Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening. Issue 1 (4th October 2022)
- Record Type:
- Journal Article
- Title:
- Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening. Issue 1 (4th October 2022)
- Main Title:
- Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening
- Authors:
- Mütze, Ulrike
Garbade, Sven F.
Gleich, Florian
Lindner, Martin
Freisinger, Peter
Hennermann, Julia B.
Thimm, Eva
Gramer, Gwendolyn
Posset, Roland
Krämer, Johannes
Grünert, Sarah C.
Hoffmann, Georg F.
Kölker, Stefan - Abstract:
- Abstract: Newborn screening (NBS) for inherited metabolic diseases (IMDs) substantially shortens a patient's journey. It enables the early start of metabolic treatment which might prevent potentially lethal neonatal disease manifestations, while promoting favorable development and long‐term clinical outcomes. This study aims to assess growth in screened individuals with IMDs under different dietary regimes. Anthropometric data (3585 prospective measures) of 350 screened individuals with IMDs born between 1999 and 2018 and participating in a German prospective multicenter observational study were evaluated. Overall, birth measures were within the reference ranges, suggesting unaffected prenatal growth, except for phenylketonuria (weight) and glutaric aciduria Type 1 (head circumference). After birth, longitudinal analysis of anthropometric measures revealed a loss of height standard deviation score (SDS; −0.5 SDS; p < 0.0001), head circumference SDS (−0.2 SDS; p = 0.0028), but not for weight SDS (0.1 SDS; p = 0.5097) until the age of 18 years, while BMI SDS increased (0.4 SDS; p < 0.0001). The significant interaction with age and diet groups was pronounced for the linear growth in individuals receiving diets being low in protein, long‐chain triglycerides, and galactose ( p < 0.001). Identification by NBS and subsequent early (dietary) treatment cannot completely protect against alterations in growths. Disease‐specific (e.g., metabolic impairments, neurotoxins) andAbstract: Newborn screening (NBS) for inherited metabolic diseases (IMDs) substantially shortens a patient's journey. It enables the early start of metabolic treatment which might prevent potentially lethal neonatal disease manifestations, while promoting favorable development and long‐term clinical outcomes. This study aims to assess growth in screened individuals with IMDs under different dietary regimes. Anthropometric data (3585 prospective measures) of 350 screened individuals with IMDs born between 1999 and 2018 and participating in a German prospective multicenter observational study were evaluated. Overall, birth measures were within the reference ranges, suggesting unaffected prenatal growth, except for phenylketonuria (weight) and glutaric aciduria Type 1 (head circumference). After birth, longitudinal analysis of anthropometric measures revealed a loss of height standard deviation score (SDS; −0.5 SDS; p < 0.0001), head circumference SDS (−0.2 SDS; p = 0.0028), but not for weight SDS (0.1 SDS; p = 0.5097) until the age of 18 years, while BMI SDS increased (0.4 SDS; p < 0.0001). The significant interaction with age and diet groups was pronounced for the linear growth in individuals receiving diets being low in protein, long‐chain triglycerides, and galactose ( p < 0.001). Identification by NBS and subsequent early (dietary) treatment cannot completely protect against alterations in growths. Disease‐specific (e.g., metabolic impairments, neurotoxins) and dietary‐specific (e.g., diets reduced in protein) factors may have an amplified impact on longitudinal growth. Therefore, alongside other important follow‐ups, the continuous observation of the anthropometric development of screened individuals with IMDs needs special attention to early identify and support individuals at risk. … (more)
- Is Part Of:
- Journal of inherited metabolic disease. Volume 46:Issue 1(2023)
- Journal:
- Journal of inherited metabolic disease
- Issue:
- Volume 46:Issue 1(2023)
- Issue Display:
- Volume 46, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 46
- Issue:
- 1
- Issue Sort Value:
- 2023-0046-0001-0000
- Page Start:
- 15
- Page End:
- 27
- Publication Date:
- 2022-10-04
- Subjects:
- growth -- height -- neonatal screening -- weight
Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- http://www.springer.com/gb/ ↗
- DOI:
- 10.1002/jimd.12563 ↗
- Languages:
- English
- ISSNs:
- 0141-8955
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5006.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25080.xml