GRIN-related disorders, a novel group of IEM (inborn errors of metabolism): Mutations on GRIN
genes, encoding for the N-methyl-D-Aspartate receptor (NMDAR) subunits, have been recently
associated with autosomic dominant GRIN-related disorders (Lemke et al., 2016; Platzer et
al., 2017; XiangWei et al., 2018; Strehlow et al., 2019). These rare conditions represent a
subtype of paediatric encephalopathies leading to intellectual disability, hypotonia,
communication deficits and motor impairment (Orphanet entries: 178469, 289266, 101685, for
GRIN1, GRIN2A and GRIN2B, respectively).
There are about 200 patients affected with these diseases in Europe according to a data
collection study conducted by the patients' families and presented at the first European
meeting of GRIN disorders in October 2018 (Barcelona, Hospital Sant Joan de Déu).
Along the last years, our research efforts were focused to delineate the pathophysiology and
personalized therapies for these diseases that are now considered as a new category of IEM.
In particular, the recent nosology of inherited metabolic disorders (Ferreira et al, 2018)
classifies GRIN-related disorders in the category: "DISORDERS OF NITROGEN CONTAINING
COMPOUNDS", and the subgroup: "20. Disorders of glutamate metabolism":
GRIN1 (OMIM138249): Ionotropic glutamate receptor NMDA type subunit 1 dysregulation (AD, AR):
Autosomal dominant mental retardation type 8; neurodevelopmental disorder with or without
hyperkinetic movements and seizures. GRIN2A (OMIM138253): Ionotropic glutamate receptor NMDA
type subunit 2A dysregulation (AD): Non related to human disease so far. GRIN2B (OMIM138252):
Inotropic glutamate receptor NMDA type subunit 2B dysregulation (AD): Early infantile
epileptic encephalopathy type 27; autosomal dominant mental retardation type 6. GRIN2D
(OMIM602717): Ionotropic glutamate receptor NMDA type subunit 2D superactivity (AD): Early
infantile epileptic encephalopathy type 46.
Indeed, in a proof-of-concept, the investigators have determined that a GRIN2B
loss-of-function variant can be rescued in vitro, by means of elevated doses of D-serine
(NMDAR coagonist) administration. More importantly, the investigators showed that L-serine
(the D-serine natural precursor) dietary supplement was associated with a significant
improvement of motor and communication skills of the patient harbouring GRIN2B hypofunctional
variant (Soto et al., 2019).
Serine enantiomers: cognitive enhancement and potential use in GRIN-related disorders
L-serine (C3H7NO3; 105.09 g/mol; synonym (S)-2-amino-3-hydroxypropanoic acid) is a
naturally-occurring dietary amino acid. It is abundant in soy products, some edible seaweeds,
sweet potatoes, eggs, and meat. Since some L-serine is produced by astrocytes in the brain,
it is considered a non-essential amino acid. L-serine is directly involved in the
biosynthesis of purines, pyrimidines, and other amino acids. Serine residues are found in
most proteins and within proteins function as a site for phosphorylation.
L-serine is considered as GRAS (generally recognized as safe) by the FDA and has been
approved as a normal food additive under CFR172.320. It is widely sold as a dietary
supplement. A randomized trial of L-serine in 18 patients with hereditary sensory and
autonomic neuropathy type 1 has been published (ClinicalTrials.gov identifier NCT01733407).
High-dose oral L-serine supplementation (400 mg/kg/day) appears safe in patients with HSAN1
and is potentially effective at slowing disease progression.The authors did not report
adverse effects at doses of 400mg/kg/day (Eichler et al) Further, L-serine dietary supplement
has been used in Paediatrics at doses of 400 to 600 mg/kg/day since several decades ago for
the treatment of a group of inherited metabolic disorders, namely: 3-phosphoglycerate
dehydrogenase deficiency, phosphoserine aminotransferase deficiency and phosphoserine
phosphatase deficiency, with no reported adverse effects. In patients with 3-phosphoglycerate
dehydrogenase deficiency, neither 100 nor 200 mg/kg per day had any effects on the patients'
symptoms or on CSF serine and glycine concentrations (de Koning et al 1998). Only with
L-serine 500 mg/kg per day was a reduction in seizure activity noted and an increase in
serine CSF concentrations observed (Koning 2006).
D-serine, the natural coagonist of the NMDA receptor, results from the racemisation of
L-serine in brain, and its biosynthetic alteration can lead to neuronal dysfunction (van de
Crabben et al., 2013). In addition to its homeostatic role in neuronal function, the
beneficial effect of D-serine supplement has been recently shown in healthy individuals
(Levin et al., 2015). Heresco-Levy's group showed the procognitive effects of D-serine
throughout NMDA receptor function. D-serine deficits have been associated with aging in rats,
with a functional rescue observed following D-serine administration (Turpin et al., 2011;
Billard, 2015).
Additionally, L-serine biosynthesis defects (de Koning, 2006) cause neurological phenotypes
(psychomotor retardation, microcephaly, seizures) that can be safely treated by L-serine.
Moreover, and as already mentioned, our group has recently described the beneficial effect of
a chronic L-serine dietary (500 mg/kg/per day) supplement in a 5 years GRIN2B patient (Soto
et al., 2019). The patient has shown notable improvements in motor and cognitive performance
and communication after 11 and 17 months of L-serine dietary supplementation. These data
suggest that L-serine supplementation might ameliorate GRIN2B-related severe encephalopathy
and other neurological conditions caused by glutamatergic signaling deficiency.
Besides this direct effect, D-serine can prevent behavioral abnormalities in adult mice
challenged by maternal immune activation (Fujita et al., 2016), and induces hippocampal
neurogenesis (Sultan et al., 2015).
These evidences indicate that 500 mg/kg/per day is a safe and effective dose, that could be
used in patients with GRIN related disorders.
HYPOTHESIS Overall, these evidences indicate that, independently on the molecular aetiology,
NMDAR activity potentiation throughout L-serine dietary supplement can ameliorate
glutamatergic function and improve the life quality of children suffering from GRIN-related
disorders, a novel IEM. Dietary supplement of L-serine results on increased D-serine plasma
levels and potentiates NMDA receptors leading to NMDA receptors functionality increase and
hypofunctionality rescue, as shown in a pilot study (Soto et al., 2019).
AIM The purpose of this study is to determine L-Serine dietary supplement efficacy for the
treatment of patients with GRIN-related disorders caused by the presence of GRIN genetic
variants leading to hypofunctional (loss-of-function) NMDA receptors.