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1.
Indian J Clin Biochem ; 39(3): 408-414, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-39005865

RESUMO

Chronic kidney disease (CKD) is one of the leading causes of mortality across the globe. Early diagnosis of the disease is important in order to prevent the adverse outcome related to CKD. Many laboratories adopt creatinine-based e-GFR equations which yields imprecise results leading to misdiagnosis of CKD. Emerging studies indicated cystatin C as a better renal marker than creatinine. The aim of the study is to compare the efficacy of CKD epidemiology collaboration (CKD-EPI) creatinine e-GFR equations with (CKD EPI) cystatin-based e-GFR equations alone and in combination with creatinine for early detection of CKD. A cross-sectional study employing 473 patients was conducted. Three estimating GFR equations were calculated based on creatinine and cystatin C. Pearson Correlation study was done to assess the correlation of creatinine and cystatin C with their respective GFRs. A predictive model was developed, and ROC curve was constructed to compare efficacy, sensitivity and specificity of the creatinine and cystatin C based equations. Cystatin C exhibited better negative correlation with GFR than creatinine in correlation study performed with three commonly employed eGFR equations including  CKD EPI Creatine cystatin C combined  equation (2021), cys C alone and CKD EPI  creatinine (2021)  equations respectively[r=(-) 0.801 vs. r=(-)0.786 vs. r=(-)0.773]. Predictive model demonstrated highest efficiency, sensitivity and specificity for creatinine-cystatin C combined equation (88%, 81% and 93%) followed by cystatin C alone equation (73%,63% and 82%) and creatinine-based equation  (61%, 56% and 66% respectively). The study showed better performance of cystatin C based equations for early detection of advance stages in chronic kidney disease as compared to creatinine-based e-GFR equation.

2.
BMC Res Notes ; 15(1): 329, 2022 Oct 22.
Artigo em Inglês | MEDLINE | ID: mdl-36273211

RESUMO

OBJECTIVE: Measurement of total vitamin B12 (vit B12) concentration raised concerns over early detection of vit B12 deficiency due to its clinical unreliability. In this present article we aimed to assess the efficacy of holo-transcobolamin (active vit B12) for true evaluation of vit B12 deficiency. METHODS: This retrospective study included 100 participants referred for vit B12 assay. Serum total vit B12, active vit B12 and homocysteine were estimated. RESULTS: Our study showed 59% of the total participants with vit B12 deficiency (185 ± 64.62 pg/ml) and 18% with hyper-cobalaminemia (1666.9 ± 367.13 pg/ml) based on their total vit B12 concentrations. A comparative study on total vit B12 and active vit B12 was done which reflected a striking disparity in results. Active vit B12 reported 28.8% patients with vit B12 deficiency (19.8 ± 17.48 pg/ml) and only 16.6% patients with hyper-cobalaminemia (224.14 ± 10 pg/ml). Active vit B12 appeared to be more sensitive (82.35% vs 65%) and specific (46.6% vs. 43.8%) diagnostic marker compared to total vit B12. Pearson Correlation study indicated a strong positive correlation (r = 0.695 at p < 0.01) hence justified use of the two methods. CONCLUSION: We claim that active vit B12 is a much more reliable biomarker than total vit B12 for early diagnosis of vit B12 deficiency.


Assuntos
Transcobalaminas , Deficiência de Vitamina B 12 , Humanos , Estudos Retrospectivos , Reprodutibilidade dos Testes , Deficiência de Vitamina B 12/diagnóstico , Vitamina B 12 , Biomarcadores , Homocisteína
3.
Cytokine ; 146: 155644, 2021 10.
Artigo em Inglês | MEDLINE | ID: mdl-34298483

RESUMO

PURPOSE: The present study was intended to investigate whether monocyte immune activation shapes plasma positive to negative acute phase reactants (APRs) ratio and predicts disease severity in dengue infection. METHODS: Serum level of ferritin, ceruloplasmin and transferrin was measured by means of electrochemiluminescence and immunoturbidimetry, respectively. Gene expression and plasma level for TNF-α, IL-6 and IL1-ß was measured by means of RT-qPCR and ELISA. RESULTS: A significant increased serum ferritin to transferrin [6.6 (3-11.7) vs 3.4 (1.9-6.1)] and ceruloplasmin to transferrin ratio [0.48 (0.21-0.87) vs 0.22 (0.13-0.43)] has been detected among the subjects with secondary dengue infection (SDENI) compared to primarily infected (PDENI) subjects (P < 0.001). Significant increased expression for CD14+ monocyte TNF-α, IL-6 and IL-1ß has been detected in SDENI patients (vs PDENI and control, P < 0.001). Plasma ferritin to transferrin ratio was found in a significant association with high level of plasma TNF-α [ρ = 0.6522, 95% CI (0.4714-0.7805)], IL-6 [ρ = 0.6181, 95% CI (0.4257-0.7571)] and IL- 1ß [ρ = 0.4119, 95% CI (0.1689-0.6077)] level among SDENI patients at 5th day time point after progression of the disease, with significantly low platelet [P < 0.001] and prolonging prothrombin time [P < 0.001] compared to control and PDENI subjects, respectively. CONCLUSION: Acute proinflammatory cytokine response is significantly associated with increased positive to negative APRs ratio in SDENI patients, which predicts intense immune activation, and renders SDENI patients extremely susceptible to hemostatic derangement.


Assuntos
Proteínas de Fase Aguda/metabolismo , Dengue/sangue , Dengue/patologia , Hemostasia , Inflamação/patologia , Monócitos/patologia , Adulto , Ceruloplasmina/metabolismo , Citocinas/sangue , Citocinas/metabolismo , Dengue/virologia , Vírus da Dengue/fisiologia , Feminino , Ferritinas/sangue , Humanos , Inflamação/sangue , Mediadores da Inflamação/metabolismo , Masculino , Prognóstico , Índice de Gravidade de Doença , Transferrina/metabolismo
4.
Int J Occup Med Environ Health ; 30(2): 271-279, 2017 Mar 30.
Artigo em Inglês | MEDLINE | ID: mdl-28366956

RESUMO

OBJECTIVES: To study any possible correlation between arsenic toxicity and the development of oral carcinoma in West Bengal population. MATERIAL AND METHODS: Ethical clearance for this study was obtained from the Vivekananda Institute of Medical Sciences. Out of 30 785 patients attending our hospital from November 2012 to July 2015, 107 cases and 50 control individuals were selected. The hair and buccal smear samples were obtained upon their consent for the purpose of the analysis of arsenic count and cytogenetic damage, respectively. RESULTS: Ninety-six percent of cases came from the highly arsenic affected districts and 81.3% showed their arsenic count above the safe limit (0.8 µg/g) whereas 96% of the controls' arsenic count was within the safe limit. The study showed a significant difference of the micronuclei and apoptosis frequency between the cases and controls. CONCLUSIONS: The difference of micronuclei and apoptosis frequency between cases and controls was significant. The maximum number of cases came from highly arsenic affected areas and a higher percentage of cases showed elevated arsenic count, as compared to controls, which may indicate a possible link between arsenic toxicity and this disease. However, a larger sample size is required for a proper correlation. Int J Occup Med Environ Health 2017;30(2):271-279.


Assuntos
Intoxicação por Arsênico/epidemiologia , Carcinoma/epidemiologia , Neoplasias Bucais/epidemiologia , Neoplasias Orofaríngeas/epidemiologia , Adolescente , Adulto , Idoso , Apoptose , Arsênio/análise , Intoxicação por Arsênico/patologia , Água Potável/química , Feminino , Cabelo/química , Humanos , Índia/epidemiologia , Masculino , Testes para Micronúcleos , Pessoa de Meia-Idade , Mucosa Bucal/citologia
5.
Genet Test Mol Biomarkers ; 15(1-2): 93-6, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21117952

RESUMO

This article reports the incidence of hemoglobin H (HbH) disease among the nontribe Bengali population living in South 24-Parganas of West Bengal. Among 105 patients with unexplained anemia with moderate hematological parameters referred to our laboratory over a period of 2 years, 17 cases (16.19%) were found to have HbH disease identified by hemoglobin electrophoresis. Molecular investigation for two common mutations of α-thalassemia (-3.7α, -4.2α) was carried out in these 17 cases using DNA extraction followed by multiplex polymerase chain reaction. Presence of these common mutations were identified in 10 of the 17 cases. Of them, -3.7α homozygotes (-3.7α/-3.7α), -3.7α/-4.2α double heterozygotes, and -4.2α homozygotes (-4.2α/-4.2α) were found in three, five, and one patient, respectively. The South East Asian (- -SEA) mutation was searched for in one Chinese patient because this mutation is very common among the Chinese population, and he showed the presence of this mutation. Seven patients with HbH disease did not show any of these mutations. These patients may have other α mutations, which need to be studied further. The need to screen for α-thalassemia at the molecular level in patients with unexplained anemia and its implication in the future generation of our society have been discussed in this article.


Assuntos
Hemoglobina H/genética , Talassemia alfa/genética , Adolescente , Adulto , Criança , Pré-Escolar , Feminino , Hematologia , Humanos , Índia , Masculino , Pessoa de Meia-Idade
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