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  • Open Access

Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia

  • 1,
  • 2, 3,
  • 2, 4,
  • 2, 3,
  • 5, 6 and
  • 2, 4, 7, 8Email author
Annals of General Psychiatry201413:18

  • Received: 17 November 2013
  • Accepted: 29 May 2014
  • Published:



Neuregulins are a family of signalling proteins that orchestrate a broad range of cellular responses. Four genes encoding Neuregulins 1–4 have been identified so far in vertebrates. Among them, Neuregulin 1 and Neuregulin 3 have been reported to contribute to an increased risk for developing schizophrenia. We hypothesized that three specific variants of these genes (rs6994992 and rs3924999 for Neuregulin 1 and rs10748842 for Neuregulin 3) that have been related to this illness may modify information processing capacity in the cortex, which would be reflected in electrophysiological parameters (P3b amplitude or gamma noise power) and/or cognitive performance.


We obtained DNA from 31 patients with schizophrenia and 23 healthy controls and analyzed NRG1 rs6994992, NRG1 rs3924999 and NRG3 rs10748842 promoter polymorphisms by allelic discrimination with real-time polymerase chain reaction (PCR). We compared cognitive outcome, P300 amplitude parameters and an electroencephalographic measure of noise power in the gamma band between the groups dichotomized according to genotype.


Contrary to our hypothesis, we could not detect any significant influence of variation in Neuregulin 1/Neuregulin 3 polymorphisms on cognitive performance or electrophysiological parameters of patients with schizophrenia.


Despite our findings, we cannot discard that other genetic variants and, more likely, interactions between those variants and with genetic variation related to different pathways may still influence cerebral processing in schizophrenia.


  • Schizophrenia
  • Brain wave
  • Auditory evoked potential
  • NRG1 protein
  • NRG3 protein


It is possible that the link between genetic variation in neuregulin (NRG) and the increased risk of developing schizophrenia could be established through the influence NRG has on the regulation of distributed cerebral activity. NRGs are a family of signalling proteins containing an epidermal growth factor (EGF)-like domain that activates ErbB receptor-tyrosine kinases, which orchestrate a broad range of cellular responses [13]. Among them, Neuregulin 1 (NRG1) has a significant impact upon differentiation, migration and maturation of gamma-Aminobutyric acid (GABA) interneurons [4]. The influence attributed to NRG1-ErbB4 signaling network may have relevant consequences on information processing in the brain, as suggested by the enhancing effect NRG1 displayed on gamma oscillations [5].

Genetic variation in NRG1 was associated to an increased risk for developing schizophrenia [6]. Among the several markers in this gene, the single-nucleotide polymorphism (SNP) rs6994992 (SNP8NRG243177) in the promoter region is particularly interesting because of its effect on the expression levels of type-IV NRG1 in human post-mortem brain samples and in luciferase in vitro assays [7, 8]. Other genetic variants related to NRG1 have been associated to schizophrenia, such as the non-synonymous (Arg/Gln) SNP rs3924999 [9]. This SNP, which maps to exon E344/E178 (Ig domain), has been associated to higher latency of the P300 potential [10].

Less information is available on the biological functions and possible relevance of Neuregulin 3 (NRG3) for mental illness. However, it is well established that NRG3 is a specific ligand for ErbB4 [11] and plays an outstanding role in the development of the cerebral cortex [12]. Four main classes of NRG3 are generated by alternative splicing [13]. Genetic variation in NRG3 (1.1 Mb, chr.10q23.1), rs10748842 at intron 1, has also been reported to increase the risk for schizophrenia and to exert a functional effect on the expression of class II and III NRG3 isoforms [13].

Among the possible electrophysiological correlates for genetic variation in NRG, we can highlight the P300 potential amplitude and cortical noise power. Cortical noise power refers to the amount of scalp-recorded power not temporally locked to stimuli, quantified as the difference in each band between the mean power of single trials and the power magnitude in the averaged potential [14, 15]. P3b amplitude decrease and gamma noise power excess have been previously reported in schizophrenia, the latter inversely correlated to cognitive performance and directly to negative symptoms [1618].

We hypothesized that NRG variants (i.e., rs6994992 and rs3924999 for NRG1 and rs10748842 for NRG3) may modify the information processing capacity in the cortex, which would be reflected in electrophysiological parameters (P3b amplitude or gamma noise power) and/or cognitive performance.


We included 31 patients with paranoid schizophrenia (DSM-IV-TR criteria) and 23 healthy controls (HC). This sample partly overlaps with that of our previous reports on noise power in schizophrenia [16, 17].

The schizophrenia cases included 10 stable, treated in the long-term, and 21 untreated cases who received a minimal treatment prior to the electroencephalographic (EEG) examination (minimally treated patients; 12 males), of which 12 were first episodes (7 males). During the preceding year, the stable patients had been treated with risperidone (7 cases (2 to 6 mg/day)) or olanzapine (3 cases (5 to 15 mg/day)). Doses and drugs were unchanged during the 3 months preceding EEG recordings. Prior to their inclusion, minimally treated patients had not received any previous treatment (first episode patients) or they had dropped their medications for a period longer than 1 month. Owing to an acute psychotic state of these patients prior to inclusion, we administered a small amount of haloperidol (2 to 4 mg) 2 days before the EEG study, with a wash-out period of approximately 24 h before EEG. The objective was to minimize the likely bias of only including patients able to cooperate with the EEG recording during an acute psychotic episode. As we reported elsewhere [16, 17], this treatment had no significant effect on gamma noise power measurements.

We scored the clinical status of the patients using the Positive and Negative Syndrome Scale (PANSS) [19]. Marital status was stratified into single (single, divorced, separated) or living in couple, and employment status as employed (currently studying or working) or unemployed (looking for a job or retired for health reasons). Education was quantified as completed academic courses; the number of years within the education system since the first official academic year (usually at 6 years old) until the last completed course before dropping out of the system.

We recruited HC through newspaper advertisements and remunerated their cooperation. They were previously assessed using a semi-structured psychiatric interview by one investigator (VM) to discard major psychiatric antecedents (personal or familial) and treatments.

The exclusion criteria included intelligence quotient (IQ) below 70; a history of any neurological illness; cranial trauma with loss of consciousness; past or present substance abuse, except nicotine or caffeine; the presence of any other psychiatric process or treatment and treatment with drugs known to act on the central nervous system. Toxic use was discarded in patients and HC with the information gathered in the interview and a urinalysis.

We obtained written informed consent from the patients and HC after providing full written information. The research board (University Hospital of Salamanca) endorsed the study according to The Code of Ethics of the World Medical Association (Declaration of Helsinki).

Cognitive assessment

We acquired cognitive assessment using the direct scores from the following subscales of the Spanish version of Brief Assessment in Cognition in Schizophrenia Scale (BACS) [20], administered by trained researchers (VS, ÁD): verbal memory (words list learning), working memory (digit span), motor speed (token motor task), verbal fluency (categories), attention and processing speed (symbol coding), and executive function/problem solving (tower of London). We used the Spanish version of the Wechsler Adult Intelligence Scale 3rd Edition (WAIS-III) [21] to assess IQ.

EEG methods

The EEG methods have been reported in detail elsewhere [16, 17]. Essentially, EEG recordings were performed during an odd-ball task in which P3a and P3b were elicited and measured in the Pz site (see Additional file 1 for details). The EEG was recorded by the Brain Vision® (Brain Products GmbH; Munich, Germany) equipment from 17 tin electrodes mounted in an electrode cap (Electro-Cap International, Inc.; Eaton, OH, USA), impedance kept under 5 kΩ. The on-line register was referenced over Cz electrode and re-referenced off-line to the electrodes' average activity [22]. The sampling rate was 250 Hz, and the signal was recorded continuously. We selected noise power values at F3, F4, P3 and P4 electrodes for the analysis according to our a priori hypothesis. See Additional file 1 for detailed information on EEG recording.

For quantitative event-related EEG analysis, the recorded signals (−50 to 600 ms post-stimulus, target condition) were submitted to specific band filtering and spectrum analysis using a fast Fourier transform yielding spectral values. The absolute magnitude (averaged total power) in gamma band (35 to 45 Hz) was computed and expressed in μV2.

As described in previous articles [16, 17], we calculated noise magnitude, which is subsequently denoted as ‘noise power’. This calculation was based on signal-to-noise ratio (SNR), a measure of the quality of the EEG signal applied to each band; it is calculated using the Brain Vision® software (Brain Products GmbH; Munich, Germany) [23] for the time window from −50 to 600 ms for the target stimuli.

For every individual participant, band and electrode, we calculated the averaged noise power from the already extracted average total power (the sum of the signal and noise power) and SNR (the average signal power quotient divided by the average noise power) using the following formula:
Avg noise power = Avg total power SNR + 1

This way, a quantification of the noise part of the activity related to the event is approximated and ‘noise’ is equivalent with activity that is not time-locked to the stimuli (see Additional file 1 for details).

Genetic methods

DNA extraction

High molecular weight DNA obtained from peripheral leukocyte blood was isolated using standard procedures with proteinase K and phenol-chloroform purification.

We extracted buccal cells using simple and sterile swabs, without medium (Aptaca, Canelli, Italy). The procedure for the DNA extraction was similar to the protocol for obtaining DNA from peripheral blood except for the proteinase K incubation, which in this case was longer.

Some of the samples extracted from buccal cells have shown a very low DNA concentration. In these cases, we amplified genomic DNA with DNA IllustraTM Amplication GenomiPhi V2 Kit (GE Healthcare, Buckinghamshire, UK).

Allelic discrimination by real-time PCR

The analysis of NRG1 rs6994992, NRG1 rs3924999 and NRG3 rs10748842 promoter polymorphisms was carried out using allelic discrimination with real-time polymerase chain reaction (PCR). The final volume of the reaction consisted of 10 μl and we used commercial mixtures of primers and TaqMan MGB® probes (C_22019_10, C_359159_10 and C_1266043_10, respectively) with the sequences VIC: AAGCACCATGCAGGGTTCAAGTGAAC GTATACTGGAGGCCAGACCTGCCCA and FAM: AAGCACCATGCAGGGTTCAAGTGAAT GTATACTGGAGGCCAGACCTGCCCA for the first polymorphism; VIC: TTTCTTCTTTTAGCCTTGCCTCCCCA ATTGAAAGAGATGAAAAGCCAGGAA and FAM: TTTCTTCTTTTAGCCTTGCCTCCCCG ATTGAAAGAGATGAAAAGCCAGGAA for the second one; and VIC: TTGCATTGTGAGAGGCTCTGAGTAAC TTATGATAAATAATGAAATGCTGTT and FAM: TTGCATTGTGAGAGGCTCTGAGTAAT TTATGATAAATAATGAAATGCTGTT for the third (Applied Biosystems, Foster City, CA, USA). We used TaqMan® Universal PCR Master Mix No AmpErase® UNG (Applied Biosystems, Foster City, CA, USA) containing the DNA polymerase. The amplification program had a denaturing temperature of 94°C, annealing of 60°C and extension of 72°C for 1 min each during 40 cycles.

Statistical analyses

By using Chi squared test or Student's t test for independent samples when appropriate, we compared demographic scores between groups. We also used Student's t test for comparing neurocognitive and neurophysiological parameters between patients and HC groups.

We studied the possible effect of long-term illness and medication over cognition and neurophysiology by comparing chronic and minimally treated patients' outcome using a non-parametrical test (Mann-Whitney's U test).

In order to test the study's main hypotheses (differences in cognition, gamma noise power and P300 parameters related to genetic variation), we dichotomized the variable rs6994992 into carriers (T+) or non-carriers (T−) of this risk allele (i.e., TT and TC group vs. CC group). Variable rs3924999 variation was dichotomized into carriers and non-carriers of the A allele (AA and AG vs. GG homozygous). As for NRG3 rs10748842, our sample only included TT and CT participants.

We used Mann-Whitney's U tests to compare total IQ and BACS scores, P300 amplitude (P3a and P3b) and gamma noise power at F3, F4, P3 and P4 electrodes between the groups dichotomized according to their genotype. Moreover, using the same test, we compared each group of patients with the HC carrying the same variation. We repeated these analyses only including the minimally treated patients' subgroup in order to discard the effects of treatment and chronicity on the arising differences. However, on account of our sample size, the results yielded by these secondary analyses were only considered as informational. Given the number of planned comparisons (gamma noise power in four electrodes, P3a and P3b amplitudes and 6 cognitive variables × 3 genetic variants = 36 comparisons), we set the level of corrected significance at p = 0.001 (0.05 × 36 = 0.00138). Accordingly, trend level was set at p = 0.006. These restrictions were not applied to the initial comparisons between patients and HC that did not consider genotype because these comparisons were descriptive and did not explore the study's hypothesis.

Finally, taking into account our limited sample size, we performed a power analysis for each of the comparisons involving genetic variants (Bonferroni-corrected significance level of p = 0.001; see Additional file 1 for details).


Patients vs. HC comparisons

There were no significant differences in age (t = 1.306, df = 52, p = 0.197) or sex distribution (χ2 = 0.013, df = 1, p = 0.910) between patients and HC. Marital (χ2 = 7.014, df = 1, p = 0.008) and employment status (χ2 = 5.994, df = 1, p = 0.014) were significantly different between groups. IQ and all BACS scores were significantly lower in patients (Table 1).
Table 1

Sociodemographic, clinical, cognitive and neurophysiological values in patients and healthy controls


All patients (N = 31)

Healthy controls (N = 23)


36.42 (12.07)

31.91 (13.14)

Sex (M:F)



Marital status (% singles)**



Employment status (% employed)*



Education (completed courses)

10.94 (3.81)

11.50 (3.00)

Total IQ**

81.68 (14.20)

104.00 (13.09)

PANSS positive

20.25 (4.33)


PANSS negative

19.68 (5.54)


PANSS total

75.46 (12.11)


BACS - verbal memory***

36.18 (12.38)

54.87 (7.68)

BACS - working memory***

16.93 (5.16)

22.17 (3.77)

BACS - motor speed***

50.24 (15.52)

64.61 (14.85)

BACS - verbal fluency***

16.41 (4.76)

25.48 (4.84)

BACS - processing speed***

37.32 (14.72)

58.57 (12.24)

BACS - problem solving***

12.33 (6.12)

17.52 (3.10)

P3b valid segments (n)



Pz amplitude S2 (P3a; μV)

0.870 (1.125)

1.297 (0.981)

Pz amplitude S3 (P3b; μV)**

0.815 (1.587)

1.935 (0.910)

Gamma noise power F3 (μV2)

0.012 (0.012)

0.009 (0.015)

Gamma noise power F4 (μV2)

0.012 (0.013)

0.008 (0.009)

Gamma noise power P3 (μV2)**

0.012 (0.009)

0.006 (0.004)

Gamma noise power P4 (μV2)**

0.012 (0.007)

0.007 (0.004)

Data specified as percentage (%), simple distribution or pertaining to Mean (S.D.); *p < 0.05; **p < 0.01; ***p < 0.001 (Chi square test or Student's t test when corresponding); N/A, not applicable.

Patients showed a significant reduction in P3b amplitude (t = 3.029; df = 52; p = 0.004) and a significantly higher gamma noise power at P3 (t = 2.971; df = 52; p = 0.004) and P4 (t = 2.669; df = 52; p = 0.010) electrodes in comparison to HC (Table 1).

Chronic vs. minimally treated patients

Chronic patients were significantly older and had more negative symptoms than minimally treated patients (p < 0.01). There were no significant differences between these groups in the main cognitive and neurophysiological measures (Additional file 1: Table S1).

Genetic-related differences

NRG1 rs6994992

There were 21 T + (TT homozygous or TC heterozygous) and 10 T − (CC) in the patient group (13 and 8 respectively for minimally treated patients). In the HC group, there were 12 T + and 11 T−. This difference was not significant (χ2 = 1.347, df = 1, p = 0.246).

There were no significant differences in cognitive performance between T + vs. T − patients or between T + and T − HC, even at uncorrected p < 0.05 level (Table 2). Power values were low in all cases (P < 18%) (Additional file 1: Table S3).
Table 2

Sociodemographic, clinical, cognitive and neurophysiological values according to NRG1 rs6994992 and rs3924999, and NRG3 rs10748842 genotypes


NRG1 rs6994992

NRG1 rs3924999

NRG3 rs10748842



Healthy controls


Healthy controls


Healthy controls


T + (N = 21)

T − (N = 10)

T + (N = 12)

T − (N = 11)

A + (N = 18)

A − (N = 13)

A + (N = 16)

A − (N = 7)

C + (N = 8)

C − (N = 23)

C + (N = 4)

C − (N = 19)

Age (years)

36.24 (12.26)

36.80 (12.33)

33.92 (14.86)

29.73 (11.25)

35.50 (14.02)

37.69 (9.10)*

33.69 (13.42)

27.86 (12.44)

35.38 (8.40)

36.78 (13.26)

40.25 (21.22)

30.16 (10.82)

Total IQ

82.16 (15.85)***

80.67 (10.62)**

101.92 (11.91)

106.27 (14.50)

81.13 (14.74)***

82.42 (14.04)**

104.19 (14.10)

103.57 (11.47)

83.67 (10.58)*

81.14 (15.20)***

106.25 (14.34)

103.53 (13.19)

PANSS positive

20.05 (3.56)

20.75 (6.14)



20.94 (4.48)

19.33 (4.14)



19.86 (5.11)

20.38 (4.18)



PANSS negative

20.10 (5.77)

18.63 (5.13)



17.69 (5.10)*

22.33 (5.14)



20.29 (7.89)

19.48 (4.75)



PANSS total

75.75 (11.00)

74.75 (15.37)



71.88 (11.62)

80.25 (11.48)



75.00 (11.66)

75.62 (12.53)



BACS verbal memory

35.44 (14.14)**

37.50 (8.90)***

51.75 (8.71)

58.27 (4.69)

37.53 (13.30)***

34.09 (11.09)*

55.50 (6.61)

53.43 (10.18)

34.86 (14.04)

36.62 (12.12)***

50.25 (9.91)

55.84 (7.07)

BACS working memory

16.33 (5.82)**

18.11 (3.48)*

22.17 (4.34)

22.18 (3.25)

17.13 (5.15)**

16.67 (5.38)

22.50 (3.18)

21.43 (5.09)

16.83 (4.54)*

16.95 (5.43)**

23.00 (1.41)

22.00 (4.11)

BACS motor speed

48.63 (17.03)*

53.30 (12.37)

65.33 (15.69)

63.82 (14.60)

52.18 (14.63)

47.50 (16.95)**

60.75 (14.23)

73.43 (13.10)

50.43 (13.76)

50.18 (16.34)**

59.50 (23.74)

65.68 (12.98)

BACS verbal fluency

16.32 (5.38)***

16.60 (3.53)***

25.17 (5.37)

25.82 (4.42)

16.12 (5.13)***

16.83 (4.34)*

27.13 (3.38)

21.71 (5.79)

17.43 (3.60)**

16.09 (5.10)***

27.75 (4.35)

25.00 (4.91)

BACS processing speed

38.33 (17.47)**

35.50 (8.25)***

57.17 (11.47)

60.09 (13.42)

38.24 (16.74)***

35.91 (11.53)**

60.13 (13.02)

55.00 (10.21)

37.86 (14.46)

37.14 (15.15)***

49.75 (5.44)

60.42 (12.54)

BACS problem solving

13.41 (5.48)

10.50 (7.00)*

16.92 (3.06)

18.18 (3.16)

11.50 (6.20)**

13.55 (6.09)

17.25 (3.32)

18.14 (2.67)

12.86 (5.61)

12.15 (6.42)**

15.75 (3.77)

17.89 (2.92)

P3b valid segments (n)

45.76 (18.53)

43.00 (26.62)

53.25 (25.03)

61.36 (24.33)

43.00 (21.01)

47.46 (21.68)

54.94 (25.72)

62.14 (22.41)

47.38 (27.51)

44.00 (18.99)

54.00 (17.42)

57.79 (26.07)

Pz amplitude S2 (P3a; μV)

0.968 (1.127)

0.666 (1.154)

1.485 (0.762)

1.093 (1.179)

0.929 (1.193)

0.789 (1.066)

1.210 (0.982)

1.497 (1.025)

0.707 (1.052)

0.927 (1.167)

1.114 (0.691)

1.336 (1.043)

Pz amplitude S3 (P3b; μV)

0.735 (1.509)**

0.983 (1.814)

2.033 (0.680)

1.827 (1.136)

0.769 (1.449)*

0.878 (1.821)*

1.623 (0.873)

2.647 (0.532)

0.623 (1.553)*

0.882 (1.628)*

1.915 (0.400)

1.939 (0.993)

Gamma Noise Power F3 (μV2)

0.012 (0.012)

0.011 (0.011)

0.007 (0.003)

0.013 (0.022)

0.014 (0.014)*

0.009 (0.005)

0.007 (0.005)

0.016 (0.026)

0.013 (0.012)*

0.011 (0.012)

0.004 (0.000)

0.011 (0.016)

Gamma Noise Power F4 (μV2)

0.009 (0.006)

0.018 (0.021)

0.006 (0.003)

0.011 (0.013)

0.015 (0.017)

0.007 (0.003)

0.007 (0.004)

0.012 (0.016)

0.013 (0.016)

0.011 (0.012)

0.005 (0.001)

0.009 (0.010)

Gamma Noise Power P3 (μV2)

0.011 (0.009)*

0.015 (0.010)**

0.006 (0.003)

0.007 (0.004)

0.013 (0.010)**

0.012 (0.008)

0.006 (0.004)

0.006 (0.002)

0.013 (0.009)*

0.012 (0.010)**

0.004 (0.002)

0.007 (0.004)

Gamma Noise Power P4 (μV2)

0.012 (0.008)*

0.011 (0.005)

0.007 (0.005)

0.007 (0.004)

0.013 (0.009)**

0.009 (0.003)

0.007 (0.004)

0.009 (0.006)

0.011 (0.006)

0.012 (0.008)*

0.005 (0.004)

0.008 (0.005)

No within-group significant differences were detected between patients or HC subgroups classified according to their genotype. Differences between patients and HC with the same SNP variation are displayed in the Patients column. Data exhibited as Mean (S.D.); *p < 0.05; **p < 0.01; ***p < 0.001; Significant results after Bonferroni correction (p < 0.00138) are in italics (Mann-Whitney's U test); N/A, not applicable.

T + and T − patients showed worse cognitive performance than the corresponding T + and T − HC, reaching the required level of significance (p < 0.001; P > 96%) for total IQ (T + patients vs. T + HC), verbal memory (T − patients vs. T − HC), verbal fluency (T + patients vs. T + HC and T − patients vs. T − HC) and processing speed (T − patients vs. T − HC) (Table 2 and Additional file 1: Table S3); in the minimally treated patients considered alone, the level of significance held up at p < 0.001 (Additional file 1: Table S2).

Gamma noise power was not significantly different between T + and T − patients or between T + and T − HC, with power values always below 7% (Table 2 and Additional file 1: Table S3).

T + and T − patients did not show significant differences in P3a, P3b or gamma noise power at any electrode site in comparison to T + and T − HC, with power value below 26% (Additional file 1: Table S3).

NRG1 rs3924999

There were 18 A + (AA or AG) and 13 A − (GG) in the patient group (12 and 9 respectively for minimally treated patients). In the HC group, there were 16 A + and 7 A−. This difference was non-significant (χ2 = 0.749, df = 1, p = 0.387).

There were no significant differences in cognitive performance between A + and A − patients or between A + and A − HC, even at uncorrected p < 0.05 level (Table 2). Power values were below 25% in all cases (Additional file 1: Table S3).

A + patients showed significantly worse cognitive performance than the corresponding A + HC (p < 0.001; P > 83%) for total IQ, verbal memory, verbal fluency and processing speed (Table 2 and Additional file 1: Table S3). These differences also held up for the minimally treated patients considered alone (Additional file 1: Table S2).

There were no significant differences in gamma noise power or in P3b and P3a amplitudes between A + and A − patients or between A + and A − HC, with power values always below 16% (Table 2 and Additional file 1: Table S3).

A + and A − patients did not show significant differences in P3a, P3b or gamma noise power at any electrode site in comparison to A + and A − HC, with power value below 36% (Additional file 1: Table S3).

NRG3 rs10748842

There were 8 C + (only CT heterocygotes), and 23 C − (TT homocygotes) in the patient group (5 and 16 respectively for minimally treated patients). In the HC group, there were 4 C + and 19 C−. This difference was not significant (χ2 = 0.541, df = 1, p = 0.462).

There were no significant differences in cognitive performance between subgroups of patients depending on their genotype, with power values always below 13% (Table 2 and Additional file 1: Table S3).

C − patients showed significantly lower total IQ, verbal memory, verbal fluency and processing speed scores than C − HC (p < 0.001; P > 98%; Table 2 and Additional file 1: Table S3). This result was also found in the comparison between minimally treated patients and HC (Additional file 1: Table S2).

There were no significant differences between C + and C − patients in gamma noise power or P3b and P3a amplitudes (Table 2). Power values were low (P < 8%) in all cases (Additional file 1: Table S3).

C + and C − patients did not show significant differences in P3a, P3b or gamma noise power at any electrode site in comparison to C + and C − HC, with power value below 26% (Additional file 1: Table S3).


We examined possible abnormal cerebral information processing in a group of chronic and minimally treated patients with schizophrenia using electrophysiological and cognitive data of interest and the association with genetic variation in three SNPs related to increased risk of suffering this disease.

We could not detect any significant influence of variation in NRG1/NRG3 polymorphisms on the cognitive performance of patients with schizophrenia. This negative finding is coherent with previous data, which did not show an association between cognition and genetic variation in NRG in schizophrenia [24]. The variety of functions subserved by NRG in the brain's development suggests the possibility that other SNP or haplotypes related to NRG1 and/or ERBB4 may be associated to cognitive deficit and/or disorganized cortical activity in schizophrenia [25, 26].

Variation in NRG polymorphisms included in our study may have a significant effect on other relevant functional parameters in schizophrenia that were not assessed in our study: the T allele for rs6994992 has been associated to prepulse inhibition deficits [27], fronto-temporal activation and cognitive deficits [28], and white matter integrity [29] in schizophrenia.

We did not find an association between electrophysiological parameters of activation (P3b amplitude or gamma noise power) and any of the explored genetic variation in NRG, in spite of previous suggestive evidence obtained with functional magnetic resonance (fMRI) in relation to rs6994992 variant [28]. In the abovementioned study, the authors compared differences in task-related activation, while our aim was to compare the amount of gamma activity unrelated to task performance. Therefore, it seems possible that rs6994992 variant may have an effect on task-related activation but not on basal activity.

Other NRG variants not included in our study may have an influence on relevant activation patterns in schizophrenia. For example, SNP8NRG221533 (rs35753505) was associated to a longer latency [30] of the P300 potential in this illness. In healthy participants, the number of risk alleles of rs35753505 variant correlated with hyperactivation of the frontal gyrus during a working memory test [31] and other regions during memory encoding [32]. Finally, NRG1 5′ and 3′ SNPs rs4560751 and rs3802160 polymorphisms (likelihood ratio test p = 0.00020) interacted with schizophrenia, and contributed to inefficient cortical activation during a working memory task in HC [33]. It could be interesting to investigate if these polymorphisms have an effect on EEG variables such as the ones we assessed in this work.

Epistatic effects may contribute to explain the lack of influence of the polymorphisms selected in our study on complex phenotypic features, such as cortical activation and cognition. Previous findings suggest epistasis between NRG1 (rs10503929; Thr286/289/294Met) and its receptor ERBB4 (rs1026882) as well as a three-way interaction with these two SNPs and AKT1 (rs2494734) [33]. Epistatic effects may be especially important between genetic variations concerning NRG1 and, on the other hand, ErbB4 receptors and/or N-methyl-d-aspartic acid (NMDA) transmission [25]. However, one of our study limitations is that we did not assess possible epistatic interactions between genotypes and cognitive and electrophysiological parameters.

Another limitation is the possible effects of chronicity and medication on cortical processing, which may mask the interaction with the studied genetic variations. According to our results, chronicity does not seem to alter patients' cognitive or neurophysiological outcome. However, even though we attempted to control for this possible effect by repeating the analyses only including the minimally treated patients' subgroup, the sample size reduction may limit any further conclusions. Finally, our sample size is limited as evidenced by the power analyses, especially for the neurophysiological comparisons between subgroups according to their genetic variants. Therefore, the absence of differences depending on the genotypes might be due to type II errors; nevertheless, this would be contradictory with the similar direction of the exhibited differences between our patients with any variant for each genotype and the corresponding HC.


We could not detect any significant influence of variation in the studied Neuregulin 1 and Neuregulin 3 polymorphisms on cognitive performance or on gamma noise power magnitudes in patients with schizophrenia. Variation at these loci may have a significant effect on other relevant functional parameters not assessed in our study.



Brief Assessment in Cognition in Schizophrenia Scale




epidermal growth factor


functional magnetic resonance imaging


gamma-Aminobutyric acid


healthy controls


intelligence quotient


N-methyl-d-aspartic acid




Positive and Negative Syndrome Scale


polymerase chain reaction


single-nucleotide polymorphism


signal-to-noise ratio


Wechsler Adult Intelligence Scale 3rd Edition.



Funding for this study was provided by the Instituto de Salud Carlos III Grants 080017 and 1102203 to VM, Gerencia Regional de Salud de Castilla y León GRS 249/A/08 and 613/A/11, a postdoctoral Marie Curie Intra European Fellowship within the 7th European Commission Framework Programme for Research and Innovation (330156-CODIP) to ÁD, a predoctoral research grant from the Consejería de Educación - Junta de Castilla y León and the European Social Fund to ÁD (EDU/1486/2008) and CC (EDU/1064/2009), a predoctoral scholarship from the University of Salamanca and Santander Bank to VS, and the FIS Grant PI 1000219 to RG.

Authors’ Affiliations

Division of Psychiatry, Faculty of Brain Sciences, University College London, London, W1W, 7EJ, UK
Institute of Biomedical Research of Salamanca (IBSAL), Salamanca, 37007, Spain
Molecular Medicine Unit, Department of Medicine and Institute of Molecular and Cellular Cancer Biology (IBMCC), University of Salamanca & CSIC, Salamanca, 37007, Spain
Neuroscience Institute of Castilla y León (INCYL), University of Salamanca, Salamanca, 37007, Spain
Anthropology Unit, Animal Biology Department, University of Barcelona, Barcelona, 08028, Spain
Clinical Neuroscience Section, Max Planck Institute of Experimental Medicine, Göttingen, 37075, Germany
Psychiatry Department, School of Medicine, University of Valladolid, Valladolid, 47005, Spain
Psychiatry Service, University Hospital of Valladolid, Avenida Ramón y Cajal, 7, Valladolid, 47005, Spain


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