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 |
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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. |
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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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CitedBy_id | crossref_primary_10_1530_EC_22_0028 crossref_primary_10_3389_fendo_2023_1131438 crossref_primary_10_3389_fendo_2022_1056871 crossref_primary_10_1007_s00431_023_05174_y crossref_primary_10_3389_fendo_2022_836527 |
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Keywords | Obesity CPP HDLc Cardiometabolic factors Leptin CSF zBMI LDLc TGLs Central precocious puberty Adiponectin ELISA |
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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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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 |
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