Influence of hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency on diagnosis of diabetes by HbA1c among Tanzanian adults with and without HIV: A cross-sectional study

被引:11
作者
Kweka, Belinda [1 ]
Lyimo, Eric [1 ]
Jeremiah, Kidola [1 ]
Filteau, Suzanne [2 ]
Rehman, Andrea M. [2 ]
Friis, Henrik [3 ]
Manjurano, Alphaxard [1 ]
Faurholt-Jepsen, Daniel [4 ]
Krogh-Madsen, Rikke [5 ]
PrayGod, George [1 ]
Heimburger, Douglas C. [6 ,7 ]
机构
[1] Natl Inst Med Res, Mwanza Res Ctr, Mwanza, Tanzania
[2] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, London, England
[3] Univ Copenhagen, Dept Nutr Exercise & Sports, Copenhagen, Denmark
[4] Rigshosp, Dept Infect Dis, Copenhagen, Denmark
[5] Univ Copenhagen, Rigshosp, Ctr Phys Act Res, Copenhagen, Denmark
[6] Vanderbilt Univ, Med Ctr, Vanderbilt Inst Global Hlth, Nashville, TN USA
[7] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
基金
美国国家卫生研究院;
关键词
SICKLE-CELL TRAIT; ALPHA; ANEMIA;
D O I
10.1371/journal.pone.0244782
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction Hemoglobin A1c (HbA1c) is recommended for diagnosing and monitoring diabetes. However, in people with sickle cell disease (SCD), sickle cell trait (SCT), alpha-thalassemia or glucose-6-phosphate dehydrogenase (G6PD) deficiency, HbA1c may underestimate the prevalence of diabetes. There are no data on the extent of this problem in sub-Saharan Africa despite having high prevalence of these red blood cell disorders. Methods Blood samples from 431 adults in northwestern Tanzania, randomly selected from the prospective cohort study, Chronic Infections, Comorbidities and Diabetes in Africa (CICADA), were analysed for SCT/SCD, alpha-thalassemia and G6PD deficiency and tested for associations with the combined prevalence of prediabetes and diabetes (PD/DM) by HbA1c, using the HemoCue 501 HbA1c instrument, and by 2-hour oral glucose tolerance test (OGTT). Results The mean age of the participants was 40.5 (SD11.6) years; 61% were females and 71% were HIV-infected. Among 431 participants, 110 (25.5%) had SCT and none had SCD. Heterozygous alpha-thalassemia (heterozygous alpha+ AT) was present in 186 (43%) of the participants, while 52 participants (12%) had homozygous alpha-thalassemia (homozygous alpha+ AT). Furthermore, 40 (9.3%) participants, all females, had heterozygous G6PD deficiency while 24 (5.6%) males and 4 (0.9%) females had hemizygous and homozygous G6PD deficiency, respectively. In adjusted analysis, participants with SCT were 85% less likely to be diagnosed with PD/DM by HbA1c compared to those without SCT (OR = 0.15, 95% CI: 0.08, 0.26, P < 0.001). When using OGTT, in adjusted analysis, SCT was not associated with diagnosis of PD/DM while participants with homozygous alpha(+) AT and hemizygous G6PD deficiency were more likely to be diagnosed with PD/DM. Conclusions HbA1c underestimates the prevalence of PD/DM among Tanzanian adults with SCT. Further research using other HbA1c instruments is needed to optimize HbA1c use among populations with high prevalence of hemoglobinopathies or G6PD deficiency.
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相关论文
共 27 条
[1]  
Al-Fadhli SM, 2001, SAUDI MED J, V22, P686
[2]   High birth prevalence of sickle cell disease in Northwestern Tanzania [J].
Ambrose, Emmanuela E. ;
Makani, Julie ;
Chami, Neema ;
Masoza, Tulla ;
Kabyemera, Rogatus ;
Peck, Robert N. ;
Kamugisha, Erasmus ;
Manjurano, Alphaxard ;
Kayange, Neema ;
Smart, Luke R. .
PEDIATRIC BLOOD & CANCER, 2018, 65 (01)
[3]   Pattern of Hemolytic Anemia Among Egyptian Pediatric Emergency Department Patients [J].
Badr, Mai Saad Eldin Mahmoud ;
Afifi, Rasha Abdel-Raouf Abdel-Aziz .
PEDIATRIC EMERGENCY CARE, 2020, 36 (03) :153-157
[4]  
Begum A, 2016, Mymensingh Med J, V25, P721
[5]   The impact of sickle cell trait on glycated haemoglobin in diabetes mellitus [J].
Bleyer, A. J. ;
Vidya, S. ;
Sujata, L. ;
Russell, G. B. ;
Akinnifesi, D. ;
Hire, D. ;
Shihabi, Z. ;
Knovich, M. A. ;
Daeihagh, P. ;
Calles, J. ;
Freedman, B. I. .
DIABETIC MEDICINE, 2010, 27 (09) :1012-1016
[6]   Anemia in Clinical Practice-Definition and Classification: Does Hemoglobin Change With Aging? [J].
Cappellini, M. Domenica ;
Motta, Irene .
SEMINARS IN HEMATOLOGY, 2015, 52 (04) :261-269
[7]   High Risk of Severe Anaemia after Chlorproguanil-Dapsone plus Artesunate Antimalarial Treatment in Patients with G6PD (A-) Deficiency [J].
Fanello, Caterina I. ;
Karema, Corine ;
Avellino, Pamela ;
Bancone, Germana ;
Uwimana, Aline ;
Lee, Sue J. ;
d'Alessandro, Umberto ;
Modiano, David .
PLOS ONE, 2008, 3 (12)
[8]   Estimating wealth effects without expenditure data - Or tears: An application to educational enrollments in states of India [J].
Filmer, D ;
Pritchett, LH .
DEMOGRAPHY, 2001, 38 (01) :115-132
[9]   Diabetes prevalence by HbA1c and oral glucose tolerance test among HIV-infected and uninfected Tanzanian adults [J].
Jeremiah, Kidola ;
Filteau, Suzanne ;
Faurholt-Jepsen, Daniel ;
Kitilya, Brenda ;
Kavishe, Bazil B. ;
Krogh-Madsen, Rikke ;
Olsen, Mette F. ;
Changalucha, John ;
Rehman, Andrea M. ;
Range, Nyagosya ;
Kamwela, Jerome ;
Ramaiya, Kaushik ;
Andersen, Aase B. ;
Friis, Henrik ;
Heimburger, Douglas C. ;
PrayGod, George .
PLOS ONE, 2020, 15 (04)
[10]   Association of Sickle Cell Trait With Hemoglobin A1c in African Americans [J].
Lacy, Mary E. ;
Wellenius, Gregory A. ;
Sumner, Anne E. ;
Correa, Adolfo ;
Carnethon, Mercedes R. ;
Liem, Robert I. ;
Wilson, James G. ;
Sacks, David B. ;
Jacobs, David R., Jr. ;
Carson, April P. ;
Luo, Xi ;
Gjelsvik, Annie ;
Reiner, Alexander P. ;
Naik, Rakhi P. ;
Liu, Simin ;
Musani, Solomon K. ;
Eaton, Charles B. ;
Wu, Wen-Chih .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2017, 317 (05) :507-515