Gruneberg MM, Morris PE. 1988, Oxford, England: John Wiley & Sons, 1: 415-420.Google Scholar
- Vicente-Torres MA, Munoz E, Davila D, Gil-Loyzaga P: Changes in the cochlear dopaminergic system of the aged rat. Brain Res. 2001, 917: 112-117. 10.1016/S0006-8993(01)02931-6.View ArticlePubMedGoogle Scholar
- Boonstra AM, Kooij JJ, Oosterlaan J, Sergeant JA, Buitelaar JK: Does methylphenidate improve inhibition and other cognitive abilities in adults with childhood-onset ADHD?. J Clin Exp Neuropsychol. 2005, 27: 278-298. 10.1080/13803390490515757.View ArticlePubMedGoogle Scholar
- Volkow ND, Wang GJ, Fowler JS, Telang F, Maynard L, Logan J, Gatley SJ, Pappas N, Wong C, Vaska P: Evidence that methylphenidate enhances the saliency of a mathematical task by increasing dopamine in the human brain. Am J Psychiatry. 2004, 161: 1173-1180. 10.1176/appi.ajp.161.7.1173.View ArticlePubMedGoogle Scholar
- Volkow ND, Fowler JS, Wang G, Ding Y, Gatley SJ: Mechanism of action of methylphenidate: insights from PET imaging studies. J Attent Disord. 2002, 6 (Suppl 1): S31-43.Google Scholar
- Stein RB, Gossen ER, Jones KE: Neuronal variability: noise or part of the signal?. Nat Rev Neurosci. 2005, 6: 389-397. 10.1038/nrn1668.View ArticlePubMedGoogle Scholar
- Li SC, Sikström S: Integrative neurocomputational perspectives on cognitive aging, neuromodulation, and representation. Neurosci Biobehav Rev. 2002, 26: 795-808. 10.1016/S0149-7634(02)00066-0.View ArticlePubMedGoogle Scholar
- Sergeant JA: Modeling attention-deficit/hyperactivity disorder: a critical appraisal of the cognitive-energetic model. Biol Psychiatry. 2005, 57: 1248-1255. 10.1016/j.biopsych.2004.09.010.View ArticlePubMedGoogle Scholar
- van der Meere JJ, Shalev RS, Borger N, Wiersema JR: Methylphenidate, Interstimulus Interval, and Reaction Time Performance of Children with Attention Deficit/Hyperactivity Disorder: A Pilot Study. Child Neuropsychol. 2009, 1-13.Google Scholar
- Baker MA, Holding DH: The effects of noise and speech on cognitive task performance. J Gen Psychol. 1993, 120: 339-355. 10.1080/00221309.1993.9711152.View ArticlePubMedGoogle Scholar
- Holding DH, Baker MA: Toward meaningful noise research. J Gen Psychol. 1987, 114: 395-410. 10.1080/00221309.1987.9711078.View ArticlePubMedGoogle Scholar
- Harrison DW, Kelly PL: Age differences in cardiovascular and cognitive performance under noise conditions. Percept Mot Skills. 1989, 69: 547-554.View ArticlePubMedGoogle Scholar
- Broadbent DE: Noise, paced performance and vigilance tasks. Br J Psychol. 1953, 44: 295-303.PubMedGoogle Scholar
- Broadbent DE: Some effects of noise on visual performance. Q J Exp Psychol. 1954, 6: 1-5. 10.1080/17470215408416643.View ArticleGoogle Scholar
- Broadbent DE: The twenty dials and twenty lights test under noise conditions. M R C, Appl Psychol Res Unit Report. 1951, 160: 8-Google Scholar
- Smith AP, Broadbent DE: The effects of noise on recall and recognition of instances of categories. Acta Psychol. 1982, 51: 257-271. 10.1016/0001-6918(82)90038-5.View ArticleGoogle Scholar
- Smith AP, Jones DM, Broadbent DE: The effects of noise on recall of categorized lists. Br J Psychol. 1981, 72: 299-316.View ArticleGoogle Scholar
- Willcutt EG, Pennington BF, Boada R, Ogline JS, Tunick RA, Chhabildas NA, Olson RK: A comparison of the cognitive deficits in reading disability and attention-deficit/hyperactivity disorder. J Abnorm Child Psychol. 2001, 110: 157-172.View ArticleGoogle Scholar
- Kibby MY, Cohen MJ: Memory functioning in children with reading disabilities and/or attention deficit/hyperactivity disorder: a clinical investigation of their working memory and long-term memory functioning. Child Neuropsychol. 2008, 14: 525-546. 10.1080/09297040701821752.PubMed CentralView ArticlePubMedGoogle Scholar
- Papageorgiou C, Giannakakis GA, Nikita KS, Anagnostopoulos D, Papadimitriou GN, Rabavilas A: Abnormal auditory ERP N100 in children with dyslexia: comparison with their control siblings. Behav Brain Funct. 2009, 5: 26-10.1186/1744-9081-5-26.PubMed CentralView ArticlePubMedGoogle Scholar
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