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1.
Scand J Clin Lab Invest ; 83(1): 64-67, 2023 02.
Artículo en Inglés | MEDLINE | ID: mdl-36534490

RESUMEN

Prolonged icterus is an important and common problem in neonatology and accurate determination of the different bilirubin species, including differentiation between delta-bilirubin and mono- and di-conjugated bilirubin, is useful for diagnostic purposes. However, most bilirubin measurements routinely performed in the clinical laboratory are hampered by the lack of separation of the four bilirubin fractions (unconjugated bilirubin, mono-conjugated bilirubin, di-conjugated bilirubin, and delta-bilirubin). Herein, we propose a high-performance liquid chromatography-based method, independent of commercially available standards or reliable molar absorption coefficients, for the determination of bilirubin fractions in blood samples from icteric patients. The method is a robust and reliable candidate for a semi-automatized setup for measuring the various bilirubin fractions in a specialized laboratory handling samples from clinics with expertise in biliary disease.


Asunto(s)
Bilirrubina , Enfermedades de la Vesícula Biliar , Humanos , Cromatografía Líquida de Alta Presión/métodos
2.
J Am Acad Dermatol ; 83(3): 817-823, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-31374307

RESUMEN

BACKGROUND: Porphyria cutanea tarda (PCT) is a rare hepatocutaneous disease for which the prognosis is largely unknown. OBJECTIVE: To compare all-cause and cause-specific mortality between a nationwide cohort of patients with PCT and a matched population sample. METHODS: We included all Danish patients who received a diagnosis of PCT from 1989 through 2012. Each patient was matched by age and sex to 10 random population control individuals. We compared survival and cause-specific mortality between patients and control individuals and adjusted for confounding from alcohol-related diseases, hepatitis, hemochromatosis, HIV, diabetes, acute myocardial infarction, stroke, cancer, chronic obstructive pulmonary disease, and cirrhosis. RESULTS: The 20-year survival was 42.9% (95% confidence interval [CI], 36.9-48.7) for patients with PCT compared with 60.5% (95% CI, 58.6-62.4) for matched control individuals. All-cause mortality hazard ratio (HR) was 1.80 (95% CI, 1.56-2.07) before adjustment and 1.22 (95% CI, 1.04-1.44) after adjustment. The cause-specific mortality was markedly increased for nonmalignant gastrointestinal diseases (HR, 5.32; 95% CI, 2.71-10.43) and cancers of the gut (HR, 2.05; 95% CI, 1.24-3.39), liver/gallbladder (HR, 11.24; 95% CI, 4.46-28.29), and lungs (HR, 2.17; 95% CI, 1.41-3.33). LIMITATIONS: We had no data on lifestyle factors. CONCLUSIONS: Patients with PCT have increased mortality, primarily explained by an increased mortality from gastrointestinal diseases and from cancers of the gut, liver/gallbladder, and lungs.


Asunto(s)
Causas de Muerte , Enfermedades Gastrointestinales/mortalidad , Estilo de Vida , Neoplasias/mortalidad , Porfiria Cutánea Tardía/mortalidad , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Comorbilidad , Dinamarca/epidemiología , Femenino , Estudios de Seguimiento , Humanos , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad , Sistema de Registros/estadística & datos numéricos , Factores de Riesgo , Adulto Joven
4.
Ugeskr Laeger ; 176(8A): V06130413, 2014 Feb 17.
Artículo en Danés | MEDLINE | ID: mdl-25350307

RESUMEN

Porphyrias are rare, distinct and well characterized diseases due to impairment of one of the eight steps in the biosynthesis of haem, which is the functional group of haemoglobin, myoglobin and cytochromes, including the cytochrome P-450 family. The actual strategies for diagnosis and biochemical control of the five most common porphyrias are described.


Asunto(s)
Porfirias/diagnóstico , Enfermedad Aguda , Hemo/biosíntesis , Humanos , Porfirias/enzimología , Porfirias/genética , Porfirinas/biosíntesis , Enfermedades Raras
5.
Liver Transpl ; 13(5): 655-7, 2007 May.
Artículo en Inglés | MEDLINE | ID: mdl-17377916

RESUMEN

Erythropoietic protoporphyria (EPP) is a disease of the heme metabolism due to a deficiency of ferrochelatase, leading to accumulation of protoporphyrin (PPIX) in the erythrocyte (red blood cell [RBC]). The major clinical manifestation in EPP is photosensitivity; however, in a small number of patients liver failure is a significant complication and liver transplantation is the only treatment option. Damage to both abdominal skin and organs occurs when exposed to operating light; however, this problem can be ameliorated by the use of filters that block the transmission of light with wavelength below 470 nm. A more unusual but very serious complication postoperatively is severe motor neuropathy, with few or no known acute available precautions. An effective treatment option is needed to manage EPP crises and to prevent complications after liver transplantation. We successfully treated a patient with EPP-induced liver failure with the molecular adsorbents recirculating system (MARS) and Prometheus in independent sessions. Following treatment with MARS we found a 9.1% reduction of the RBC-PPIX concentration and a 5.9% reduction after treatment with the Prometheus system. Plasmapheresis made a reduction in RBC-PPIX concentration of 0.8%. Following treatment sessions with MARS and Prometheus, the clinical condition was markedly improved and orthotopic liver transplantation was performed without further complications. In conclusion, extracorporeal therapy with MARS or Prometheus seems to be efficient in reducing RBC-PPIX concentration in comparison to plasma exchange.


Asunto(s)
Trasplante de Hígado , Cuidados Preoperatorios , Protoporfiria Eritropoyética/terapia , Diálisis Renal , Adulto , Eritrocitos/metabolismo , Humanos , Fallo Hepático/etiología , Masculino , Concentración Osmolar , Trastornos por Fotosensibilidad/etiología , Plasmaféresis , Protoporfiria Eritropoyética/sangre , Protoporfiria Eritropoyética/complicaciones , Protoporfirinas/sangre , Albúmina Sérica , Resultado del Tratamiento
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