Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Mar 25;12(1):5182.
doi: 10.1038/s41598-022-09096-x.

Predictive factors of responsiveness to a body weight reduction program in Prader-Willi patients at 6 years of follow-up

Affiliations

Predictive factors of responsiveness to a body weight reduction program in Prader-Willi patients at 6 years of follow-up

Stefano Lazzer et al. Sci Rep. .

Erratum in

Abstract

Prader-Willi syndrome (PWS), a multisystemic disorder caused by lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region, is characterized by hyperphagia and childhood-onset morbid obesity, A retrospective cohort study of 60 PWS patients, 38 females and 22 males, undergoing a 6-year rehabilitation program was analysed. Mean age at the time of first admission was 27 ± 7 years, body weight (BW) was 97 kg ± 29 kg and height was 1.53 ± 0.09 m. Twenty-four patients (40%) showed BW loss after 6 years of follow-up, seventeen (28%) remained stable and nineteen (32%) gained BW. Responsiveness in term of BW reduction was less frequent in patients with the UPD karyotype, karyotype del15 being more frequent among responsive patients. Furthermore, responsive PWS subjects had a higher BMI (47 vs. 36 kg/m2), waist (123 vs. 106 cm) and hip (136 vs. 118 cm) circumferences than non-responsive at the time of first hospitalization. Baseline body composition and metabolic parameters did not differentiate between responsive and non-responsive patients. Given the rarity of PWS and relative lack of studies, these results can be considered relevant because based on a relatively large number of PWS patients followed up for a long term period.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

References

    1. Bar C, et al. Early diagnosis and care is achieved but should be improved in infants with Prader–Willi syndrome. Orphanet. J. Rare Dis. 2017;12:118. doi: 10.1186/s13023-017-0673-6. - DOI - PMC - PubMed
    1. Angulo MA, Butler MG, Cataletto ME. Prader–Willi syndrome: A review of clinical, genetic, and endocrine findings. J. Endocrinol. Invest. 2015;38:1249–1263. doi: 10.1007/s40618-015-0312-9. - DOI - PMC - PubMed
    1. Butler MG, et al. Molecular genetic classification in Prader–Willi syndrome: A multisite cohort study. J. Med. Genet. 2019;56:149. doi: 10.1136/jmedgenet-2018-105301. - DOI - PMC - PubMed
    1. Miller JL, et al. Nutritional phases in Prader–Willi syndrome. Am. J. Med. Genet. A. 2011;155:1040–1049. doi: 10.1002/ajmg.a.33951. - DOI - PMC - PubMed
    1. Proffitt J, et al. Contributing factors of mortality in Prader–Willi syndrome. Am. J. Med. Genet. A. 2019;179:196–205. doi: 10.1002/ajmg.a.60688. - DOI - PMC - PubMed

Publication types