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Diagnostics of preeclampsia based on Congo red binding to urinary components: Rationales and limitations.
Fedotov, Sergei A; Khrabrova, Maria S; Vashukova, Elena S; Glotov, Andrey S; Anpilova, Anastasia O; Dobronravov, Vladimir A; Velizhanina, Maria E; Rubel, Aleksandr A.
Afiliação
  • Fedotov SA; Laboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.
  • Khrabrova MS; Laboratory of Toxinology and Molecular Systematics, L.A. Orbeli Institute of Physiology, National Academy of Sciences of the Republic of Armenia, Yerevan, Armenia.
  • Vashukova ES; Laboratory of Comparative Behavioral Genetics, Pavlov Institute of Physiology, Russian Academy of Sciences, St. Petersburg, Russia.
  • Glotov AS; Laboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.
  • Anpilova AO; Department of Propaedeutics of Internal disease, Pavlov University, St. Petersburg, Russia.
  • Dobronravov VA; Department of Genomic Medicine, D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology, St. Petersburg, Russia.
  • Velizhanina ME; Department of Genomic Medicine, D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology, St. Petersburg, Russia.
  • Rubel AA; Laboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.
PLoS One ; 19(1): e0297144, 2024.
Article em En | MEDLINE | ID: mdl-38241324
ABSTRACT
Preeclampsia is a disorder that can occur during pregnancy and is one of the leading causes of death among pregnant women. This disorder occurs after the 20th week of pregnancy and is characterized by arterial hypertension, proteinuria, fetoplacental, and multiple organ dysfunctions. Despite the long history of studying preeclampsia, its etiology and pathogenesis remain poorly understood, and therapy is symptomatic. One of the factors of the disorder is believed to be misfolded proteins that are prone to form amyloid aggregates. The CRD tests, utilizing the binding of the amyloid-specific dye Congo red to urine components, demonstrate high efficiency in diagnosing preeclampsia. However, these tests have also been found to be positive in other disorders with proteinuria, presumably associated with concomitant amyloidosis. To assess the limitations of the CRD tests, we examined urine congophilia and protein components mediating Congo red positivity in patients with proteinuria, including preeclampsia, amyloid and non-amyloid nephropathies. We stained the urine samples and calculated congophilia levels. We also assessed the contribution of large protein aggregates to congophilia values using ultracentrifugation and determined the molecular weights of congophilic urinary proteins using centrifugal concentrators. All proteinuric groups demonstrate positive results in the CRD tests and congophilia levels were more than two times higher compared with the control non-proteinuric groups (p <0.01). There was a strong correlation between urine protein excretion and congophilia in amyloid nephropathy (rs = 0.76), non-amyloid nephropathies (rs = 0.90), and preeclampsia (rs = 0.90). Removal of large aggregates from urine did not affect the congophilia levels. Separation of urine protein fractions revealed congophilic components in the range of 30-100 kDa, including monomeric serum albumin. Our results indicate limitations of CRD tests in preeclampsia diagnostics in women with renal disorders and underscore the need for further research on the mechanisms of Congo red binding with urine components.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / Amiloidose / Hipertensão Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / Amiloidose / Hipertensão Idioma: En Ano de publicação: 2024 Tipo de documento: Article