<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-30T03:56:58Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18239" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18239</identifier><datestamp>2024-11-28T14:55:20Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</setSpec><setSpec>col_20.500.12105_16982</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Boughanem, Hatim</subfield>
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      <subfield code="a">Yubero-Serrano, Elena M.</subfield>
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      <subfield code="a">López-Miranda, José</subfield>
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      <subfield code="a">Tinahones, Francisco J.</subfield>
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      <subfield code="a">Macias-Gonzalez, Manuel</subfield>
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      <subfield code="c">2021-01-24</subfield>
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      <subfield code="a">Evidence from observational and in vitro studies suggests that insulin growth-factor-binding protein type 2 (IGFBP2) is a promising protein in non-communicable diseases, such as obesity, insulin resistance, metabolic syndrome, or type 2 diabetes. Accordingly, great efforts have been carried out to explore the role of IGFBP2 in obesity state and insulin-related diseases, which it is typically found decreased. However, the physiological pathways have not been explored yet, and the relevance of IGFBP2 as an important pathway integrator of metabolic disorders is still unknown. Here, we review and discuss the molecular structure of IGFBP2 as the first element of regulating the expression of IGFBP2. We highlight an update of the association between low serum IGFBP2 and an increased risk of obesity, type 2 diabetes, metabolic syndrome, and low insulin sensitivity. We hypothesize mechanisms of IGFBP2 on the development of obesity and insulin resistance in an insulin-independent manner, which meant that could be evaluated as a therapeutic target. Finally, we cover the most interesting lifestyle modifications that regulate IGFBP2, since lifestyle factors (diet and/or physical activity) are associated with important variations in serum IGFBP2.</subfield>
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      <subfield code="a">10.3390/ijms22031133</subfield>
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      <subfield code="a">1422-0067</subfield>
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      <subfield code="a">International Journal of Molecular Sciences</subfield>
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      <subfield code="a">http://hdl.handle.net/10668/4187</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/18239</subfield>
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      <subfield code="a">IGFBP2</subfield>
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      <subfield code="a">Obesity</subfield>
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      <subfield code="a">Insulin resistance</subfield>
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      <subfield code="a">Lifestyle modification</subfield>
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      <subfield code="a">Proteína 2 de unión a factor de crecimiento similar a la insulina</subfield>
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      <subfield code="a">Potential Role of Insulin Growth-Factor-Binding Protein 2 as Therapeutic Target for Obesity-Related Insulin Resistance</subfield>
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