Altered cardiometabolic profile in girls with central precocious puberty and adipokines: A propensity score matching analysis

•Patients with CPP have an increased cardiovascular risk in adulthood.•Since the diagnosis of CPP, the girls have an altered cardiometabolic profile.•CPP girls at diagnosis have higher free leptin levels and hypertriglyceridemia.•In CPP, the altered cardiometabolic profile is independent of BMI. To...

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Published in:Cytokine (Philadelphia, Pa.) Vol. 148; p. 155660
Main Authors: Zurita-Cruz, Jessie N., Villasís-Keever, Miguel A., Manuel-Apolinar, Leticia, Damasio-Santana, Leticia, Gutierrez-Gonzalez, Alejandro, Wakida-Kusunoki, Guillermo, Padilla-Rojas, Michel, Maldonado-Rivera, Cesar, Garrido-Magaña, Eulalia, Rivera-Hernández, Aleida de J., Nishimura-Meguro, Elisa
Format: Journal Article
Language:English
Published: England Elsevier Ltd 01-12-2021
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Abstract •Patients with CPP have an increased cardiovascular risk in adulthood.•Since the diagnosis of CPP, the girls have an altered cardiometabolic profile.•CPP girls at diagnosis have higher free leptin levels and hypertriglyceridemia.•In CPP, the altered cardiometabolic profile is independent of BMI. To compare cardiometabolic factors and adipokines between patients with recently diagnosed CPP and controls without CPP, paired by BMI Z scores (BMIz) and classified into girls with adequate nutritional status and girls who are overweight or obese. This cross-sectional study was performed from January 2012 to May 2015 at two tertiary care pediatric centers in Mexico City. We included female patients with idiopathic CPP without other chronic pathology and healthy controls. Patients were divided into groups, BMI < 85th and BMI ≥ 85th percentile, according to 2000 CDC Growth Charts. Anthropometric data and fasting plasma concentrations of lipids, glucose, insulin, and leptin were assessed. There were 73 patients with CPP and 82 without CPP. Sixty-six patients were matched between the groups; no significant difference was noted between the groups according to zBMI. However, differences in the bone/chronological age relationship, birth weight and proportions in different Tanner stages were observed. Among girls with normal BMI, the percentage of body fat (24.6% vs 18.9%, p < 0.001), serum triglycerides (102.9 vs 54.3 mg/dl, p < 0.001), leptin (7.46 vs 5.4 ng/ml, p = 0.010) and free leptin (0.44 vs 0.29 ng/ml, p = 0.044) were higher in those with CPP; additionally, girls with CPP presented a higher proportion of hypertriglyceridemia. In the overweight/obese group, adiponectin levels were lower in girls with CPP (6.23 vs 7.28 pg/ml, p = 0.011). Girls with CPP and normal BMI at diagnosis had a worse cardiometabolic profile, as reflected by higher levels of free leptin, and higher proportion of hypertriglyceridemia than girls without CPP.
AbstractList OBJECTIVETo compare cardiometabolic factors and adipokines between patients with recently diagnosed CPP and controls without CPP, paired by BMI Z scores (BMIz) and classified into girls with adequate nutritional status and girls who are overweight or obese. METHODSThis cross-sectional study was performed from January 2012 to May 2015 at two tertiary care pediatric centers in Mexico City. We included female patients with idiopathic CPP without other chronic pathology and healthy controls. Patients were divided into groups, BMI < 85th and BMI ≥ 85th percentile, according to 2000 CDC Growth Charts. Anthropometric data and fasting plasma concentrations of lipids, glucose, insulin, and leptin were assessed. RESULTSThere were 73 patients with CPP and 82 without CPP. Sixty-six patients were matched between the groups; no significant difference was noted between the groups according to zBMI. However, differences in the bone/chronological age relationship, birth weight and proportions in different Tanner stages were observed. Among girls with normal BMI, the percentage of body fat (24.6% vs 18.9%, p < 0.001), serum triglycerides (102.9 vs 54.3 mg/dl, p < 0.001), leptin (7.46 vs 5.4 ng/ml, p = 0.010) and free leptin (0.44 vs 0.29 ng/ml, p = 0.044) were higher in those with CPP; additionally, girls with CPP presented a higher proportion of hypertriglyceridemia. In the overweight/obese group, adiponectin levels were lower in girls with CPP (6.23 vs 7.28 pg/ml, p = 0.011). CONCLUSIONSGirls with CPP and normal BMI at diagnosis had a worse cardiometabolic profile, as reflected by higher levels of free leptin, and higher proportion of hypertriglyceridemia than girls without CPP.
•Patients with CPP have an increased cardiovascular risk in adulthood.•Since the diagnosis of CPP, the girls have an altered cardiometabolic profile.•CPP girls at diagnosis have higher free leptin levels and hypertriglyceridemia.•In CPP, the altered cardiometabolic profile is independent of BMI. To compare cardiometabolic factors and adipokines between patients with recently diagnosed CPP and controls without CPP, paired by BMI Z scores (BMIz) and classified into girls with adequate nutritional status and girls who are overweight or obese. This cross-sectional study was performed from January 2012 to May 2015 at two tertiary care pediatric centers in Mexico City. We included female patients with idiopathic CPP without other chronic pathology and healthy controls. Patients were divided into groups, BMI < 85th and BMI ≥ 85th percentile, according to 2000 CDC Growth Charts. Anthropometric data and fasting plasma concentrations of lipids, glucose, insulin, and leptin were assessed. There were 73 patients with CPP and 82 without CPP. Sixty-six patients were matched between the groups; no significant difference was noted between the groups according to zBMI. However, differences in the bone/chronological age relationship, birth weight and proportions in different Tanner stages were observed. Among girls with normal BMI, the percentage of body fat (24.6% vs 18.9%, p < 0.001), serum triglycerides (102.9 vs 54.3 mg/dl, p < 0.001), leptin (7.46 vs 5.4 ng/ml, p = 0.010) and free leptin (0.44 vs 0.29 ng/ml, p = 0.044) were higher in those with CPP; additionally, girls with CPP presented a higher proportion of hypertriglyceridemia. In the overweight/obese group, adiponectin levels were lower in girls with CPP (6.23 vs 7.28 pg/ml, p = 0.011). Girls with CPP and normal BMI at diagnosis had a worse cardiometabolic profile, as reflected by higher levels of free leptin, and higher proportion of hypertriglyceridemia than girls without CPP.
To compare cardiometabolic factors and adipokines between patients with recently diagnosed CPP and controls without CPP, paired by BMI Z scores (BMIz) and classified into girls with adequate nutritional status and girls who are overweight or obese. This cross-sectional study was performed from January 2012 to May 2015 at two tertiary care pediatric centers in Mexico City. We included female patients with idiopathic CPP without other chronic pathology and healthy controls. Patients were divided into groups, BMI < 85th and BMI ≥ 85th percentile, according to 2000 CDC Growth Charts. Anthropometric data and fasting plasma concentrations of lipids, glucose, insulin, and leptin were assessed. There were 73 patients with CPP and 82 without CPP. Sixty-six patients were matched between the groups; no significant difference was noted between the groups according to zBMI. However, differences in the bone/chronological age relationship, birth weight and proportions in different Tanner stages were observed. Among girls with normal BMI, the percentage of body fat (24.6% vs 18.9%, p < 0.001), serum triglycerides (102.9 vs 54.3 mg/dl, p < 0.001), leptin (7.46 vs 5.4 ng/ml, p = 0.010) and free leptin (0.44 vs 0.29 ng/ml, p = 0.044) were higher in those with CPP; additionally, girls with CPP presented a higher proportion of hypertriglyceridemia. In the overweight/obese group, adiponectin levels were lower in girls with CPP (6.23 vs 7.28 pg/ml, p = 0.011). Girls with CPP and normal BMI at diagnosis had a worse cardiometabolic profile, as reflected by higher levels of free leptin, and higher proportion of hypertriglyceridemia than girls without CPP.
ArticleNumber 155660
Author Damasio-Santana, Leticia
Nishimura-Meguro, Elisa
Zurita-Cruz, Jessie N.
Maldonado-Rivera, Cesar
Villasís-Keever, Miguel A.
Padilla-Rojas, Michel
Garrido-Magaña, Eulalia
Gutierrez-Gonzalez, Alejandro
Wakida-Kusunoki, Guillermo
Manuel-Apolinar, Leticia
Rivera-Hernández, Aleida de J.
Author_xml – sequence: 1
  givenname: Jessie N.
  surname: Zurita-Cruz
  fullname: Zurita-Cruz, Jessie N.
  email: zuritajn@hotmail.com
  organization: Clinical Research Department, Hospital Infantil de México Federico Gómez, and Medicine Faculty of Autonomous National University, Calle Doctor Márquez 162 Col. Doctores, C.P. 06720 Mexico City, Mexico
– sequence: 2
  givenname: Miguel A.
  surname: Villasís-Keever
  fullname: Villasís-Keever, Miguel A.
  email: miguel.villasis@gmail.com, miguel.villasis@imss.gob.mx
  organization: Unit of Analysis and Synthesis of the Evidence, National Medical Center XXI Century, Instituto Mexicano del Seguro Social, Av. Cuauhtemoc 330, Col. Doctores, C.P. 06720 México City, Mexico
– sequence: 3
  givenname: Leticia
  surname: Manuel-Apolinar
  fullname: Manuel-Apolinar, Leticia
  email: letymanu@yahoo.com.mx
  organization: Department of Endocrinology Research, Hospital of Medical Specialties, National Medical Center XXI Century, Instituto Mexicano del Seguro Social, Av. Cuauhtemoc 330, Col. Doctores, CP 06720 México City, Mexico
– sequence: 4
  givenname: Leticia
  surname: Damasio-Santana
  fullname: Damasio-Santana, Leticia
  email: ldamasiosantana@yahoo.com.mx
  organization: Department of Endocrinology Research, Hospital of Medical Specialties, National Medical Center XXI Century, Instituto Mexicano del Seguro Social, Av. Cuauhtemoc 330, Col. Doctores, CP 06720 México City, Mexico
– sequence: 5
  givenname: Alejandro
  surname: Gutierrez-Gonzalez
  fullname: Gutierrez-Gonzalez, Alejandro
  email: zottacko@gmail.com
  organization: Computer Research Center of Instituto Politecnico Nacional, Av. Luis Enrique Erro S/N, Unidad Profesional Adolfo López Mateos, Zacatenco, C.P. 07738 Mexico City, Mexico
– sequence: 6
  givenname: Guillermo
  surname: Wakida-Kusunoki
  fullname: Wakida-Kusunoki, Guillermo
  email: guillewakida@yahoo.com.mx
  organization: Pediatrics Service, South Central Hospital of High Specialty of Petroleos Mexicanos, Health Services of Petroleos Mexicanos, Anillo Periferico 4091, Col. Fuentes del Pedregal, Tlalpan, C.P. 14140 Mexico City, Mexico
– sequence: 7
  givenname: Michel
  surname: Padilla-Rojas
  fullname: Padilla-Rojas, Michel
  email: mitchellmartinpadillarojas@yahoo.com.mx
  organization: Pediatrics Service, South Central Hospital of High Specialty of Petroleos Mexicanos, Health Services of Petroleos Mexicanos, Anillo Periferico 4091, Col. Fuentes del Pedregal, Tlalpan, C.P. 14140 Mexico City, Mexico
– sequence: 8
  givenname: Cesar
  surname: Maldonado-Rivera
  fullname: Maldonado-Rivera, Cesar
  email: dr.cesarmaldonado@gmail.com
  organization: Pediatrics Service, South Central Hospital of High Specialty of Petroleos Mexicanos, Health Services of Petroleos Mexicanos, Anillo Periferico 4091, Col. Fuentes del Pedregal, Tlalpan, C.P. 14140 Mexico City, Mexico
– sequence: 9
  givenname: Eulalia
  surname: Garrido-Magaña
  fullname: Garrido-Magaña, Eulalia
  email: garridolulu@hotmail.com
  organization: Department of Pediatric Endocrinology, Children’s Hospital, National Medical Center XXI Century, Instituto Mexicano del Seguro Social, Av. Cuauhtemoc 330, Col. Doctores, C.P. 06720 México City, Mexico
– sequence: 10
  givenname: Aleida de J.
  surname: Rivera-Hernández
  fullname: Rivera-Hernández, Aleida de J.
  email: riha0306@yahoo.com.mx
  organization: Department of Pediatric Endocrinology, Children’s Hospital, National Medical Center XXI Century, Instituto Mexicano del Seguro Social, Av. Cuauhtemoc 330, Col. Doctores, C.P. 06720 México City, Mexico
– sequence: 11
  givenname: Elisa
  surname: Nishimura-Meguro
  fullname: Nishimura-Meguro, Elisa
  email: erinishimura@prodigy.net.mx
  organization: Department of Pediatric Endocrinology, Children’s Hospital, National Medical Center XXI Century, Instituto Mexicano del Seguro Social, Av. Cuauhtemoc 330, Col. Doctores, C.P. 06720 México City, Mexico
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Keywords Obesity
CPP
HDLc
Cardiometabolic factors
Leptin
CSF
zBMI
LDLc
TGLs
Central precocious puberty
Adiponectin
ELISA
Language English
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Snippet •Patients with CPP have an increased cardiovascular risk in adulthood.•Since the diagnosis of CPP, the girls have an altered cardiometabolic profile.•CPP girls...
To compare cardiometabolic factors and adipokines between patients with recently diagnosed CPP and controls without CPP, paired by BMI Z scores (BMIz) and...
OBJECTIVETo compare cardiometabolic factors and adipokines between patients with recently diagnosed CPP and controls without CPP, paired by BMI Z scores (BMIz)...
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StartPage 155660
SubjectTerms Adipokines - blood
Adiponectin
Cardiometabolic factors
Central precocious puberty
Child
Female
Humans
Leptin
Lipids - blood
Myocardium - metabolism
Obesity
Propensity Score
Puberty, Precocious - blood
Title Altered cardiometabolic profile in girls with central precocious puberty and adipokines: A propensity score matching analysis
URI https://dx.doi.org/10.1016/j.cyto.2021.155660
https://www.ncbi.nlm.nih.gov/pubmed/34334260
https://search.proquest.com/docview/2557540143
Volume 148
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