Insulin resistance and glycine metabolism in humans

Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decr...

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Published inAmino acids Vol. 50; no. 1; pp. 11 - 27
Main Authors Adeva-Andany, M., Souto-Adeva, G., Ameneiros-Rodríguez, E., Fernández-Fernández, C., Donapetry-García, C., Domínguez-Montero, A.
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Published Vienna Springer Vienna 01.01.2018
Springer Nature B.V
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Abstract Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans.
AbstractList Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans.
Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans.Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In prospective studies, hypoglycinemia at baseline predicts the risk of developing type 2 diabetes and higher serum glycine level is associated with decreased risk of incident type 2 diabetes. Consistently, plasma glycine concentration is lower in the lean offspring of parents with type 2 diabetes compared to healthy subjects. Among patients with type 2 diabetes, hypoglycinemia occurs before clinical manifestations of the disease, but the pathophysiological mechanisms underlying glycine deficit and its potential clinical repercussions are unclear. Glycine participates in several metabolic pathways, being required for relevant human physiological processes. Humans synthesize glycine from glyoxylate, glucose (via serine), betaine and likely from threonine and during the endogenous synthesis of L-carnitine. Glycine conjugates bile acids and other acyl moieties producing acyl-glycine derivatives. The glycine cleavage system catalyzes glycine degradation to carbon dioxide and ammonium while tetrahydrofolate is converted into 5,10-methylene-tetrahydrofolate. Glycine is utilized to synthesize serine, sarcosine, purines, creatine, heme group, glutathione, and collagen. Glycine is a major quantitative component of collagen. In addition, the role of glycine maintaining collagen structure is critical, as glycine residues are required to stabilize the triple helix of the collagen molecule. This quality of glycine likely contributes to explain the occurrence of medial arterial calcification and the elevated cardiovascular risk associated with diabetes and chronic kidney disease, as emerging evidence links normal collagen content with the initiation and progression of vascular calcification in humans.
Author Donapetry-García, C.
Adeva-Andany, M.
Souto-Adeva, G.
Fernández-Fernández, C.
Domínguez-Montero, A.
Ameneiros-Rodríguez, E.
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  surname: Souto-Adeva
  fullname: Souto-Adeva, G.
  organization: National Institutes of Health, National Institute of Arthritis and Metabolic Diseases
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  surname: Ameneiros-Rodríguez
  fullname: Ameneiros-Rodríguez, E.
  organization: Internal Medicine Department, Hospital General Juan Cardona
– sequence: 4
  givenname: C.
  surname: Fernández-Fernández
  fullname: Fernández-Fernández, C.
  organization: Internal Medicine Department, Hospital General Juan Cardona
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  fullname: Donapetry-García, C.
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  surname: Domínguez-Montero
  fullname: Domínguez-Montero, A.
  organization: Internal Medicine Department, Hospital General Juan Cardona
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29094215$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright Springer-Verlag GmbH Austria 2017
Amino Acids is a copyright of Springer, (2017). All Rights Reserved.
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ID FETCH-LOGICAL-c471t-a89fa39bf10914a71bc0582b0d7869571b4058f4200d8bbf285234a26c83f4113
IEDL.DBID 7X7
ISSN 0939-4451
1438-2199
IngestDate Thu Jul 10 17:52:19 EDT 2025
Fri Jul 11 10:42:35 EDT 2025
Fri Jul 25 11:06:20 EDT 2025
Wed Feb 19 02:43:30 EST 2025
Tue Jul 01 04:05:59 EDT 2025
Thu Apr 24 22:48:46 EDT 2025
Fri Feb 21 02:37:24 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Obesity
Insulin resistance
One-carbon metabolism
Diabetes
Glycine
Serine hydroxymethyl transferase
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c471t-a89fa39bf10914a71bc0582b0d7869571b4058f4200d8bbf285234a26c83f4113
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content type line 23
PMID 29094215
PQID 1992787900
PQPubID 1456339
PageCount 17
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proquest_miscellaneous_1959324326
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pubmed_primary_29094215
crossref_citationtrail_10_1007_s00726_017_2508_0
crossref_primary_10_1007_s00726_017_2508_0
springer_journals_10_1007_s00726_017_2508_0
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PublicationDate 2018-01-01
PublicationDateYYYYMMDD 2018-01-01
PublicationDate_xml – month: 01
  year: 2018
  text: 2018-01-01
  day: 01
PublicationDecade 2010
PublicationPlace Vienna
PublicationPlace_xml – name: Vienna
– name: Austria
PublicationSubtitle The Forum for Amino Acid, Peptide and Protein Research
PublicationTitle Amino acids
PublicationTitleAbbrev Amino Acids
PublicationTitleAlternate Amino Acids
PublicationYear 2018
Publisher Springer Vienna
Springer Nature B.V
Publisher_xml – name: Springer Vienna
– name: Springer Nature B.V
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Snippet Plasma glycine level is low in patients with obesity or diabetes and the improvement of insulin resistance increases plasma glycine concentration. In...
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StartPage 11
SubjectTerms Ammonium
Analytical Chemistry
Arteriosclerosis
Betaine
Bile acids
Biochemical Engineering
biochemical pathways
Biochemistry
Biomedical and Life Sciences
blood serum
Calcification
Calcification (ectopic)
Carbon dioxide
Cardiovascular diseases
Carnitine
Collagen
Creatine
Diabetes
Diabetes mellitus
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - metabolism
Diabetes Mellitus, Type 2 - physiopathology
glucose
Glutathione
Glycine
Glycine - biosynthesis
Glycine - blood
Glycine - deficiency
Glycine - metabolism
Heme
Humans
Insulin
Insulin resistance
Insulin Resistance - physiology
kidney diseases
Kidney transplantation
L-Carnitine
Life Sciences
Metabolic pathways
Metabolism
Models, Biological
moieties
Neurobiology
noninsulin-dependent diabetes mellitus
obesity
Parents
Patients
progeny
prospective studies
Proteomics
Purines
Review Article
Risk
risk reduction
Sarcosine
Serine
Synthesis
Tetrahydrofolic acid
Threonine
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Title Insulin resistance and glycine metabolism in humans
URI https://link.springer.com/article/10.1007/s00726-017-2508-0
https://www.ncbi.nlm.nih.gov/pubmed/29094215
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Volume 50
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