CLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.

BACKGROUND: Clinical laboratory reference intervals have not been established in many African countries, and non-local intervals are commonly used in clinical trials to screen and monitor adverse events (AEs) among African participants. Using laboratory reference intervals derived from other populat...

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Auteurs principaux: Karita, E, Ketter, N, Price, M, Kayitenkore, K, Kaleebu, P, Nanvubya, A, Anzala, O, Jaoko, W, Mutua, G, Ruzagira, E, Mulenga, J, Sanders, E, Mwangome, M, Allen, S, Bwanika, A, Bahemuka, U, Awuondo, K, Omosa, G, Farah, B, Amornkul, P, Birungi, J, Yates, S, Stoll-Johnson, L, Gilmour, J, Stevens, G, Shutes, E, Manigart, O, Hughes, P, Dally, L, Scott, J, Stevens, W, Fast, P, Kamali, A
Format: Journal article
Langue:English
Publié: Public Library of Science 2009
_version_ 1826281761301069824
author Karita, E
Ketter, N
Price, M
Kayitenkore, K
Kaleebu, P
Nanvubya, A
Anzala, O
Jaoko, W
Mutua, G
Ruzagira, E
Mulenga, J
Sanders, E
Mwangome, M
Allen, S
Bwanika, A
Bahemuka, U
Awuondo, K
Omosa, G
Farah, B
Amornkul, P
Birungi, J
Yates, S
Stoll-Johnson, L
Gilmour, J
Stevens, G
Shutes, E
Manigart, O
Hughes, P
Dally, L
Scott, J
Stevens, W
Fast, P
Kamali, A
author_facet Karita, E
Ketter, N
Price, M
Kayitenkore, K
Kaleebu, P
Nanvubya, A
Anzala, O
Jaoko, W
Mutua, G
Ruzagira, E
Mulenga, J
Sanders, E
Mwangome, M
Allen, S
Bwanika, A
Bahemuka, U
Awuondo, K
Omosa, G
Farah, B
Amornkul, P
Birungi, J
Yates, S
Stoll-Johnson, L
Gilmour, J
Stevens, G
Shutes, E
Manigart, O
Hughes, P
Dally, L
Scott, J
Stevens, W
Fast, P
Kamali, A
author_sort Karita, E
collection OXFORD
description BACKGROUND: Clinical laboratory reference intervals have not been established in many African countries, and non-local intervals are commonly used in clinical trials to screen and monitor adverse events (AEs) among African participants. Using laboratory reference intervals derived from other populations excludes potential trial volunteers in Africa and makes AE assessment challenging. The objective of this study was to establish clinical laboratory reference intervals for 25 hematology, immunology and biochemistry values among healthy African adults typical of those who might join a clinical trial. METHODS AND FINDINGS: Equal proportions of men and women were invited to participate in a cross sectional study at seven clinical centers (Kigali, Rwanda; Masaka and Entebbe, Uganda; two in Nairobi and one in Kilifi, Kenya; and Lusaka, Zambia). All laboratories used hematology, immunology and biochemistry analyzers validated by an independent clinical laboratory. Clinical and Laboratory Standards Institute guidelines were followed to create study consensus intervals. For comparison, AE grading criteria published by the U.S. National Institute of Allergy and Infectious Diseases Division of AIDS (DAIDS) and other U.S. reference intervals were used. 2,990 potential volunteers were screened, and 2,105 (1,083 men and 1,022 women) were included in the analysis. While some significant gender and regional differences were observed, creating consensus African study intervals from the complete data was possible for 18 of the 25 analytes. Compared to reference intervals from the U.S., we found lower hematocrit and hemoglobin levels, particularly among women, lower white blood cell and neutrophil counts, and lower amylase. Both genders had elevated eosinophil counts, immunoglobulin G, total and direct bilirubin, lactate dehydrogenase and creatine phosphokinase, the latter being more pronounced among women. When graded against U.S. -derived DAIDS AE grading criteria, we observed 774 (35.3%) volunteers with grade one or higher results; 314 (14.9%) had elevated total bilirubin, and 201 (9.6%) had low neutrophil counts. These otherwise healthy volunteers would be excluded or would require special exemption to participate in many clinical trials. CONCLUSIONS: To accelerate clinical trials in Africa, and to improve their scientific validity, locally appropriate reference ranges should be used. This study provides ranges that will inform inclusion criteria and evaluation of adverse events for studies in these regions of Africa.
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spelling oxford-uuid:80aca22d-70f9-4f6c-a9c7-b4e1ff8743542022-03-26T21:25:03ZCLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:80aca22d-70f9-4f6c-a9c7-b4e1ff874354EnglishSymplectic Elements at OxfordPublic Library of Science2009Karita, EKetter, NPrice, MKayitenkore, KKaleebu, PNanvubya, AAnzala, OJaoko, WMutua, GRuzagira, EMulenga, JSanders, EMwangome, MAllen, SBwanika, ABahemuka, UAwuondo, KOmosa, GFarah, BAmornkul, PBirungi, JYates, SStoll-Johnson, LGilmour, JStevens, GShutes, EManigart, OHughes, PDally, LScott, JStevens, WFast, PKamali, ABACKGROUND: Clinical laboratory reference intervals have not been established in many African countries, and non-local intervals are commonly used in clinical trials to screen and monitor adverse events (AEs) among African participants. Using laboratory reference intervals derived from other populations excludes potential trial volunteers in Africa and makes AE assessment challenging. The objective of this study was to establish clinical laboratory reference intervals for 25 hematology, immunology and biochemistry values among healthy African adults typical of those who might join a clinical trial. METHODS AND FINDINGS: Equal proportions of men and women were invited to participate in a cross sectional study at seven clinical centers (Kigali, Rwanda; Masaka and Entebbe, Uganda; two in Nairobi and one in Kilifi, Kenya; and Lusaka, Zambia). All laboratories used hematology, immunology and biochemistry analyzers validated by an independent clinical laboratory. Clinical and Laboratory Standards Institute guidelines were followed to create study consensus intervals. For comparison, AE grading criteria published by the U.S. National Institute of Allergy and Infectious Diseases Division of AIDS (DAIDS) and other U.S. reference intervals were used. 2,990 potential volunteers were screened, and 2,105 (1,083 men and 1,022 women) were included in the analysis. While some significant gender and regional differences were observed, creating consensus African study intervals from the complete data was possible for 18 of the 25 analytes. Compared to reference intervals from the U.S., we found lower hematocrit and hemoglobin levels, particularly among women, lower white blood cell and neutrophil counts, and lower amylase. Both genders had elevated eosinophil counts, immunoglobulin G, total and direct bilirubin, lactate dehydrogenase and creatine phosphokinase, the latter being more pronounced among women. When graded against U.S. -derived DAIDS AE grading criteria, we observed 774 (35.3%) volunteers with grade one or higher results; 314 (14.9%) had elevated total bilirubin, and 201 (9.6%) had low neutrophil counts. These otherwise healthy volunteers would be excluded or would require special exemption to participate in many clinical trials. CONCLUSIONS: To accelerate clinical trials in Africa, and to improve their scientific validity, locally appropriate reference ranges should be used. This study provides ranges that will inform inclusion criteria and evaluation of adverse events for studies in these regions of Africa.
spellingShingle Karita, E
Ketter, N
Price, M
Kayitenkore, K
Kaleebu, P
Nanvubya, A
Anzala, O
Jaoko, W
Mutua, G
Ruzagira, E
Mulenga, J
Sanders, E
Mwangome, M
Allen, S
Bwanika, A
Bahemuka, U
Awuondo, K
Omosa, G
Farah, B
Amornkul, P
Birungi, J
Yates, S
Stoll-Johnson, L
Gilmour, J
Stevens, G
Shutes, E
Manigart, O
Hughes, P
Dally, L
Scott, J
Stevens, W
Fast, P
Kamali, A
CLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.
title CLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.
title_full CLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.
title_fullStr CLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.
title_full_unstemmed CLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.
title_short CLSI-derived hematology and biochemistry reference intervals for healthy adults in eastern and southern Africa.
title_sort clsi derived hematology and biochemistry reference intervals for healthy adults in eastern and southern africa
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