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Comparison of haematology and biochemistry parameters in healthy South African infants with laboratory reference
B-M Schmidt1, M Tameris1, H Geldenhuys1
1South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine and Division of Immunology, Department of Pathology, University of Cape Town, Cape Town, South Africa.
Insights
Paediatric reference intervals for blood tests in South African infants often differ from established norms. Local data is crucial for accurate diagnosis and healthcare in developing nations.
Area of Science:
- Paediatric Haematology and Biochemistry
- Clinical Laboratory Science
- Global Health
Background:
- Paediatric laboratory reference intervals used in Africa and Asia are often based on Caucasian populations.
- These historical intervals may not accurately reflect the health status of infants in developing countries.
- There is a need to establish local reference intervals for accurate clinical interpretation.
Purpose of the Study:
- To compare haematology and biochemistry parameters in healthy South African infants with local laboratory reference intervals.
- To identify deviations from established national reference intervals.
- To highlight the importance of locally derived reference ranges.
Main Methods:
- A cross-sectional study of 634 HIV-unexposed infants (3-6 months old) in rural Western Cape, South Africa.
- Baseline haematology and biochemistry results were collected.
- Observed values were compared against South African National Health Laboratory Services (NHLS) reference intervals.
Main Results:
- Significant deviations were observed in platelet counts, mean corpuscular volume (MCV), and mean corpuscular haemoglobin (MCH).
- Abnormalities in haematocrit, alkaline phosphatase (ALP), alanine transaminase (ALT), and gamma-glutamyl transferase (GGT) were also noted.
- These deviations suggest potential subclinical conditions like hypochromic microcytic anaemia.
Conclusions:
- Healthy South African infants frequently show haematology and biochemistry parameters outside national reference intervals.
- Local derivation of paediatric laboratory reference intervals is essential for accurate diagnosis.
- Adopting local norms is critical as clinical trials increasingly occur in sub-Saharan Africa.
Objective:
Paediatric laboratory reference intervals used in Africa and Asia may be derived from historical intervals of predominantly Caucasian infants in Europe or North America. These intervals may therefore not be compatible with the range of normality for developing country populations. We aimed to compare haematology and biochemistry parameters in healthy South African infants with local laboratory reference intervals.
Methods:
We compared the baseline haematology and biochemistry results of 634 (316 male and 318 female) HIV-unexposed infants, aged 3-6 months, living in a rural area of the Western Cape Province, South Africa, against laboratory reference intervals supplied by the South African National Health Laboratory Services (NHLS). We calculated the percentage of observed values out of bound (in terms of lower and upper limits) compared to laboratory reference intervals.
Results:
Of the 634 healthy infants screened, 316 (49.84%) were male and 318 (50.16%) female. A majority (91.05%) had platelet counts above the laboratory reference interval upper limit (350 × 109 cells/l), while over half, 54.85% and 56.98% had mean corpuscular volume (MCV) and mean corpuscular haemoglobin (MCH) values below the lower limits of 77.0-105.0 fl and 26.0-34.0 pg, respectively. A small proportion were outside the reference limits for haematocrit, namely 15.71% below and 7.14% above the normal limits of 0.31-0.38 l/l. For male and female infants, 33.65% and 18.04% of alkaline phosphatase (ALP) values and 7.01% and 14.56% of alanine transaminase (ALT) values were above the upper limits, respectively. For male infants, 10.83% of gamma-glutamyl transferase (GGT) values, and for female infants, 31.11% of GGT values were below the lower limits of 12 U/l for males and 15 U/l for females. We observed no significant deviations (>10% out of bound) from NHLS reference intervals in the remaining haematology and biochemistry parameters measured.
Conclusions:
Haematology and biochemistry parameters in apparently healthy South African infants deviate frequently from national laboratory reference intervals, including abnormalities consistent with subclinical hypochromic microcytic anaemia. It is important that clinical laboratory reference intervals for children are derived locally, rather than being adopted from Caucasian norms in developed countries, because clinical trials of vaccines, drugs and diagnostics are increasingly conducted in sub-Saharan Africa.
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