Autoimmune glial fibrillary acid protein (GFAP) astrocytopathy
Autoimmune glial fibrillary acid protein (GFAP) astrocytopathy, or simply GFAP astrocytopathy, is a rare inflammatory central nervous system (CNS) disorder.
Given the rarity of the condition, epidemiological data pertaining to autoimmune GFAP astrocytopathy are not well established. Based on existing case series-level data, it tends to manifest in middle-aged adults and there may be a slight female preponderance 1.
Autoimmune GFAP astrocytopathy has a broad clinical neuropsychiatric and temporal spectrum 1-6. The most common phenotypical syndromes are those of meningoencephalitis or meningoencephalomyelitis 1-6, which can manifest over an acute, subacute, or chronic time-frame 4. Within those syndromes, the most common clinical features include 1-6:
- neck stiffness
- psychiatric symptoms (e.g. psychosis)
- blurred vision (due to optic papillitis)
- motor and sensory changes (due to myelopathy)
- cerebellar ataxia
- movement disorders (e.g. tremor, chorea, myoclonus)
- drug-refractory seizures
- autonomic dysfunction
- bulbar symptoms
Additionally, a coryzal or flu-like prodrome is also a common clinical feature, being present in 30-67% of patients 4-6.
The pathophysiology of autoimmune GFAP astrocytopathy has not been fully elucidated and is not well understood. It is known that GFAP is an intracellular protein that forms an integral component of astrocyte cytoskeletons and also plays a pivotal role in multiple astrocytic functions 4. In autoimmune GFAP astrocytopathy, there are IgG autoantibodies that target GFAP in astrocytes, which leads to an eventual loss of astrocytes, and presumably the resultant clinical phenotype 1-6. These autoantibodies may have a paraneoplastic or parainfectious etiological basis 1.
The key marker is the GFAP antibody, which has a higher positive predictive value when present in the CSF than in the serum 5. Additionally, CSF will often have an inflammatory phenotype, with high protein and a pleocytosis 1-6. Co-existing autoantibodies (e.g. NMDA receptor antibody, aquaporin-4 antibody) may also be present 1-6.
Typical neuropathological features include 1,3:
- extensive perimicro-vascular inflammation, sparing the vessel itself
- microglial activation
Radiographic abnormalities of the neuraxis are very common in autoimmune GFAP astrocytopathy 1-6.
Typical findings include:
- T2/FLAIR: hyperintense, diffuse, confluent, periventricular white matter lesions 1-6, often extending into the centrum semiovale, deeper brain structures, and/or brainstem 1,3
- DWI: normal 6
T1 C+ (Gd): characteristic linear, perivascular pattern of contrast-enhancement extending radially from the periventricular surface and through the cerebral white matter 1-6
- other less characteristic and less common patterns of enhancement include leptomeningeal and periependymal 1,2,4-6
- MR angiogram: normal 6
Notably, in patients with a predominantly cerebellar ataxia phenotype, diffuse cerebellar atrophy may be the only radiographic feature 4. Furthermore, despite visual changes being a relatively common feature of autoimmune GFAP atstrocytopathy, optic nerves often appear normal on imaging.
Typical findings, most commonly in the cervicothoracic spinal cord, include:
T2: hyperintense longitudinally extensive spinal cord lesion(s), often pericentrally located 1-6
- lesions are described as having “hazy” borders 6
- may also have focal cord atrophy 3
- T1 C+ (Gd): may have contrast-enhancement 1-6
FDG PET-CT of the neuraxis may reveal increased FDG uptake indicative of hypermetabolism, often corresponding with regions of signal abnormality on MRI brain and/or spinal cord 1-3,5,6.
Treatment and prognosis
Autoimmune GFAP astrocytopathy is typically steroid-responsive 1-6. In cases that are steroid-refractory, often in the setting of concurrent underlying malignancy or co-existing autoantibody, there may be response to other immunotherapy (e.g. rituximab, mycophenolate mofetil, azathioprine, cyclophosphamide, intravenous immunoglobulin) 5.
The disease is most often monophasic, however may have a relapsing course in approximately 20% of patients 6. Overall, the prognosis is generally good 6.
History and etymology
Autoimmune GFAP astrocytopathy was first described by Boyan Fang, Vanda Lennon, and colleagues from the Mayo Clinic in their 2016 seminal paper 2. It is thought that some cases previously labeled as 'nonvasculitic autoimmune inflammatory meningoencephalitis' may actually have been autoimmune GFAP astrocytopathy 3.
- 1. Shan F, Long Y, Qiu W. Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy: A Review of the Literature. (2018) Frontiers in immunology. 9: 2802. doi:10.3389/fimmu.2018.02802 - Pubmed
- 2. Fang B, McKeon A, Hinson SR, Kryzer TJ, Pittock SJ, Aksamit AJ, Lennon VA. Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy: A Novel Meningoencephalomyelitis. (2016) JAMA neurology. 73 (11): 1297-1307. doi:10.1001/jamaneurol.2016.2549 - Pubmed
- 3. Long Y, Liang J, Xu H, Huang Q, Yang J, Gao C, Qiu W, Lin S, Chen X. Autoimmune glial fibrillary acidic protein astrocytopathy in Chinese patients: a retrospective study. (2018) European journal of neurology. 25 (3): 477-483. doi:10.1111/ene.13531 - Pubmed
- 4. Iorio R, Damato V, Evoli A, Gessi M, Gaudino S, Di Lazzaro V, Spagni G, Sluijs JA, Hol EM. Clinical and immunological characteristics of the spectrum of GFAP autoimmunity: a case series of 22 patients. (2018) Journal of neurology, neurosurgery, and psychiatry. 89 (2): 138-146. doi:10.1136/jnnp-2017-316583 - Pubmed
- 5. Dubey D, Hinson SR, Jolliffe EA, Zekeridou A, Flanagan EP, Pittock SJ, Basal E, Drubach DA, Lachance DH, Lennon VA, McKeon A. Autoimmune GFAP astrocytopathy: Prospective evaluation of 90 patients in 1 year. (2018) Journal of neuroimmunology. 321: 157-163. doi:10.1016/j.jneuroim.2018.04.016 - Pubmed
- 6. Kunchok A, Zekeridou A, McKeon A. Autoimmune glial fibrillary acidic protein astrocytopathy. (2019) Current opinion in neurology. 32 (3): 452-458. doi:10.1097/WCO.0000000000000676 - Pubmed
Related Radiopaedia articles
White matter disorders
- white matter
- normal myelination
white matter disorders
- anti-MOG associated encephalomyelitis
- Guillain-Barré syndrome (GBS)
- chronic inflammatory demyelinating polyneuropathy (CIDP)
- transverse myelitis
- tumefactive demyelinating lesions
- acute disseminated encephalomyelitis (ADEM)
- acute hemorrhagic encephalomyelitis (AHEM)
- neuromyelitis optica (NMO) (Devic disease)
multiple sclerosis (MS)
McDonald diagnostic criteria for MS (current 2017 revision)
- previous 2016 MAGNIMS consensus
- McDonald diagnostic criteria for MS (current 2017 revision)
- radiologically isolated syndrome (RIS)
- clinically isolated syndrome (CIS)
- early-onset neuronal degenerative disorders
- GM1 & GM2 gangliosidoses (e.g. Tay Sachs disease)
- giant axonal neuropathy
- hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC)
- hypomyelination with congenital cataract
- leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
- hypomyelination with brainstem and spinal cord involvement and leg spasticity
- Pol III-related leukodystrophies
- early-onset neuronal degenerative disorders
- myelin disorders
- myelin vacuolisation
- adult-onset autosomal dominant leukodystrophy
- cerebrotendinous xanthomathosis
- cystic leukoencephalopathy without megalencephaly
- L-2-hydroxyglutaric aciduria
- lysosomal storage diseases
- peroxisomal disorders
- Sjögren-Larsson syndrome