Emerging trends in management of propionic acidemia

Tendências emergentes no manejo da academia propiônica

Muhammad Rafique About the author

Abstracts

Objetivo

: To evaluate the therapeutic agents used during metabolic crises and in long-term management of patients with propionic acidemia (PA).

Materials and methods

: The records of PA patients were retrospectively evaluated.

Results

: The study group consisted of 30 patients with 141 admissions. During metabolic crises, hyperammonemia was found in 130 (92%) admissions and almost all patients were managed with normal saline, ≥ 10% dextrose, and restriction of protein intake. In 56 (40%) admissions, management was done in intensive care unit, 31 (22%) with mechanical ventilation, 10 (7%) with haemodialysis, 16 (11%) with vasopressor agents, and 12 (9%) with insulin. In the rescue procedure, L-carnitine was used in 135 (96%) patients, sodium bicarbonate in 116 (82%), sodium benzoate in 76 (54%), and metronidazole in 10 (7%), biotin in about one-quarter, L-arginine in one third, and antibiotics in three-quarter of the admissions. Blood/packed RBCs were used in 28 (20%) patients, platelets in 26 (18%), fresh frozen plasma in 8 (6%), and granulocyte-colony stimulating factors in 10 (7%) admissions. All patients were managed completely/partially with medical nutrition formula plus amino acid mixture, vitamins and minerals. For long-term management 24 (80%) patients were on L-carnitine, 22 (73%) on sodium benzoate, 6 (20%) on biotin, one half on alkaline therapy and 4 (13%) on regular metronidazole use. Almost all patients were on medical formula and regular follow-up.

Conclusion

: Aggressive and adequate management of acute metabolic crises with restriction of protein intake, stabilization of patient, reversal of catabolism, and removal of toxic metabolites are essential steps. Concerted efforts to ensure adequate nutrition, to minimize the risk of acute decompensation and additional therapeutic advances are imperative to improve the outcome of PA patients. Arq Bras Endocrinol Metab. 2014;58(3):237-42

Propionate; therapeutic agents; management; latest trends; metabolic crises; hyperammonaemia


Objetivo

: Avaliar os agentes terapêuticos usados durante as crises metabólicas e para o manejo de longo prazo de pacientes com academia propiônica (AP).

Materiais e métodos

: Avaliação retrospectiva das fichas médicas de pacientes com AP.

Resultados

: O grupo estudado consistiu de 30 pacientes com 141 hospitalizações. Durante as crises metabólicas, a hiperamonemia foi observada em 130 (92%) pacientes hospitalizados e quase todos foram tratados com solução salina regular, ≥ 10% dextrose e restrição da ingestão de proteína. Em 56 (40%) das hospitalizações, o manejo foi feito na unidade de terapia intensiva, 31(22%) com ventilação mecânica, 10 (7%) com hemodiálise, 16 (11%) com vasopressores e 12 (9%) com insulina. Para o resgate, a L-carnitina foi usada em 135 (96%) pacientes, o bicarbonato de sódio em 116 (82%), o benzoato de sódio em 76 (54%), o metronidazole em 10 (7%), a biotina em cerca de um quarto, a L-arginina em um quarto e antibióticos em três quartos dos pacientes hospitalizados. Sangue/concentrado de hemácias foram usados em 28 (20%), plaquetas em 26 (18%), plasma fresco congelado em 8 (6%) e fatores estimulantes de colônias de granulócitos em 10 (7%) pacientes hospitalizados. Todos os pacientes foram manejados completamente/parcialmente com fórmula de nutrição hospitalar mais uma mistura de aminoácidos, vitaminas e minerais. Para o manejo de longo prazo, 24 (80%) dos pacientes foram tratados com L-carnitina, 22 (73%) com benzoato de sódio, 6 (20%) com biotina, a metade com tratamento alcalino e 4 (13%) com uso regular de metronidazole. Quase todos os pacientes foram tratados com fórmulas médicas e acompanhamento regular.

Conclusão

: O manejo adequado e agressivo de crises metabólicas com restrição da ingestão de proteína, estabilização do pacientes e reversão do catabolismo, e remoção dos metabólitos tóxicos são passos essenciais. Esforços concentrados para garantir a nutrição adequada, minimizar o risco de descompensação aguda e avanços terapêuticos adicionais são imperativos na melhora dos desfechos de pacientes com AP. Arq Bras Endocrinol Metab. 2014;58(3):237-42

Propionato; agentes terapêuticos; manejo; últimas tendências; crises metabólicas; hiperamonemia


INTRODUCTION

Propionic acidemia (PA) is a rare metabolic disorder, caused by deficiency of a mitochondrial enzyme propionyl CoA carboxylase (PCC) resulting in accumulation of highly toxic metabolites. The disorder is unusually frequent in Saudi Arabia, and has been reported to occur in 1 in 2,000 to 1 in 5,000 live births in this region (1. Al Essa M, Rahbeeni Z, Jumaah S, Joshi S, Al Jishi E, Rashed MS, et al. Infectious complications of propionic acidemia in Saudi Arabia. Clin Genet. 1998;54:90-5.). About 80% PA patients are early-onset cases (diagnosed < 3 months of age). They have more severe disease and classically present, in the neonatal period, lethargy, vomiting, refusal to feed, hypotonia and, less frequently, dehydration and seizures. Some patients have late-onset disease (manifested any time after three months of age), show milder symptoms, and long survival rate. PA is usually associated with long-term neurological complications and is characterized by recurrent episodes of metabolic crises (2. van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, et al. Clinical outcome and long term management of 17 patients with propionic acidemia. Eur J Pediatr. 1996;155:205-10.). Several metabolites and physiological stressors are thought to account for many of the acute and chronic disease manifestations. Common findings include metabolic acidosis, ketosis, hyperammonemia, increased incidence of infections and bone marrow suppression. During metabolic crises, total protein restriction, reversal of catabolism and rapid detoxification are essential life-saving steps to prevent acute brain injury, severe morbidity and mortality (2. van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, et al. Clinical outcome and long term management of 17 patients with propionic acidemia. Eur J Pediatr. 1996;155:205-10.). Treatment options include low protein diet, carnitine, biotin, a precursor free amino acid formula and alkaline therapy. Hemodiafilteration/hemodialysis is recommended for severe hyperammonemia, extreme acidosis, and dangerous electrolyte imbalance (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.). Packed red blood cells (RBCs) transfusion and/or granulocyte colony stimulating factors (G-CSF) are recommended in anemia, neutropenia, or bone marrow suppression (2. van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, et al. Clinical outcome and long term management of 17 patients with propionic acidemia. Eur J Pediatr. 1996;155:205-10.). Antibiotics are commonly used during metabolic crises, which have strong association with immuno-suppression and sepsis (1. Al Essa M, Rahbeeni Z, Jumaah S, Joshi S, Al Jishi E, Rashed MS, et al. Infectious complications of propionic acidemia in Saudi Arabia. Clin Genet. 1998;54:90-5.).

The objective of this study was to evaluate the therapeutic agents used for acute management during metabolic crisis and those used on a regular basis for long term management of the PA patients to minimize the risk of recurrent metabolic decompensation.

MATERIALS AND METHODS

This retrospective study was conducted in a tertiary care public hospital from January 2001 to March 2013. Our study group included 30 children, in a total of 141 admissions. The records of all patients who were admitted in the Department of Pediatrics with confirmed diagnosis of PA during the study period were evaluated. The patients were diagnosed based on high propionylcarnitine level in blood, detected by Tandem Mass Spectrometry; high level of propionate excreted in the urine; enzyme analysis; and genetic studies. All cases were reviewed for the following variables – age of the patients at diagnosis, age at last admission before this study, family history of PA, therapeutic agents/blood products used, and procedures carried out to manage acute problems/imbalances developed during metabolic crises. Prophylactic agents regularly used for long-term management to avoid metabolic decompensations were also recorded. Information was gathered regarding admissions in neonatal intensive care unit (NICU), pediatric intensive care unit (PICU), mechanical ventilation during metabolic decompensation. The percentage of patients discharged after recovery and who died during metabolic crises was also calculated. Weight and height/length of the patients were recorded. These anthropometric parameters were plotted on growth charts specific for Saudi children and their normal-for-age percentages were calculated. Percentages of under-nutrition/wasting (weight < normal for age) and short stature/stunting (height < normal for age) of the PA patients were calculated. The data were analysed using Microsoft Excel spread sheets. The results were expressed in percentages. The study was approved by the Research and Ethical Committee of the institution (Record # 2012 - 10 - 08).

RESULTS

We studied thirty patients and their 141 admissions were analysed. Table 1 demonstrates demographic characteristics of patients with PA. Twenty eight (93%) patients were early presenters (diagnosed within three months of age) and two (7%) children manifested their disease after three months of age (late-onset cases). Our 24 (80%) patients were undernourished/wasted (weight < 90% expected for age) and 19 (63%) were stunted/short stature (length/height < 95% expected for age) (4. Keane V. Assessment of growth. In: Kleigman RM, Behrman RE, Jenson HB, Stanton BF.18th ed. Philadelphia PA: W.B. Saunders; 2007. p. 70-4.). Table 2 shows detail of therapeutic agents and blood products used during acute metabolic crises and prophylactic agents used regularly for long-term management to avoid metabolic decompensations. During metabolic crises, medical nutrition therapy (MNT), intravenous (IV) dextrose and normal saline were used for all patients to correct dehydration and to reverse catabolism. In 12 (8.5%) admissions of PA patients, insulin was also added to drive glucose into the cells to rapidly achieve anabolism. Mean hospital stay of the patients was 9.32 ± 8.15 days. In 56 (39.71%) admissions, patients were admitted in the PICU, with mean duration of stay 8.9 ± 8.47 days. In 31 (22%) admissions, patients were mechanically ventilated with mean duration of 7.9 ± 6.97 days. In 10 (7.1%) admissions of our patients, hemodialysis was performed for quick recovery of metabolic crisis.

Table 1
Data of patients with PA. Values are given in n (%)/mean [SD]

Table 2
Therapeutic agents used during metabolic crises and for long-term management in n = 141 admissions of 30 patients with PA

DISCUSSION

Stabilization, if critical

In stressful conditions, acute metabolic crises with hyperammonemia are common in PA individuals. For their management, patients should be stabilized with IV fluid, glucose, restriction of proteins, vasopressors (if hypotension persists), and mechanical ventilation (if oxygen saturation is not maintained by alternative measures) (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.). In this study, almost all the patients were managed with parenteral normal saline, ≥ 10% dextrose (1.5 times maintenance requirement of IV fluids), and restriction of protein intake. In 22% admissions, patients were mechanically ventilated, and in 11% admissions, inotropic agents were used to maintain blood pressure.

Reversal of catabolism

  •  Acute episode of hyperammonemia is always an emergency and a life-threatening episode (5. Haberle J. The management of hyperammonaemia. Eur J Pediatr. 2011;170:21-34.). We found hyperammonemia in 95% admissions. Its treatment consists of hydration, correction of acidosis with IV glucose, insulin, carnitine, sodium benzoate, and vitamin therapy associated with a hypercaloric, protein-free diet (6. Daniotti M, la Marca G, Fliorini P, Filippi L. New development in the treatment of hyperammonemia: emerging use of carglumic acid. Int J Gen Med. 2011;4:21-8.). During metabolic decompensation, stop all sources of protein (enteral and parenteral) to cut exogenous propionate production, and to inhibit catabolism of endogenous proteins. Give non-protein calory in the form of parenteral dextrose ≥ 10% with necessary electrolytes. Intralipids can be added to provide more calories, if needed. To drive glucose into the cells and reverse catabolism, insulin infusion can be added (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.). In the current study, almost all patients were managed along the same lines. Insulin infusion was used in 9% admissions. In a few patients, intralipids were also added. Hemodialysis is recommended in cases of ammonia levels > 300 umol/L, extreme acidosis/electrolyte imbalance, coma, deterioration, and failure to improve. In 7% admissions, hemodialysis was performed, whereas Grunert and cols. reported this figure as 15% (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.). In 40% admissions, our patients were managed in the PICU, which is compatible with another case series (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.).

  •  L-carnitine conjugates with propionate and promotes transfer out of the mitochondria, so it can be excreted in the urine. It is helpful to eliminate the use of sodium bicarbonate for metabolic correction, and to correct its deficiency, which is a common finding in PA (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.). Broadly in line with another report (equal to 93%) (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.), L-carnitine was used in 96% admissions of our patients, while other authors reported it as equal to 82% (2. van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, et al. Clinical outcome and long term management of 17 patients with propionic acidemia. Eur J Pediatr. 1996;155:205-10.).

  •  In the acute phase of a not yet diagnosed metabolic patient with hyperammonemia, it is useful to start a nitrogen scavenger, sodium benzoate (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.). In a case series, alternative pathway medications included sodium benzoate in 80% patients, sodium phenyl acetate in 40%, metronidazole in 40%, and sodium bicarbonate in 20% (8. Vara R, Turner C, Mundy H, Heaton ND, Rela M, Mieli-Vergani G, et al. Liver transplantation for propionic acidemia in children. Liver Transpl. 2011;17:661-7.). In children with inborn error of metabolism with continued production of acid (despite normal tissue perfusion and oxygenation); sodium bicarbonate is usually an essential part of treatment of metabolic acidosis (9. Jones SA, Walter JH. Diagnosis and treatment of severe metabolic acidosis. Paediatr Child Health. 2007;17(7):260-5.). In the present study, sodium bicarbonate was used in 82% admissions, sodium benzoate in 54%, and metronidazole in 7%. A big portion of propionate (20-30%) is produced as food is metabolised by bacteria in the gut, which can be alleviated by using non-absorbable oral antibiotics, such as metronidazole/neomycin, which have been reported to be helpful in improving metabolic crises. Laxative agents, such as lactulose, increase gut motility and acidify the intestine, thus decreasing ammonia uptake (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.,5. Haberle J. The management of hyperammonaemia. Eur J Pediatr. 2011;170:21-34.,1111 . Tuchman M, Caldovic L, Daikhin Y, Horyn O, Nissim I, Nissim I, et al. N-carbamylglutamate markedly enhances ureagenesis in N-acetylglutamate deficiency and propionic acidemia as measured by isotopic incorporation and blood biomarkers. Pediatr Res. 2008;64(2):213-7.). During decompensation, we used metronidazole in 7% admissions, and laxatives in 4%. However, a report of metronidazole use in PA patients was as high as 47% (8. Vara R, Turner C, Mundy H, Heaton ND, Rela M, Mieli-Vergani G, et al. Liver transplantation for propionic acidemia in children. Liver Transpl. 2011;17:661-7.), and another one was as 40% (metronidazole alone in 20% patients, and metronidazole plus colistin in another 20%) (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.).

  •  N-carbamylglucomate has been shown to be beneficial in decreasing ammonia levels in acute hyperammonemia in patients with PA (6. Daniotti M, la Marca G, Fliorini P, Filippi L. New development in the treatment of hyperammonemia: emerging use of carglumic acid. Int J Gen Med. 2011;4:21-8.,1010 . Gosen LV. Organic acidemias: a methylmalonic and propionic acidemia. J Pediatr Nurs. 2008;23(3):225-33.,1111 . Tuchman M, Caldovic L, Daikhin Y, Horyn O, Nissim I, Nissim I, et al. N-carbamylglutamate markedly enhances ureagenesis in N-acetylglutamate deficiency and propionic acidemia as measured by isotopic incorporation and blood biomarkers. Pediatr Res. 2008;64(2):213-7.).

  •  PCC is a biotin-dependent enzyme responsible for propionate metabolism in mitochondria. Biotin has been used by some researchers during metabolic crises (6. Daniotti M, la Marca G, Fliorini P, Filippi L. New development in the treatment of hyperammonemia: emerging use of carglumic acid. Int J Gen Med. 2011;4:21-8.,8. Vara R, Turner C, Mundy H, Heaton ND, Rela M, Mieli-Vergani G, et al. Liver transplantation for propionic acidemia in children. Liver Transpl. 2011;17:661-7.). This data is in agreement with our study, in which biotin was used in about one quarter of the admissions of PA patients.

  •  In some case series, L-arginine has also been used in acute management of hyperammonemia (5. Haberle J. The management of hyperammonaemia. Eur J Pediatr. 2011;170:21-34.,1212 . Lehnert W, Sperl W, Suormala T, Baumgartner ER, et al. Propionic acidemia: clinical, biochemical and therapeutic aspects. Eur J Pediatr. 1994;153(7 Suppl 1):S68-80.). Consistently, we also used it in about one third of the admissions.

  •  Antimicrobial therapy is recommended during metabolic decompensation as PA is associated with suppression of the immune system and increased risk of infections (1010 . Gosen LV. Organic acidemias: a methylmalonic and propionic acidemia. J Pediatr Nurs. 2008;23(3):225-33.). In line with Al Essa and cols. (1. Al Essa M, Rahbeeni Z, Jumaah S, Joshi S, Al Jishi E, Rashed MS, et al. Infectious complications of propionic acidemia in Saudi Arabia. Clin Genet. 1998;54:90-5.) antibiotics were used in three quarter of the admissions of our patients. Similarly, in some patients of this study, antifungal and antiviral therapy was also used.

  •  Proteins should be re-introduced within 24-36 hours of initiation of therapy during metabolic crisis. Consistently, within 24-48 hours, we also re-started proteins in our patients in the form of MNT (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.).

  •  Packed RBCs and other blood product transfusions are recommended if patients are anemic, immunocompromised or have bone marrow suppression (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.,1212 . Lehnert W, Sperl W, Suormala T, Baumgartner ER, et al. Propionic acidemia: clinical, biochemical and therapeutic aspects. Eur J Pediatr. 1994;153(7 Suppl 1):S68-80.). In this study, blood/Packed RBCs were transfused in 20% admissions, platelets in 18%, and fresh frozen plasma in 6%. G-CSF was used in 7% admissions to counteract neutropenia caused by bone marrow suppression, which is consistent with another report (1313 . Land MH, Roberts RL. Neutropenia and hypo-gammaglobulinemia in propionic acidemia. J Allergy Clin Immunol. 2006(Suppl 1);117(2):S172.).

  •  In agreement with Land and Roberts’ report, immunoglobulins were used in some of our patients to enhance their immunity (1313 . Land MH, Roberts RL. Neutropenia and hypo-gammaglobulinemia in propionic acidemia. J Allergy Clin Immunol. 2006(Suppl 1);117(2):S172.).

Transition from acute to chronic management

  •  For long-term management of PA patients, nutritional support regimen is performed with MNT. It has been described that, with advancing age, tolerance to natural proteins increases, and metabolic decompensation occur less frequently. In a case series, most of the patients received a diet that restricted natural protein. In addition, a nonpropiogenic amino acid mixture was supplemented to meet age-appropriate protein intake recommendations (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.,1414 . Ogier de Boulny H, Dionisi-Vici C, Wendel U. Branched-chain organic acidurias/acidemias. In: Saudubray JM, van den Berghe G, Walter JH (eds). Inborn metabolic diseases. Diagnosis and treatment, 5th edn. Springer, Heidelberg; 2012. p. 277-96.,1515 . Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, et al. Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. 2012;105:26-33.). In the present study, almost all patients were found to be managed completely/partially with MNT, amino acid mixture, vitamins, and minerals.

  •  Many PA patients were poor oral feeders. Nasogastric/gastrostomy (NG/G) tube feeding can be used to meet daily metabolic nutrition therapy goals when patients are anorexic, as it is often seen in PA (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.,1515 . Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, et al. Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. 2012;105:26-33.). Our 20% children were exclusively on NG/G tube feeding. However, Grunert and cols. reported this figure as 15% (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.).

  •  Regular use of carnitine is required to avoid metabolic decompensations and to prevent secondary deficiency of this agent (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.,1515 . Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, et al. Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. 2012;105:26-33.). In accordance with another report (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.), 92% of our patients used it regularly.

  •  Some patients need alkaline therapy for long-term management (9. Jones SA, Walter JH. Diagnosis and treatment of severe metabolic acidosis. Paediatr Child Health. 2007;17(7):260-5.). This is consistent with our study. One half of our patients were on regular sodium bicarbonate therapy.

  •  In addition to prevention of constipation, for gut flora control, long-term oral antimicrobial (metronidazole) therapy may offer significant clinical benefits in children with PA (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.,1515 . Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, et al. Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. 2012;105:26-33.). In line with another report, 13% of our patients were on long-term metronidazole therapy (7. Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.).

  •  Screening studies, such as electrocardiogram, echocardiogram, hearing screening, and optic field assessment are regularly recommended in PA patients (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.,1515 . Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, et al. Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. 2012;105:26-33.). Most of our patients were on regular follow-up, at the current/another centre.

  •  Physical and occupational therapy should start as soon as possible in patients with physical disabilities (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.). This is compatible with our management of PA patients.

  •  Similar to our policy, parental education about the disease and management has also been considered to be crucial (3. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.,1212 . Lehnert W, Sperl W, Suormala T, Baumgartner ER, et al. Propionic acidemia: clinical, biochemical and therapeutic aspects. Eur J Pediatr. 1994;153(7 Suppl 1):S68-80.).

  •  Some researchers have described the role of growth hormone to improve lean body mass and linear growth and to increase tolerance to natural proteins in PA patients (1515 . Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, et al. Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. 2012;105:26-33.).

  •  Long-term management of the individuals with PA is imperative. The severity of radiological abnormalities seems to correlate with the degree of compliance to therapy, but not with the number of hospital or PICU admissions (1616 . Brismar J, Ozand PT. CT and MRI of the brain in disorders of the propionate and methylmelonate metabolism AJNR Am J Neuroradiol. 1994;15:1459-73.). Liver transplantation may be considered in individuals with recurrent episodes of hyperammonemia/metabolic decompensation that are not adequately controlled with medical therapy (9. Jones SA, Walter JH. Diagnosis and treatment of severe metabolic acidosis. Paediatr Child Health. 2007;17(7):260-5.,1515 . Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, et al. Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. 2012;105:26-33.). Last, development in the field of somatic gene therapy are also very promising (8. Vara R, Turner C, Mundy H, Heaton ND, Rela M, Mieli-Vergani G, et al. Liver transplantation for propionic acidemia in children. Liver Transpl. 2011;17:661-7.).

There were some limitations in this study due to unavailability of complete records of some patients, especially those who were being followed up at other centres.

CONCLUSION

Aggressive identification of PA patients and initiation of therapy are necessary to prevent severe morbidity and mortality. During metabolic decompensation, reversal of catabolism and removal of toxic compounds is a life-saving measure. Concerted efforts are needed to ensure adequate nutrition of PA patients, to minimize the risk of acute decompensation, and to treat episodes of metabolic crises promptly. The long-term, firm education and guidance of parents and patients by established diagnostic and therapeutic centers, and additional therapeutic advances are indispensible for a beneficial outcome.

REFERENCES

  • 1
    Al Essa M, Rahbeeni Z, Jumaah S, Joshi S, Al Jishi E, Rashed MS, et al. Infectious complications of propionic acidemia in Saudi Arabia. Clin Genet. 1998;54:90-5.
  • 2
    van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, et al. Clinical outcome and long term management of 17 patients with propionic acidemia. Eur J Pediatr. 1996;155:205-10.
  • 3
    Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16-25.
  • 4
    Keane V. Assessment of growth. In: Kleigman RM, Behrman RE, Jenson HB, Stanton BF.18th ed. Philadelphia PA: W.B. Saunders; 2007. p. 70-4.
  • 5
    Haberle J. The management of hyperammonaemia. Eur J Pediatr. 2011;170:21-34.
  • 6
    Daniotti M, la Marca G, Fliorini P, Filippi L. New development in the treatment of hyperammonemia: emerging use of carglumic acid. Int J Gen Med. 2011;4:21-8.
  • 7
    Grunert SC, Mullerleile S, De Silva L, Barth M, Walter M, Walter K, et al. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013;8:6-14.
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  • Grant/support: no financial support was provided by any organization for this study

Publication Dates

  • Publication in this collection
    Apr 2014

History

  • Received
    23 May 2013
  • Accepted
    24 Jan 2014
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