TY - JOUR
T1 - Impact of newborn screening for very-long-chain acyl-CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes
AU - Bleeker, Jeannette C.
AU - Kok, Irene L.
AU - Ferdinandusse, Sacha
AU - van der Pol, W. Ludo
AU - Cuppen, Inge
AU - Bosch, Annet M.
AU - Langeveld, Mirjam
AU - Derks, Terry G.J.
AU - Williams, Monique
AU - de Vries, Maaike
AU - Mulder, Margot F.
AU - Gozalbo, Estela R.
AU - de Sain-van der Velden, Monique G.M.
AU - Rennings, Alexander J.
AU - Schielen, Peter J.C.I.
AU - Dekkers, Eugenie
AU - Houtkooper, Riekelt H.
AU - Waterham, Hans R.
AU - Pras-Raves, Mia L.
AU - Wanders, Ronald J.A.
AU - van Hasselt, Peter M.
AU - Schoenmakers, Marja
AU - Wijburg, Frits A.
AU - Visser, Gepke
N1 - Funding Information:
First, we would like to thank all the patients and their families for participating in our study. Second, we would like to thank Jos Ruiter for his help with enzymatic analyses and Astrid Verhoef, Sanna Kulik, Ellen Blok and Debbie Spiekman for their help in coordinating clinical evaluation in the Dutch Fatty Acid Oxidation Expertise Center. This work was supported by grants from ZonMW and Metakids.
Publisher Copyright:
© 2019 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM
PY - 2019/5
Y1 - 2019/5
N2 - Most infants with very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD) identified by newborn screening (NBS) are asymptomatic at the time of diagnosis and remain asymptomatic. If this outcome is due to prompt diagnosis and initiation of therapy, or because of identification of individuals with biochemical abnormalities who will never develop symptoms, is unclear. Therefore, a 10-year longitudinal national cohort study of genetically confirmed VLCADD patients born before and after introduction of NBS was conducted. Main outcome measures were clinical outcome parameters, acyl-CoA dehydrogenase very long chain gene analysis, VLCAD activity, and overall capacity of long-chain fatty acid oxidation (LC-FAO flux) in lymphocytes and cultured skin fibroblasts. Median VLCAD activity in lymphocytes of 54 patients, 21 diagnosed pre-NBS and 33 by NBS was, respectively, 5.4% (95% confidence interval [CI]: 4.0-8.3) and 12.6% (95% CI: 10.7-17.7; P < 0.001) of the reference mean. The median LC-FAO flux was 33.2% (95% CI: 22.8-48.3) and 41% (95% CI: 40.8-68; P < 0.05) of the control mean, respectively. Clinical characteristics in 23 pre-NBS and 37 NBS patients revealed hypoglycemic events in 12 vs 2 patients, cardiomyopathy in 5 vs 4 patients and myopathy in 14 vs 3 patients. All patients with LC-FAO flux <10% developed symptoms. Of the patients with LC-FAO flux >10% 7 out of 12 diagnosed pre-NBS vs none by NBS experienced hypoglycemic events. NBS has a clear beneficial effect on the prevention of hypoglycemic events in patients with some residual enzyme activity, but does not prevent hypoglycemia nor cardiac complications in patients with very low residual enzyme activity. The effect of NBS on prevalence and prevention of myopathy-related complications remains unclear.
AB - Most infants with very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD) identified by newborn screening (NBS) are asymptomatic at the time of diagnosis and remain asymptomatic. If this outcome is due to prompt diagnosis and initiation of therapy, or because of identification of individuals with biochemical abnormalities who will never develop symptoms, is unclear. Therefore, a 10-year longitudinal national cohort study of genetically confirmed VLCADD patients born before and after introduction of NBS was conducted. Main outcome measures were clinical outcome parameters, acyl-CoA dehydrogenase very long chain gene analysis, VLCAD activity, and overall capacity of long-chain fatty acid oxidation (LC-FAO flux) in lymphocytes and cultured skin fibroblasts. Median VLCAD activity in lymphocytes of 54 patients, 21 diagnosed pre-NBS and 33 by NBS was, respectively, 5.4% (95% confidence interval [CI]: 4.0-8.3) and 12.6% (95% CI: 10.7-17.7; P < 0.001) of the reference mean. The median LC-FAO flux was 33.2% (95% CI: 22.8-48.3) and 41% (95% CI: 40.8-68; P < 0.05) of the control mean, respectively. Clinical characteristics in 23 pre-NBS and 37 NBS patients revealed hypoglycemic events in 12 vs 2 patients, cardiomyopathy in 5 vs 4 patients and myopathy in 14 vs 3 patients. All patients with LC-FAO flux <10% developed symptoms. Of the patients with LC-FAO flux >10% 7 out of 12 diagnosed pre-NBS vs none by NBS experienced hypoglycemic events. NBS has a clear beneficial effect on the prevention of hypoglycemic events in patients with some residual enzyme activity, but does not prevent hypoglycemia nor cardiac complications in patients with very low residual enzyme activity. The effect of NBS on prevalence and prevention of myopathy-related complications remains unclear.
KW - cardiomyopathy
KW - fatty acid oxidation
KW - hypoglycemia
KW - myopathy
KW - newborn screening
KW - very-long-chain acyl-CoA dehydrogenase deficiency
UR - http://www.scopus.com/inward/record.url?scp=85064015724&partnerID=8YFLogxK
U2 - 10.1002/jimd.12075
DO - 10.1002/jimd.12075
M3 - Article
C2 - 30761551
SN - 0141-8955
VL - 42
SP - 414
EP - 423
JO - Journal of Inherited Metabolic Disease
JF - Journal of Inherited Metabolic Disease
IS - 3
ER -