Abstract
A summit held March 2023 in Scottsdale, Arizona (USA) focused on the intronic hexanucleotide expansion in the C9ORF72 gene and its relevance in frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS; C9ORF72-FTD/ALS). The goal of this summit was to connect basic scientists, clinical researchers, drug developers, and individuals affected by C9ORF72-FTD/ALS to evaluate how collaborative efforts across the FTD-ALS disease spectrum might break down existing disease silos. Presentations and discussions covered recent discoveries in C9ORF72-FTD/ALS disease mechanisms, availability of disease biomarkers and recent advances in therapeutic development, and clinical trial design for prevention and treatment for individuals affected by C9ORF72-FTD/ALS and asymptomatic pathological expansion carriers. The C9ORF72-associated hexanucleotide repeat expansion is an important locus for both ALS and FTD. C9ORF72-FTD/ALS may be characterized by loss of function of the C9ORF72 protein and toxic gain of functions caused by both dipeptide repeat (DPR) proteins and hexanucleotide repeat RNA. C9ORF72-FTD/ALS therapeutic strategies discussed at the summit included the use of antisense oligonucleotides, adeno-associated virus (AAV)-mediated gene silencing and gene delivery, and engineered small molecules targeting RNA structures associated with the C9ORF72 expansion. Neurofilament light chain, DPR proteins, and transactive response (TAR) DNA-binding protein 43 (TDP-43)–associated molecular changes were presented as biomarker candidates. Similarly, brain imaging modalities (i.e., magnetic resonance imaging [MRI] and positron emission tomography [PET]) measuring structural, functional, and metabolic changes were discussed as important tools to monitor individuals affected with C9ORF72-FTD/ALS, at both pre-symptomatic and symptomatic disease stages. Finally, summit attendees evaluated current clinical trial designs available for FTD or ALS patients and concluded that therapeutics relevant to FTD/ALS patients, such as those specifically targeting C9ORF72, may need to be tested with composite endpoints covering clinical symptoms of both FTD and ALS. The latter will require novel clinical trial designs to be inclusive of all patient subgroups spanning the FTD/ALS spectrum.
Plain Language Summary
The C9ORF72 Summit was held in March 2023 in Scottsdale, Arizona (USA). Some people who have the disease frontotemporal dementia or the disease amyotrophic lateral sclerosis have a change in one of their genes; the name of the gene is C9ORF72. People who carry this genetic difference usually inherited it from a parent. Researchers are improving their understanding of how the change in the C9ORF72 gene affects people, and efforts are being made to use this knowledge to develop treatments for amyotrophic lateral sclerosis and frontotemporal dementia. In addition to studying the cellular and molecular mechanisms of how the C9ORF72 mutation leads to cellular dysfunction and frontotemporal dementia and amyotrophic lateral sclerosis clinical symptoms, a large effort of the research community is aimed at developing measurements, called biomarkers, that could enhance therapy development efforts in multiple ways. Examples include monitoring of disease activity, identifying those at risk of developing amyotrophic lateral sclerosis or frontotemporal dementia, predicting which people might benefit from a particular treatment, and showing that a drug has had a biological effect. Markers that identify healthy people who are at risk of developing amyotrophic lateral sclerosis or frontotemporal dementia could be used to test treatments that would start before a person shows any symptoms and hopefully would delay or even prevent their onset.
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Why was this summit held? |
This summit was held to foster a breakdown of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) disease silos. Areas included all levels of investigation, from basic research through biomarker development, therapeutic target discovery and therapeutics development, and clinical trial design. Additional aims were evaluate the most effective treatment and care of individuals affected by FTD/ALS, including the most prevalent familial form of FTD/ALS, C9ORF72-related FTD/ALS, discussions, and collaborative efforts. |
What were key takeaways from this summit? |
Critical information in our understanding of the biology around the C9ORF72 expansion is still lacking, and many questions remain unanswered: What molecular and cellular changes occur at pre-symptomatic stages and how early do they occur? Why are some individuals only affected with ALS-associated symptoms, while others show FTD-associated clinical symptoms, and yet others have symptoms of both diseases? How do non-neuronal cells respond to the C9ORF72 repeat expansion, how do they contribute to neuronal degeneration, and do these contributions differ between the frontal cortex and spinal cord? |
Biomarkers, based on both imaging and on molecular readouts, are crucial to improving disease modeling, predicting disease progression, predicting onset of symptoms spanning ALS and FTD, and determining which therapies are engaging their targets in all affected brain regions. |
Basket and/or platform trials are needed that include all patient subgroups, including mutation carriers and patients experiencing the FTD/ALS disease spectrum. |
Commentary
A mutation in the C9ORF72 gene is one of the most common causes of both frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). To explore the convergence of these two diseases with a common genetic root, a summit was held. Participants in this summit, held March 2023 in Scottsdale, Arizona (USA), discussed the biology (genetics, RNA, proteins) of C9ORF72-related FTD and ALS (C9ORF72-FTD/ALS) and the potential relevance of this biology to biomarkers, therapeutic target identification, and the design of clinical trials in the affected and pre-symptomatic populations. The information presented and discussed at the summit is presented in this article.
The contents of this manuscript are based on discussions at the C9ORF72 Summit and did not entail any animal or human subjects research that required review/approval by the Institutional Animal Care & Use Committee (IACUC) or Institutional Review Board (IRB).
Translating Genetic Discoveries into Therapies
Researchers have identified genetic causes for 60–70% of familial ALS and familial FTD and about 10% of sporadic ALS and sporadic FTD [1, 2]. Interestingly, the C9ORF72 locus was identified as the most commonly linked genetic factor to both ALS and FTD [3]. A pathological intronic hexanucleotide repeat expansion (HRE) that is believed to have arisen around the fall of Rome is recognized as the source of a common founder, and Viking conquests have been postulated as the mechanism of dissemination of C9ORF72 [4,5,6]. The age range at symptom onset is broad for patients who carry the C9ORF72 repeat expansion [7, 8]. This expansion is known to have incomplete, but age-dependent, penetrance; while patients may occasionally develop ALS or FTD in their 20s, others survive into their ninth decade without developing symptoms [7].
Screening for the C9ORF72 HRE and other genes associated with ALS and FTD became common with the advent of next-generation sequencing [9], and it has become standard practice in many places across the world for both familial and apparently sporadic cases. Genomic approaches are also beginning to unravel the mystery of the biology of ALS and FTD. Cellular pathways that have been linked to ALS and FTD based on genomic discoveries include neuronal projection, cytoskeleton alterations, membrane trafficking, and cyclic-nucleotide-mediated signaling [10, 11].
The discovery of the C9ORF72 gene as the most common genetic cause of ALS and FTD has yielded novel opportunities for therapeutic intervention (e.g., gene therapy trials [discussed below]). The failure of these trials, however, has illuminated the limits of the current understanding of the biology of C9ORF72-FTD/ALS, as well as the critical importance of improving this understanding to help ensure that future trials have a greater likelihood of success.
Overall, numerous novel therapies for ALS and FTD are emerging, but the belief is that these are likely be most effective when patients are treated as early as possible in their disease course. With advanced technologies in genome sequencing and gene therapy approaches, one could speculate that whole-genome sequencing early in life might become available to everyone and would pave the road for future precision medicine approaches for ALS and FTD patients as well as for gene carriers.
C9ORF72 Disease Biology
Mutations in the C9ORF72 gene are characterized by a GGGGCC (G4C2)n HRE in a non-coding region on chromosome 9p21; these mutations represent the most common genetic abnormality in FTD (10%-30%) and are also highly prevalent in ALS (20%-50%) and the spectrum disease of FTD-ALS (30%) [4, 12]. Extensive research over the past 10 years on the role of the (G4C2)n repeat expansion in C9ORF72 has led to the proposals of different disease-causing mechanisms for mutant C9ORF72: (1) protein loss of function; (2) toxic RNA gain of function; and (3) toxicity caused by repeat-associated non-ATG initiated (RAN) translation, which leads to the accumulation of dipeptide repeats (DPR) [13]. Ongoing studies are investigating the cellular consequences of these mechanistic pathways, including defects in nuclear-cytoplasmic trafficking of RNAs and proteins due to RNA toxicity and DPR formation, such as transactive response DNA-binding protein 43 (TDP-43) [14, 15], which further contribute to C9ORF72 disease pathogenesis.
Loss of C9ORF72 Function in C9ORF72-FTD/ALS
The repeat expansion causes C9ORF72 haploinsufficiency in ALS/FTD through the downregulation of C9ORF72 transcripts and reduced C9ORF72 protein expression (Fig. 1) [4, 12, 16,17,18,19,20]. Mechanisms that suppress C9ORF72 expression include DNA methylation [21], histone trimethylation [22], and nucleotide repeat structures that form G-quadraplexes and promote R-loops [23].
Proposed C9ORF72 disease mechanisms. The C9ORF72 (GGGGCC) hexanucleotide repeat expansion is thought to contribute to disease pathogenesis in frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) via three non-mutually exclusive mechanisms: (1) a loss of function due to impaired transcription leading to a reduction in C9ORF72 protein levels; (2) a toxic gain of function due to the formation of secondary RNA structures which sequester RNA binding proteins and consequently a loss of function of these proteins; (3) a toxic gain of function due to repeat-associated non-ATG (RAN) translation from both the sense and antisense strand, which generates potentially toxic dipeptide repeats (DPRs; poly-GP, poly-GA, poly-GR, poly-PA, poly-PR)
Transcription of the C9ORF72 locus gives rise to three distinct messenger RNA (mRNA) isoforms (V1-V3), which encode for two proteins: C9ORF72-long (C9-L), which is a 481-amino acid protein encoded by NM_001256054.3 and NM_018325.5, and C9ORF72-short (C9-S), which is a C-terminally truncated protein isoform of 222 amino acids encoded by NM_14500.57 [4, 12]. Multiple other sense and antisense transcripts are generated through the use of different transcriptional start sites which exhibit expression profiles that are specific to different cell types [24]. Although C9-L is conserved between human and mouse, C9-S is a human-specific isoform [25]. Most research has focused upon the long isoform, since it is more abundant and its expression is significantly reduced by the pathogenic C9ORF72 HRE.
C9ORF72 transcript expression is highest in myeloid cells, which is consistent with the observation that homozygous C9ORF72 knockout mice exhibit peripheral immune phenotypes by activating the protein pathway known as stimulator of interferon genes (STING) [26,27,28]. Remarkably, these phenotypes can be rescued by reducing immune-stimulating bacteria in the gut, which suggests a role for C9ORF72 in autoimmunity [29]. C9ORF72 knockout mice exhibit mild motor and cognitive deficits [30, 31], and a recent study demonstrated TDP-43 pathology in aged C9ORF72 knockout animals [32]. These neurological deficits occur in the absence of overt neurodegeneration but are associated with increased synaptic pruning by overactive microglia [33]. Notably, C9ORF72 deficiency exacerbates phenotypes derived from (G4C2)n repeat expression in human-induced pluripotent stem cell (iPSC)-derived neurons [34, 35] and rodent models [36,37,38,39], and predisposes neurons to glutamate-induced excitotoxicity [35, 39].
The neuronal-specific roles for C9ORF72 are less clear. C9-L interacts with SMCR8 through its DENN (differentially expressed in normal cells and neoplasia) domain and, when C9-L-SMCR8 is in complex with WDR41, this protein complex acts as a GTPase-activating protein that may have roles in membrane trafficking, such as endolysosomal pathways and autophagy [40]. Loss of C9ORF72 in mice and in motor neurons derived from iPSC causes changes in synaptic plasticity and defects in glutamate receptor homeostasis [18, 35, 41,42,43]. Finally, recent studies have also identified a role for C9ORF72 in regulating neuronal nucleocytoplasmic transport through disruption of importin β1 and nucleoporin interactions [44].
The involvement of C9ORF72 function in many neuronal processes illustrates the complexity of dysfunctions caused by the HRE-induced haploinsufficiency. For example, autophagy is an important mechanism for regulating synaptic plasticity [45], and disruption of the nuclear pore can cause defects in autophagy through reducing nuclear import of an autophagy-inducing transcription factor known as TFEB [46]. Another converging mechanism may be the role of C9ORF72 in regulating actin dynamics through an interaction with cofilin [47]. Loss of C9ORF72 in mouse motor neurons causes cofilin inactivation through phosphorylation at serine 3 by LIM domain kinase 1 (LIMK1), which causes defects in neuronal outgrowth. The regulation of actin dynamics is a fundamental process in synaptic plasticity, in glutamate receptor trafficking [48], and in maintaining nuclear homeostasis [49]. Further, the modulation of actin dynamics in motor neurons by the interactions of C9ORF72 with cofilin may explain the functions of the C9ORF72 protein in autophagy and endosomal-lysosomal pathways [47, 50].
Role of RNA Toxicity in C9ORF72-FTD/ALS
RNA toxicity is one of three non-exclusive mechanisms—along with loss of function of the C9ORF72 protein and gain-of-toxic function through DPR protein toxicity—that can cause ALS and FTD (Fig. 1) [51]. It is important to note that both sense and antisense repeat RNA strands are thought to be involved in the RNA-associated mechanisms of C9ORF72 disease. In addition, studies suggest that the expression of sense RNA is greater than that of antisense RNA [52, 53], yet it is still unknown whether both strands contribute equally to disease pathogenesis, and this lack of knowledge raises questions about which strand to target therapeutically, if not both.
The exact impact of foci-containing repeat RNA is unclear. These repeat RNAs are found in complex with several RNA-binding proteins in neurons, astrocytes, microglia, and oligodendrocytes. In addition, they are mostly intranuclear but also found as cytoplasmic RNA foci and at the edge of the nucleus. RNA foci are equally prevalent in the frontal cortex of affected FTD patients and in spinal cord–affected ALS patients [54].
It is often difficult to discriminate repeat RNA toxicity from DPR toxicity in animal models. For example, in zebrafish, both sense and antisense repeat RNA have been shown to be toxic, whereas DPRs could not be detected and a similar toxicity could be obtained with RNA-only constructs containing stop codons [55].
One hypothesis of the observed repeat RNA toxicity is the sequestration of RNA-binding proteins and their subsequent loss of function, which could be corrected by overexpression of the specific sequestered protein. In support of this hypothesis, several studies identified RNA-binding proteins that interact with the sense and/or antisense C9ORF72 repeat RNA, including MBNL1, CUGBP1, PURA, HNRNPA2, HNRNPK, SRSF1, and SRSF2 [54]. One example that overexpression of such an RNA-binding protein can counteract the disease process is the RNA-binding protein heterogeneous nuclear ribonucleoprotein K (HNRNPK). Together with its downstream target ribonucleotide reductase regulatory subunit M2 (RRM2), it can also rescue the DNA damage in the zebrafish model of repeat RNA toxicity [56]. Overexpression of this protein also rescued the reduction in axonal length and abnormal axonal branching in this zebrafish model of C9ORF72 RNA toxicity.
It is clear that repeat RNA-induced RNA toxicity can play roles in different RNA processing mechanisms, including splicing, nuclear-cytoplasmic transport, mRNA nuclear retention, and nucleolar stress [57]. The therapeutic implications of the RNA toxicity–related findings are that strategies to prevent the formation of both sense and antisense repeat RNA through antisense oligonucleotides (ASOs) or through small molecules could be successful. In addition, overexpression of RNA-binding proteins and targeting downstream mechanisms relevant to all forms of ALS and FTD (e.g., DNA damage) might be considered [54].
Protein Dyshomeostasis in C9ORF72-FTD/ALS
The pathology of C9ORF72-ALS and FTD features a diverse set of protein aggregates, including those composed of SQSTM1/p62, DPRs, and TDP-43 [58]. Loss of C9ORF72 due to the above-described HRE-associated haploinsufficiency leads to inefficient autophagy, the accumulation of autophagy adapter proteins such as SQSTM1/p62, and, in some cases, autophagy substrates, including TDP-43.
Translation of the pathogenic C9ORF72 HRE results in five different DPRs: poly(GA), poly(GP), poly(GR), poly(PA), and poly(PR). Rather than affecting a single pathway, DPRs are likely to impact several distinct processes, culminating in neurodegeneration through a variety of mechanisms. Poly(GA) accumulation impairs endosomal transport and protein turnover via the proteasome [59, 60]. Conversely, the arginine-rich DPRs (poly[GR] and poly[PR]) lead to deficits in nucleocytoplasmic transport, autophagy, the stress response [61, 62], translation [63], protein quality control [64], and DNA damage repair [65, 66].
Although TDP-43 mislocalization and cytoplasmic deposition are hallmarks of C9ORF72-FTD/ALS, the underlying reasons for these changes remain mysterious. Given the myriad consequences associated with DPR production, however, it is possible that TDP-43 mislocalization may be secondary to impaired nucleocytoplasmic transport, nuclear protein quality control mechanisms, or cytoplasmic clearance pathways such as autophagy.
Genetic evidence suggests that autophagy impairment can lead to ALS and FTD, but it is unclear whether inducing autophagy can prevent or halt neurodegeneration in these conditions. Autophagy induction may be helpful or harmful, depending on the therapeutic mechanism of action and the pathophysiology of disease [67]. For example, strategies that enhance autophagy induction may enhance rather than reduce toxicity if autophagosome maturation (a late step in the pathway) is impaired by genetic insults or other disease-related changes. Related work highlights cell type–specific mechanisms regulating autophagy, raising the possibility of targeted approaches for selectively stimulating autophagy in affected cell types such as neurons [68].
Drug screens in model systems have identified several emerging candidates for interventions targeting proteinopathies in ALS. One recent example is the small molecule apilimod, which has been shown to inhibit PIKFYVE kinase [69]. Inhibition of PYKFYVE shows promise for ameliorating ALS pathology and extending survival, but more research is needed.
Summary of the Working Group Discussions on C9ORF72 Disease Biology
Attendees split up into working groups to discuss in more detail each of the three major topics of this summit and to define the priorities of the community for the focus of future research. Table 1 summarizes the highlights of the C9ORF72 Disease Biology working group.
Biomarkers for C9ORF72-FTD/ALS
Both ALS and FTD are complex neurological system disorders with effects spanning ‘nucleic acid to networks,’ so that multiple tools are required to appreciate the whole pathology from cellular to cerebral levels. A key research priority is the development of biomarkers to predict prognosis for patients with C9ORF72-FTD/ALS and to evaluate the effects of candidate therapies more efficiently and sensitively. Current biomarker research involves investigations into circulating biomarkers in cerebrospinal fluid (CSF) and/or plasma, but also imaging-based biomarkers such as magnetic resonance imaging (MRI) and positron emission tomography (PET).
Fluid Biomarkers to Assess Prognosis, Risk and Susceptibility, and Biological Response in C9ORF72-FTD/ALS
Neurofilament proteins, such as neurofilament light (NfL) and phosphorylated neurofilament heavy (pNfH), are among the most studied biomarkers across neurodegenerative diseases. Because they are released from degenerating and dying neurons, the biomarker potential of neurofilaments in the CSF and blood has been extensively characterized in ALS and FTD [70].
CSF and blood concentrations of neurofilaments are elevated in ALS, FTD, and other neurodegenerative diseases in comparison to their concentrations in healthy controls [71,72,73]. However, since increases in neurofilaments are not disease specific, they are unlikely to be diagnostic for ALS or FTD on their own; nonetheless, neurofilaments can help distinguish ALS or FTD from disease mimics [74,75,76,77]. Neurofilament concentrations show promise as prognostic biomarkers for C9ORF72-FTD/ALS, with higher levels predicting faster rates of disease progression, shorter survival and, in patients with FTD, greater rate of cortical volume loss [73, 78, 79].
NfL is also being evaluated as a candidate risk/susceptibility biomarker among asymptomatic carriers of the C9ORF72 repeat expansion who are at risk of developing ALS or FTD [72, 80,81,82,83]. Monitoring CSF or blood neurofilaments in these individuals could inform impending phenoconversion. However, because pre-symptomatic increases in NfL are not seen as consistently among C9ORF72 repeat expansion carriers as is observed for rapidly progressive forms of ALS linked to mutations in the superoxide dismutase 1 gene (SOD1-ALS), alternate biomarkers or a multimodal approach will likely be needed to predict phenoconversion in C9ORF72 expansion carriers [84].
Both the prognostic utility of neurofilaments and their use as response biomarkers could improve clinical trial design and inform interpretation of clinical trial data. The latter would additionally benefit from the use of DPR proteins, which have potential pharmacodynamic information on upstream target engagement. Indeed, early investigations to identify approaches to neutralize or degrade C9ORF72 repeat RNA enabled the monitoring of the intended effects of putative therapeutics, such as a lowering of DPR proteins [85,86,87,88,89,90,91]. While assays to measure poly(GP) DPR proteins in human CSF were developed first, poly(GP), poly(GA), and poly(GR) have since been detected in CSF from asymptomatic and symptomatic C9ORF72 repeat expansion carriers, and these two groups have levels of DPR proteins that are generally similar [78, 92]. Despite the fact that CSF DPR proteins in symptomatic C9ORF72 expansion carriers do not associate with clinical traits such as age at disease onset, revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R) score, rate of decline of ALSFRS-R score, or survival, data from preclinical models and human studies support the use of CSF DPR proteins as pharmacodynamic biomarkers.[78, 85, 86, 90, 92,93,94,95] In fact, measures of DPR proteins have been used as an exploratory endpoint in clinical trials of investigational agents, such as antisense oligonucleotides (ASOs), for C9ORF72-FTD/ALS.
Biomarkers of C9ORF72-FTD/ALS Based on TDP-43–Associated Pathology
Loss of splicing repression by the TDP-43 is linked to ALS and FTD pathology [96]. TDP-43 has been explored extensively as a fluid biomarker for ALS and FTD, including in CSF, plasma, circulating lymphomonocytes, and platelets, but no robust measure of pathological TDP-43 protein itself has been developed as of yet.
In brains of patients with ALS or FTD, TDP-43 is compromised in its function of repressing the splicing of cryptic exons [97]. The stathmin-2 (STMN2) cryptic exon is a biomarker for both ALS and FTD [98,99,100]. Additionally, the cryptic exon splicing event in the UNC13A locus is a biomarker that results from loss of TDP-43 [101, 102]. Researchers used a monoclonal antibody specific to a TDP-43–dependent cryptic epitope to show that C9ORF72-associated ALS, including in pre-symptomatic mutation carriers, involves losing TDP-43 splicing repression [103]. With the use of mass spectrometry, TDP-43–dependent cryptic peptides can also be detected in C9ORF72-associated ALS [104]. These findings have two major implications. First, therapeutic strategies could overcome the loss of TDP-43 splicing repression for C9ORF72-related and sporadic ALS and FTD. Second, developing TDP-43 cryptic peptides as functional biomarkers could lead to early-stage diagnosis of ALS and FTD and could aid in monitoring the biological response of therapeutic treatment in clinical trials.
Neuroimaging of the C9ORF72 FTD/ALS Syndrome
Advances in neuroimaging sequences and computation have allowed the non-invasive quantification of cerebral structural (MRI, grey matter volumetry, and white matter tractography), functional (blood oxygen level-dependent [BOLD] MRI), and metabolic (fluorodeoxyglucose [FDG] PET) changes that have been applied to the study of the C9ORF72-related syndrome (comprehensively reviewed in [105]).
Symptomatic C9ORF72-related FTD and ALS has been consistently associated with more widespread cortical and subcortical grey and white matter changes—more so than has non-C9ORF72 FTD or ALS [106]—with longitudinal changes detectable in some patients over months [107]. Consistent thalamic involvement, particularly of the pulvinar sub-region, occurs in both FTD and ALS [108], with an overlapping regional hypometabolic thalamic signature also seen in ALS cases using FDG PET [109]. Alterations in cerebral networks, as demonstrated in resting state BOLD MRI, have been associated with both ALS and FTD phenotypes [110, 111].
In asymptomatic C9ORF72 expansion carriers, substantial MRI changes have been detected, including grey and white matter loss [112, 113], gyrification abnormalities [114], hypothalamic atrophy [115], changes in resting-state network connectivity [116], and reduced cerebral perfusion [117]. FDG PET has demonstrated regional hypometabolism encompassing the cingulate gyrus, frontal and temporal neocortices, and thalami [118, 119]. Future studies might usefully exploit the unrivaled sensitivity of magnetoencephalography (MEG) to subtle changes in cortical motor neurophysiology, as noted in a small study of asymptomatic carriers of varied ALS-causing genotypes [120]. In relation to understanding the different phenotypic outcomes, a study of the cervical spinal cord showed that a sub-group of asymptomatic C9ORF72 expansion carriers aged over 40 years who were relatives of those affected by ALS (rather than FTD) showed evidence of early pathology of the white matter of the corticospinal tract [121].
The differing clinical needs of patients tend to result in the dichotomization of symptomatic neuroimaging cohorts into either ALS or FTD. Through the increasing partnership with families affected by C9ORF72 and international data-sharing platforms, the opportunity to study larger numbers of younger asymptomatic expansion carriers (including those aged < 18 years) will deepen the understanding of a syndrome that may have a broader neurodevelopmental dimension than previously realized [122].
Summary of the Working Group Discussions on C9ORF72 Biomarkers
Table 2 summarizes the highlights of the C9ORF72 Biomarker working group.
C9ORF72-FTD/ALS Gene Therapy and Small Molecule Approaches
Gene therapy is a potential treatment approach for C9ORF72-FTD/ALS with the primary goal of targeting the underlying disease-causing genetic mutation. Specifically, gene therapy strategies aim to reduce the abnormal HRE within the C9ORF72 gene. One approach involves using small RNA molecules, known as ASOs, to target and bind to the expanded repeat sequences. Parallel approaches explore the design of small molecule compounds that can inhibit the activity of the abnormal repeat expansion in the C9ORF72 gene. Finally, small molecule compounds targeting the underlying mechanisms and pathological processes associated with C9ORF72 repeat expansion are also being investigated as therapeutic avenues for C9ORF72-FTD/ALS.
Gene Therapy for C9ORF72-FTD/ALS: Challenges and Opportunities
The entire field of gene therapy has been very active recently, with many clinical trials underway in an array of different diseases. The approaches being investigated for C9ORF72-FTD/ALS include ASOs, adeno-associated virus (AAV)–mediated gene silencing using CRISPR or RNA interference (RNAi) technology, and AAV-mediated gene delivery of therapeutic proteins [123, 124]. ASO treatments are a great way to explore the possibility of modifying mutant gene expression in ALS using a reversible system whereas AAV methods using constitutive promoter systems are permanent and cannot be switched off if problems are encountered. However, while ASOs require constant delivery through clinical visits and a lumbar puncture, AAV infusions are “one and done,” which is more practical for patients. Newer technologies to allow regulated expression of therapeutic genes are an exciting area that may allow more flexible use of AAV constructs in the clinic. Using gene therapy to deliver therapeutic proteins to the brain is another exciting area—either directly or “ex vivo” using cells as a delivery vehicle.
The major challenge for using gene therapy to modify C9ORF72 toxicity in patients is the complexity of how the HREs cause cell death, as discussed throughout this article. As there is both a loss of function due to reduced C9ORF72 protein levels and a gain of function due to toxic products driven by the repeats, any gene therapy approach has to take both of these processes into consideration. As of the writing of this article, there have been three clinical trials in this area. In the first trial, mutant C9ORF72 expression was suppressed by a mixed backbone ASO targeting the antisense strand in an N-of-one study, which resulted in a drop in the DPR protein poly(GP), but the patient’s ALS functional rating score was unchanged and neurofilament levels actually increased [86]. A larger study led by Biogen Inc. (Cambridge, MA, USA) used an ASO against C9ORF72 (BIIB078) in a phase 1 study; however, patients on the higher dose of the drug trended towards greater decline, so the clinical development was halted. Wave Life Sciences (Cambridge, MA, USA) used a similar ASO-targeting strategy, and this phase 1b/2 trial was also halted (ClinicalTrials.gov: NCT04931862). While there are no current trials using AAV and gene editing techniques to correct the C9ORF72 repeat expansion, many studies are under development, as described extensively in two reviews [123, 124].
In addition to gene editing approaches to treat C9ORF72, other gene therapy approaches are also applicable to all forms of ALS, as they focus on replacing cells expressing the mutation while at the same time being engineered to release powerful growth factors. One recent study showed that this approach is safe in patients with sporadic ALS [125] and opens up other opportunities for similar approaches in C9ORF72 patients.
Small Molecule Approaches to Degrade the HRE in C9ORF72-FTD/ALS
Another way to target the HRE in C9ORF72 is via a small molecule approach, which would have the advantage of being delivered orally as a pill. A particular small molecule, known as an RNase recruiting chimera (RIBOTAC), was engineered to eliminate (G4C2)n through the use of a heterobifunctional compound that selectively binds the target with one end and depletes it with the other end by activating ribonuclease L that can cleave RNA when it is in close proximity [126]. This approach decreased the abundance of (G4C2)n in vitro by being selective for the very thermodynamically stable hairpin RNA structures. After being delivered intracerebroventricularly in mice, the RIBOTAC displayed prolonged activity and decreased pathological aggregates in the cortex.
An additional small molecule approach used a nuclear RNA exosome to degrade RNA and was designed to be a blood–brain penetrant [127]. This RNA-targeted small molecule is selective in induced pluripotent stem cells and bioactive in multiple mouse models of C9ORF72-FTD/ALS upon delivery by injection. Multiple mechanisms are available to affect the decay of (G4C2)n in cells and mouse models, and dual-functioning compounds can affect the RNA in both the nucleus and cytoplasm.
Small molecules can affect RNA biology in many ways, including affecting the degradation of RNA. Known drug collections can be used to find ligands that bind RNA and that can be optimized, including being designed to be brain penetrant.
Clinical Trial Design for C9ORF72-FTD/ALS
Experiences from Alzheimer’s disease (AD) and spinal muscular atrophy suggest that treating FTD and ALS will be most successful if treatment is initiated early—ideally in pre-symptomatic stages. Such a prevention approach has been implemented in the DIAN-TU AD trial [128]. However, unlike AD, in FTD, little is known about the progression of biomarker and clinical changes that could be used to determine the criteria for enrollment or to identify the best clinical trial endpoints at different disease stages. Similar difficulties are found in ALS. The onset of genetic FTD or ALS, particularly for C9ORF72-associated FTD and ALS, is difficult to predict [8]. Further, the number of eligible patients, especially for C9ORF72-FTD, is limited, so it is challenging to power trials for efficacy.
Clinical Trials for C9ORF72—Current Landscape and Hopes for the Future
Current clinical trials for C9ORF72 ALS include both trials that enroll gene-targeted and gene-enriched clinical cohorts of patients affected by C9ORF72, respectively (Table 3) [129]. As highlighted above, the gene-targeted trials are focused on using ASOs to reduce the repeat-containing toxic RNA transcripts and DPR, while RNAi using AAV vectors for degrading the C9ORF72 repeat-containing RNAs is in pre-clinical development [129]. A recently halted trial of the ASO known as WVE-004 was selective against the RNA V1 and V3 repeat-containing transcript variants [129]. The discontinued trial of the ASO known as BIIB078 in adults with C9ORF72-associated ALS showed reduced concentrations of DPRs (poly[GP] and poly[GA]) in CSF, indicating target engagement, but results showed increased concentrations of CSF NfL compared with concentrations in the placebo group and poorer trends in measures of clinical functional outcomes [129]. Cohorts of patients with C9ORF72-ALS have been the focus of trials targeting downstream pathways of autophagy or neuroinflammation via drugs such as the oral PIKFYVE inhibitor apilimod (LAM-002a, also known as AIT-101) [69], the LINE-1 retrotransposon inhibitor TPN-101 [129], and metformin [129].
Currently, nearly all C9ORF72 ALS clinical trials are in phase 1 or 2a testing, and there are no late-phase clinical efficacy trials yet. As more C9ORF72-targeted experimental compounds move into later phases of clinical trials, it is critical to develop innovative clinical trial designs that efficiently utilize the relatively small and available pool of C9ORF72-FTD and -ALS trial participants for all phases of clinical trial testing and for all concurrently available experimental therapies. This could be achieved by more innovative and efficient early clinical phase trial designs that have small sample sizes and short treatment durations yet are adequately powered for biomarker-driven primary outcomes and enriched by trial cohorts of clinically homogenous individuals with early FTD and ALS. Such trials could aid in efficient screening of experimental compounds and assist in making sound go/no-go decisions based on in vivo human biological efficacy, CNS target engagement, pharmacokinetic signals, and safety signals. Subsequently, successful compounds could be brought forward for late-phase testing in large, traditional, randomized, placebo-controlled, clinical efficacy trials.
Preparing for FTD/ALS Prevention Trials
We have already entered an era of ALS prevention trials with the initiation of the ATLAS study in the SOD1-ALS population [130]. This trial builds on the observation that a pre-symptomatic rise in NfL predicts imminent phenoconversion to clinically manifest ALS, at least in a subset of people with highly penetrant SOD1 mutations associated with rapidly progressive disease [80]. While additional biomarkers will be needed to empower similar disease prevention trials among pre-symptomatic C9ORF72 mutation carriers, the ATLAS study has forged a path that will shed important light on future FTD/ALS prevention trials.
The FTD Prevention Initiative (www.thefpi.org) seeks to bring together global FTD cohorts to prepare for clinical trials. The majority (approx. 80%) of C9ORF72 mutation carriers in this worldwide network of approximately 1000 mutation carriers do not meet diagnostic criteria for ALS or motor neuron disease (MND), suggesting that ALS may not be the most common phenotype for C9ORF72 mutation carriers. Some individuals meet diagnostic criteria for a FTD subtype, while others have intermediate FTD-ALS phenotype and may not fully meet either diagnostic criterion. The approach to modeling disease progression jointly includes both clinical endpoints and biomarkers, determines latent “disease age” as the years to/since clinical onset, and uses Bayesian priors derived from estimates of years since onset based on clinician report of symptoms or age relative to the mutation’s mean for pre-symptomatic patients; the controls use disease age, which is based on the mutation that their family carries, such as C9ORF72, GRN, or MAPT [84]. The baseline sample population included 796 patients who are carriers of genes for FTD: 347 carriers of C9ORF72, 281 carriers of GRN, and 168 carriers of MAPT. MRI-measured NfL chain and brain atrophy were observed to diverge 20–30 years before the disease had clinical impact on carriers of C9ORF72, and the dynamics differ between the genetic groups. Disease progression and selection of endpoints are specific to the mutation that carriers have.
Prevention trials may require informative biomarkers to serve as surrogate endpoints, whereas clinical endpoints are sufficient for trials of treatments in fully symptomatic individuals. Whether someone will develop ALS, FTD, a movement disorder, or some mixed phenotype because of a C9ORF72 expansion is currently not predictable. Therefore, prevention trials that begin treatment prior to symptom onset will need to consider the potential development of multiple C9ORF72 phenotypes. The sample size of a prevention trial can be reduced by using disease age as an inclusion criterion. Clinical trial power may be further increased by Bayesian efficacy analyses and model-derived endpoints, which may be necessary for addressing rare mutations such as MAPT and GRN.
Summary of the Working Group Discussions on C9ORF72 Therapeutics and Clinical Trial Design
The highlights of the C9ORF72 Therapeutics and Clinical Trials working group are summarized in Table 4.
Conclusion
Families who live with C9ORF72 typically understand all too well that ALS and FTD exist on a spectrum. Genetic carriers are at risk of developing ALS, FTD, or a combination thereof, with no ability at this time to predict which disease may emerge in which person. Basic scientists working on C9ORF72 recognize that their research has equal applicability to both ALS and FTD, with little ability—to date—to identify which laboratory models are relevant to which clinical disease. However, medical care and clinical research are often siloed with ALS and FTD patients seen by different clinical care centers with distinct training.
Working in silos has helped clinics to develop the specialization needed to tend to each of these highly complex diseases. However, the full spectrum of symptoms can go unrecognized, something that can be particularly painful to families dealing with unrecognized behavioral FTD symptoms in loved ones with ALS, and vice versa.
The clinical research silos of FTD versus ALS also create a number of specific problems. Both fields are actively working to detect the earliest manifestation of clinical disease in genetic carriers, a critical step to design clinical trials to test the ability of disease-modifying therapies that might protect against the development of disease. Collaboration across the two fields of expertise is critical—including an awareness of the respective bodies of literature in the two fields—with a willingness of researchers to learn from each other. This is especially important given that it is not currently known which disease will emerge in these genetic carriers. Sponsors seeking to test the effectiveness of a given treatment for C9ORF72 or shared causes of FTD/ALS must usually select one or the other condition. Two phase 2 basket trials are underway in 2023 for C9ORF72 FTD and C9ORF72 ALS, but the lack of a unified outcome measure of efficacy means that one or the other condition must be selected for phase 3 trials. Biorepositories are often built for either ALS or FTD, with different core data elements, tissue processing protocols, and participant profiles, and those differences challenge the ability to leverage resources in rare diseases where every sample and every data point are of critical importance.
The ALS and FTD communities can work together to understand genetics, pathophysiology, and disease progression. Families who carry C9ORF72 require holistic support. Specific tools may help to overcome these challenges; these include: (1) the development and use of tools to promote linkage and collaboration of care and research resources across ALS and FTD, such as minimal dataset or usage of the same tokenization tools; (2) collaboration on the inclusion criteria and outcome measures for prodromal prevention clinical trials in genetic carriers at risk of ALS and FTD; (3) increased collaboration across FTD and ALS in the support of families and individuals at risk of disease; and (4) development of training and communication resources to make it easier for ALS clinics and families to understand and support FTD-related symptoms.
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Acknowledgements
We would like to acknowledge the recent passing of Mr. Mark Nilsson who attended this summit with his wife and caretaker Ms. Paula Nilsson. We are honored to have met Mark and appreciated his perspectives as an individual living with ALS during our discussions. We would also like to thank David and Weezie Reese for their support and encouragement to host this summit, and Karis Anderson for her support towards the organization of this summit.
Medical Writing/Editorial Assistance
Kathy Boltz, PhD, of On Point Scientific, LLC, provided medical writing support, and Sharese Terrell Willis, PhD, of Doc’s Editing Shop, LLC, provided editorial support. This assistance was funded by the authors.
Funding
The summit was funded by the Arizona Community Foundation through a generous donation to the Barrow Neurological Foundation. This work was also supported by the Intramural Research Program of the NIH, National Institute on Aging (ZIAAG000933-15) to BJT. The journal’s fee was waived.
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Rita Sattler: drafting, finalizing and submitting the manuscript. Bryan J. Traynor: drafting the manuscript. Janice Robertson: drafting the manuscript. Ludo Van Den Bosch: drafting the manuscript. Sami J. Barmada: drafting the manuscript. Clive Svendsen: drafting the manuscript. Matthew D. Disney: drafting the manuscript. Tania F. Gendron: drafting the manuscript. Philip C. Wong: drafting the manuscript. Martin R. Turner: drafting the manuscript. Adam Boxer: drafting the manuscript. Suma Babu: drafting the manuscript. Michael Benatar: drafting the manuscript. Michael Kurnellas: drafting the manuscript. Jonathan D. Rohrer: drafting the manuscript. Christopher J. Donnelly: drafting the manuscript. Lynette M. Bustos: generating figure. Kendall Van Keuren-Jensen: drafting the manuscript. Penny A. Dacks: drafting the manuscript. Marwan N. Sabbagh: drafting the manuscript.
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Conflict of Interest
Janice Robertson, Sami J. Barmada, Clive Svendsen, Tania F. Gendron, Philip C. Wong, Martin R. Turner, Adam Boxer, Michael Kurnellas, Lynette M Bustos, Kendall Van Keuren-Jensen have nothing to disclose. Rita Sattler is a member of the Scientific Advisory Board of Spinogenix Inc, the LiveLikeLou Foundation, the Robert Packard Center and Northeast ALS consortium. Bryan J. Traynor holds patents on the diagnostic and therapeutic implications of the C9orf72 repeat expansion. Ludo Van Den Bosch is head of the Scientific Advisory Board of Augustine Therapeutics (Leuven, Belgium) and is part of the Investment Advisory Board of Droia Ventures (Meise, Belgium). Jonathan D Rohrer has provided consultancy or been on an advisory board for Novartis, Wave Life Sciences, Prevail, Alector, Aviado Bio, Arkuda Therapeutics, and Denali Therapeutics. Matthew D. Disney is a founder of Expansion Therapeutics. Christopher J Donnelly is cofounder and advisor for Confluence Therapeutics. Michael Benatar reports grants from the National Institutes of Health, the Muscular Dystrophy Association, and the ALS Association; and receives consulting fees for Alector, Alexion, Annexon, Arrowhead, Biogen, Cartesian, Denali, Eli Lilly, Horizon, Immunovant, Novartis, Roche, Sanofi, Takeda, UCB, and UniQure. The University of Miami has licensed intellectual property to Biogen Inc. to support the design of the ATLAS study. He has a provisional patent ‘Determining Onset of ALS’ (US Patent No. 17/941,117). He serves as a member of the Board of Trustees for the ALS Association. Suma Babu has received research funding from Biogen Inc. (including the BIIB078 ASO trial for C9ORF72 ALS), AI therapeutics, Novartis, Orion, Voyager Therapeutics, Medicinova, Ionis, American Academy of Neurology, AANEM Foundation, and Muscular Dystrophy Association. Penny A. Dacks is an employee of the Association for Frontotemporal Degeneration (AFTD), King of Prussia, PA, USA. Marwan N. Sabbagh is a consultant for Roche-Genentech, Eisai, Lilly, Synaptogenix, NeuroTherapia, T3D, Signant Health, Novo Nordisk, Corium, Prothena, KeiferRx; is on the board of directors at CervoMed; and receives stock options/owns stocks from Athira, Lighthouse Pharmaceuticals, Alzheon. Michael Kurnellas, new affiliation: Neuron23, Inc., South San Francisco, CA, USA. Lynette M Bustos, new affiliation: Ionis Pharmaceuticals, Inc., Carlsbad, CA, USA.
Ethical Approval
The contents of this manuscript are based on discussions at the C9orf72 Summit and did not entail any animal or human subjects research that required review/approval by the IACUC or IRB. All patients and pre-symptomatic gene mutation carriers who participated and/or disclosed their gene mutation status, did so of their own volition.
Additional information
The members of the Attendees of the inaugural C9ORF72 FTD/ALS Summit are listed in the online Supplementary material.
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Below is the link to the electronic supplementary material.
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Sattler, R., Traynor, B.J., Robertson, J. et al. Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit. Neurol Ther 12, 1821–1843 (2023). https://doi.org/10.1007/s40120-023-00548-8
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DOI: https://doi.org/10.1007/s40120-023-00548-8