Postmortem studies in human infants have shown that in the primary somatosensory areas, thalamic axons grow through the subplate, a transient fetal structure underneath the cortical plate, between the 17 and 26th gestational weeks (GW²) (Kostovic and Rakic, 1990; Kostovic et al., 1995). During the early preterm period (26th–34th GW), these axons grow to the cortical plate and form the first thalamo-cortical connections, constituting the anatomical pathway for sensory impulses from the periphery to the cortex. Myelination starts in the human telencephalon around the 14th GW (Zecevic et al., 1998). In the pre- and post-central gyri, myelin is detectable around the 35th GW (Iai et al., 1997). Myelination then proceeds actively during the first postnatal year (Brody et al., 1987) and continues at a slower pace thereafter. In accordance with changes caused by pre-myelination and myelination, in vivo DTI data show a basic pattern of white matter maturation both before and after term-age. As a function of gestational age, mean diffusivity decreases and fractional anisotropy (a measure of relative degree of directionality of diffusion in a voxel) increases in a posterior-to-anterior and a central-to-peripheral order (Hüppi et al., 1998a; Berman et al., 2005; Yoshida et al., 2013).

In human infants, the functionality of the early connections from the periphery through thalamus to the primary somatosensory cortex (SI) can be explored in vivo with somatosensory evoked potentials (SEPs) recorded on the scalp, or with SEFs recorded extracranially with MEG. In preterm infants, median nerve SEPs are recordable on the scalp already by the 25th GW (Hrbek et al., 1973). In the youngest preterm infants (<30 GW), the most striking feature of the scalp SEP is a large negative wave with a mean duration of 1500 ms (Hrbek et al., 1973; Vanhatalo et al., 2009). This slow wave can be detected without averaging when a tactile stimulus is given between bursts of the tracé discontinue EEG pattern of preterm infants (Milh et al., 2007; Vanhatalo et al., 2009). A concerted action of the subplate and cortex may be required for generation of this component (Kanold, 2009; Vanhatalo et al., 2009). With increasing gestational age, the amplitude of this slow wave gradually decreases and an earlier component, usually referred to as N1 in the literature, becomes detectable with a latency of approximately 90 ms somewhere between the 27th (Taylor et al., 1996) and 29th GW (Hrbek et al., 1973). Toward term-age, the N1 latency rapidly decreases (Hrbek et al., 1973; Klimach and Cooke, 1988a; Karniski et al., 1992; Taylor et al., 1996; Smit et al., 2000), reaching approximately 30 ms at term-age (sep_MN30), though with considerable inter-individual variability (Desmedt and Manil, 1970; Hrbek et al., 1973; Laget et al., 1976; Zhu et al., 1987; Laureau et al., 1988; Laureau and Marlot, 1990; George and Taylor, 1991; Gibson et al., 1992; Karniski, 1992).

In term-age infants, primary somatosensory responses have also been studied with MEG. In accordance with the neonatal sep_MN30, the initial SEF to median nerve stimulation in full-term newborns peaks at around 30 ms (sef_MN30). The MEG data together with earlier EEG findings suggest that this earliest cortical response in newborns reflects activation of a similar cortical ensemble as the earliest SEF_MN response in adults (SEF_MN20 peaking at 20 ms) (Lauronen et al., 2006) – that is, summated intracellular currents in cortical pyramidal cells in SI, specifically area 3b in the anterior wall of postcentral gyrus (Allison et al., 1989a). Since the current direction in SI pyramidal cells during this early response is oriented from deeper to more superficial cortical layers, MEG source modeling yields an anteriorly pointing current dipole, which in SEP is recorded as a posterior negativity (SEP_MN20 in adults and sep_MN30 in infants).

The development of this early response during childhood is primarily reflected in its latency (Figure 3). Although the absolute latencies differ between studies (due to, e.g., different stimulation method, filter settings, vigilance state/anesthesia), the general rule is that until the age of approximately 3–5 years, the sep_MN30 and sef_T30 latency decreases and slightly increases thereafter (e.g., Laget et al., 1976; Lauronen et al., 1997; Boor and Goebel, 2000; Gondo et al., 2001; Bercovici et al., 2008; Doria-Lamba et al., 2009; Pihko et al., 2009). These latency changes reflect the increasing neural conduction velocities following myelination and maturation opposed by physical growth of the body and limbs (Müller et al., 1994; Boor and Goebel, 2000; García et al., 2000).

Besides the wiring of thalamo-cortical connections, major developmental changes also occur within the cortex during the second and third trimester as well as postnatally (Marin-Padilla, 1970). Between the 28 and 40th GW, the brain volume more than doubles and cortical gray matter volume extends fourfold (Hüppi et al., 1998b). Postmortem data of human infants show that development of dendrites of cortical pyramidal cells begins during the second trimester from the deeper cortical layers, followed by more superficial layers (Mrzljak et al., 1992). The number of basal dendrites stabilizes around the 27th GW, but their growth in length accelerates during the third trimester and continues postnatally (Mrzljak et al., 1992). Along with dendritic development, the number of synaptic connections increases, starting in the primary sensory areas during the second trimester and proceeding toward higher-order areas. The “boom time” for cortical synaptogenesis in the primary sensory areas extends over the third trimester and the first three postnatal months, resulting in a sixfold increase in synaptic density (Huttenlocher and Dabholkar, 1997). Of intracortical connections in the visual cortex, the first to form are the vertical intracolumnar connections around the 26–29th GW. Horizontal connections follow with intercolumnar projections within layers IVB/V forming around 37th GW and long-range horizontal connections within layer II/III only after 16 postnatal weeks (Burkhalter et al., 1993). These changes in cortical neural structures are also observable in vivo with DTI of the gray matter, where both the mean diffusivity (reflecting an increase in neurite number, cellular complexity, and synapse formation), and fractional anisotropy decline (reflecting an increase in dendritic elongation and branching orthogonal to cortical columns) (Ball et al., 2013). After the third postnatal month, the synaptic density in primary sensory areas decreases gradually, reaching adult levels around puberty (Huttenlocher and Dabholkar, 1997). Some studies on monkeys suggest that the most rapid phase of synapse elimination may occur as late as puberty (Bourgeois and Rakic, 1993).

Marked changes in several neurotransmitter systems also take place around term. One example is the effect of gamma-aminobutyric acid (GABA) on the post-synaptic neuron. In the adult brain, GABA is an inhibitory neurotransmitter. At early stages of development, however, GABA_A receptor activation leads to depolarization (i.e., synaptic excitation) of the post-synaptic neuron due to high intracellular Cl⁻ concentration (Ben-Ari et al., 2004). The change from GABAergic excitation to inhibition in humans likely takes place around or shortly after term (Dzhala et al., 2005).

Evaluating the effects of these changes in the intracortical wiring and “chemistry” of cortical neural processing in vivo is not straight forward, but some inferences can be made from careful examination of neurophysiological data. The deflections following the adult SEF_MN20/SEP_MN20 or neonatal sef_MN30/sep_MN30 are considered to represent a “higher” level of information processing either within local neural circuits of the primary cortical area or in higher-order cortical areas. In a developmental SEP study, Laget and coworkers (Laget et al., 1976) describe substantial changes in the early sep_MN sequence as a function of age. In awake term-age newborns, the early cortical sep_MN usually consisted of a wide initial surface negative potential in the parietal area, peaking at around 40 ms and lasting up to 100 ms. Already during the first postnatal month, a notch directed toward the baseline divided this wide neonatal response into two distinct peaks, the first of which peaked at 30 ms. The notch then grew in amplitude with increasing age and crossed the baseline at around 3–4 months of age. The overall sep_MN morphology attained an adult-like form by age 3 years (Laget et al., 1976). However, as only four recording electrodes were used and, consequently, no source modeling was applicable, it is difficult to infer whether the described changes represent the development of local or larger-scale processing.

Modeling the neural sources underlying the early cortical somatosensory responses in MEG has revealed fundamental, qualitative differences in the cortical activity pattern of neonates compared with school-age children or adults. In adults, regardless of the method of somatosensory stimulation, the hallmark of the early SEF in central contralateral areas is a quick transition from the initial, anteriorly pointing dipolar source (i.e., SEF_MN20/SEF_T30, Figure 2) to a more prominent posteriorly pointing source (i.e., SEF_MN35/SEF_T50, Figure 2). In neonates, no such posteriorly pointing source has been detected at all. Instead, in newborns, the activity of the initial anteriorly pointing source continues over the first 100 ms after both median nerve and tactile stimulation. This difference between adults and newborns holds with different interstimulus intervals (ISI) as well as different vigilance states (particularly also when adults are examined during sleep) (Nevalainen et al., 2008; Pihko et al., 2009). Thus, the neural populations generating the posteriorly pointing neural current source in adult SI are not similarly activated in neonates.

Some previous neonatal SEP studies seemingly disagree with the MEG data by reporting an “adult-like” initial parietal negativity followed by a positivity in the same area with only slightly prolonged latencies (Willis et al., 1984; Laureau et al., 1988; George and Taylor, 1991). This may, however, be an artificial effect of the highpass filter setting applied in these studies (see Pihko and Lauronen, 2004). Others using a lower highpass cutoff value showed a clearly distinct morphology of early neonatal SEPs compared with those of adults (Desmedt and Manil, 1970; Hrbek et al., 1973; Laget et al., 1976; Karniski, 1992; Karniski et al., 1992). Part of the differences between the SEF and SEP data also naturally arises from the different sources preferentially detected by the two methods: tangential in MEG and both tangential and radial in EEG/SEP.

The exact reason for the lack of a posteriorly pointing SI SEF component in newborns can only be speculated, since no general agreement exists on the cellular-level generation mechanism, even in adults (see, e.g., Huttunen, 1997). Whereas the earliest cortical response (SEF_MN20/SEF_T30 and SEP_MN20) is generally agreed to represent thalamo-cortical excitation of pyramidal cells in area 3b of SI (Allison et al., 1989a), the mechanism underlying SEF_MN35/SEF_T50 is not as straight forward. During the SEF_MN35/SEF_T50, the intracellular current flow is directed from superficial to deeper cortical layers (i.e., opposite to that of SEF_MN20/SEF_T30). Such intracellular current could be generated by either inhibition in deeper cortical layers (Huttunen and Hömberg, 1991; Wikström et al., 1996; Restuccia et al., 2002; Huttunen et al., 2008), or by excitation of the pyramidal cell apical dendrites in layers I/II (Allison et al., 1989a). In area 1 of monkeys, both mechanisms seem important in the generation of a similar “superficial-to-deep” intracellular current dipole following the initial “deep-to-superficial” dipole (Gardner and Costanzo, 1980; Gardner et al., 1984; Kulics and Cauller, 1986; Cauller and Kulics, 1991; Nicholson Peterson et al., 1995). In newborns, the absence of a posteriorly pointing source could reflect a lack of functional cortico-cortical connectivity necessary for mediating the response, since many of these connections are established postnatally (Burkhalter et al., 1993; Kostovic and Jovanov-Miloševic, 2006). Alternatively, the possibly still immature GABAergic inhibition could result in absence of the posteriorly pointing SI SEF, since such response is also absent in patients with Angelman syndrome, a disorder caused by a deletion in the GABA_A receptor subunit gene (Egawa et al., 2008). Furthermore, the long-duration of the initial neonatal response might reflect prolonged excitation in the proximal parts of apical dendrites of the pyramidal cells in area 3b, due to, e.g., slow kinetics of intrinsic membrane conductances (Kim et al., 1995; Moody and Bosma, 2005) and immature neurotransmitter receptors.

Though the exact mechanism for the lack of a posteriorly pointing SI SEF component in newborns remains unclear, it clearly reflects immaturity of somatosensory cortical processing. Consequently, emergence of the posteriorly pointing SI SEF likely reflects maturation of the functional somatosensory network. The transition from the neonatal SI response to the adult-like response occurs gradually during the first couple of years of life (Figure 4, Pihko et al., 2009). By 6 months of age, the originally wide U-shaped neonatal tactile SEF-response has turned into a W-shaped response with an emerging notch (Gondo et al., 2001; Pihko et al., 2009). This notch gradually grows in amplitude and crosses the baseline at around age 2 years, when the field pattern, location and direction of the underling currents begin to resemble those of the adult SEF_MN35/SEF_T50. After 2 years of age, the morphology of the responses gradually turns into the mature form with the posteriorly pointing source becoming more and the anteriorly pointing less prominent (Figure 4, Pihko et al., 2009). In school-age children and adolescents, the SEF-response sequence (i.e., anteriorly pointing dipolar source followed by a prominent posteriorly pointing source), is very similar to that of adults (Lauronen et al., 1997; Lauronen, 2001; Xiang et al., 2003; Bast et al., 2007; Nevalainen et al., 2012a). In general, the developmental pattern observed with MEG has a lot in common with the SEP morphology development described by Laget et al. (1976). However, the developmental changes occur at a younger age in SEPs than SEFs, for which there are several possible explanations. First, the SEP study used median nerve stimulation, whereas the developmental SEF study applied tactile stimulation of the index finger. Second, the SEP recordings were performed in awake infants and children, whereas SEFs were recorded during sleep. Third, neural activity in gyri may have a greater contribution to the change in SEPs, whereas MEG mainly reflects activity within sulci. For example, the notch in Laget et al.’s (1976) data may represent activity in the crown of the postcentral gyrus (area 1), which could go unnoticed in MEG. A combined multielectrode EEG–MEG study would clearly provide invaluable information about the differences and similarities in SEP and SEF development and clarify the underlying developmental phenomena.

Relatively little is known about the development of long cortico-cortical connections and the functionality of large-scale neural networks in the prenatal and neonatal period. In humans, callosal unmyelinated fibers are detectable in DTI around the 28th GW (Hüppi et al., 1998a). Postmortem anatomical studies show that after the 35th GW, the long cortico-corticals (e.g., callosal fibers) grow into the cortical plate (Kostovic and Jovanov-Miloševic, 2006). In mice, the region- and layer-specific targeting of callosal projections in the contralateral SI is dependent on electrical excitation and synaptic output of the callosal neurons (Wang et al., 2007). Furthermore, in rhesus monkeys, callosal axons are first overproduced, being three to four times more numerous in newborn than adult monkeys, and their refinement takes place postnatally through callosal axon elimination (LaMantia and Rakic, 1990). Maturation of the callosal connections in humans continues years after birth, as indicated by DTI anisotropy of the corpus callosum, which increases between childhood (7–11 years) and adolescence (15–17 years) (Koerte et al., 2009). Specific knowledge about the development of non-callosal, long cortico-cortical connections is sparse. In general, cortical projection neurons initially have relatively widespread distributions, which become more restricted during development through elimination of functionally inappropriate axon segments and branches (O’Leary et al., 2007).

Recent fMRI data suggest that several resting-state functional networks, including a network encompassing bilateral sensorimotor regions, are present at term-equivalent age (Fransson et al., 2007, 2009; Lin et al., 2008). The neonatal resting-state networks are, however, relatively restricted to homotopic counterparts in the two hemispheres with strong interhemispheric but limited intrahemispheric connectivity, whereas in adults, highly integrated interhemispheric and intrahemispheric connections between disparate regions exist (e.g., Biswal et al., 2010). In general, an increase in strength, complexity, and regional variability of networks are the hallmarks of resting-state fMRI across all periods of development that have been investigated (Lin et al., 2008; Fair et al., 2009; Gao et al., 2009; Supekar et al., 2009; Smyser et al., 2010). Accordingly, the interhemispheric connectivity between the left and right sensorimotor cortices increases both during the preterm period (Doria et al., 2010; Smyser et al., 2010) as well as between birth and age 2 years (Lin et al., 2008; however, see also Liu et al., 2008). Differences in the architecture of the resting-state networks between newborns and adults have also been demonstrated with a graph-theoretical analysis approach to fMRI data. In the adult brain, cortical hubs (brain areas with a disproportionately high degree of functional connectivity, suggesting an important role in the control of information flow) and their related cortical networks are mainly located in higher-order association areas such as posterior cingulate, lateral temporal, lateral parietal, and medial/lateral prefrontal cortices (Achard et al., 2006; Buckner et al., 2009). In contrast, in newborns, cortical hubs and their associated cortical networks are mainly found in primary sensory and motor brain regions (Fransson et al., 2011). However, the resting-state (or background) neural activity during early development and adulthood are different both in terms of generative mechanisms and function. Consequently, the results of developmental resting-state studies using indirect measures of neural activity (such as hemodynamic changes in fMRI) should be interpreted conservatively (Colonnese and Khazipov, 2012). In adults resting-state fMRI activity is thought to reflect the slow modulation of ongoing oscillatory activity generated by dense cortico-cortical networks. During early development (particularly during prematurity), however, the source of the slow fluctuations in resting-state fMRI may reflect alternating periods of electrical silence and bursts generated in sensory networks, driven by spontaneous activity in the periphery that interacts with the thalamo-cortical networks (Colonnese and Khazipov, 2012).

Altogether, studies of resting-state networks and brain anatomy suggest that at the time of full-term birth, the large-scale brain networks are immature and their connectivity patterns restricted. However, both fMRI and MEG studies in newborns have demonstrated ipsilateral SI responses, and MEG studies have revealed bilateral SII responses at term-age.

In fMRI, unilateral passive finger extension–flexion movements elicited BOLD (blood-oxygen-level dependent) responses in contra- and ipsilateral SI without significant differences between the hemispheres. This was interpreted as immature lateralization of somatosensory processing in newborns (Erberich et al., 2006; Heep et al., 2009). MEG responses from ipsilateral SI are detectable only in a minority of healthy newborns, however, and have longer latencies (approximately 20-100 ms) than the contralateral responses (Nevalainen et al., 2008). This suggests that the ipsilateral SEFs are unlikely to represent cortical activation via direct thalamo-cortical pathways, but could be generated through callosal connections that can be relatively abundant at term-age (LaMantia and Rakic, 1990). The millisecond scale latency difference between the contra- and ipsilateral MEG SI activations in neonates would go unnoticed in fMRI, likely explaining the lack of difference between signals at contra- and ipsilateral SI reported by Erberich et al. (2006). Interestingly, at 3 months of age follow-up, the BOLD fMRI signal changes already exhibit an adult-like contralateral SI activation, which persisted at 6 and 9 months (Erberich et al., 2006; Heep et al., 2009). No MEG or EEG reports exist on ipsilateral SI response development in early childhood after the neonatal period.

In adults, unilateral tactile stimulation elicits ipsilateral positive BOLD signals in the posterior parts of SI, probably area 2, in agreement with the bilateral representation of digits in area 2 in monkeys (Fabri et al., 1999; Polonara et al., 1999; Iwamura et al., 2002). With MEG, activation of ipsilateral SI in adult subjects has been detected in some studies (Korvenoja et al., 1995; Kanno et al., 2003; Hadoush et al., 2010; Pihko et al., 2010). Intracranial recordings confirm the presence of ipsilateral SEPs in some epilepsy and tumor patients. In contrast to contralateral responses, they originate only from Brodmann areas 1 and 2, have longer latencies, smaller amplitudes, and no initial surface negativity or phase reversal across the central sulcus (Allison et al., 1989b; Noachtar et al., 1997). The difference in sensitivity to the direction of underlying currents (mostly radial from area 1) and synchronization of activity could explain why ipsilateral responses from areas 1 and 2 are detected better with fMRI than MEG. Another explanation for the rarely reported ipsilateral SI responses in adults may involve transcallosal inhibition of ipsilateral area 3b after unilateral somatosensory stimulation (Hlushchuk and Hari, 2006). In the motor system, transcallosal inhibition is absent in infancy and early childhood (Müller et al., 1997; Heinen et al., 1998). The presence of ipsilateral SI responses could reflect lack of transcallosal inhibition in the somatosensory system in early childhood.

Knowledge of somatosensory processing beyond SI was limited before the era of MEG and modern neuroimaging. Since then, these methods have shown that, in the mature somatosensory system, information processing takes place in a wide network, including at least frontoparietal operculum (e.g., the bilateral SII), posterior parietal cortex, and mesial paracentral lobule (see, e.g., Hari and Forss, 1999 for MEG and Disbrow et al., 2000 for fMRI).

Neonatal MEG studies have demonstrated that, after tactile and median nerve stimulation, a prominent deflection in the contralateral hemisphere peaks at about 230 ms (sef_MN230/sef_T230; Figure 5). The generator source underlying this deflection has been localized to the parietal operculum and thus sef_T230 most likely represents activity in SII (Pihko et al., 2005; Nevalainen et al., 2008, 2012b). This indicates that the connections to and the neurons in SII are sufficiently developed to produce a detectable SEF response at full-term-age, although with a longer peak latency (approximately 230 ms) than in adulthood (approximately 100 ms; e.g., Hari and Forss, 1999). The neonatal SII response does have some similar characteristics with the mature SII response: it is often detectable not only contralaterally but also ipsilaterally and is diminished with the shortening of the ISI (Nevalainen et al., 2008). Interestingly though, the neonatal SII response is particularly prominent in quiet sleep (Pihko et al., 2004; Nevalainen et al., 2008), whereas in adults it is diminished or even vanishes in non-REM sleep (Kitamura et al., 1996; Kakigi et al., 2003; our own unpublished observation). Thus, from an ontogenetic point of view, SII activation in quiet sleep in newborns may have a function in the maturation of the somatosensory neural network. No reports exist about the development of SII responses in early childhood after the neonatal period.

In neonatal SEP studies, several investigators consistently detected a peak at a latency of around 230 ms (Desmedt and Manil, 1970; Hrbek et al., 1973; Laget et al., 1976; Karniski, 1992; Pihko and Lauronen, 2004; Pihko et al., 2004), with a positivity at the vertex (Desmedt and Manil, 1970; Pihko and Lauronen, 2004; Pihko et al., 2004). Although this SEP response was usually recorded with only a few electrodes, and hence no source modeling was applicable, in retrospect with knowledge from MEG studies, it can be interpreted to represent activity from SII. SEP studies on the evolution of this response with age are also lacking.

Although the survival of very preterm infants has increased significantly during recent decades (Vohr et al., 2005), many of these infants still develop with neurological impairments. Neonatal neurological examination is challenged by the non-specificity of signs of neural dysfunction (discussed above) and, consequently, complementary biomarkers for adverse outcome have been sought from neuroimaging and neurophysiology. As the period of active dendritic development and synapse formation is likely to offer better possibilities for rehabilitation than later periods (Kolb, 1999), interventions need to be started at an early age (note, however, the suggested reasons for restricting interventions before term-age: De Graaf-Peters and Hadders-Algra, 2006). Consequently, early prediction of outcome is essential for rehabilitation resources to be offered to those most in need.

Classical risk factors for adverse neurological outcome, including cystic periventricular leukomalacia (PVL) and grade III–IV IVH picked up by cranial ultrasound (Neil and Inder, 2004), are seen ever more rarely, and preterm infants with normal cranial ultrasound may have adverse outcomes (Laptook et al., 2005). At present, the type of pathology suggested to account for most of the neurological problems of preterm infants is diffuse white matter injury (WMI) (Khwaja and Volpe, 2008). WMI is further associated with impaired cerebral cortical development (Inder et al., 1999) and is also likely to lead to impaired development of cortico-cortical connectivity (Mathur and Inder, 2009). In preterm infants, moderate to severe white matter abnormalities in MRI at term-age are associated with severe cognitive and motor dysfunction at 2 years of age (Woodward et al., 2006) and cognitive, language and executive function impairment at 4 and 6 years of age (Woodward et al., 2012).

Furthermore, defects in the microstructural development of the cortex, reflected in DTI as higher mean diffusivity and fractional anisotropy in gray matter in preterm vs. term infants at term-equivalent age, may underlie adverse neurodevelopmental outcome. A slower decline in mean diffusivity during the preterm period was associated with lower overall developmental scores in Griffiths Mental Development Scales at 2 years corrected age (Ball et al., 2013). Moreover, at term-equivalent age, fMRI data have demonstrated significant differences between the resting-state networks of preterm infants and term-born controls. Specifically, functional connectivity between thalamus and sensorimotor cortex was weaker in the preterm infants than in the full-term infants (Smyser et al., 2010).

Possible injury to the thalamo-cortical connections due to periventricular pathology has also motivated a wealth of SEP studies in preterm infants to assess the predictive value of abnormal (absent or delayed depending on the study) median nerve sep_MN30 (usually referred to as N1 in the literature; Klimach and Cooke, 1988b; Willis et al., 1989; de Vries et al., 1992; Pierrat et al., 1997) and the earliest posterior tibial nerve SEP (referred to as P1) from SI for future cerebral palsy (CP) (White and Cooke, 1994; Pierrat et al., 1997; Pike and Marlow, 2000). Results have been, however, somewhat contradictory, with specificity, sensitivity, and positive and negative predictive values varying markedly between studies. At least part of this variation is probably explained by differences in patient inclusion criteria, methods of SEP assessment, and outcome measure as well as technical difficulties in reliably recording the responses, particularly in the youngest infants (Smit et al., 2000).

A recent MEG study has expanded the somatosensory response evaluation from SI to SII, thus including cortico-cortical processing assessment. SEFs were recorded at term-age from 39 extremely preterm infants (born <28 GW) whose neurodevelopmental outcome was assessed at 2 years corrected age (Rahkonen et al., 2013). MEG data showed that, while SI responses were present in all the preterm infants, the SII response was absent uni- or bilaterally in a third of them. At follow-up, those infants with SII responses missing at term had worse neuromotor and overall developmental scores in the Griffiths Mental Developmental Scales assessment than the preterm infants with normal SII response present at term (Rahkonen et al., 2013). On the contrary, in this study, mild white matter abnormalities in MRI at term-age were not associated with adverse neurodevelopment (the study group did not include infants with moderate/severe WMI) (Rahkonen et al., 2013). It was speculated that the absence of SII responses may reflect not only damage to the connections within the sensorimotor networks but also more widespread disturbances in the development of cortico-cortical connectivity. Behaviorally, SII areas are considered to be involved in the integration of somatic inputs across large portions of the hand, sensorimotor integration, and bimanual coordination (see, e.g., Disbrow et al., 2000 for a discussion), motivating further SII response studies in preterm infants. Many such infants develop with minor neuromotor dysfunction and poor coordination (Hadders-Algra, 2002; Saigal and Doyle, 2008).

Cerebral palsy, caused by an early lesion to the developing brain, is a persistent disorder of movement and posture often accompanied by various sensory deficits. When the early lesion is unilateral and severe enough, in some individuals the sensorimotor networks may develop into an unusual configuration. During normal development, the originally bilateral cortico-spinal motor innervation (Eyre et al., 2001; Eyre, 2003) is reduced to mainly contralateral connections during the first two postnatal years through elimination of most ipsilateral projections. However, after an early unilateral brain insult, the ipsilateral cortico-spinal projections can be, to a great extent, maintained. In such cases of hemiplegic CP, instead of the normal contralateral motor representation, transcranial magnetic stimulation (TMS) may demonstrate bilateral or completely ipsilateral motor representation of the plegic extremity depending on the timing, location, and extent of the lesion (Staudt et al., 2002, 2004, 2006; Eyre, 2007). The mechanisms for preservation of the ipsilateral cortico-spinal projections are thought to involve activity-dependent competition for spinal synaptic space (Eyre, 2007).

Contrary to the motor system, after both subcortical and cortico-subcortical early brain lesions, primary somatosensory representation of the affected hand generally remains in the contralateral (i.e., ipsilesional) hemisphere as demonstrated by MEG (Gerloff et al., 2006; Staudt et al., 2006; Wilke et al., 2009; Nevalainen et al., 2012a; Pihko et al., 2014), SEPs (Guzzetta et al., 2007), and fMRI (Wilke et al., 2009). Consequently, contralesionally organized motor representation results in the dissociation of somatosensory and motor cortical representations (Staudt et al., 2006; Guzzetta et al., 2007; Wilke et al., 2009). With limited interhemispheric and intrahemispheric reorganization capability, the somatosensory system seems to be particularly vulnerable to lesions extending to the neocortex (Wilke et al., 2009), especially those including areas SI, SII, and/or inferior parietal cortex (Juenger et al., 2011). When the cortex is spared, ascending thalamo-cortical tracts are able to bypass subcortical periventricular white matter lesions, as shown by DTI, and connect to their normal destinations in SI, even in patients with extensive subcortical lesions and ipsilateral motor representation (Staudt et al., 2006). Clinically, somatosensory abilities in such patients are relatively well preserved (Wilke et al., 2009), despite the fact that the fiber count in the thalamo-cortical somatosensory tract may be reduced (Thomas et al., 2005).

In CP patients with unilateral subcortical lesions and contralateral somatosensory representation, somatosensory MEG data reveal alterations in cortical somatosensory processing in both hemispheres (Nevalainen et al., 2012a). First, after median nerve stimulation, the normal activation sequence of SI (SEF_MN20–SEF_MN35) was disrupted in both hemispheres by an additional peak, SEF_MN25, with posterior current orientation, preceding a delayed SEF_MN35. Second, within SI, the cortical representations of contralateral digits II and V were located abnormally close to each other in both hemispheres. Unilateral spatial alterations in the hand representation area have been detected by fMRI, where the area activated by passive hand movement showed larger inter-individual spatial variability in the affected than unaffected hemisphere in patients with CP (Wilke et al., 2009). Third, compared with typically developing adolescents, in the CP patients, SEFs from ipsilateral SI in response to stimulation of the normal hand were more frequent. Thus, the ipsilateral responses in the CP patients do not suggest contralesional (i.e., ipsilateral) reorganization of the somatosensory representation from the affected hand (Nevalainen et al., 2012a). They may, however, reflect another form of unusual organization of the sensorimotor networks and/or lack of the usual ipsilateral area 3b inhibition (Hlushchuk and Hari, 2006). Deficient transcallosal inhibition between the motor cortices has been demonstrated with TMS in some (Heinen et al., 1999), though not all, diplegic CP patients (Koerte et al., 2011).

The dissociation of primary motor and somatosensory representations into different hemispheres in some individuals with CP offers a unique opportunity to study reactivity of sensorimotor oscillations separately from SI and the primary motor area (MI). (Usually, SI and MI locations in the post- and precentral gyri are in such close proximity to each other that separating sources originating from the two areas with certainty in MEG is difficult.) In three CP patients, Gerloff et al. (2006) observed using MEG the corticomuscular coherence to voluntary, paretic hand isometric contraction in the ipsilateral precentral gyrus at a location similar to where TMS evoked responses in the paretic hand muscles. This result suggests that the cortical signal coherent with electromyography during isometric contraction represents the driving volley from MI, and not sensory feedback processing within SI. In another study, in two CP patients with dissociation of motor and somatosensory representations, stimulation of the median nerve of the affected hand did not modulate the sensorimotor beta-band oscillations in either hemisphere, even though oscillations in alpha-band were modulated in both hemispheres (Pihko et al., 2014). These data suggest that the somatosensory afferent flow to the contralateral cortex was unable to influence the excitability of the motor cortex in the ipsilateral hemisphere controlling the affected hand.

Discoveries of the large-scale alterations in the wiring of the sensorimotor brain networks in people with CP clearly demonstrate the power of multimodal functional investigation of the developing brain. MEG is an essential tool in the brain development investigation toolbox, particularly when used in combination with other non-invasive methods, such as DTI, fMRI, and TMS. The puzzle of brain network organization after early insults of different scale, timing, and etiology, however, still remains only partly solved. The heterogeneity in this patient population calls for large multi-methodological studies to reveal the principles of vulnerability vs. plastic potential in brain organization after early brain insults.