Scholarly article on topic 'The cognitive neuropsychological phenotype of carriers of the FMR1 premutation'

The cognitive neuropsychological phenotype of carriers of the FMR1 premutation Academic research paper on "Clinical medicine"

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Academic research paper on topic "The cognitive neuropsychological phenotype of carriers of the FMR1 premutation"

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The cognitive neuropsychological phenotype of carriers of the FMR1 premutation

Jim Grigsby1,2*, Kim Cornish3, Darren Hocking4, Claudine Kraan3, John M Olichney5,6, Susan M Rivera5,7,8, Andrea Schneider5,8, Stephanie Sherman9, Jun Yi Wang5,10 and Jin-Chen Yang5,6


The fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder affecting a subset of carriers of the FMR1 (fragile X mental retardation 1) premutation. Penetrance and expression appear to be significantly higher in males than females. Although the most obvious aspect of the phenotype is the movement disorder that gives FXTAS its name, the disorder is also accompanied by progressive cognitive impairment. In this review, we address the cognitive neuropsychological and neurophysiological phenotype for males and females with FXTAS, and for male and female unaffected carriers. Despite differences in penetrance and expression, the cognitive features of the disorder appear similar for both genders, with impairment of executive functioning, working memory, and information processing the most prominent. Deficits in these functional systems may be largely responsible for impairment on other measures, including tests of general intelligence and declarative learning. FXTAS is to a large extent a white matter disease, and the cognitive phenotypes observed are consistent with what some have described as white matter dementia, in contrast to the impaired cortical functioning more characteristic of Alzheimer's disease and related disorders. Although some degree of impaired executive functioning appears to be ubiquitous among persons with FXTAS, the data suggest that only a subset of unaffected carriers of the premutation - both female and male - demonstrate such deficits, which typically are mild. The best-studied phenotype is that of males with FXTAS. The manifestations of cognitive impairment among asymptomatic male carriers, and among women with and without FXTAS, are less well understood, but have come under increased scrutiny.

Keywords: Fragile X-associated tremor/ataxia syndrome, FXTAS, FMR1, Fragile X, Executive function, Cognition disorders, Fragile X premutation

The fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder associated with trinucleotide (CGG) repeat expansions of the FMR1 (fragile X mental retardation 1) gene. The most obvious signs and symptoms of FXTAS include action tremor, ataxia, parkinsonism, and peripheral neuropathy, but circumscribed aspects of cognition are impaired as well. FXTAS affects persons who have CGG expansions in the premutation range (that is, 55-200 CGG repeats), as opposed to fragile X syndrome (FXS), which is associated with the full mutation (over 200 CGG repeats) at FMR1. FXTAS and FXS have very different phenotypes, the latter

* Correspondence:

department of Psychology, University of Colorado Denver, Denver, CO, USA 2Department of Medicine; Division of Health Care Policy and Research, University of Colorado Schoolof Medicine, Aurora, CO, USA Fulllist of author information is available at the end of the article

Bio Med Central

involving an early childhood-onset intellectual development disorder, often with autistic features, while FXTAS affects persons who previously were cognitively normal, in the sixth or seventh decade of life.

The basic cognitive phenotype of FXTAS is relatively well understood. However, at the time of the initial identification of FXTAS, it was thought that women who carry the premutation might have little susceptibility to the disorder, perhaps because of the presence of a normal allele among female heterozygotes. Penetrance, and possibly expression, is significantly higher in males than females, and because men with FXTAS were more readily identified than females with FXTAS, they have been more extensively studied, and more is known about the nature, severity, and course of cognitive impairment among men. The objective of this paper is to review the cognitive neuropsychological phenotype of carriers of the fragile X

© 2014 Grigsby et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

(FX) premutation, both those who have FXTAS, and those who are clinically unaffected.


Cognitive neuropsychological phenotype among males with FXTAS

Since the first case reports [1], it has been apparent that FXTAS is associated with a progressive decline in cognitive functioning. Although deficits in several aspects of cognition have been reported [2-4], the evidence appears to support the idea that the primary disorder is a disturbance of executive functioning (EF) [5]. The executive functions represent an important subset of cognitive abilities. In essence, EF is the capacity for the autonomous regulation of one's own behavior and attention. Fuster [6,7] maintains that EF represents the temporal organization of behavior, allowing one to initiate purposeful behavior, and to inhibit irrelevant or inappropriate activity.

Early studies of FXTAS reported deficits in EF, working memory, speed/capacity of information processing and learning [2,3,8]. The first systematic study of cognition essentially replicated the early results, and showed that males with FXTAS ranged from high average through severely impaired in these areas of functioning, the group mean representing moderate impairment [4]. FXTAS patients performed significantly worse on several EF measures than did a sample of controls.

General cognitive functioning among FXTAS patients is typically impaired [2-4], although intelligence quotient (IQ) scores are in the normal range. In the largest study of men with FXTAS to date, mean Wechsler Adult Intelligence Scale-III (WAIS-III) verbal and performance (nonverbal) IQ scores were 106.6 and 97.7, respectively [4]. Lower performance IQs may be a function of the greater dependence of the nonverbal scale on processing speed, working memory, and EF [5]. On the Mini Mental State Exam [9], a measure of general mental status, the difference in mean scores of FXTAS patients and controls was statistically, but not clinically, significant (27.6 vs 29.2). Nevertheless, a subset of individuals with FXTAS - most with advanced disease -demonstrates frank dementia [10,11]. Performance on measures of declarative memory is impaired, likely reflecting the effects of executive dysfunction (that is, problems with active learning and active retrieval) rather than a primary memory disorder.

Neither expressive nor receptive language appears to be affected in FXTAS. Repetition, naming, reading, comprehension of complex material, and following spoken commands differed little across groups. Performance on most visuospatial measures was unimpaired, although men with FXTAS performed more poorly than controls on the WAIS-III Block Design subtest - probably in

association with reduced processing speed and deficient organizational ability [4,5].

In a study of functional status (basic physical functioning, activities of daily living, and instrumental activities of daily living), men with FXTAS, but not unaffected carriers, were impaired in all three functional areas. This effect appeared to be mediated by both executive and motor functioning [12].

It is not possible to localize the cognitive deficits of FXTAS to a specific brain region. Although the event-related brain potential (ERP) studies of Yang and colleagues [13,14] may implicate prefrontal cortex, EF is a widely distributed functional system that also may be affected by lesions of other areas, in particular the cerebellum [15,16]. To a large extent, FXTAS is a white matter disease [17-19], and the cognitive phenotype observed among men with FXTAS is similar to what has been called white matter dementia [16,20,21], in which the extent of executive deficits is correlated with the burden of white matter abnormalities distributed throughout the brain [22].

Cognitive neuropsychological phenotype among females with FXTAS

The manifestation of neuropsychological signs and symptoms in female carriers can be diverse with low penetrance of FXTAS and milder phenotypes than those observed in males. Based on current diagnostic criteria, estimates suggest that as few as 8 to 16 % of female carriers will develop FXTAS [23,24]. Moreover, in comparison with males, the onset of FXTAS for females tends to occur later in life, and is anatomically less severe, with a lower penetrance of middle cerebellar peduncle and pontine white matter hyperintensities, less brain atrophy, and less severe white matter disease overall [25,26]. This milder phenotype is thought to stem from protective mechanisms associated with X-inactivation and hormonal differences [27-29]. However, this notion does not have full support [23].

Although studies of FXTAS among males suggest that the presenting cognitive profile is predominantly one of executive dysfunction, there is a dearth of research systematically examining the cognitive profile in females with FXTAS. Indeed, existing studies have been inconsistent in demonstrating interrelationships between neuro-psychological profiles, imaging correlates, and standardized clinical measures [25,30-32]. Recent neuropsychological and neurophysiological studies have shown that females with FXTAS present with executive dysfunction as the primary cognitive impairment, similar to the male cognitive profile [32,33]. Most significantly, a neuropathological case study series reported dementia in 4 of 8 autopsied female carriers, in conjunction with an increased number of intranuclear inclusions, suggesting that dementia may be

more prevalent than previously thought in women with FXTAS [34].

With regard to psychological symptoms in females with FXTAS, neuroimaging studies have shown an association between hippocampal abnormalities and anxiety in unaffected carriers [35]. Although these results suggest that females show mild early-onset neuropsychological pheno-types irrespective of FXTAS, further research is needed to understand the synergistic effects of age, psychological vulnerability, and risk factors for FXTAS. Indeed, given that prevalence rates for probable attention deficit hyper-activity disorder (4.5 to 25%), anxiety (20.9 to 30%) and depression (14.03 to 47.3%) far exceed the risk of FXTAS (8 to 16%) in women [23,24,36-40], the molecular and environmental factors contributing to gender-divergent trajectories are yet to be fully characterized.

Neurophysiology of cognition in FXTAS

Much of what is known of the cognitive electrophysiology of FXTAS patients has been found using the ERP technique. Cognitive ERPs, primarily representing the summated activity of post-synaptic potentials, offer an excellent non-invasive measure for characterizing different stages of cognitive processing due to their millisecond-level temporal resolution [41].

While performing an auditory "oddball" task requiring dual-response, a predominantly male group of participants with FXTAS had longer N100 latency and smaller P200 amplitude than normal controls, indicating some impairment of early-stage attention [13]. Furthermore, these individuals showed decreased amplitude and prolonged latency of P300, a component believed to reflect late-stage "controlled" attention and working memory updating. P300 abnormalities in these FXTAS patients were observed over fronto-central and parietal scalp, and the frontal P300 measures correlated with executive function test scores, working memory, FMR1 mRNA level, and CGG repeat length [13]. The frontal P300 impairments have been replicated in a second study including 29 female FXTAS patients, with correlations also obtained between P300 measures and executive function, working memory, and information processing speed [32]. Therefore, it has been suggested [13,32] that abnormal fronto-parietal attentional network dynamics may play an important role in executive dysfunction, the primary cognitive impairment in FXTAS [5].

Verbal memory and language processes in FXTAS also have been probed via an ERP word repetition paradigm/ category judgment task, in which semantically congruous (50%) and incongruous words are repeated after an interval of between 10 and 140 seconds. This word repetition paradigm was employed in the first published ERP study of FXTAS [42], in which it was demonstrated that FXTAS patients had a significantly reduced N400 word

repetition effect (new-old incongruous words), an elec-trophysiological marker of semantic processing load and implicit memory previously shown to be sensitive to early Alzheimer's disease (AD) [43,44]. Unlike persons with AD, however, FXTAS patients displayed a preserved P600 word repetition effect (new-old congruous words) that has been linked to episodic/declarative memory. Yang and colleagues [45] examined a group of FXTAS females and found a relatively normal N400 repetition effect, but decreased N400 congruity effect (incongruous-congruous new words), suggesting abnormal semantic activation and/or semantic network disorganization, which they attributed to executive dysfunction.

Electrophysiology has also been used to assess the effectiveness of potential pharmacologic treatments for FXTAS. Because the N400 measures are sensitive to both FXTAS and glutamatergic signaling [46], the method was utilized to evaluate the treatment effects of memantine (an un-competitive N-methyl-D-aspartate receptor antagonist approved for treatment of AD) in a substudy of the first placebo-controlled, double-blind, randomized clinical trial in FXTAS [47,48]. Results indicated a tendency toward larger N400 repetition effect amplitude after 12 months on memantine, and patients who had increased N400 repetition effects showed the largest improvements in cued-recall of the experimental verbal stimuli. Although the main memantine trial in FXTAS showed no significant treatment effects on the primary outcome measures of executive function and intention tremor [48], the ERP results suggest the need for further studies of memantine and/or other therapeutic agents for this neurodegenerative disorder, which currently has no proven therapies.

There is a paucity of other published studies on the central neurophysiology of FXTAS, with a few case report studies showing abnormal electroencephalogram (for example, [49]). One noteworthy study of people with FXTAS found decreased auditory prepulse inhibition [50], an electromyography index of sensorimotor gating also affected in FXS. Thus, abnormalities of the frontal P300, N400 brain potentials, and prepulse inhibition should all be considered putative electrophysio-logical trait markers of the FMR1 premutation.

Cognition among unaffected male premutation carriers

The cognitive phenotype of unaffected male carriers of the FMR1 premutation, although not as extensively researched as that of males with FXTAS, is relatively well understood. There is general agreement that some males demonstrate a progressive age-related decline in executive function skills that is greater than that displayed by males with a normal allele, matched on age and IQ. In a series of published papers, Cornish and colleagues have isolated a subtle age-related decline of inhibitory control (as measured by the Haylings Task) and

working memory (as measured by the Letter-Number sequencing task [51-53]) that begins in early adulthood and continues across the lifespan. Interestingly, males with more than 100 CGG repeats may be especially at risk for cognitive difficulties [51]. Grigsby and colleagues [4] reported a similar profile of difficulties in executive functioning, with unaffected carriers performing worse than normal-allele controls on a composite measure of EF, and on immediate and delayed recall on the Logical Memory subtest of the Wechsler Memory Scale-III [54].

In addition, recent functional magnetic resonance imaging (fMRI) data indicate changes in prefrontal activity in premutation carriers, irrespective of FXTAS diagnosis, during performance of a working memory task [55]. These preliminary findings provide the first evidence to suggest the involvement of specific brain regions associated with neural networks mediating EF among persons in the premutation range, with or without FXTAS. However, several studies have failed to find differences in cognitive performance between non-affected male carriers and typically developing males [56,57]. One possibility is that relatively small samples sizes and variability in age range and CGG repeat distribution across studies may explain some of the discrepant findings.

To address this concern, Hunter and colleagues [58] combined their samples to form a multi-center database with 100 asymptomatic premutation males and 216 non-carriers. In line with previous reports by Cornish and Grigsby [4,5,51], analyses across shared measures of inhibition and working memory detected very subtle differences (which were of minimal clinical significance) on a measure of response inhibition (Stroop task), but on no other cognitive measures. Taken together, current findings provide evidence of a subtle, suboptimal level of cognitive performance among a subset of unaffected carriers, involving mild deficits in inhibition and working memory among a subset of male carriers, results which are relatively consistent with earlier research [59-61].

Cognition among unaffected female premutation carriers

Although the presence of a neuropsychological phenotype in unaffected female premutation carriers is controversial [56,57], recent studies have shown that a subset of young adult female carriers exhibit subtle deficits in executive function and inhibitory control [33,37,62], visuospatial processing [63,64], mathematical reasoning [65,66], and tasks dependent on processing speed and working memory [32]. It has been argued that targeted, domain-specific measures may more sensitively identify subtle neurocognitive deficits than gross neuropsychological tests [67]. Indeed, more targeted measures have identified enhanced psycho-motor ability [68,69], motor programming deficits [70], increased balance and memory problems [70,71], and age- and CGG-dependent changes in the attentional

demands of postural control [72]. Collectively, these findings point to early at-risk phenotypic features suggesting cerebellar dysfunction in a subgroup of female premutation carriers; however, prospective longitudinal studies will be needed to determine who will eventually develop cognitive impairment and neurodegenerative decline.

With regard to the neuropsychiatric phenotype, it has been shown that a subgroup of women who carry the FMR1 premutation, but who do not have FXTAS, may also be more vulnerable to elevated symptoms of anxiety and depression compared to the general population [40,73,74]. At least in part this may be the result of genetic variation (for example, CRHR1 polymorphisms and release of cortisol) moderating the stress of raising a child with FXS [75,76]. However, one recent study has shown that poorer inhibitory control and working memory are associated with elevated social anxiety, depression, and attention deficit hyperactivity disorder (predominantly inattentive symptoms) among women with the FMR1 premutation [37].

These data are novel in that they indicate early changes within frontally-mediated networks that may increase the risk of neuropsychiatric dysfunction. However, evidence for a contribution by other factors, such as expanded CGG repeats, and reproductive history in depressive female carriers, and anxiety symptoms in female carriers, has been inconsistent [37,75,76]. A recent study using more detailed clinical interviews from the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition has provided evidence that comorbid depressive and anxiety disorders are associated with significantly expanded CGG repeats, but not with reproductive or menstrual history [77]. Thus, a complex set of factors may contribute to executive and neuropsychiatric dysfunction in female carriers, involving genetic and epigenetic factors, caregiver burden, hormonal changes, and hypothalamic-pituitary-adrenal axis function. The precise relationships among these factors remain unclear.

Neuroimaging and cognition

The FMR1 gene and its protein product, fragile X mental retardation protein (FMRP), are expressed in brain areas important for high-level cognitive functioning [78,79]. Consequently, both subtle FMRP deficit and excessive FMR1 mRNA may affect the brain during development and aging in the FMR1 premutation, which ultimately lead to the cognitive phenotype in FX premutation carriers. Neuroimaging is a useful tool for non-invasive investigations of the impact of the FMR1 premutation on the brain and neural substrates underlying the cognitive deficits. Two main imaging modalities provide complementary insights into the mechanisms: functional MRI, which examines brain activation during cognitive tasks, and structural

MRI, which provides a quantification of volume, morph-ometry, and white matter structural integrity/connectivity.

Consistent with the FMRP expression profile in the brain [80], both functional and structural MRI studies have shown a dose-response of FMR1 gene expression on brain regions important for working memory. In a functional MRI study examining verbal working memory in male and female premutation carriers [55], reduced activation was observed in the right inferior frontal cortex and left premotor cortex in both asymptomatic pre-mutation carriers and carriers with FXTAS. Reduced activation was found in right premotor/inferior frontal cortex in the FXTAS group. The reduced activation in the right inferior frontal cortex exhibited a significant correlation with high lymphocytic FMR1 mRNA levels. In a structural MRI study [80] of male premutation carriers, while individuals with FXTAS showed diffuse gray matter loss most prominent in areas important for working memory (including prefrontal cortex, anterior cingu-late cortex, and cerebellum) only the anterior cerebellar vermis and hemisphere displayed volume loss in those premutation carriers without FXTAS. Importantly, the reduced gray matter density of the inferior frontal and anterior cingulate cortices correlated significantly with low working memory performance, and the reduced gray matter density in the dorsomedial frontal cortex correlated with long CGG repeat length in premutation carriers.

Functional MRI studies have also revealed differences in brain activation in young adult premutation carriers asymptomatic for FXTAS, even where subtle differences in cognition cannot be measured by standard behavioral techniques. In a study of delayed recall memory, premutation carriers showed no deficits (relative to control participants) in ability to recall pairings on an associative memory task a day later, but were found to exhibit reduced left hippocam-pal activation, and activity in the left hippocampus was also negatively correlated with both FMR1 mRNA level and psychiatric symptomatology [81].

Likewise, in a study examining magnitude estimation processing, young asymptomatic adult carriers showed significantly attenuated bilateral intraparietal sulcus (IPS) activity that is commonly associated with the numerical distance effect (that is, greater effort/brain activation when the two displays to be compared are closer in numerosity), despite comparable behavioral task performance with the control group [82]. While both elevated FMR1 mRNA and increased CGG repeat expansion were associated with reduced IPS activation, the results of multiple regression suggested that increased CGG repeat size was the primary contributor to aberrant IPS function.

Molecular mechanisms of FXTAS

Although the data suggest that FXTAS may result from a toxic gain of function associated with excessive levels

of FMR1 mRNA, the mechanism, and variables that influence it, remain unclear [83]. Although CGG repeat size in the premutation range is a diagnostic indicator and genetic marker for those who may develop FXTAS, repeat length predicts only a portion of risk and severity of FXTAS [84,85], and there are other yet unidentified factors involved. Repeat length does not elucidate the mechanism of cellular or central nervous system pathology, or the relationship of cellular pathology to clinical disease.

Treatment of FXTAS

There are as yet no effective therapies for the treatment of FXTAS. As noted previously, one 12-month randomized controlled trial of memantine showed no difference from placebo on measures of tremor severity and executive functioning [48]. The limited literature is based largely on case studies (for example, [86]) and treatment has largely been directed toward symptom amelioration, with inconsistent results [87,88].


The cognitive phenotype of FXTAS for both sexes appears to be characterized by a progressive impairment of executive functioning, working memory, and speed of information processing. This is characteristic of the pattern observed in fronto-cerebellar and white matter disease. The degree of impairment may become severe, and in advanced stages people with FXTAS may have very significant cognitive problems, even demonstrating problems ordinarily associated with cortical disorders. The dysexe-cutive syndrome that accompanies FXTAS appears to play a significant role, along with the movement disorder, in a significant decline in functional independence, and the development of psychiatric symptomatology.

Among carriers of the FMR1 premutation who do not have FXTAS, the data suggest that a subset of individuals has mild executive impairment. Whether the cognitive deficits shown by these people indicate preclinical FXTAS, or are neurodevelopmental features of a premutation pheno-type, is uncertain, although some imaging data suggest that both are possibilities [89]. Also unclear is whether cognitive problems precede, follow, or are contemporaneous with the onset of tremor and ataxia, and whether these may be associated with neuropathologic and/or neurora-diologic anomalies. Neurophysiologic and neuroimaging data, in conjunction with neuropsychological examination, may help to answer this question.


AD: Alzheimer's disease; EF: executive functioning; ERP: event-related potential; FMR1: fragile X mentalretardation 1; FMRP: fragile X mental retardation protein; FX: fragile X; FXS: fragile X syndrome; FXTAS: fragile X-associated tremor/ataxia syndrome; IPS: intraparietalsulcus; IQ: intelligence quotient; MRI: magnetic resonance imaging; WAIS: Wechsler Adult Intelligence Scale.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

Allauthors contributed to the writing of this review. Allauthors read and approved the finalmanuscript.

Author details

department of Psychology, University of Colorado Denver, Denver, CO, USA. 2Department of Medicine; Division of Health Care Policy and Research, University of Colorado Schoolof Medicine, Aurora, CO, USA. 3Schoolof Psychology & Psychiatry; Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia. 4Olga Tennison Autism Research Centre, Schoolof PsychologicalScience, La Trobe University, Melbourne, Victoria, Australia. 5Center for Mind and Brain, University of California, Davis, CA, USA. 6Department of Neurology, University of California, Davis, Sacramento, CA, USA. 'Department of Psychology, University of California-Davis, Sacramento, CA, USA. 8MIND Institute, University of California-Davis MedicalCenter, Sacramento, CA, USA. 9Department of Human Genetics, Emory University, Atlanta, GA, USA. 10Department of Pediatrics, University of California, Davis, Sacramento, CA, USA.

Received: 31 October 2013 Accepted: 27 January 2014 Published: 30 July 2014


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Cite this article as: Grigsby et al.: The cognitive neuropsychological phenotype of carriers of the FMR1 premutation. Journal of Neurodevelopmental Disorders 2014 6:28.

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