Low haemoglobin oxygen saturation (SpO2) predicts complications in children with sickle cell anaemia (SCA) in the North but there are few data from Africa, where the majority of the patients reside. We measured daytime and overnight SpO2 in children with SCA in routine follow-up clinic, and controls without symptoms of SCA, comparing rural (Kilifi, Kenya) and urban (Dar-es-Salaam, Tanzania) cohorts. Daytime SpO2 was lower in 65 Tanzanian children with SCA (TS; median 97 (IQR 94–100)%); p<0.0001) than in 113 Kenyan children with SCA (KS; 99 (98–100)%) and 20 Tanzanian controls (TC; 100 (98–100)%). Compared with 95 Kenyan children with SCA, in 54 Tanzanian children with SCA and 19 TC who returned for overnight oximetry, mean (KS 99.0 (96.7–99.8)%; TS 97.9 (95.4–99.3)%; TC 98.4 (97.5–99.1)%; p=0.01) and minimum nocturnal SpO2 (92 (86–95)%; 87 (78.5–91)%; 90 (83.5–93)% p=0.0001) were lower. The difference between children with SCA persisted after adjustment for haemoglobin (p=0.004). Urban Tanzanian children, with and without SCA, experience greater exposure to low daytime and night-time SpO2 compared with rural Kenyan children with SCA. Possible explanations include differences in the prevalence of obstructive sleep apnoea or asthma, alterations in the oxyhaemoglobin desaturation curve or cardiovascular compromise, for example, to shunting at atrial or pulmonary level secondary to increased pulmonary artery pressure. The fact that non-SCA siblings in the urban area are also affected suggests that environmental exposures, for example, air pollution, nutrition or physical exercise, may play a role. Further studies should determine aetiology and clinical relevance for the SCA phenotype in children resident in Africa.
- sickle cell
- haemoglobin oxygen saturation
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What is already known on this topic
Low daytime haemoglobin oxygen saturation is common in sickle cell anaemia, and may be exacerbated overnight by dips secondary to obstructive and central apnoea.
Low haemoglobin oxygen saturation appears to be associated with complications of sickle cell anaemia including central nervous system events.
Markers of severity of sickle cell anaemia, including abnormally high transcranial Doppler velocities and left ventricular hypertrophy, are associated with low haemoglobin oxygen saturation.
What this study adds
In sickle cell anaemia, compared with rural Kenyan children, urban Tanzanian children had low daytime and mean and minimum overnight haemoglobin oxygen saturation.
Sibling controls in Tanzania also had low daytime and mean and minimum overnight haemoglobin oxygen saturation, consistent with environmental factors in the aetiology.
Haemoglobin levels were similar in the Tanzanian and Kenyan children with sickle cell anaemia and the difference in haemoglobin oxygen saturation survived adjustment for haemoglobin.
Homozygous sickle cell anaemia (SCA) is one of the most common monogenetic conditions in the world, with more than 70% of sufferers living in sub-Saharan Africa. Approximately 98% of oxygen carried in the blood is transported by haemoglobin with the remainder dissolved in plasma. The dysfunctional haemoglobin and right-shifted oxyhaemoglobin dissociation curve in SCA affect haemoglobin oxygen saturation, which can be measured by pulse oximetry (SpO2). Children spend half their lives asleep; sleep is associated with a natural fall in SpO2 as minute ventilation falls. Daytime and night-time (episodic and continuous) desaturation is common in Western populations with SCA and predicts complications.
In a Jamaican study, rural SCA populations achieved higher physical and mental health scores, with fewer limitations in daily living activities and better quality of life.1 In non-SCA adults enrolled in the Sleep Heart health study, sleep-disordered breathing and nocturnal hypoxaemia correlated with short-term changes in particulate matter pollutant level.2 Even though the major burden of SCA remains in sub-Saharan Africa, where air quality in cities is often poor (http://www.unep.org/transport/pcfv/PDF/DART-OVERVIEWAIRPOLLUTION.pdf; http://www.unep.org/urban_environment/PDFs/EABAQ2008-ProgressregionKeziaMbwambo.pdf),3 few studies have compared childhood SpO2 in urban with rural paediatric SCA populations in the African setting, particularly with respect to sleep.
Overnight pulse oximetry with signal extraction technology (Masimo) provides an inexpensive and accessible method of recording nocturnal SpO2. The objective of this study was to characterise daytime and overnight SpO2 in African children with SCA and compare those living in rural and urban settings.
The study was approved by the Kenya National Ethical committee (SCC 688) and the Muhimbili University College of Health Sciences research committee (MU/RP/ AECNoI.XII/77). Children were recruited from confirmed HbSS, but otherwise unselected, cohorts of patients attending outpatient clinics in rural Kenya (Kilifi) in 20044 and urban Tanzania (Dar-es-Salaam) in 2009.5 In Tanzania, household controls without symptoms of SCA were also recruited.5 Blood samples and pulse oximetry were obtained >12 weeks post-transfusion, and >12 weeks following acute illness. Resting daytime and overnight recordings of SpO2 were recorded by pulse oximetry (Masimo Irvine, California, USA) using a 2 s averaging time continuously during sleep. The data were analysed using Download 2001 software (Stowood Scientific, UK). Any residual movement artefact was excluded manually. We examined the overnight data for mean SpO2, and percentage of time spent with SpO2<90%.
Data entry and analysis
Analyses were performed using the statistical software package SPSS V.21.0. χ2 was used to compare prevalence of symptoms of sleep-disordered breathing. Non-parametric statistics (median and IQR as descriptives; Kruskal–Wallis test for comparison between groups) are reported for non-normally distributed variables. A two-tailed p value of p<0.05 was considered to be significant. Scheffe's test was used for post hoc testing to compare means of the Kenyan and Tanzanian children with SCA and the controls.
The study included 113 Kenyan children with SCA (median age 6.4 years) consecutively recruited at Kilifi District Hospital in the first half of 2004 from a cohort of 124 (median age 6.3 years)4 and 65 (median age 7.3 years) recruited5 from a cohort of 263 potentially eligible Tanzanian children with SCA without stroke aged 3–16 years (median 10.1 years) seen in clinic from mid-March to mid-June 2009 (table 1; figure 1). The study was not offered to all potentially eligible Tanzanian children with SCA because of lack of equipment during the study period but there was no attempt to recruit children with specific symptoms, for example, respiratory or snoring. Additionally, 20 Tanzanian children without symptoms of SCA were assessed in 2009 (figure 1).5
Mean daytime SpO2 was significantly lower in the urban Tanzanian children with SCA compared with the rural Kenyan children with SCA, including after adjustment for haemoglobin and nutritional status, which varied between groups (p=0.01) (table 1).
Ninety-five Kenyan and 54 Tanzanian children with SCA and 19 Tanzanian controls returned for overnight oximetry (figure 1). Table 1 shows age, body mass index-z-scores, haemoglobin, and daytime and overnight oximetry measures in the three groups. There was no difference in the prevalence of snoring at least half the week in the children with SCA who attended for overnight pulse oximetry compared with those who did not in either the Kenyan or the Tanzanian SCA cohort (χ2 p=0.6 and 0.7, respectively). Overnight mean SpO2 was significantly lower in urban Tanzanian children with SCA compared with rural Kenyan children with SCA (table 1), including after adjustment for haemoglobin (p=0.004), and was similar to Tanzanian controls. Similarly, minimum SpO2 was lower in urban Tanzanian children with SCA than in rural Kenyan children with SCA (table 1).
Urban children with SCA in Tanzania experience greater exposure to intermittent and continuous nocturnal haemoglobin oxygen desaturation in comparison with rural Kenyan children with SCA despite similar haemoglobin levels and both living at sea level. This may indicate that these two otherwise similar East African coastal populations may follow a different clinical course of disease, perhaps related to genetic or environmental factors such as nutrition or pollution.3
The aetiology of the differences in haemoglobin oxygen saturation is not clear. The α-thalassaemia 3.7 deletion is associated with daytime and nocturnal SpO2 in the Tanzanian SCA population, but this is unlikely to explain the difference as the prevalence is very similar in the two SCA populations (Williams-TN, personal communication). Obstructive sleep apnoea is a possible explanation. The lack of difference in symptom prevalence and absence of overweight children in the samples provide no positive evidence and central apnoeas are also relatively common in SCA; investigation of their relative importance with polysomnography in this setting would require considerable funding. Asthma and previous acute chest syndrome might play a role, but are rare in African settings and were not diagnosed in our patients. A vascular effect of air pollution,6 for example, increased pulmonary artery pressures with right-to-left shunting, might be an explanation in the context; the prevalence of high tricuspid jet velocities is similar to studies in the North in Dar-es-Salaam7 but there are currently no data for Kilifi. There might also be differences in the oxyhaemoglobin dissociation curve, although both Kilifi and Dar-es-Salaam are at sea level and in fact, exposure to carbon monoxide in polluted air may ameliorate SCA,6 at least in part by shifting the curve, typically right shifted in SCA, to the left. Another possible explanation is that living in a rural environment provides an opportunity for greater time spent in the natural environment engaging in unstructured outdoor activities, shown to be associated with physical health benefits in children, while children in a rural environment may also be less exposed to pollutants than those living in rapidly developing cities such as Dar-es-Salaam.3
A limitation of this study is the potential for a recruitment bias, as families may prioritise an opportunity to participate in research if they are concerned about their children's health, and to return for overnight oximetry if concerned about their sleep. Although the majority of Kenyan clinic population was studied, for the larger Tanzanian population, a convenience sample of consecutive patients with SCA and household controls was recruited from clinic over a 3-month period. Tanzanian children participating were a little younger than the remainder seen in clinic, comparable with the Kenyan patients with SCA and mainly in the age group most vulnerable to sleep-disordered breathing. Confidence that this is a real difference between populations is increased by the differences in daytime SpO2 in the larger clinical samples. The majority of the Tanzanian children recruited returned for overnight pulse oximetry; those returning did not have more clinical evidence for sleep-disordered breathing than those who did not.
In summary, urban Tanzanian children, with and without SCA, experience greater exposure to low daytime and night-time SpO2 compared with rural Kenyan children with SCA. The aetiology of the desaturation is uncertain but differences in air quality might be a factor. The clinical relevance in an African setting requires further investigation.
VSL and TE contributed equally.
Contributors FJK, SEC, CRN and JM designed the study with VSL and TE. VSL undertook data collection in Dar-es-Salaam, Tanzania together with DS, SEC and JM. TE (nee Ajala-Agbo) undertook data collection in Kilifi, Kenya, together with AK. VSL, TE, SEC, FJK and CMH analysed the data. VSL and TE wrote the first draft of the paper which was edited by DS, AK, CRN, SEC, JM, FJK and CMH. All authors read and approved the final version for submission.
Funding VSL and TE were awarded Wellcome Trust student elective prizes to undertake this work. This work was also supported through funding from the following Wellcome Trust grants (SEC) project grant 080025; (JM) personal fellowship 072064; strategic awards 084538 and 095009.
Competing interests None declared.
Ethics approval Muhimbili University College of Health Sciences research committee (MU/RP/AECNoI.XII/77).
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement We are willing to share our unpublished data on request after appropriate consultation with the principal investigators and the Wellcome Trust.