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1.
Int. j. cardiovasc. sci. (Impr.) ; 34(1): 10-18, Jan.-Feb. 2021. tab
Article in English | LILACS | ID: biblio-1154531

ABSTRACT

Abstract Background Lipoprotein (a) is a cardiovascular risk factor in adult. Studies have shown the presence of this emergent risk factor in school children, which may contribute to the development of atherosclerosis in adulthood. Objective To evaluate the association between lipoprotein (a) and cardiovascular risk factors in school children. Methods Lipoprotein (a) levels were measured in 320 school children (6-14 years) selected from a population survey carried out in Ouro Preto (southeast of Brazil). Demographic (sex and age), biochemical (total cholesterol, high-density lipoprotein-cholesterol, low-density lipoprotein-cholesterol, triglycerides, and glucose), anthropometric (body mass index, waist circumference, body fat percentage), clinical (arterial blood pressure, pubertal stage and birth weight) and economic (family income) parameters, as well as family history (obese and/or hypertensive parents) were analyzed. Non-parametric analysis was used to evaluate lipoprotein (a) levels in each subgroup. Variables with p≤0.20 in the univariate analysis were included in binary regression logistic model. Differences with p < 0.05 were considered significant. Results Lipoprotein (a) levels were associated with total cholesterol (p=0.04), body fat (p=0.009), and mother´s systolic (p=0.02) and diastolic blood pressure (p=0.04). In a logistic regression analysis, children with high lipoprotein (a) levels and body fat, and children born from hypertensive mothers were, respectively, at 3.2(p=0.01) and 1.4 (p=0.03) times higher risk than other children. In clustering these factors, elevated lipoprotein (a) was 2.6 times more likely to be seen in school children with high body fat and born hypertensive mothers. Conclusions Lipoprotein (a) was correlated with cardiovascular risk factors in children and adolescents. Persistence of these risk factors in childhood suggests a contribution of elevated lipoprotein (a) to future cardiovascular disease. (Int J Cardiovasc Sci. 2020; [online].ahead print, PP.0-0)


Subject(s)
Humans , Male , Female , Child , Adolescent , Cardiovascular Diseases/etiology , Lipoprotein(a)/blood , Heart Disease Risk Factors , Cardiovascular Diseases/prevention & control , Cardiovascular Diseases/epidemiology , Demography , Cholesterol , Cross-Sectional Studies , Atherosclerosis/etiology , Adiposity , Hypertension
3.
Arch. argent. pediatr ; 115(1): 50-57, feb. 2017. tab
Article in English, Spanish | LILACS | ID: biblio-1038346

ABSTRACT

Antecedentes/Objetivo. El objetivo de nuestro estudio fue analizar el lipidograma y ciertos factores de riesgo de ateroesclerosis, tales como las lipoproteínas de baja densidad oxidadas (ox-LDL, por su sigla en inglés) y las lipoproteínas de baja densidad pequeñas y densas (sdLDL, por su sigla en inglés) en los hijos de pacientes con cardiopatía coronaria (CC) prematura. Población y métodos. Hijos de padres con CC de inicio temprano emparejados con pares de su misma edad y mismo sexo. Se analizaron las concentraciones de lípidos, apolipoproteínas (ApoA, B, E), ox-LDL, sdLDL y lipoproteína (a) [Lp(a)] en los niños de estudio y de referencia. Los datos se evaluaron con el programa SPSS, junto con la prueba t de Student y la prueba U de Mann-Whitney. Resultados. Los niños del grupo de estudio (n: 43) tenían niveles más elevados de LDL, Lp(a) y ox-LDL y cocientes mayores de CT/HDL, ApoB/ApoA, LDL/HDL y ox-LDL/HDL (p < 0,05) que los del grupo de referencia. Conclusión. Con base en estos hallazgos, se sugiere que la dislipidemia y las concentraciones elevadas de LDL, Lp(a) y ox-LDL son frecuentes en los hijos de pacientes con CC de inicio temprano y representan gran parte de la predisposición familiar a tener CC


Background/Aim: The objective of our study was to analyze the lipid profile and some risk factors of atherosclerosis such as oxidized-low density lipoprotein (ox-LDL), small dense LDL (sd LDL) in the offspring of patients with premature coronary heart disease (CHD). Population and Methods: Children whose parents had early onset CHD were matched with age and sex pairs. Study and controls were analyzed for lipid levels, apolipoproteins (Apo- A,B,E), ox-LDL, sd LDL and lipoprotein (a) [Lp(a)]. The data were evaluated with SPSS using "Student tand Mann-Whitney U" tests. Results: Thestudy group children (n: 43) had higher LDL, Lp(a) and ox-LDL levels, ratios of TC/HDL, Apo-B/A, LDL/HDL and ox-LDL/HDL (p<0.05) than control group. Conclusion: These findings suggest that dyslipidemia and increased LDL, Lp(a) and ox-LDL levels are common in the offspring of patients with early onset CHD and account largely for their familial predisposition for CHD.


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Young Adult , Parents , Apolipoproteins/blood , Triglycerides/blood , Coronary Artery Disease , Lipoprotein(a)/blood , Atherosclerosis/blood , Lipoproteins, LDL/blood , Prospective Studies , Risk Factors
4.
Braz. j. med. biol. res ; 50(8): e5979, 2017. tab, graf
Article in English | LILACS | ID: biblio-888982

ABSTRACT

As a mechanism compensating for obstructive coronary artery disease, coronary collateral circulation (CCC) has attracted cardiologists for a long time to explore its potential impact. In the present study, Chinese patients suffering from ≥95% coronary stenosis, as diagnosed by angiography, have been investigated for the correlation between CCC and lipoprotein(a) [Lp(a)] levels. A cohort of 654 patients was divided into four categories according to Rentrop grades 0, 1, 2, and 3. Lp(a) levels were divided into model 1, discretized with critical values of 33 and 66%, and model 2, discretized with a cutoff value of 30.0 mg/dL. Furthermore, we evaluated the correlation between CCC and serum Lp(a) levels. The four groups had significantly different Lp(a) levels (25.80±24.72, 18.99±17.83, 15.39±15.80, and 8.40±7.75 mg/dL; P<0.001). In model 1, concerning R0, the risk in the third Lp (a) tertile (OR=3.34, 95%CI=2.32-4.83) was greater than that in the first tertile. In model 2, concerning R0, the risk in Lp(a) >30.0 group (OR=6.77, 95%CI=4.44-10.4) was greater than that of Lp(a) <30.0 mg/dL. The worst condition of CCC can be predicted independently by Lp(a) levels. In addition to clinical usage, Lp(a) levels can also be utilized as biological markers.


Subject(s)
Humans , Male , Female , Middle Aged , Collateral Circulation/physiology , Coronary Artery Disease/blood , Coronary Artery Disease/diagnostic imaging , Coronary Circulation/physiology , Coronary Occlusion/blood , Lipoprotein(a)/blood , Biomarkers/blood , Cohort Studies , Coronary Angiography , Coronary Artery Disease/physiopathology , Coronary Occlusion/diagnostic imaging , Coronary Occlusion/physiopathology , Predictive Value of Tests , Risk Factors
5.
Rev. méd. Chile ; 143(1): 85-95, ene. 2015. ilus, tab
Article in Spanish | LILACS | ID: lil-742555

ABSTRACT

Background: There is growing interest in the treatment and return-to-work of workers with labor related mental illnesses. Aim: To perform a systematic review of practices and interventions that improve return to work. Material and Methods: Systematic literature review. Thirty articles were selected for in- depth analysis. Results: Self efficacy perception, work motivation, a lower age and a better socioeconomic status were identified as worker-related return to work facilitators. Among work environment facilitators, good communication practices, supervisor support, a good assessment and modification of work load, adjustment of expectations, a good relationship between employers and employees and positive work experiences were identified. Treatment may improve return to work using a multidisciplinary approach, reducing stress and identifying psychosocial determinants of mental problems rather than symptoms and providing a timely health care. Conclusions: Return to work of workers with labor related mental illnesses requires a constant sharing of information between health care workers, employers and employees to identify common therapeutic objectives.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , White People/genetics , Genetic Loci , Lipoprotein(a)/blood , Lipoprotein(a)/genetics , Polymorphism, Single Nucleotide , Cohort Studies , Europe , Genetic Association Studies , Genotype , Oligonucleotide Array Sequence Analysis , Phenotype
6.
Rev. paul. pediatr ; 31(4): 531-537, dez. 2013. tab
Article in English | LILACS | ID: lil-698037

ABSTRACT

OBJECTIVE: To review the relationship between lipoprotein (a) [Lp(a)] and other risk factors for cardiovascular disease (CVD) in children and adolescents. DATA SOURCES: This systematic review included studies from 2001 to 2011, a ten-year time period. Epidemiological studies with children and/or adolescents published in English, Portuguese or Spanish and fully available online were included. The searches were performed in Science Direct, PubMed/Medline, BVS (Biblioteca Virtual em Saúde) and Cochrane Library databases, using the following combination of key-words: "lipoprotein a" and "cardiovascular diseases" and "obesity". DATA SYNTHESIS: Overall, 672 studies were obtained but only seven were included. Some studies assessed the family history for CVD. In all of them, Lp(a) levels were increased in patients with family history for CVD. There was also a positive correlation between Lp(a) and LDL-cholesterol, total cholesterol, and apolipoprotein B levels, suggesting an association between Lp(a) levels and the lipid profile. CONCLUSIONS: The evidence that CVD may originate in childhood and adolescence leads to the need for investigating the risk factors during this period in order to propose earlier and possibly more effective interventions to reduce morbidity and mortality rates. .


OBJETIVO: Revisar la relación de la lipoproteína (a) {Lp(a)} con otros factores de riesgo para enfermedades cardiovasculares (ECV) en niños y adolescentes. FUENTES DE DATOS: Se trata de una revisión sistemática, realizada de julio a agosto de 2011, con estudios del periodo de 2001 a 2011, caracterizando un recorte temporal de diez años. Se incluyeron estudios epidemiológicos realizados en niños y/o adolescentes, publicados en inglés, portugués o español, disponibles integralmente en línea. Se realizó la búsqueda en las bases de datos Science Direct, PubMed/Medline, Biblioteca Virtual en Salud y Biblioteca Cochrane, utilizándose la combinación de los descriptores "lipoproteína a", "enfermedades cardiovasculares" y "obesidad". SÍNTESIS DE LOS DATOS: Se encontraron 672 estudios, pero solamente siete fueron incluidos en la revisión. Algunos trabajos evaluaron el histórico familiar para ECV. En todos, los niveles de Lp (a) eran aumentados en los pacientes con ese histórico. Se observó además la correlación positiva entre Lp(a) y colesterol LDL, colesterol total y apolipoproteína B, sugiriendo una asociación entre concentraciones de Lp(a) y perfil lipídico. CONCLUSIONES: La evidencia de que las ECV pueden tener su origen en la infancia y adolescencia lleva a la necesidad de investigar los factores de riesgo en ese periodo, para planear intervenciones cada vez más tempranas y, posiblemente, más efectivas, reduciendo la morbimortalidad. .


OBJETIVO: Revisar a relação da lipoproteína (a) [Lp(a)] com outros fatores de risco para doenças cardiovasculares (DCV) em crianças e adolescentes. FONTES DE DADOS: Revisão sistemática, com estudos do período de 2001 a 2011, caracterizando um recorte temporal de dez anos. Incluíram-se estudos epidemiológicos realizados com crianças e/ou adolescentes, publicados em inglês, português ou espanhol, disponíveis integralmente on-line. Realizou-se a busca nas bases de dados Science Direct, PubMed/Medline, Biblioteca Virtual em Saúde e Biblioteca Cochrane, utilizando-se a combinação dos descritores "lipoproteína a" e "doenças cardiovasculares" e "obesidade". SÍNTESE DOS DADOS: Encontraram-se 672 estudos, porém apenas sete foram incluídos na revisão. Alguns trabalhos avaliaram o histórico familiar para DCV. Em todos, os níveis de Lp(a) eram aumentados nos pacientes com esse histórico. Observou-se também correlação positiva entre Lp(a) e colesterol LDL, colesterol total e apolipoproteína B, sugerindo uma associação entre concentrações de Lp(a) e perfil lipídico. CONCLUSÕES: A evidência de que as DCV podem ter sua origem na infância e na adolescência leva à necessidade de se investigarem os fatores de risco nesse período, para planejar intervenções cada vez mais precoces e, possivelmente, mais efetivas, reduzindo a morbimortalidade. .


Subject(s)
Adolescent , Child , Humans , Cardiovascular Diseases/blood , Cardiovascular Diseases/epidemiology , Lipoprotein(a)/blood , Cardiovascular Diseases/etiology , Risk Factors
7.
Arq. bras. cardiol ; 100(4): 322-327, abr. 2013. graf, tab
Article in Portuguese | LILACS | ID: lil-674194

ABSTRACT

FUNDAMENTO: A prevalência das doenças cardiovasculares (DCV) tem aumentado nos últimos anos. A literatura revela que cerca de 35% dos eventos ateroscleróticos ocorrem na ausência dos fatores de risco clássicos, requerendo uma avaliação individual minuciosa para melhor caracterizar o risco. Os índices lipídicos tetravalente (LTI) e pentavalente (LPI) constituem uma nova e eficiente forma de avaliação do perfil lipídico e do risco para DCV. OBJETIVO: O presente estudo avaliou o LTI e o LPI em estudantes de graduação, estabelecendo estes índices em indivíduos saudáveis e correlacionando-os com o perfil lipídico tradicional. MÉTODOS: Participaram do estudo 110 estudantes, 48 (44%) do sexo masculino e 62 (56%) do sexo feminino, com média de idade de 20,9 ± 1,7 anos. Apolipoproteína-AI, apolipoproteína B, colesterol total, lipoproteína (a), triglicérides, HDL e LDL foram analisados usando-se métodos diagnósticos específicos. LTI e LPI foram calculados por meio das equações LTI = [colesterol total x triglicérides x lipoproteína (a) / HDL] e LPI = [colesterol total x triglicérides x lipoproteína (a) x apolipoproteína B / apolipoproteína A-I], respectivamente. RESULTADOS: Os valores de LTI e de LPI foram significativamente maiores nas mulheres quando comparados aos dos homens. Para os outros parâmetros, houve diferenças significativas entre os gêneros apenas para colesterol total, HDL e apolipoproteína A-I. Houve correlações positivas e significativas entre LDL e LTI e entre LDL e LPI. CONCLUSÃO: Os achados indicam que LTI e LPI estavam associados com LDL, um parâmetro não utilizado para calcular os índices lipídicos e amplamente usado na prática clínica para investigação do risco cardiovascular.


BACKGROUND: The prevalence of cardiovascular disease (CVD) has increased steadily in recent years. Literature data show that about 35% of atherosclerotic events occur in the absence of classic risk factors, requiring a broader assessment of the individual to better characterize the risk. Lipid Tetrad Index (LTI) and Lipid Pentad Index (LPI) constitute a new and efficient evaluation of the lipid profile and CVD risk. OBJECTIVE: This study assessed LTI and LPI in undergraduate students, seeking to establish the parameters of these indices in healthy subjects and correlate them with the conventional lipid profile. METHODS: The study included 110 students, 48 (44%) males and 62 (56%) females, mean age 20.9 ± 1.7. Apolipoprotein-AI, apolipoprotein B, total cholesterol, lipoprotein(a), triglycerides, high-density lipoprotein (HDL) and low-density lipoprotein (LDL) were assessed, using specific diagnostic methods. LTI and LPI indices were calculated using the equations LTI = [total cholesterol x triglycerides x lipoprotein(a) / HDL] and LPI = [total cholesterol x triglycerides x lipoprotein(a) x apolipoprotein B/apolipoprotein-AI], respectively. RESULTS: LTI and LPI values were significantly higher in females compared to males. As for the other parameters, there were significant differences between males and females only regarding total cholesterol, HDL and apolipoprotein-AI. There were significant and positive correlations between LDL and LTI and between LDL and LPI. CONCLUSIONS: Findings indicate that both LTI and LPI were associated with LDL, a parameter not used to calculate lipid indices and widely used in clinical practice for cardiovascular risk assessment.


Subject(s)
Female , Humans , Male , Young Adult , Apolipoprotein A-I/blood , Apolipoproteins B/blood , Cardiovascular Diseases/diagnosis , Cholesterol/blood , Lipoprotein(a)/blood , Students/statistics & numerical data , Triglycerides/blood , Biomarkers/blood , Risk Factors , Statistics, Nonparametric
8.
Rev. SOCERJ ; 22(5): 318-325, set.-out. 2009.
Article in Portuguese | LILACS | ID: lil-540222

ABSTRACT

As doenças cardiovasculares estão relacionadas com o processo aterosclerótico e o metabolismo lipídico. Apesar da importância dos lipídios sanguíneos na doença cardiovascular, 50 % dos infartos do miocárdio ocorrem em indivíduos sem hiperlipidemia. Nos últimos anos, estudos demonstram fatores de risco emergentes como marcadores de aterosclerose. Lipoproteína-A consiste essencialmente de uma partícula de LDL, limitada pela apoliproteína-a. Lipoproteína-A é associada à presença e extensão da doença coronariana. Proteína-C reativa desempenha um papel na terosclerose e complicações cardiovasculares. Evidências experimentais sugerem que a homocisteína pode estar envolvida na aterogênese e trombogênese. A importância da hiperfibrinogenemia como um fator de risco de aterotrombose...


Subject(s)
Humans , Female , Adult , Aged , Atherosclerosis/diagnosis , Homocysteine/urine , Lipoprotein(a)/blood , C-Reactive Protein/urine , Cholesterol/blood , Endothelium/anatomy & histology , Risk Factors , Triglycerides/blood
9.
Arq. bras. cardiol ; 93(1): 28-33, jul. 2009. tab, graf
Article in English, Spanish, Portuguese | LILACS | ID: lil-528233

ABSTRACT

FUNDAMENTO: Ainda não foi claramente estabelecido se a resistência/deficiência insulínica leva diretamente à aterogênese ou através de sua associação com outros fatores de risco como os níveis de lipoproteína (a)[Lp(a)]. OBJETIVO: O objetivo do estudo foi estabelecer a relação entre os níveis basais de insulina, lípides e lipoproteína (a) em pacientes com diabetes mellitus (DM) tipo 2. MÉTODOS: Amostras de sangue foram colhidas em jejum e os níveis de insulina, lipoproteína (a), colesterol total (CT), triglicérides (TG), lipoproteína de baixa densidade (LDL-C), lipoproteína de alta densidade (LDL-C), glicose e hemoglobina glicada (HbA1c) foram medidos em 60 pacientes com DM tipo 2 e 28 indivíduos saudáveis. Nós dividimos os pacientes em dois grupos baseados nos níveis basais de insulina: > 10 µIU/ml e < 10 µIU/ml. RESULTADOS: Os níveis de insulina eram mais altos nos indivíduos diabéticos do que nos controles [p < 0,05]. Os níveis de CT (p< 0,01), LDL-C (p< 0,05), razão CT/HDL (p< 0,01), e TG (p< 0,05) eram mais altos e os níveis de HDL- C eram significantemente mais baixos em ambos os grupos de diabéticos, quando comparados aos controles. Os níveis de Lp(a) eram significantemente mais baixos em diabéticos com insulina basal > 10 µIU/ml comparados com aqueles que apresentavam insulina basal < 10 µIU/ml (p < 0.05). A análise de regressão mostrou uma relação significante da Lp(a) com os níveis de insulina (r = 0,262, p < 0,05) e razão Insulina/Glicose(r = 0,257, p < 0,05). CONCLUSÃO: Os níveis de Lp(a) se correlacionam inversamente com os níveis de insulina em pacientes com DM tipo 2. Os níveis de Lp(a) podem ser um dos fatores de risco cardiovascular em pacientes com DM tipo 2 com maior duração da doença. (Arq Bras Cardiol 2009;93(1):28-33)


BACKGROUND: It has not been clearly established whether insulin resistance/deficiency leads directly to atherogenesis or through its association with other risk factors such as Lipoprotein(a) [Lp(a)]. OBJECTIVE: This project aimed at studying the association between basal Insulin, Lipids and Lipoprotein(a) levels in Patients with Type 2 Diabetes Mellitus. METHODS: Fasting blood samples were analyzed for Insulin, Lipoprotein(a), total cholesterol (TC), triglycerides (TG), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glucose and glycosylated hemoglobin (HbA1c) levels in 60 patients with type 2 Diabetes Mellitus (DM) and 28 healthy subjects. We divided patients into two groups based on basal insulin levels: > 10 µIU/ml and < 10 µIU/ml. RESULTS: Insulin levels were higher in diabetic versus control individuals [p < 0.05]. TC (p< 0.01), LDL-C (p< 0.05), TC/HDL ratio (p< 0.01) and TG levels (p< 0.05) were higher and HDL- C levels were significantly lower (p < 0.001) in both diabetic groups as compared to control. Lp(a) levels were significantly higher in both diabetic groups, when compared to the control group. Lp(a) levels were significantly lower in diabetics with basal insulin > 10 µIU/ml when compared to those with basal insulin < 10 µIU/ml (p < 0.05). Regression analysis revealed a significant relationship of Lp(a) with insulin levels (r = 0.262, p < 0.05) and Insulin Glucose ratio (r = 0.257, p < 0.05). CONCLUSION: Lp(a) levels correlate inversely with insulin levels in Type 2 diabetic patients. Lp(a) may be one of the cardiovascular risk factor in type 2 diabetic patients with longer duration of DM.


FUNDAMENTO: Todavía no se aclaró totalmente si la resistencia/deficiencia insulínica lleva directamente a la aterogénesis o a través de su asociación con otros factores de riesgo como los niveles de lipoproteína (a) [Lp(a)]. OBJETIVO: : El objetivo del estudio fue establecer la relación entre los niveles basales de insulina, lípidos y lipoproteína (a) en pacientes con diabetes mellitus (DM) tipo 2. MÉTODOS: Se extrajeron muestras de sangre en ayuno y se determinaron los niveles de insulina, lipoproteína (a), colesterol total (CT), triglicéridos (TG), lipoproteína de baja densidad (LDL-C), lipoproteína de alta densidad (LDL-C), glucosa y hemoglobina glicosilada (HbA1c) en 60 pacientes con DM tipo 2 y 28 individuos sanos. Dividimos a los pacientes en dos grupos basados en los niveles basales de insulina: > 10 µIU/ml y < 10 µIU/ml. RESULTADOS: : Los niveles de insulina eran más altos en los individuos diabéticos que en los controles [p < 0,05]. Los niveles de CT (p< 0,01), LDL-C (p< 0,05), razón CT/HDL (p< 0,01), y TG (p< 0,05) eran más altos y los niveles de HDL- C eran significantemente más bajos en ambos grupos de diabéticos, cuando comparados a los controles. Los niveles de Lp(a) eran significantemente más bajos en diabéticos con insulina basal > 10 µIU/ml comparados con aquellos que presentaban insulina basal < 10 µIU/ml (p < 0.05). El análisis de regresión evidenció una relación significante de la Lp(a) con los niveles de insulina (r = 0,262, p < 0,05) y razón insulina glucosa(r = 0,257, p < 0,05). CONCLUSIÓN: Los niveles de Lp(a) se correlacionan inversamente con los niveles de insulina en pacientes con DM tipo 2. Los niveles de Lp(a) pueden ser uno de los factores de riesgo cardiovascular en pacientes con DM tipo 2 con mayor duración de la enfermedad.


Subject(s)
Adult , Female , Humans , Male , Blood Glucose/analysis , /blood , Insulin/blood , Lipoprotein(a)/blood , Biomarkers/blood , Case-Control Studies , Cholesterol/blood , Fasting/blood , Triglycerides/blood
10.
Journal of Tehran University Heart Center [The]. 2008; 3 (3): 163-167
in English | IMEMR | ID: emr-143374

ABSTRACT

The potential role of lipoprotein [a] changes and also inflammation in coronary artery disease [CAD] have rendered these processes one of the most interesting objects of study in patients affected by type 2 diabetes mellitus. The aim of the current study was to evaluate lipoprotein [a] and other lipid profiles and also C-reactive protein [CRP] as the predictors of cardiovascular disease severity in non-insulin dependent diabetic subjects in comparison with non-diabetic CAD patients. Between June and September 2004, 372 patients with CAD were enrolled at Tehran Heart Center. Non-insulin dependent diabetics accounted for 102 of the cases, and the remaining 270 were non-diabetics. The severity of CAD was evaluated using the Gensini score, and the effect of patient variables such as serum lipid concentrations and CRP on CAD severity in the diabetics was investigated and compared with that of the non-diabetics. The mean of the Gensini score, CRP, and serum concentrations of all the lipid profiles were similar between the diabetic and non-diabetic patients. In the diabetic group, a high CRP concentration [?=0.200, Rs= 0.040; P=0.046] was effective on the Gensini score, whereas lipoprotein [a] and lipid profiles did not influence CAD severity. In the non-diabetics, no significant relationships were found between the Gensini score and all the studied laboratory indices. A high CRP level is an important predictor of the severity of CAD in diabetic patients with CAD


Subject(s)
Humans , Male , Female , Diabetes Mellitus, Type 2 , Severity of Illness Index , Lipids/blood , C-Reactive Protein/blood , Lipoprotein(a)/blood , Lipoprotein(a) , C-Reactive Protein , Retrospective Studies
11.
Arq. bras. endocrinol. metab ; 51(3): 472-477, abr. 2007. tab
Article in Portuguese | LILACS | ID: lil-452190

ABSTRACT

O hipotireoidismo subclínico (HS) já foi associado a aumento do risco cardiovascular. Na avaliação desse risco, a medida da espessura íntima-média (EIM) carotídea por ultra-sonografia é capaz de detectar alterações iniciais da aterosclerose. O objetivo deste estudo foi avaliar a EIM carotídea em pacientes com HS e sua associação com um provável aumento do risco cardiovascular. Não foi encontrada diferença significativa nas medidas da EIM das pacientes com HS e das controles. Os resultados encontrados nos dois grupos estudados foram, respectivamente: 0,573 ± 0,070 mm vs. 0,576 ± 0,068 mm para as carótidas comuns (p= 0,904) e 0,602 ± 0,079 mm vs. 0,617 ± 0,102 mm para as bifurcações (p= 0,714). Mesmo após estratificação das pacientes de acordo com o TSH e com a presença ou não de auto-imunidade, a diferença entre os sub-grupos permaneceu sem significância estatística. As medidas da EIM nesses grupos nos sítios avaliados foram: TSH 4-8 mUI/L: 0,579 ± 0,070 mm e 0,586 ± 0,063 mm; TSH > 8 mUI/L: 0,569 ± 0,073 mm e 0,616 ± 0,091 mm; anti-TPO+: 0,585 ± 0,070 mm e 0,621 ± 0,085 mm; anti-TPO-: 0,554 ± 0,072 mm e 0,571 ± 0,066 mm. Também não houve diferença no lipidograma e nas dosagens de apoproteína B e de lipoproteína (a). Este fato sugere que o HS, quando leve, sem alterações metabólicas associadas, não promove aumento do risco cardiovascular.


Subclinical hypothyroidism (SH) has been associated with an increased risk for coronary disease. Carotid intima-media thickness (IMT), as assessed by ultrasonography, is a precise marker of atherosclerotic changes and can be used as an endpoint for cardiovascular events. Aims of this study were to determine carotid IMT in a group of patients with SH and its possible association with an increase in cardiovascular risk. There were no significant differences in mean carotid IMT between patients and controls. Results of both groups were, respectively: common carotid arteries, 0.573 ± 0.070 mm and 0.576 ± 0.068 mm (p= 0.904); carotid bifurcation, 0.602 ± 0.079 mm and 0.617 ± 0.102 mm (p= 0.714). Similar results were obtained when analyzing subgroups with serum TSH < or > 8 mIU/L and with positive or negative titers of TPOAb. The mean carotid IMT in these subgroups were: TSH 4-8 mIU/L: 0.579 ± 0.070 mm and 0.586 ± 0.063 mm; TSH > 8 mIU/L: 0.569 ± 0.073 mm and 0.616 ± 0.091 mm; TPOAb+: 0.585 ± 0.070 mm and 0.621 ± 0.085 mm; TPOAb-: 0.554 ± 0.072 mm and 0.571 ± 0.066 mm. No differences in the lipid profile and in the apoprotein B and lipoprotein (a) levels between the groups were found. These findings suggest that mild SH with no related metabolic changes is not associated with an increase in cardiovascular risk, as assessed by carotid IMT.


Subject(s)
Adult , Female , Humans , Middle Aged , Carotid Artery, Common , Coronary Artery Disease/etiology , Hypothyroidism/complications , Lipids/blood , Tunica Intima , Apolipoproteins B/blood , Body Mass Index , Biomarkers/blood , Case-Control Studies , Carotid Artery, Common/pathology , Coronary Artery Disease/pathology , Coronary Artery Disease , Hypothyroidism/blood , Lipid Metabolism/physiology , Lipoprotein(a)/blood , Risk Factors , Sex Factors , Tunica Intima/pathology
12.
J Indian Med Assoc ; 2006 Nov; 104(11): 622-4, 626
Article in English | IMSEAR | ID: sea-98067

ABSTRACT

Subclinical hypothyroidism is characterised by elevated serum thyroid stimulating hormone (TSH) concentrations in association with normal free thyroid hormones. The aim of the study was to evaluate the prevalence and pattern of serum lipid alterations in patients with stable subclinical hypothyroidism in comparison to age- as well as sex-matched euthyroid group and also subgroup analysis between them in regard to age of presentation, sex, antithyroperoxidase (anti TPO) positivity, and TSH value. In this study, 100 patients of SCH were recruited, age ranged 17-68 years, majority (78%) being females, presenting mainly with non-specific symptoms and compared with 52 euthyroid control regarding lipid parameters. Of the subclinical hypothyroidism patients, only 10% had goitre and anti TPO was positive in 52% cases. Serum lipoprotein (a) above the age of 20 years, and total cholesterol, triglyceride and low density liporpotein cholesterol in the age group of 40-50 years were significantly elevated. In addition, total cholesterol, triglyceride and low density lipoprotein cholesterol levels in anti TPO positive cases and serum triglyceride and low density lipoprotein cholesterol in anti TPO negative patients showed statistically significant higher levels. In males only lipoprotein (a), but in females total cholesterol, triglyceride, low density lipoprotein cholesterol and liproprotein (a)--all were significantly elevated.


Subject(s)
Adolescent , Adult , Aged , Case-Control Studies , Comorbidity , Dyslipidemias/epidemiology , Female , Humans , Hypothyroidism/complications , India/epidemiology , Lipids/blood , Lipoprotein(a)/blood , Male , Middle Aged , Prevalence , Thyrotropin/blood
14.
Arq. bras. cardiol ; 87(3): 260-266, set. 2006. ilus, tab
Article in Portuguese, English | LILACS | ID: lil-436185

ABSTRACT

OBJETIVO: Determinar os níveis plasmáticos de lipoproteína(a) e perfil lipídico de um grupo de indivíduos submetidos à angiografia coronariana, buscando estabelecer a possível correlação entre estes parâmetros e a gravidade da doença coronariana. MÉTODOS: Níveis plasmáticos de colesterol total, HDL C, LDL C, triglicérides, lipoproteína(a), apolipoproteínas A-I e B foram medidos em amostras de sangue de 17 indivíduos com ausência de ateromatose nas coronárias (controles), 12 indivíduos apresentando ateromatose leve/moderada e 28 indivíduos apresentando ateromatose grave. RESULTADOS: Não foram encontradas diferenças estatisticamente significativas entre as médias dos três grupos para os parâmetros avaliados, exceto para os níveis plasmáticos de lipoproteína(a) que apresentaram diferenças significativas entre as médias dos grupos controle, ateromatose leve/moderada e ateromatose grave (p<0,001). CONCLUSÃO: As médias obtidas nos três grupos para Lp(a) sinalizam um aumento progressivo nos níveis plasmáticos deste parâmetro, de acordo com a gravidade da ateromatose coronariana. Estes achados sugerem a necessidade de estudos adicionais, visando obter suficiente evidência para a introdução rotineira da avaliação dos níveis de Lp(a) em laboratórios clínicos, no monitoramento de pacientes apresentando risco para doença arterial coronariana (DAC).


OBJECTIVE: To determine serum levels of lipoprotein(a) and lipid profile of a group of individuals submitted to coronary angiography, with the aim of establishing the possible correlation between these parameters and the severity of coronary artery disease. METHODS: Serum levels of total cholesterol, HDL C, LDL C, triglycerides, lipoprotein(a), apolipoproteins A-I and B were measured in blood samples of 17 subjects with absence of atheromatosis in the coronary arteries (control), 12 subjects presenting mild/moderate atheromatosis and 28 subjects presenting severe atheromatosis. RESULTS: No significant statistical differences were found between the means of the three groups for the parameters assessed, except for lipoprotein(a) serum levels which presented significant differences between the means of the control, mild/moderate atheromatosis and severe atheromatosis groups (p<0.001). CONCLUSION: The means obtained in the three groups for Lp(a) indicate a progressive increase in the serum levels of this parameter according to the severity of coronary atheromatosis. These findings suggest the need of additional studies in order to obtain enough evidence to support the introduction of routine assessment of Lp(a) levels in clinical laboratories in the monitoring of patients at risk for coronary artery disease (CAD).


Subject(s)
Humans , Male , Female , Middle Aged , Coronary Angiography , Coronary Artery Disease/blood , Lipoprotein(a)/blood , Biomarkers/blood , Case-Control Studies , Coronary Artery Disease , Lipoproteins/blood , Severity of Illness Index
15.
Rev. méd. Chile ; 133(11): 1285-1293, nov. 2005. tab, graf
Article in Spanish | LILACS | ID: lil-419931

ABSTRACT

Background: The use of new biomarkers improved risk stratification for patients with acute coronary syndromes (ACS). Aim: To evaluate the relationship between multiple biomarkers and long-term clinical outcome in ACS without ST segment elevation. Patients and Methods: Consecutive patients presenting with suspected ACS were studied. On admission to the emergency room, serum was obtained to determine highly sensitive C reactive protein (hsCRP), erythrocyte sedimentation rate (ESR), lipoprotein (a) (LPa) and soluble P selectin (sPS). Clinical endpoints were mortality and a composite endpoint of major adverse cardiovascular events (MACE) including death, re-infarction, and angina. Results: Seventy patients, aged 63±13 years, 54 males, were studied. Final diagnosis was unstable angina in 71% and non-ST-segment elevation myocardial infarction in 29%. MACE and mortality rate were 17% and 5.8%, respectively. We found higher plasma levels of hsCRP, ESR and Lp(a) in patients with MACE (p=0.032, p=0.015 and p=0.010, respectively). Plasma levels of hsCRP and ESR were also higher in patients who died during the follow up (p=0.002 y p=0.045, respectively). Conclusion: Plasma levels of inflammatory markers and atherosclerosis biomarkers are associated with a worse long-term clinical outcome in ACS without ST segment elevation. The inclusion of these biomarkers in the routine blood test on admission, could improve risk stratification of patients with ACS in the future.


Subject(s)
Female , Humans , Male , Middle Aged , Angina, Unstable/blood , Blood Sedimentation , C-Reactive Protein/analysis , Creatine Kinase, MB Form/blood , Lipoprotein(a)/blood , P-Selectin/blood , Acute Disease , Angina, Unstable/mortality , Biomarkers/blood , Coronary Artery Disease/blood , Coronary Artery Disease/mortality , Epidemiologic Methods , Inflammation/blood
16.
Article in English | IMSEAR | ID: sea-1107

ABSTRACT

A case control study done to evaluate the Lipoprotein(a) [LP(a)] as a risk factor for CVD (cerebrovascular disease). 150 non-smokers, non-alcoholic subjects free from DM, renal disease, thyroid disease and liver disease were included in the study. Among them 120 were CVD cases and 30 were age and sex matched healthy control. Subjects were grouped as group-I (30, healthy control), Group-II (60, Hemorrhagic CVD) and group-III (60, Ischemic CVD). Fasting (12 hr) blood samples were collected from all subjects and in CVD cases samples were collected after 24 hr of attack. Lipid profile and LP(a) conc. were measured in all samples. Mean serum LP(a) conc. in Group-I, Group-II and Group-III were found to be 17.6 7.4 mg/dl, 31.9 15.6 mg/dl and 44.8 24.0 mg/dl respectively. Both the groups of CVD cases showed significantly higher level of serum LP(a) conc. compared to healthy control. CVD cases did not differ statistically in respect of their lipid profile when compared with control. Moreover the serum LP (a) conc. of CVD cases found to show no correlation with their lipid profile, suggesting the serum LP(a) conc. a possible independent risk factor for CVD.


Subject(s)
Adult , Aged , Cerebrovascular Disorders/blood , Female , Humans , Lipoprotein(a)/blood , Male , Middle Aged , Risk Factors
17.
Article in English | IMSEAR | ID: sea-1073

ABSTRACT

A case-control study was done to evaluate the association of Lipoprotein(a)[LP(a)] with CVD (Cerebrovascular disease) and also to assess the implication of serum LP(a) concentration as a differentiating marker between ICVD (Ischemic CVD) & HCVD (Hemorrhagic CVD). 150 non-smokers, non-alcoholic subjects free from DM, renal disease, thyroid disease and liver disease were studied. Among them 120 were CVD cases and 30 were age & sex matched healthy control. Fasting (12 hr.) blood samples were collected from all subjects and in CVD cases samples were collected after 24 hr. of attack. Serum LP(a) concentration were measured in all samples. Mean serum LP(a) concentration in control, HCVD & ICVD were found to be 17.6 +/- 7.4 mg/dl, 31.9 +/- 15.6 mg/dl and 44.8 +/- 24.0 mg/dl respectively. Both HCVD & ICVD cases showed significantly higher level of serum LP(a) concentration compared to control. Moreover ICVD cases showed significantly higher level of serum LP(a) concentration compared to HCVD cases. The exquisite athero-thrombo-embolic potential of LP(a) explain its involvement with CVD but more with ICVD in comparison to HCVD; This finding apparently suggest the prospect of serum LP(a) concentration to be used as a promising laboratory maker to differentiate clinically the ICVD from HCVD following determination of cut-off value between ICVD & HCVD by broad based comprehensive study.


Subject(s)
Adult , Aged , Biomarkers/blood , Case-Control Studies , Cerebrovascular Disorders/blood , Female , Humans , Lipoprotein(a)/blood , Male , Middle Aged
18.
Article in English | IMSEAR | ID: sea-22842

ABSTRACT

Lipoprotein (a) [LP(a)] is a genetic variant of low density lipoprotein (LDL) and is mainly synthesized in liver. We conducted a study to evaluate the association of serum [Lp(a)] level with hepatitis viral infections. A total of 130 patients including 50 patients with acute viral hepatitis (AVH), 30 with chronic active hepatitis (CAH), 30 with cirrhosis of liver and 20 patients with fulminant hepatic failure (FHF) were analysed for different hepatitis viral markers and Lp(a) level in their serum samples. For comparison, 50 healthy persons were also tested for Lp(a) level. Serum Lp(a) level in patients in all the disease groups was significantly reduced compared to that observed in controls. Lp(a) level could not be detected in 40 per cent cases with AVH, 46.6 per cent with CAH, 70 per cent with cirrhosis and 80 per cent of FHF patients. On correlating Lp(a) level to viral etiology in these patients, it was found that the extent of diminution in Lp(a) level did not follow any trend with some particular viral infection and was recorded nearly same in all the infections. The findings of this study suggested that serum Lp(a) level was significantly (P<0.001) reduced in patients with liver diseases irrespective of the viral etiology.


Subject(s)
Adult , Hepatitis, Viral, Human/blood , Humans , Lipoprotein(a)/blood , Liver Diseases/etiology , Middle Aged
19.
Indian Heart J ; 2004 Nov-Dec; 56(6): 642-5
Article in English | IMSEAR | ID: sea-3838

ABSTRACT

BACKGROUND: Carotid artery intimal medial thickness is a simple, non-invasive and reproducible clinical tool to evaluate atherosclerosis and predict coronary artery disease. Lipoprotein(a) levels are related to both atherogenesis and thrombogenesis and may be a key link between lipid and coronary artery disease. This study evaluated the association of carotid intimal medial thickness and lipoprotein(a) with coronary artery disease. METHODS AND RESULTS: We studied 185 randomly selected patients hospitalized for coronary angiogram in our institute. There were 110 angiographically proven patients of coronary artery disease with mean age of 55.8 +/- 9 years (range 34-72 years) and 75 subjects with normal coronary artery anatomy with mean age of 54.8 +/- 8 years (range 34-68 years). The mean carotid intimal medial thickness of subjects with coronary artery disease was significantly higher than in subjects without coronary artery disease (0.84 +/- 0.16 mm v. 0.65 +/- 0.15 mm, p<0.001). The mean carotid intimal medial thicknesses in patients with triple vessel, double vessel and single vessel disease were 0.96 +/- 0.12 mm, 0.84 +/- 0.11 mm and 0.78 +/- 0.13 mm, respectively (p=0.05). The mean lipoprotein(a) of subjects with coronary artery disease was significantly higher than in subjects without coronary artery disease (35.9 +/- 22.3 mg/dl v. 19.1 +/- 21.2 mg/dl, p<0.001). Mean lipoprotein(a) levels in subjects with carotid intimal medial thickness <0.80 was 26.4 +/- 24.2 mg/dl and in subjects with carotid intimal medial thickness > or = 0.80 was 32.1 +/- 22.1 mg/dl (p=0.05). CONCLUSIONS: There is a strong correlation between carotid and coronary atherosclerosis and carotid intimal medial thickness is a good predictor of presence and extent of coronary artery disease. Lipoprotein(a) level is a powerful independent risk factor for atherosclerosis. Carotid intimal medial thickness and lipoprotein(a) in conjoint can predict coronary artery disease reliably.


Subject(s)
Adult , Aged , Biomarkers/blood , Carotid Arteries/diagnostic imaging , Cholesterol/blood , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Coronary Angiography/methods , Coronary Artery Disease/blood , Cross-Sectional Studies , Female , Humans , India/epidemiology , Lipoprotein(a)/blood , Male , Middle Aged , Predictive Value of Tests , Risk Factors , Severity of Illness Index , Triglycerides/blood , Tunica Intima/diagnostic imaging
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