Changes in Branched-Chain Amino Acids One Year after Sleeve Gastrectomy in Youth with Obesity and Their Association with Changes in Insulin Resistance.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
30 Aug 2023
Historique:
received: 11 08 2023
revised: 25 08 2023
accepted: 28 08 2023
medline: 11 9 2023
pubmed: 9 9 2023
entrez: 9 9 2023
Statut: epublish

Résumé

Adults with obesity have a reduction in branched-chain amino acid (BCAA) levels following metabolic and bariatric surgery (MBS), which is hypothesized to contribute to the metabolic advantages of MBS. We examined this relationship in 62 youth 13-24 years old with severe obesity (47 female) over 12 months. Thirty had sleeve gastrectomy (SG) and 32 were non-surgical controls (NS). We measured fasting insulin, glucose, glycated hemoglobin (HbA1c), isoleucine, leucine, and valine concentrations, and post-prandial insulin and glucose, following a mixed meal tolerance test. Twenty-four-hour food recalls were collected. At baseline, groups did not differ in the intake or the serum levels of BCAAs, HbA1C, HOMA-IR, Matsuda index, insulinogenic index, or oral Disposition index (oDI). Over 12 months, SG vs. NS had greater reductions in serum BCAAs, and SG had significant reductions in BCAA intake. SG vs. NS had greater reductions in HbA1c and HOMA-IR, with increases in the Matsuda index and oDI. In SG, baseline leucine and total BCAA concentrations were negatively correlated with the baseline Matsuda index. Reductions in serum leucine were positively associated with the reductions in HOMA-IR over 12 months. These associations suggest a potential role of BCAA in regulating metabolic health. Reducing dietary intake and serum BCAA concentrations may reduce insulin resistance.

Identifiants

pubmed: 37686833
pii: nu15173801
doi: 10.3390/nu15173801
pmc: PMC10489782
pii:
doi:

Substances chimiques

Amino Acids, Branched-Chain 0
Leucine GMW67QNF9C
Glycated Hemoglobin 0
Insulin 0
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK103946
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002541
Pays : United States
Organisme : NICHD NIH HHS
ID : K24 HD071843
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK057521
Pays : United States
Organisme : NIDDK NIH HHS
ID : K24 DK109940
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001102
Pays : United States
Organisme : NCRR NIH HHS
ID : S10 RR023405
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK110419
Pays : United States

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Auteurs

Imen Becetti (I)

Division of Pediatric Endocrinology, Mass General for Children and Harvard Medical School, Boston, MA 02114, USA.
Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

Meghan Lauze (M)

Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

Hang Lee (H)

Biostatistics Center, Massachusetts General Hospital, Boston, MA 02114, USA.

Miriam A Bredella (MA)

Department of Radiology, Musculoskeletal Imaging and Interventions, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

Madhusmita Misra (M)

Division of Pediatric Endocrinology, Mass General for Children and Harvard Medical School, Boston, MA 02114, USA.
Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

Vibha Singhal (V)

Division of Pediatric Endocrinology, Mass General for Children and Harvard Medical School, Boston, MA 02114, USA.
Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Pediatric Program, MGH Weight Center, Massachusetts General Hospital, Boston, MA 02114, USA.

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Classifications MeSH