MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1016/j.lansea.2025.100571

Медицинская библиотека · The Lancet regional health. Southeast Asia · 2025

Evaluation of low-cost techniques to detect sickle cell disease and β-thalassemia: an open-label, international, multicentre study.

Shrestha Pranav, Lohse Hendrik, Bhatla Christopher, McCartney Heather, Alzaki Alaa, Sandhu Navdeep, Oli Pardip Kumar, Chaudhary Sanjeev, Amid Ali, Onell Rodrigo, Au Nicholas, Merkeley Hayley, Kapoor Videsh, Pande Rajan, Stoeber Boris

СтатьяПеревод в очереди

Аннотация

BACKGROUND

Sickle cell disease (SCD) persists as a major global health problem, disproportionately affecting children in low- and middle-income countries (LMIC). Accurate and low-cost point-of-care techniques are urgently needed in LMIC to detect carrier or disease forms with haemoglobin S (HbS) and other variants like β-thalassemia.

METHODS

An open-label, international, multicentre study was conducted at clinical sites in Nepal and Canada. Blood samples were collected from healthy volunteers (HbAA) and participants with known haemoglobinopathies (HbA/β-thalassemia, HbAS, HbS/β-thalassemia, HbSS). The performance of six low-cost tests (Conventional sickling test; HbS solubility test; HemoTypeSC; Sickle SCAN; Gazelle Hb variant test; Automated sickling test using automated microscopy and machine learning) was evaluated against HPLC (ClinicalTrials.gov Identifier: NCT05506358).

FINDINGS: Between September 2022 and March 2023, we enrolled 138 participants (aged 2-74 years; 59% female, 41% male) at clinical sites in Nepal and Canada. Four low-cost tests (HemoTypeSC, Sickle SCAN, Gazelle, and automated sickling), which could identify phenotypes, detected severe SCD (HbSS, HbS/β-thalassemia) accurately (sensitivity >96%; specificity >99%). In contrast, for carrier forms, HemotypeSC and Sickle SCAN only detected HbAS (sensitivity >97%; specificity 100%) and not HbA/β-thalassemia (sensitivity 0%; specificity 100%), while Gazelle detected HbAS (sensitivity 100%, specificity 100%) and HbA/β-thalassemia (sensitivity 91%, specificity 99%), and automated sickling test detected both trait conditions (HbAS and HbA/β-thalassemia; sensitivity 85%, specificity 85%).

INTERPRETATION: When HbS co-exists with β-thalassemia, Gazelle and automated sickling test accurately identify severe SCD and carrier forms. However, HemotypeSC and Sickle SCAN miss β-thalassemia trait, and need to be complemented with other low-cost tests.

FUNDING: UBCPSI, Canada Research Chairs, UBC HIFI Awards, UBC 4YF, Naiman Vickars Endowment fund.

Для цитирования: Shrestha Pranav, Lohse Hendrik, Bhatla Christopher, McCartney Heather, Alzaki Alaa, Sandhu Navdeep, Oli Pardip Kumar, Chaudhary Sanjeev, Amid Ali, Onell Rodrigo, Au Nicholas, Merkeley Hayley, Kapoor Videsh, Pande Rajan, Stoeber Boris. Evaluation of low-cost techniques to detect sickle cell disease and β-thalassemia: an open-label, international, multicentre study.. The Lancet regional health. Southeast Asia. 2025. DOI: 10.1016/j.lansea.2025.100571.
Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.