Stimulus Orienting Versus Response Control

Models of attention include both stimulus orienting and response control. Stimulus orienting is the automatic capture of attention by salient sensations (James, Reference James1890; more recently, automatic disengaging and shifting attention, Mirsky et al., Reference Mirsky, Anthony, Duncan, Ahearn and Kellam1991; Posner & Peterson, Reference Posner and Peterson1990; filtering of salience information, Knudsen, Reference Knudsen2007; or creating saliency maps, Treue, Reference Treue2003). Response control is the voluntary direction of a motor response, corresponding to Posner and Peterson's (Reference Posner and Peterson1990) anterior attention system and to Knudsen's (Reference Knudsen2007) response selection. Being an unobservable construct, attention is inferred in both stimulus orienting and response control from manipulations of the relation between sensation and movement. In stimulus orienting, inhibition of return (IOR) is inferred from the contingencies between motor engaging and disengaging. In response control, stopping an ongoing action is inferred from the relation between go and stop actions.

A new taxonomy (Figure 1) was prompted by considerations relevant to the specific aims. First, we aimed to integrate stimulus orienting and response control into a single taxonomy. Some models of attention used in childhood clinical disorders focus on only one process; for example, Barkley's (Reference Barkley1997) model of attention considers only response control. Second, we wanted to distinguish among operations within stimulus orienting and response control. Some earlier models of attention that considered both processes (e.g., Mirsky et al., Reference Mirsky, Anthony, Duncan, Ahearn and Kellam1991; Posner & Peterson, Reference Posner and Peterson1990) have not separated activation, inhibition, and adjustment. Third, we aimed to incorporate recent parsings of attendee roles (e.g., the distinction in striatal learning between a “critic” who evaluates performance and an “actor” who performs) and cognitive phenotypes (e.g., the distinction in response control between restraining a prepotent response and canceling an ongoing response). Fourth, we wanted to integrate the three attention dimensions into a factorially structured taxonomy to identify both functional assets and deficits. Such an integration will facilitate functional comparisons both within and across clinical disorders and generate not only descriptions, but also principled inferences about the neural and behavioral correlates of attention.

Fig. 1.

Attention taxonomy.

Puppet Versus Robot Versus Critic Versus Actor

Within stimulus orienting, the attendee may be a puppet or robot. We devised the puppet metaphor to capture the idea of a passive attendee whose attention is driven by bottom-up, stimulus-driven orienting to exogenous (external) stimuli, such as a flash of light. We devised the robot metaphor to capture the idea of an active attendee whose orienting is top-down and task-driven, in accord with endogenous (internal) programs, scripts, or symbols, such as an arrow.

Within response control, the attendee may be a critic or an actor. The critic metaphor captures the idea of looped, model-driven responding, involving an active attendee who evaluates performance options and reward contingencies in light of an existing model of desired behavior. The actor metaphor captures the idea of a top-down, action-driven, active attendee responding in accordance with an instructional set and attention priorities. We adopted the actor-critic metaphors from habit-driven learning (Dayan & Balleine, Reference Dayan and Balleine2002; O'Reilly & Frank, Reference O'Reilly and Frank2006) and animal studies separating a dorsal striatum (actor) role in performance from a ventral striatum (actor and critic) role in performance and learning (Atallah et al., Reference Atallah, Lopez-Paniagua, Rudy and O'Reilly2007).

Activation Versus Inhibition Versus Adjustment

The attendee is involved in activation, inhibition, or adjustment. Activation enables directed attention towards the attended material. Inhibition refers to diverse attention processes, some of which concern automatic avoidance of previously attended locations (e.g., IOR), and some of which involve voluntary acts of inhibitory control (e.g., stopping an ongoing action in response to a signal). Adjustment refers to a number of evaluative-regulative processes by which previous attention modifies subsequent attention (Larson et al., Reference Larson, Aronoff and Stearns2007), including error detection, performance monitoring, and adjusting the contingency between present action and future reward (Holroyd & Coles, Reference Holroyd and Coles2002; Nigg et al., Reference Nigg, Willcutt, Doyle and Sonuga-Barke2005; Sagvolden et al., Reference Sagvolden, Aase, Zeiner and Berger1998).

Attention Measures Express Cognitive Phenotypes

The italicized entries in Figure 1 are cognitive phenotypes, which are overt and measurable expressions of the attention constructs. For each cognitive phenotype, we identify a representative task measure, below.

Interrelation of Attention Processes

The taxonomy parses a set of attention processes and roles that normally work together in a complex choreography (Mesulam, Reference Mesulam1990). Bottom-up, top-down, and looped operations operate in the same attention space. Stimulus orienting serves as a circuit breaker for response control (as when a flash of lightning draws attention from a book and we orient to the window). Dissociable inhibitory processes work together; for example, IOR not only aids visual search, but also helps adjust behavioral demands in a dynamic environment (Ivanoff & Taylor, Reference Ivanoff and Taylor2006). Arousal influences the level of activation. Controlled attention helps maintain instructional set, even for stimulus orienting tasks.

While the key to the taxonomy is attendee roles in stimulus orienting and response control, time is a thread throughout, and the terms time binding (Dennis, Reference Dennis, Risberg and Grafman2006) and intertemporal competence (Barkley, Reference Barkley1997) characterize temporal processes in attention, such as time estimation, time management, and rule maintenance (Barkley et al., Reference Barkley, Koplowitz, Anderson and McMurray1997). The taxonomy does not explicitly address working memory, which is the product of currently activated attention, including the activated subset that can be manipulated or inhibited (i.e., the products of the right side of Figure 1). Although it is not an account of executive function, the taxonomy does address executive constructs like response control, conflict, and monitoring.

Overview

Disordered attention characterizes several childhood conditions, including attention deficit hyperactivity disorder considered as a primary form of adaptive impairment (P-ADHD, Barkley, Reference Barkley1997), and other congenital brain malformations such as spina bifida meningomyelocele (SBM; Dennis et al., Reference Dennis, Edelstein, Copeland, Frederick, Francis, Hetherington, Blaser, Kramer, Drake, Brandt and Fletcher2005a, Reference Dennis, Edelstein, Copeland, Frederick, Francis, Hetherington, Blaser, Kramer, Drake, Brandt and Fletcher2005b) and Sotos syndrome (a haploinsufficiency of the Nuclear receptor Set Domain containing protein 1 gene, NSD 1; de Boer et al., Reference de Boer, Roder and Wit2006; Kurotaki et al., Reference Kurotaki, Imaizumi, Harada, Masuno, Kondoh, Nagai, Ohashi, Naritomi, Tsukahara, Makita, Sugimoto, Sonoda, Hasegawa, Chinen, Tomita Ha, Kinoshita, Mizuguchi, Yoshiura Ki, Ohta, Kishino, Fukushima, Niikawa and Matsumoto2002). Impaired attention is also a consequence of acquired brain insults, including traumatic brain injury (TBI; Levin et al., Reference Levin, Hanten, Max, Li, Swank, Ewing-Cobbs, Dennis, Menefee and Schachar2007), childhood brain tumors (Dennis et al., Reference Dennis, Hetherington and Spiegler1998), and acute lymphoblastic leukemia (ALL; Schatz et al., Reference Schatz, Kramer, Ablin and Matthay2004).

Using the taxonomy in Figure 1, we now review attention in four disorders that vary in prevalence, etiology, and developmental course: P-ADHD, TBI, SBM, and ALL. Attention deficits define P-ADHD, and occur in a subset of children with the three other disorders, in which the presenting problem is explicit brain injury. In P-ADHD and SBM, attention is disordered early in development; in contrast, in TBI and ALL, disordered attention is acquired after some period of normal development.

To facilitate the review, we consider two paradigmatic tasks for stimulus orienting (covert orienting, Figure 2) and response control (stop signal, Figure 3). Most components of Figure 1 can be understood in the context of these two tasks. We also summarize the review in Table 1.

Fig. 2.

Covert stimulus orienting paradigms. In exogenous orienting (left), the participant maintains central fixation and then an exogenous cue, such as a luminance change, appears to one side of fixation, followed by a target, to which the participant must respond. In this example, the brightness cue will facilitate target detection because it draws attention to the side on which the target will appear (a misleading cue would have appeared on the side opposite to the upcoming target). In endogenous orienting (right), the participant maintains central fixation, which is then replaced by a central endogenous cue, such as an arrow, followed by a target, to which the participant must respond. In this example, the arrow cue will facilitate target detection because it draws attention to the side on which the target will appear (a misleading arrow would have directed attention to the side opposite to the upcoming target).

Fig. 3.

Stop signal paradigm. The participant fixates a central dot and then a go stimulus appears, either an X indicating a left hand response (shown in figure) or an O indicating a right hand response. One-third of the trials involve a stop signal (a background color change) following the go signal to indicate that the participant should not respond. Because of the adaptively manipulated delay interval between go and stop signals, each participant will fail to stop on half of the stop trials. Failed stop trials activate the error detection system, so that go trials that follow a failed stop trial (circled in figure) will be slower than go trials that do not follow failures to stop.

Table 1.

Robots, puppets, critics, and actors: The fractionation of attention in developmental disorders

Note

Bold entries are from strong, clear data; regular text entries represent a less clear, more limited, or more qualified database, or data from related tasks or age group. Intact or impaired refer to group, not individual, data.

Primary Attention Deficit Hyperactivity Disorder

P-ADHD affects 4–7% of children worldwide (Szatmari, Reference Szatmari and Weiss1992) and is defined by hyperactive, impulsive, inattentive, and/or maladaptive behavior (Barkley, Reference Barkley2004; Goldman et al., Reference Goldman, Genel, Bezman and Slanetz1998; Jensen et al., Reference Jensen, Kettle, Roper, Sloan, Dulcan, Hoven, Bird, Bauermeister and Payne1999). P-ADHD persists into adulthood, although heterogeneity in ADHD is considerable throughout development (Barkley et al., Reference Barkley, Murphy and Fischer2008), with hyperactivity being more common in children than in adults (Biederman et al., Reference Biederman, Mick and Faraone2000).

Spina Bifida Meningomyelocele

Spina bifida is a common disabling birth defect, occurring in about 19.3 per 100,000 live births in North America (Martin et al., Reference Martin, Hamilton, Sutton, Ventura, Menacker and Kirmeyer2006). The most severe form, spina bifida meningomyelocele (SBM), occurs in 90% of cases (Detrait et al., Reference Detrait, George, Etchevers, Gilbert, Vekemans and Speer2005). Compared to siblings or to normative samples, children with SBM are more distractible and less attentive (Ammerman et al., Reference Ammerman, Kane, Slomka, Reigel, Franzen and Gadow1998; Burmeister et al., Reference Burmeister, Hannay, Copeland, Fletcher, Boudousquie and Dennis2005; Colvin et al., Reference Colvin, Yeates, Enrile and Coury2003; Rose & Holmbeck, Reference Rose and Holmbeck2007; Vachha & Adams, Reference Vachha and Adams2005) and around one-quarter to one-third is inattentive (Burmeister et al., Reference Burmeister, Hannay, Copeland, Fletcher, Boudousquie and Dennis2005; Davidovitch et al., Reference Davidovitch, Manning-Courtney, Hartmann, Watson, Lutkenhoff and Oppenheimer1999; Fletcher et al., Reference Fletcher, Copeland, Frederick, Blaser, Kramer, Northrup, Hannay, Brandt, Francis, Villarreal, Drake, Laurent, Townsend, Inwood, Boudousquie and Dennis2005). It is not clear whether attention deficits extend into adulthood.

Traumatic Brain Injury

Traumatic brain injury (TBI) is frequent in children and adolescents (180 in 100,000 youths annually, Kraus & McArthur, Reference Kraus and McArthur1996; Kraus et al., Reference Kraus, Rock and Hemyari1990), and long-term neuropsychological deficits include inattention (Yeates, Reference Yeates, Yeates, Taylor and Ris2000). Premorbid P-ADHD contributes to post-TBI attention symptoms (Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche, Bryan and Denckla1998, Reference Gerring, Brady, Chen, Quinn, Herskovits, Bandeen-Roche, Denckla and Bryan2000; Levin et al., Reference Levin, Hanten, Max, Li, Swank, Ewing-Cobbs, Dennis, Menefee and Schachar2007; Max et al., Reference Max, Lindgren, Knutson, Pearson, Ihrig and Welborn1998), although some 15–20% of TBI survivors with no ADHD history meet diagnostic criteria for secondary ADHD (S-ADHD; Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche, Bryan and Denckla1998, Reference Gerring, Brady, Chen, Quinn, Herskovits, Bandeen-Roche, Denckla and Bryan2000; Herskovits et al., Reference Herskovits, Megalooikonomou, Davatzikos, Chen, Bryan and Gerring1999; Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005b, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005c; Slomine et al., Reference Slomine, Salorio, Grados, Vasa, Christensen and Gerring2005; Yeates et al., Reference Yeates, Armstrong, Janusz, Taylor, Wade, Stancin and Drotar2005), and even more develop subthreshold attention symptoms.

S-ADHD is associated not only with severe TBI (Max et al., Reference Max, Lansing, Koele, Castillo, Bokura, Schachar, Collings and Williams2004) but also with mild or moderate TBI (Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche, Bryan and Denckla1998, Reference Gerring, Brady, Chen, Quinn, Herskovits, Bandeen-Roche, Denckla and Bryan2000; Herskovits et al., Reference Herskovits, Megalooikonomou, Davatzikos, Chen, Bryan and Gerring1999; Max et al., Reference Max, Lindgren, Knutson, Pearson, Ihrig and Welborn1998; Max et al., Reference Max, Manes, Robertson, Mathews, Fox and Lancaster2005a, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005b; Schachar et al., Reference Schachar, Levin, Max, Purvis and Chen2004a; Slomine et al., Reference Slomine, Salorio, Grados, Vasa, Christensen and Gerring2005), as well as with high levels of pre-injury behavioral difficulties (Schachar et al., Reference Schachar, Levin, Max, Purvis and Chen2004a), maladaptive function, or psychosocial adversity (Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche, Bryan and Denckla1998; Max et al., Reference Max, Lansing, Koele, Castillo, Bokura, Schachar, Collings and Williams2004, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005b, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005c). S-ADHD manifests as early as 3 months post-TBI (Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche, Bryan and Denckla1998, Reference Gerring, Brady, Chen, Quinn, Herskovits, Bandeen-Roche, Denckla and Bryan2000) and persists over years (Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche, Bryan and Denckla1998; Levin et al., Reference Levin, Hanten, Max, Li, Swank, Ewing-Cobbs, Dennis, Menefee and Schachar2007; Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005c). Inattentive symptoms peak at six months post-injury and later decline, whereas hyperactive/impulsive symptoms fluctuate for two years (Levin et al., Reference Levin, Hanten, Max, Li, Swank, Ewing-Cobbs, Dennis, Menefee and Schachar2007) and then diminish (Levin et al., Reference Levin, Hanten, Max, Li, Swank, Ewing-Cobbs, Dennis, Menefee and Schachar2007; Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005b, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005c). Although poor inhibitory control improves over time (Leblanc et al., Reference Leblanc, Chen, Swank, Ewing-Cobbs, Barnes, Dennis, Max, Levin and Schachar2005), children with TBI with or without S-ADHD exhibit impaired long-term attention (e.g., Dennis et al., Reference Dennis, Wilkinson, Koski, Humphreys, Broman and Michel1995; Konrad et al., Reference Konrad, Gauggel, Manz and Scholl2000a, Reference Konrad, Gauggel, Manz and Scholl2000b; Schachar et al., Reference Schachar, Levin, Max, Purvis and Chen2004a).

Acute Lymphoblastic Leukemia

Of the 3,000–6,000 people diagnosed with acute lymphoblastic leukemia (ALL) each year in the United States, two-thirds are children (Cortes & Kantarjian, Reference Cortes and Kantarjian1995; Parker et al., Reference Parker, Tong, Bolden and Wingo1997), and 80% will survive (Parker et al., Reference Parker, Tong, Bolden and Wingo1997). ALL is associated with cognitive deficits, including poor attention, after treatment with cranial radiation therapy (CRT) and/or chemotherapy, (Christie et al., Reference Christie, Leiper, Chessells and Vargha-Khadem1995; Cousens et al., Reference Cousens, Waters, Said and Stevens1988; Fletcher & Copeland, Reference Fletcher and Copeland1988; Goff et al., Reference Goff, Anderson and Cooper1980; Hertzberg et al., Reference Hertzberg, Huk, Ueberall, Langer, Meier, Dopfer, Skalej, Lackner, Bode, Janssen, Zintl and Beck1997; Mennes et al., Reference Mennes, Stiers, Vandenbussche, Vercruysse, Uyttebroeck, De Meyer and Van Cool2005), especially with early exposure and longer time since treatment (Cousens et al., Reference Cousens, Waters, Said and Stevens1988; Jankovic et al., Reference Jankovic, Brouwers, Valsecchi, Van Veldhuizen, Huisman, Kamphuis, Kingma, Mor, Van Dongen-Melman, Ferronato, Mancini, Spinetta and Masera1994). Attention problems are evident at least 7–14 years following ALL treatment (Lockwood et al., Reference Lockwood, Bell and Colegrove1999; Schatz et al., Reference Schatz, Kramer, Ablin and Matthay2004), especially in females and in children treated with CRT at a younger age (Lockwood et al., Reference Lockwood, Bell and Colegrove1999; Schatz et al., Reference Schatz, Kramer, Ablin and Matthay2004).

Stimulus Orienting and the Posterior Cortex, Midbrain, and Superior Colliculus

Deficits in disengaging (not shifting attentional set) are associated with superior colliculus and posterior cortex lesions in adults (Posner et al., Reference Posner, Walker, Friedrich and Rafal1984). IOR deficits in adults are associated with superior colliculus lesions (Rafal et al., Reference Rafal, Calabresi, Brennan and Sciolto1989, Reference Rafal, Henik and Smith1991; Sapir et al., Reference Sapir, Soroker, Berger and Henik1999) and midbrain lesions such as those in progressive supranuclear palsy (Rafal & Grimm, Reference Rafal and Grimm1981; Rafal et al., Reference Rafal, Posner, Friedman, Inhoff and Bernstein1988).

SBM involves malformations of the cerebellum, hindbrain, and midbrain (Fletcher et al., Reference Fletcher, Copeland, Frederick, Blaser, Kramer, Northrup, Hannay, Brandt, Francis, Villarreal, Drake, Laurent, Townsend, Inwood, Boudousquie and Dennis2005; Salman et al., Reference Salman, Blaser, Sharpe and Dennis2006a). The midbrain abnormality, tectal beaking (Barkovich et al., Reference Barkovich, Kuzniecky, Jackson, Guerrini and Dobyns2005; Fletcher et al., Reference Fletcher, Copeland, Frederick, Blaser, Kramer, Northrup, Hannay, Brandt, Francis, Villarreal, Drake, Laurent, Townsend, Inwood, Boudousquie and Dennis2005), is a mechanical consequence of brain development in a small posterior fossa (McLone & Knepper, Reference McLone and Knepper1989). Brain growth in SBM affects posterior more than anterior cortical structures, producing selective reduction in posterior cortical volume (Dennis et al., Reference Dennis, Fitz, Netley, Sugar, Harwood-Nash, Hendrick, Hoffman and Humphreys1981; Fletcher et al., Reference Fletcher, Brookshire, Landry, Bohan, Davidson, Francis, Levin, Brandt, Kramer and Morris1996a,Reference Fletcher, McCauley, Brandt, Bohan, Kramer, Francis, Thorstad and Brookshireb; Juranek et al., Reference Juranek, Fletcher, Hasan, Breier, Cirino, Alvarez, Diaz, Ewing-Cobbs, Dennis and Papanicolaou2008) and impairments in white matter integrity (Hasan et al., Reference Hasan, Eluvathingal, Kramer, Ewing-Cobbs, Dennis and Fletcher2008a), with relative preservation, even hypertrophy, of anterior cortex (Juranek et al., Reference Juranek, Fletcher, Hasan, Breier, Cirino, Alvarez, Diaz, Ewing-Cobbs, Dennis and Papanicolaou2008) and some cortical and subcortical structures (Hasan et al., Reference Hasan, Sankar, Halphen, Kramer, Ewing-Cobbs, Dennis and Fletcher2008b; Miller et al., Reference Miller, Widjaja, Blaser, Dennis and Raybaud2008).

In SBM, deficits in disengaging and shifting are associated with tectal beaking and posterior brain volume loss (Dennis et al., Reference Dennis, Edelstein, Copeland, Frederick, Francis, Hetherington, Blaser, Kramer, Drake, Brandt and Fletcher2005a), and attenuated IOR is associated with tectal beaking (Dennis et al., Reference Dennis, Edelstein, Copeland, Frederick, Francis, Hetherington, Blaser, Kramer, Drake, Brandt and Fletcher2005b). Individual differences in stimulus orienting deficits are correlated with individual differences in structural brain damage observed in children with SBM in the posterior cortex, midbrain, and superior colliculus.

The midbrain is involved in dopamine dysfunction in children with P-ADHD. Ernst et al. (Reference Ernst, Zametkin, Matochik, Pascualvaca, Jons and Cohen1999) found that accumulation of [F-18]DOPA, a measure of dopa decarboxylase activity in synaptic terminals of dopaminergic-rich regions, was nearly 50% higher in the right midbrain in children with ADHD, measures being correlated with symptom severity. However, this excess of midbrain dopamine does not disrupt stimulus orienting in P-ADHD.

We predict that structural or neurochemical damage to the midbrain should produce stimulus-orienting deficits at any age. For example, childhood acquired midbrain tumors, such as pineal germinomas, should be associated with impaired stimulus orienting.

Response Control and Frontal-Striatal Circuits

Response control develops throughout childhood (Davidson et al., Reference Davidson, Amso, Anderson and Diamond2006; Rubia et al., Reference Rubia, Smith, Woolley, Nosarti, Heyman, Taylor and Brammer2006) and involves two principal dopamine-modulated pathways: a prefrontal-dorsal striatum circuit and an orbitofrontal-ventral striatum circuit. Activation of the superior, medial, and inferior frontal gyri as well as midline networks are associated with withholding and monitoring motor responses (Chevrier et al., Reference Chevrier, Noseworthy and Schachar2007; Rubia et al., Reference Rubia, Russell, Overmeyer, Brammer, Bullmore, Sharma, Simmons, Williams, Giampietro, Andrew and Taylor2001). The withdrawal or canceling of responses has been shown to activate the right inferior frontal gyrus, the right anterior cingulate cortex (ACC), supplementary motor cortex, and caudate (Chevrier et al., Reference Chevrier, Noseworthy and Schachar2007; Rubia et al., Reference Rubia, Russell, Overmeyer, Brammer, Bullmore, Sharma, Simmons, Williams, Giampietro, Andrew and Taylor2001). These data are congruent with the idea of distinct brain systems for intentional actions and the withholding of intended actions (Brass & Haggard, Reference Brass and Haggard2007). Frontal regions are also implicated in conflict management: Better interference control is associated with activity in the right middle frontal gyrus and left inferior frontal gyrus (Bunge et al., Reference Bunge, Ochsner, Desmond, Glover and Gabrieli2001).

There is ongoing debate about the neural basis of error detection and performance monitoring. The extensive limbic connections of the ACC contribute to the modulation of emotional expression (Critchley, Reference Critchley2005), and the dorsal ACC is directly involved in higher-order cognitive functions such as attention and response selection (e.g., Bush et al., Reference Bush, Luu and Posner2000). Although the striatum has an important role as critic, the ACC also supports evaluative aspects of performance monitoring (Dias & Aggleton, Reference Dias and Aggleton2000) that require integration of cognitive and limbic input. It is activated preceding errors (Li et al., Reference Li, Yan, Bergquist and Sinha2007), responds to both internal and external error signals (Holroyd et al., Reference Holroyd, Nieuwenhuis, Yeung, Nystrom, Mars, Coles and Cohen2004), and is more activated by error responses than by correct responses and by error feedback than by correct feedback (Holroyd et al., Reference Holroyd, Nieuwenhuis, Yeung, Nystrom, Mars, Coles and Cohen2004). The dorsal ACC is particularly activated by error detection invoked by failed inhibition trials of the stop signal task (Chevrier et al., Reference Chevrier, Noseworthy and Schachar2007), and by changes in task “sets” that signal adaptive changes in response style (Woodward et al., Reference Woodward, Metzak, Meier and Holroyd2008). The role of the ACC in conflict monitoring may be domain-general because dorsal ACC activity is related to a cognitive conflict between major and minor musical modes (Mizuno & Sugishita, Reference Mizuno and Sugishita2007).

Individuals with P-ADHD show selective cortical thinning of networks serving attention and executive control (Makris et al., Reference Makris, Biederman, Valera, Bush, Kaiser, Kennedy, Caviness, Faraone and Seidman2007). Structural imaging of children with P-ADHD has identified volume reduction in the whole cerebrum (Castellanos et al., Reference Castellanos, Lee, Sharp, Jeffries, Greenstein, Clasen, Blumenthal, James, Ebens, Walter, Zijdenbos, Evans, Giedd and Rapoport2002), cortical gray matter, caudate nucleus, globus pallidus, prefrontal cortex, ACC (Castellanos et al., Reference Castellanos, Giedd, Marsh, Hamburger, Vaituzis, Dickstein, Sarfatti, Vauss, Snell, Lange, Kaysen, Krain, Ritchie, Rajapakse and Rapoport1996; Filipek et al., Reference Filipek, Semrud-Clikeman, Steingard, Renshaw, Kennedy and Biederman1997; Seidman et al., Reference Seidman, Valera, Makris, Monuteaux, Boriel, Kelkar, Kennedy, Caviness, Bush, Aleardi, Faraone and Biederman2006), and especially, the right inferior frontal cortex (Durston et al., Reference Durston, Hulshoff Pol, Schnack, Buitelaar, Steenhuis, Minderaa, Kahn and van Engeland2004; Sowell et al., Reference Sowell, Thompson, Welcome, Henkenius, Toga and Peterson2003), with relatively lesser involvement of the posterior cortex, midbrain, and cerebellum (Berquin et al., Reference Berquin, Giedd, Jacobsen, Hamburger, Krain, Rapoport and Castellanos1998). Various brain regions have been implicated in P-ADHD symptoms (Seidman et al., Reference Seidman, Valera and Makris2005), including dorsolateral prefrontal cortex and orbitofrontal cortex (Spencer et al., Reference Spencer, Biederman and Mick2007), and dysfunction has been identified in dorsolateral and orbitofrontal cortices, ACC, inferior frontal gyri, and striatal-pallidal-thalamic circuits (e.g., Bush et al., Reference Bush, Valera and Seidman2005; Spencer et al., Reference Spencer, Biederman and Mick2007).

Inhibitory control deficits associated with P-ADHD are correlated with functional alterations in a frontostriatal network. Poor interference control in children with P-ADHD is associated with decreased activation of the left inferior frontal gyrus (Vaidya et al., Reference Vaidya, Bunge, Dudukovic, Zalecki, Elliott and Gabrieli2005), and hypoactivation of the dorsal ACC occurs in adults with P-ADHD (Bush et al., Reference Bush, Frazier, Rauch, Seidman, Whalen, Jenike, Rosen and Biederman1999). During inhibition trials, children with P-ADHD fail to activate the right inferior frontal or precentral gyri (Vaidya et al., Reference Vaidya, Bunge, Dudukovic, Zalecki, Elliott and Gabrieli2005), exhibit abnormal activity in the dorsal ACC (no activation, Durston et al., Reference Durston, Tottenham, Thomas, Davidson, Eigsti, Yang, Ulug and Casey2003, hypoactivation, Tamm et al., Reference Tamm, Menon, Ringel and Reiss2004), and exhibit striatal dysfunction, including decreased left caudate activity (Durston et al., Reference Durston, Tottenham, Thomas, Davidson, Eigsti, Yang, Ulug and Casey2003; Vaidya et al., Reference Vaidya, Austin, Kirkorian, Ridlehuber, Desmond, Glover and Gabrieli1998). Poor cancellation by P-ADHD patients is associated with hypoactive mesial prefrontal cortex (i.e., near the dorsal ACC) and ventrolateral prefrontal cortex, and decreased left caudate activity (Rubia et al., Reference Rubia, Overmeyer, Taylor, Brammer, Williams, Simmons and Bullmore1999).

TBI is frequently associated with dysfunction of the prefrontal and frontal cortex (Levin et al., Reference Levin, Fletcher, Kusnerik, Kufera, Lilly, Duffy, Chapman, Mendelsohn and Bruce1996; Wilde et al., Reference Wilde, Hunter, Newsome, Scheibel, Bigler, Johnson, Fearing, Cleavinger, Li, Swank, Pedroza, Roberson, Bachevalier and Levin2005), and corpus callosum and frontal lobe white matter (Levin et al., Reference Levin, Benavidez, Verger-Maestre, Perachio, Song, Mendelsohn and Fletcher2000), with some cerebellar involvement (Spanos et al., Reference Spanos, Wilde, Bigler, Cleavinger, Fearing, Levin, Li and Hunter2007). S-ADHD is associated with damage to neural regions known to be abnormal in P-ADHD, including the orbitofrontal gyrus (Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005b), thalamus (Gerring et al., Reference Gerring, Brady, Chen, Quinn, Herskovits, Bandeen-Roche, Denckla and Bryan2000), and basal ganglia (Gerring et al., Reference Gerring, Brady, Chen, Quinn, Herskovits, Bandeen-Roche, Denckla and Bryan2000; Herskovits et al., Reference Herskovits, Megalooikonomou, Davatzikos, Chen, Bryan and Gerring1999; Max et al., Reference Max, Manes, Robertson, Mathews, Fox and Lancaster2005a; and see Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis, Saunders and Landis2005c). Children with TBI/S-ADHD also exhibit response inhibition deficits, although there is no clear association with lesion site (Leblanc et al., Reference Leblanc, Chen, Swank, Ewing-Cobbs, Barnes, Dennis, Max, Levin and Schachar2005; Levin et al., Reference Levin, Hanten, Zhang, Swank and Hunter2004). ACC activity in adults with TBI is abnormal during conflict tasks (Soeda et al., Reference Soeda, Nakashima, Okumura, Kuwata, Shinoda and Iwama2005), possibly because of diffuse axonal damage disrupting frontal-cortical and subcortical networks, leading to reduced post-error slowing (Larson et al., Reference Larson, Aronoff and Stearns2007). In children with TBI, inhibitory impairments are correlated with prefrontal injury. Restraining a prepotent response on go/no-go tasks is related to volume of left prefrontal lesions (Levin et al., Reference Levin, Culhane, Mendelsohn, Lilly, Bruce, Fletcher, Chapman, Harward and Eisenberg1993, Reference Levin, Hanten, Zhang, Swank and Hunter2004), as well as to injury severity (Konrad et al., Reference Konrad, Gauggel, Manz and Scholl2000a; Levin et al., Reference Levin, Hanten, Zhang, Swank and Hunter2004, but see Leblanc et al., Reference Leblanc, Chen, Swank, Ewing-Cobbs, Barnes, Dennis, Max, Levin and Schachar2005).

Children with P-ADHD and children with TBI have deficits in response control, with individual differences being correlated with individual differences in prefrontal-dorsal striatum and orbitofrontal-ventral striatum circuits. The caudate, putamen, and globus pallidus are part of a striatal-pallidal-thalamic circuit. In feedforward and feedback relations with the cortex, this circuit modulates inhibitory control and sensitivity to reward (Alexander et al., Reference Alexander, DeLong and Strick1986), which is consistent with the idea that dopaminergic and/or noradrenergic medications affect ADHD by increasing inhibitory effects of frontal cortical activity on subcortical brain regions (Zametkin & Rapoport, Reference Zametkin and Rapoport1987). The thalamus is part of two subcortical networks that are implicated in P-ADHD symptomatology as well as response inhibition (Gerring et al., Reference Gerring, Brady, Chen, Quinn, Herskovits, Bandeen-Roche, Denckla and Bryan2000), and damage to the thalamus produces distractibility and disinhibition (Gentilini et al., Reference Gentilini, De Renzi and Crisi1987). To be sure, there is considerable heterogeneity in the brain systems associated with inhibition. Furthermore, the link of S-ADHD or P-ADHD to the thalamus is less clear than that of either of these disorders to the caudate, putamen, or inferior frontal gyrus.

Double Dissociation Between Automatic and Controlled Attention

Within- and between-disorder comparisons in childhood conditions have provided functional and neurobiological evidence of a double dissociation between automatic and controlled forms of attention. This is congruent with a long history of adult lesion studies, and also with new evidence from markers of event-related potentials. For example, listening to Mozart's D major sonata K.448 has opposite effects on event-related potentials markers of involuntary and voluntary attention (Zhu et al., Reference Zhu, Zhao, Zhang, Ding, Liu, Ni, Ma and Zhou2008).

Inhibition Is a Diverse Attention Construct

Inhibition constitutes a diverse and often uncorrelated group of functions. In children with P-ADHD, the puppet is intact (normal IOR), but the actor is impaired (poor restrain). Different conditions have the same inhibitory impairment (P-ADHD and TBI both show impaired actor role and have restrain deficits). Adult disorders show differently dissociated forms of inhibition; for example, patients with Parkinson's disease demonstrate intact IOR but impaired endogenously evoked inhibition (NP) (Grande et al., Reference Grande, Crosson, Heilman, Bauer, Kilduff and McGlinchey2006).

Dissociations also exist within and between top-down and bottom-up processes. Children with P-ADHD are impaired on top-down response inhibition of the actor but not on endogenous top-down stimulus orienting of the robot. In children with SBM, bottom-up exogenous stimulus orienting deficits in the puppet are uncorrelated with intact top-down endogenous stimulus orienting in the robot.

Brain Injury Trumps Age at Onset

Anatomy trumps age at onset with respect to the puppet in stimulus orienting, in that SBM and ALL share deficits in this domain despite differences in age at onset, although stimulus-orienting deficits may have different anatomical origins in these two conditions. Anatomy certainly trumps age at onset for response control. Despite differences in age at onset, response control is largely unimpaired in SBM and ALL, and impaired in P-ADHD and TBI/S-ADHD, highlighting the role of anterior brain regions and the subcortical dopaminergic system in the production of response control deficits. Age at onset seems relevant to persistence of deficits in the two congenital conditions and the relative volatility over time of deficits in acquired conditions.

Although both P-ADHD and SBM are congenital conditions, they have distinct attentional and neurobiological profiles. Children with SBM have difficulties with error detection, although not with post-error adjustment. It is possible that they share error detection difficulties with children with P-ADHD because of shared midbrain dysfunction, perhaps related to mesolimbic dopamine (Di Chiara, Reference Di Chiara1998), or mesencephalic function more generally, affecting dorsal ACC and right frontal function. We predict some error detection deficits in children with other forms of structural or neurochemical midbrain dysfunction (e.g., children with pontine tumors).

Temporal Stability of Attention Deficits

Both P-ADHD and SBM have attention deficits that persist over time and, at least for P-ADHD, into adult life. Their common pattern of stability of attention problems over time is consistent with their shared status as genetically based life-long developmental conditions with no period of normal development.

Compared to P-ADHD, children with TBI and S-ADHD have more volatile attention symptoms over time. Children with P-ADHD are evaluated in the school-aged years, and are already into the chronic stage of their attention disorder. It is unclear whether the picture of enhanced symptom volatility in children with TBI and S-ADHD arises because they have been studied in relatively short terms in relation to injury onset. Perhaps S-ADHD recovers over time, while formative brain anomalies ensure that P-ADHD will persist. However, one issue is that the time frame for resolution of cognitive deficits matches long-term TBI degenerative processes (e.g., loss of axonal connections and secondary focal brain atrophy) better than the short-term recovery mechanisms known to be operative (e.g., reduction in inflammatory processes and brain swelling).

Based on our data, we predict that attention deficits, whatever their form, will be more stable over time in developmental conditions (e.g., Sotos syndrome) than in acquired conditions (e.g., childhood strokes).

Cognitive-Energetic Models, White Matter Damage, and Activating the Actor

In their cognitive-energetic model of attention, Russell et al. (Reference Russell, Oades, Tannock, Killeen, Auerbach, Johansen and Sagvolden2006) propose that P-ADHD involves inefficient astrocyte function from deficient ATP production in neurons, over milliseconds, and deficient myelination of axons during development, over months and years. Poor formation and supply of lactate produces inefficient and inconsistent performance in P-ADHD and other white matter disorders (Russell et al., Reference Russell, Oades, Tannock, Killeen, Auerbach, Johansen and Sagvolden2006).

Although ALL treatment produces cortical atrophy (Baron et al., Reference Baron, Fennell and Voeller1995), CRT and/or chemotherapy (Moore, Reference Moore2005) particularly disrupt white matter, disturbances of which range from folate deficiency and subacute myeloencephalopathy to leukoencephalopathy with myelin degeneration and white matter necrosis (Maria et al., Reference Maria, Dennis and Obonsawin1993). Antimetabolites such as methotrexate involved in ALL treatment particularly affect white matter (Cole & Kamen, Reference Cole and Kamen2006). SBM involves two types of white matter disruption, the first involving abnormal white matter development and the second, persistent white matter degeneration with increased age. Diffusion tensor tractography in children with SBM reveals abnormal development in the association pathways (e.g., poor visualization of tracts, impairment in myelination) as well as acquired abnormalities in intrinsic axonal characteristics (Hasan et al., Reference Hasan, Eluvathingal, Kramer, Ewing-Cobbs, Dennis and Fletcher2008a).

The cognitive-energetic model of Russell and colleagues (Reference Russell, Oades, Tannock, Killeen, Auerbach, Johansen and Sagvolden2006) predicts increased response variability with compromised white matter, congenital or acquired. Children with SBM or ALL have little increased variability on sustained attention tasks despite impaired white matter, so our data provide no support for this prediction.

Temporal Processing and the Cerebellum

Temporal processing has been proposed as a key deficit in P-ADHD (e.g., Barkley et al., Reference Barkley, Koplowitz, Anderson and McMurray1997), with a central importance being given to cerebellar abnormalities (Berquin et al., Reference Berquin, Giedd, Jacobsen, Hamburger, Krain, Rapoport and Castellanos1998). The cerebellar abnormalities in P-ADHD are minor compared to the massive cerebellar compromise in SBM, which is associated with abnormalities (in 98%) and volume reductions in the lateral cerebellum (Fletcher et al., Reference Fletcher, Copeland, Frederick, Blaser, Kramer, Northrup, Hannay, Brandt, Francis, Villarreal, Drake, Laurent, Townsend, Inwood, Boudousquie and Dennis2005) and with upward and downward displacement of the cerebellar vermis (Salman et al., Reference Salman, Blaser, Sharpe and Dennis2006a). Children with S-ADHD exhibit the typical P-ADHD attention profile, and are less likely than children with SBM to have cerebellar damage.

Perception of brief time intervals (around 400 ms) is consistently impaired in childhood cerebellar disease (SBM, Dennis et al., Reference Dennis, Edelstein, Hetherington, Copeland, Frederick, Blaser, Kramer, Drake, Brandt and Fletcher2004), adolescents with cerebellar degenerative disease (ataxia-telangiactiasia, Mostofsky et al., Reference Mostofsky, Kunze, Cutting, Lederman and Denckla2000), and adult survivors of childhood cerebellar tumors (Hetherington et al., Reference Hetherington, Dennis and Spiegler2000). Temporal estimation tasks, involving cognitive estimations of longer durations ranging from 4 minutes to a half hour, is intact in adult survivors of childhood cerebellar tumors (Hetherington et al., Reference Hetherington, Dennis and Spiegler2000). Children with P-ADHD cannot estimate long durations, around 4 sec, although they accurately perceive brief durations (Radonovich & Mostofsky, Reference Radonovich and Mostofsky2004), suggesting that the temporal impairment in P-ADHD involves failure to monitor temporal information in working memory rather than a cerebellar central timing deficit (Mahone et al., Reference Mahone, Prahme, Ruble, Mostofsky and Schwartz2007).

Our data temper the view that the cerebellar temporal processing is of primary importance in P-ADHD. Not only is the degree of cerebellar damage unrelated to attention profiles, but children with P-ADHD have temporal estimation rather than timing deficits.

Can Puppets as Well as Actors be Candidate Endophenotypes?

Endophenotypes are hypothetical constructs intervening between genes and symptoms (Almasy & Blangero, Reference Almasy and Blangero2001). Endophenotypes were originally proposed in the context of psychiatric disorders (Gottesman & Gould, Reference Gottesman and Gould2003), but have more recently been used in neurodevelopmental disorders such as ADHD (Aron & Poldrack, Reference Aron and Poldrack2005). Endophenotypes have more explanatory power than the cognitive phenotypes italicized in Figure 1, so we consider whether two of our cognitive phenotypes, response inhibition and IOR, might be considered as candidate endophenotypes. Crosbie et al. (Reference Crosbie, Pérusse, Barr and Schachar2008) examined the theoretical rationale and a priori criteria for validating an endophenotype in P-ADHD and, with Biederman et al. (Reference Biederman, Faraone, Mick, Spencer, Wilens, Kiely, Guite, Ablon, Reed and Warburton1995), propose that a candidate endophenotype should be common in affected individuals (sensitive), relatively unique to the disorder (specific), and relatively uncommon in the general population; they suggest, further, that a powerful way to establish endophenotype status would be to identify markers in cases with genetic, but not acquired, ADHD.

Response inhibition is a candidate endophenotype for P-ADHD (Aron & Poldrack, Reference Aron and Poldrack2005; Crosbie et al., Reference Crosbie, Pérusse, Barr and Schachar2008). While response inhibition deficits are common in P-ADHD, but not in SBM or ALL, and are relatively uncommon in the general population, they also occur in S-ADHD, an acquired condition. A convincing non-genetic etiology for acquired conditions is difficult to demonstrate (Crosbie et al., Reference Crosbie, Pérusse, Barr and Schachar2008), and children with S-ADHD, considered as a group, have elevated rates of P-ADHD. Informative comparisons for invalidating response inhibition as a putative endophenotype would be a study of response inhibition in mild TBI, and a comparison of response inhibition deficits in children with TBI and a de novo S-ADHD diagnosis and those with TBI and preexisting P-ADHD.

Endophenotypes should be state-independent (i.e., should not vary with disease progression or treatment, Crosbie et al., Reference Crosbie, Pérusse, Barr and Schachar2008). Both acquired conditions, TBI and ALL, show cognitive phenotypes that fluctuate with disease characteristics, time since diagnosis, or treatment. Attention is worsened by severe injury in TBI and by adjuvant CRT treatment in ALL, in contrast to the relatively stable patterns of congenital conditions over the lifespan (in P-ADHD and, possibly, in SBM). Cognitive phenotypes in acquired conditions are perhaps less likely than those in congenital conditions to be endophenotypes marking genetic risk.

IOR may be a candidate endophenotype. Children of mothers with a genetic mutation in the folate metabolic pathway share the genetic mutation, have the upper spinal cord lesions (Volcik et al., Reference Volcik, Blanton, Tyerman, Jong, Rott, Page, Romaine and Northrup2000) associated with tectal beaking (Fletcher et al., Reference Fletcher, Copeland, Frederick, Blaser, Kramer, Northrup, Hannay, Brandt, Francis, Villarreal, Drake, Laurent, Townsend, Inwood, Boudousquie and Dennis2005), and have IOR deficits primarily when they have tectal beaking (Dennis et al., Reference Dennis, Edelstein, Copeland, Frederick, Francis, Hetherington, Blaser, Kramer, Drake, Brandt and Fletcher2005b). Children with ALL have a dual compromise of folate metabolism. Part of their treatment-related delayed neurotoxicity is a pharmacologic disruption of CNS folate physiology (Cole & Kamen, Reference Cole and Kamen2006), and they have a genotype involving a folate metabolic mutation linked to inattentive symptoms (Krull et al., Reference Krull, Brouwers, Jain, Zhang, Bomgaars, Dreyer, Mahoney, Bottomley and Okcu2008). While it is not clear that the identical mutations are involved (the C677T methylenetetrahydrofolate is the risk factor for upper spinal lesion level deficits in SBM, Volcik et al., Reference Volcik, Blanton, Tyerman, Jong, Rott, Page, Romaine and Northrup2000, the A1298C methylenetetrahydrofolate genotype is the predominant link to inattention in ALL, Krull et al., Reference Krull, Brouwers, Jain, Zhang, Bomgaars, Dreyer, Mahoney, Bottomley and Okcu2008), there is evidence for a link between folate mutations and inattention. More broadly, candidate endophenotypes for attention disorders might exist, not only in the actor and critic, but also in the puppet and robot.