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Krabbe disease, an autosomal recessive disease, is a type of lysosomal storage disorder that results from the deficiency of the enzyme galactocerebrosidase. As a result, there is an accumulation of the toxic compound psychosine, principally in the central and peripheral nervous systems, which leads to widespread neurological symptoms. Since the outcome of this disease is profound and fatal, a meticulous diagnostic work-up, followed by early treatment, is crucial. This activity reviews the evaluation and management of Krabbe disease and highlights the role of the interprofessional team in the care of patients with this condition. Objectives: Identify the etiology of Krabbe disease. Review the appropriate evaluation of Krabbe disease. Outline the management options available for Krabbe disease. Summarize the importance of improving care coordination among interprofessional team members to improve outcomes for patients affected by Krabbe disease. Access free multiple choice questions on this topic.

Krabbe disease is an autosomal recessive neurodegenerative disorder.[1][2] The gene mutation occurs at chromosome 14, which codes for a lysosomal hydrolase known as galactosylceramide beta hydrolase (GALC). This enzyme is responsible for metabolizing galactolipids in the central nervous system and peripheral nervous system, and the failure of which will lead to the accumulation of compounds responsible for neurodegeneration. Krabbe disease is also known as globoid cell leukodystrophy because of the characteristic multinucleated globoid cells found on brain biopsy and the presence of white matter degeneration. Krabbe disease is subdivided into four subcategories based on the age of presentation of symptoms; however, many experts disagree with the age range allotted to different subtypes.[3][4] Early infantile type: 0 to 13 months Late infantile type: 13 to 36 months Juvenile type:  3 to 16 years Adult type: >16 years

Krabbe disease is due to loss of function gene mutation coding for galactosylceramide beta hydrolase (GALC). About 200 GALC gene mutations have been identified. Usually, it is challenging to establish the phenotype severity with the genotype, but large deletions like 30 kilobase (kb) gene deletions, truncations, frameshift mutations, and nonsense mutations are associated with severe clinical manifestations.[5] The 30-kilobase gene deletion is common and accounts for 40% of 45% of mutations in the infantile form in Northern Europe and 35% in Mexican patients.[6] Approximately 50% of patients with juvenile and adult types are heterozygous for 30kb gene deletion or have mutations leading to reduced GALC enzyme activity.

Krabbe disease is a genetic disorder, and its frequency varies widely with the population. It is a rare lysosomal storage disorder that is rapidly progressive and fatal. The incidence in Europe is estimated to be 1 per 100,000 live births. After analyzing death certificates, a U.S. estimate of 1 per 250,000 was made, but a more precise estimate can approach the European incidence.[7] Its rate is as high as 6 per 1000 live births in Israel's Druze community due to consanguineous marriages. Among the four subtypes, 85% to 90% of the cases are of the infantile subtype, which is also the most severe and rapidly progressing. The mortality rate is as high as 90% in the first two years of life. The late-onset type has a better prognosis, and life expectancy is 5 to 7 years after the onset of symptoms.

Krabbe disease is due to the GALC enzyme deficiency, present in the lysosomes of microglial cells of the brain and the spinal cord. Microglia cells are responsible for the physiological turnover of myelin components and the elimination of toxic compounds. GALC metabolizes two galactolipids, galactosylceramide, and psychosine. Galactosylceramide is present in high concentrations in Schwann cells and oligodendroglial cells. GALC degrades galactosylceramide; its deficiency leads to the building up of galactosylceramide in the central and peripheral nervous system. Psychosine is a cytotoxic sphingosine lipid formed as a byproduct during myelin synthesis.[8][9] The mechanism of how the accumulation of psychosine manifests its cytotoxic effect on oligodendroglia is unclear. Multiple hypotheses, like the microglia hypothesis and the psychosine hypothesis, have been formulated. The accumulation of these two compounds in the oligodendrocytes and Schwann cells leads to apoptosis of these cells and, hence, demyelination. In turn, the apoptosis leads to secondary activation of microglial cells and its transformation into multinucleated giant cells known as globoid cells, which are pathognomic of Krabbe disease.

Blood vessels will have clusters of multinucleated macrophages with abundant cytoplasm (globoid cells).[1] Neuronal degeneration at the gray matter is found. Hypomyelination and segmental demyelination occur in the early and late-onset forms, respectively. Curvilinear lamellar inclusions can be seen in Schwann cells and histiocytes on electron microscopy.

The severity of the symptoms depends on the age of presentation of symptoms. The infantile disease is rapidly progressive and fatal by age 2. Late-onset disease has relatively milder symptoms and longer life expectancy.[10][11][12] Infantile disease: The symptom progression is best explained by categorizing it into stages.[11][12][13][14][15][16] Stage 1- The child grows well until 4 to 6 months of age, when the clinical illness manifests. The symptoms commence with restlessness, irritability, vomiting, feeding difficulty, and failure to thrive. The child may be hypersensitive to touch, noise, or bright light and can develop tonic spasms in the presence of these instigating factors. Stage 2- The child develops visual difficulty, optic atrophy, and opisthotonic posturing. They experience seizure-like episodes that have to be differentiated from epilepsy as these don't respond to anticonvulsants. Stage 3- The most debilitating form of the disease is when the child develops blindness, deafness, and decerebrate posturing. Spasticity can be severe enough to halt any voluntary movement.[15] Late infantile disease: Manifests between 13 to 36 months of age with irritability, visual difficulties, and abnormal gait. As the condition progresses, these symptoms worsen with the development of seizures, apneic episodes, and temperature instability. The median age of mortality is usually six years.[4] Juvenile onset disease: The child develops visual difficulties, tremors, gait abnormalities, and attention deficit hyperactivity disorder. The rate of progression of the disease is highly variable, but the disease eventually debilitates the patient, and they die within ten years of the diagnosis. Late-onset disease: Characterized by burning paresthesias in the extremities, mood and behavior alterations, ataxia, spasticity, visual difficulty/blindness, seizures, hearing loss/deafness, and psychomotor retardation. The patients can present with motor and sensory neuropathy associated with muscular atrophy and scoliosis. Few patients present with symptoms confined to a physical weakness without intellectual disability; on the other hand, others deteriorate both mentally and physically.[17][18]

Newborn Screening Many states in the U.S. include screening for Krabbe disease in a standard newborn screening protocol. The initial screening test involves measuring the GALC enzyme activity in the peripheral leukocytes or cultured skin fibroblasts.[19][20] Values falling below 5% of the normal range confirm the diagnosis. However, it does not correlate with the severity of disease manifestation. This screening method's specificity is low; therefore, a second tier of the screening method is added to help identify the true positives. It can either be measuring blood psychosine levels or performing sequencing for the GALC gene. The high levels of psychosine are indicative of infantile Krabbe's disease. As not all laboratories are equipped to detect all GALC gene mutations and multiple variants of GALC mutations of unknown significance, measuring psychosine levels is more feasible and reliable.[9][21][22][23] Imaging Studies Computed tomographic scan: Initially shows symmetrical hyperdense areas (due to demyelination) in the cerebellum, cerebrum, thalamus, brainstem, internal capsule, and corona radiata. Later in the course, hypodense areas (due to atrophy) develop in the corona radiata, and cerebral/cerebellar atrophy develops. Magnetic resonance imaging: It is particularly useful in identifying brain lesions in Krabbe disease. In the infantile forms, there is increased T2 signal intensity in deep cerebral white matter, dentate nucleus, and cerebellar white matter. In juvenile and adult disease, there is increased T2 signal intensity in the parieto-occipital regions and the corticospinal tracts; the dentate nuclei and the cerebellar white matter are usually spared.[13][24][25] There is no contrast enhancement in the affected areas; however, optic nerve and peripheral nerve (e.g., lumbosacral plexus) thickening and enhancement can be seen. Magnetic Resonance Spectroscopy The centrum semiovale may show raised choline levels in the adult subtype.[26] Electroencephalography May show epileptiform activity. Generalized slowing or disorganized rhythms are expected. Ophthalmologic and Otolaryngologist Evaluation The child needs an otolaryngologist assessment and an eye examination to determine the degree of hearing and vision loss and to provide hearing and vision aids to the patient. Genetic Testing

Electroencephalography May show epileptiform activity. Generalized slowing or disorganized rhythms are expected. Ophthalmologic and Otolaryngologist Evaluation The child needs an otolaryngologist assessment and an eye examination to determine the degree of hearing and vision loss and to provide hearing and vision aids to the patient. Genetic Testing Molecular genetic analysis is crucial, as it identifies carriers within a family. It also identifies at-risk pregnancies, and, in some cases, predicts the phenotype based on detected genotype. Lumbar Puncture A lumbar puncture may reveal elevated cerebrospinal fluid (CSF) protein levels and an abnormal protein electrophoretic pattern. The protein analysis demonstrates an increase in albumin and alpha-1 globulin levels and decreased beta-1 globulin and gamma globulin levels. CSF protein levels greater than 61.5mg/dl are associated with low/shorter survival. Electromyography and Nerve Conduction Studies Electromyography changes are usually consistent with peripheral neuropathy. There is a significant slowing of conduction velocity in both motor and sensory nerves in most patients with the infantile type of disease and about 20% of patients with the late-onset Krabbe disease. Brain Biopsy The pathology findings show demyelination of white matter, loss of oligodendroglial cells, and areas of atrophy. The classical multinucleated globoid cells can be demonstrated on the periodic acid-Schiff stain.[11]

Currently, the therapeutic options are limited to asymptomatic or minimally symptomatic patients with Krabbe disease's infantile form. Hematopoietic Stem Cell Transplant (HSCT) The hematopoietic cells from a healthy donor are transplanted to the patient. HSCT helps the patient to populate the brain with microglia with normal function and good GALC enzyme activity. HSCT works best before the onset of symptoms and helps plateau or slow its progression. Studies have shown its efficacy in halting the cognitive and motor decline in the patient.[27][28][29][30][31] A study focused on diffusion tensor imaging in patients with Krabbe disease demonstrated that HSCT reduces the fraction anisotropy (FA) across six tracts measured. The decrease in FA in corticospinal tracts is associated with better cognitive and motor outcomes. A reduction in FA in the splenium and uncinate fasciculus is correlated with better cognitive outcomes.[32] The risk factors associated with HSCT are due to the chemotherapy the patient receives to limit the donor stem cells' immune rejection. There is ongoing research to make this treatment safer for the patient and with fewer side effects. Cord Blood Stem Cell Transfusion Cord blood stem cells collected from an unrelated donor's umbilical cord are transfused into the patient. However, this procedure has also been beneficial to only those patients treated before symptoms appear.[16] Supportive More research is required to find better treatment options for patients suffering from Krabbe disease. Until then, the patient can be provided with supportive care. Muscle relaxants for spasms Anticonvulsants might sometimes be helpful for seizures Physiotherapy to increase mobility Occupational therapy for children to improve motor function Speech therapy to maintain swallowing functioning and maximize communication Tube feedings for good nutrition if swallowing is affected

The differential diagnosis of infantile Krabbe disease is broad and includes several neurodegenerative conditions that can present with neurodevelopmental delay and white matter abnormalities on neuroimaging studies:[33][34] Alexander disease Canavan disease GM2 gangliosidoses Metachromatic leukodystrophy Sphingomyelinase deficiency Although distinguishing Krabbe disease from the disorders mentioned above can be challenging, a definitive diagnosis can be made based on targeted metabolic and molecular genetic testing.[33]

The average lifespan in patients with infantile Krabbe disease is 13 months. Most patients with late infantile disease die within two years of disease onset. The progression of disease and lifespan reduction vary in both juvenile-onset and adult-onset Krabbe disease. HSCT markedly improves short-term survival for individuals treated while asymptomatic during the early neonatal period.[30][35]

The disease is usually fatal. Most infantile cases die by two years of age, late infantile within two years of disease onset, and juvenile cases within ten years of diagnosis. It has a multitude of complications that debilitate the patient, including: Deafness Vision loss Rigid posture Cognitive deterioration Aspiration leading to infections Respiratory failure due to poor muscle tone

As it is an incapacitating disease, both patients and caretakers should be educated about the disease's genetic nature, its complications, prognosis, and the necessity of early intervention. They should be informed that a team of care providers will work with them to achieve the best possible outcomes. Genetic testing should also be offered to all parents of children suffering from Krabbe disease to understand the risk of future pregnancies being affected and have options to avoid it.[27][30]

Krabbe disease involves multiple systems, and therefore, the best outcomes can be achieved with an interprofessional approach with a team of clinicians, therapists, and social workers involved. As the disease symptoms present similarly to other leukodystrophies, prompt and accurate diagnosis is essential for an appropriate management plan. It is important to note that treatment for Krabbe disease works best when commenced before the onset of symptoms; therefore, a clinician's vigilance is essential to pick up symptoms in their early stages. Also, screening newborns can help in early identification and early intervention. An interprofessional team of specialists is employed, including a geneticist, neurologist, ophthalmologist, audiometrist, and physiotherapist. The geneticist can help the families understand the disease outcome, risk recurrence, and prenatal testing. The neurologist can provide symptomatic treatment and documentation of neurological sequelae. The social worker can assess the level of care at home and provide options to facilitate it further.