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Year : 2021  |  Volume : 46  |  Issue : 4  |  Page : 715-718

Retained splenic function in an indian population with homozygous sickle cell disease may have important clinical significance

1 The Sickle Cell Trust, 14 Milverton Crescent, Kingston 6, Jamaica
2 Sir George Alleyne Chronic Disease Research Centre, The University of the West Indies, Cave Hill, Barbados

Date of Submission28-Dec-2020
Date of Acceptance26-Aug-2021
Date of Web Publication08-Dec-2021

Correspondence Address:
Prof. Graham Serjeant
The Sickle Cell Trust, 14 Milverton Crescent, Kingston 6
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijcm.IJCM_1054_20

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Background and Objectives: To determine whether the persistence of splenomegaly characteristic of the Asian haplotype of homozygous sickle cell (SS) disease is associated with continued splenic function, a comparison of patients from Odisha, India, and Jamaica. Materials and Methods: Indian patients were examined in a cross-sectional study and compared with the Jamaican Cohort Study from birth. Splenomegaly was assessed in both populations with standard methods. Splenic function was assessed in both by counts of pitted red blood cells determined by differential interference contrast microscopy in the same laboratory. Results: In Jamaica, the spleen became palpable in 55% of patients during the 1st year of life and the prevalence declined thereafter, whereas in Indian patients, the prevalence rose steeply after the age of 4 years. Raised pitted red cell counts, consistent with loss of splenic function, were common after 2 years in Jamaicans but did not increase in Indians until after the age of 5 years. Interpretation and Conclusions: The maximal risk of invasive pneumococcal infection in SS disease falls sharply after the age of 3 years, and persistence of splenic function in Odisha patients beyond this age may explain the apparent absence of pneumococcal septicemia in Indian patients and questions the role of pneumococcal prophylaxis.

Keywords: Asian haplotype, pitted red blood cells, sickle cell disease, splenic function, splenomegaly

How to cite this article:
Serjeant B, Hambleton I, Serjeant G. Retained splenic function in an indian population with homozygous sickle cell disease may have important clinical significance. Indian J Community Med 2021;46:715-8

How to cite this URL:
Serjeant B, Hambleton I, Serjeant G. Retained splenic function in an indian population with homozygous sickle cell disease may have important clinical significance. Indian J Community Med [serial online] 2021 [cited 2022 Jun 27];46:715-8. Available from: https://www.ijcm.org.in/text.asp?2021/46/4/715/331960

   Introduction Top

The spleen is central to much of the early pathology of homozygous sickle cell (SS) disease as the less pliable red cells compromise its normal functions. The declining fetal hemoglobin (HbF) in postnatal life is associated with increasing levels of sickle hemoglobin (HbS), increasing intravascular sickling, and a tendency to splenomegaly. The time course of splenomegaly differs between patients of African origin and those with the Asian haplotype of the disease. In Jamaican patients, the majority develop splenomegaly in the 1st year of life followed by a progressive age-related decline in frequency[1] whereas splenomegaly in patients with the Asian haplotype develops later and persists for longer.[2],[3] Splenic enlargement does not necessarily imply continuing function,[4],[5] but pitted red cells, which correlate with other indices of splenic function, such as Howell–Jolly bodies and technetium (99mTc) sulfur colloid scans,[6] provide an independent assessment of splenic function. Pitted red cell counts rose with compromised splenic function in Jamaican patients[7] and pitted red cell counts increased later in disease of the Asian haplotype in eastern Saudi Arabia.[8] Genetic factors known to inhibit sickling such as high levels of HbF[1] and alpha-thalassemia[9] are associated with persistence of splenomegaly in Jamaican patients and both are common in the Asian haplotype of SS disease. Since early loss of splenic function renders patients prone to overwhelming septicemia and to acute splenic sequestration (ASS), it becomes important to establish the pattern of splenomegaly in the Asian haplotype and whether this splenomegaly is associated with evidence of continuing splenic function.

   Materials and Methods Top

The Jamaican SS Cohort Study recruited 311 patients with SS disease from newborn screening of 100,000 consecutive nonoperative deliveries at the main Government Maternity Hospital (Victoria Jubilee) in Kingston, Jamaica, between June 1973 and December 1981.[10] Patients with SS disease were followed prospectively with regular clinical assessments including routine hematology, estimations of HbF, and measurement of spleen size, so the age at which the spleen first became palpable was recorded. Deaths and emigration led to attrition of patient numbers, so data were depicted in 5-year groups from the age of 10 years. Of the 311 SS patients recruited, pitted red cell counts were measured in 242 patients aged 0.1–8.3 years between November 1976 and November 1984, and in those with multiple counts, the last count was selected for analysis.

Indian patients attended the SS Clinic operated at the VSS Medical College Hospital, Burla, Sambalpur, Odisha state.[2] Patients were seen once during the study period (February 19–March 6, 1986) and so data are entirely cross sectional. Clinical examinations included spleen size (cm) measured in the axis of the spleen below the left costal margin in all patients by a single observer (GRS).

In both groups, venous blood was taken by “Vacutainer” into ethylenediaminetetraacetic acid and one drop placed in 0.5 ml 10% formal saline. Pitted red cells in Indian patients were counted by differential interference contrast microscopy (Nomarski optics) by a single individual (BES) and in Jamaican patients by the same individual or one other physician. Counts of 10% or more were considered abnormal. HbF was measured by alkali denaturation[11] in both groups in the Jamaican laboratory. Values for HbF were entirely cross sectional in Indian patients, but as multiple values were available in Jamaican patients, the presented values are the mean of steady-state values over the age of 5 years avoiding the rapid age-related change in SS disease before this age.[12]

Statistical methods

Clinical splenomegaly at any time (yes/no) was modeled using logistic regression adjusting for age at splenomegaly, then including two potential predictors: level of HbF (%) and country of residence.

   Results Top

The frequency of splenomegaly is summarized in [Table 1] and graphically in [Figure 1]. In the Jamaican Cohort Study, splenomegaly occurred in 55% in the 1st year of life and declined progressively thereafter. In Odisha patients, splenomegaly was first seen at the age of 3 years increasing at later ages and tending to decline in frequency after 20 years. Overall, splenomegaly was significantly more frequent in Jamaican compared to Indian patients (odds ratio: 4.0, 95% confidence interval [CI]: 1.2–13.2, P = 0.03), but this finding is difficult to interpret because of the different time courses of splenomegaly in the two populations. In both groups, the prevalence increased with each 1% increase in HbF level (odds ratio: 1.09, 95% CI: 1.02–1.18, P = 0.02).
Table 1: Splenomegaly expressed as incidence in Jamaicans and prevalence in Indians from Odisha

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Figure 1: Incidence of splenomegaly in jamaicans and prevalence in indian subjects from Odisha

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Pitted red cell counts in the two populations are compared in [Table 2] and graphically in [Figure 2]. For Jamaicans, pitted red cell counts were not elevated in the 1st year of life but increased progressively from the 2nd year and were elevated in the majority from the age of 4 years, whereas in Odisha patients, the first elevated counts occurred at the age of 5 years and increased at later ages.
Table 2: Pitted red blood cells in Jamaicans and Indians from Odisha

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Figure 2: Pitted red blood cells in jamaicans and indian subjects from Odisha

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   Discussion Top

Data from whole-genome sequencing suggest that the Asian haplotype of SS disease arose from a single occurrence of the HbS mutation approximately 7300 years ago.[13] This haplotype accounts for over 90% of the disease in the Indian subcontinent[14],[15] and for almost all the diseases in the Eastern Province of Saudi Arabia.[3],[14] It is associated with elevated HbF[8],[14],[16] and with alpha-thalassemia,[8],[15],[17],[18] both of which inhibit sickling.

The spleen acts like a filter in the bloodstream taking out damaged red blood cells and bacteria that gain access to the blood. In SS disease, the many damaged or abnormal red cells clog up this filter causing initially an enlargement and later a progressive splenic fibrosis. The behavior of the spleen, therefore, gives information on the degree of intravascular sickling and its early loss of function renders patients prone to overwhelming infections.[19],[20],[21],[22],[23]

Splenomegaly has different time courses in Jamaican and Indian patients. Most Jamaican patients develop splenomegaly in the 1st year of life with subsequent declining prevalence so that few patients have a palpable spleen after the age of 10 years. In Odisha patients, splenomegaly occurs later and lasts for longer, and data in other Indian areas,[24] although limited, are consistent with this. It is of interest that this pattern occurs occasionally in Jamaican patients with high HbF levels[1] or alpha-thalassemia,[9] both factors ameliorating sickling, and both characteristic of the Asian haplotype of SS disease. It seems reasonable to conclude that splenic enlargement occurs later and lasts longer in Odisha patients compared with Jamaicans and probably other patients with SS disease of African origin.

In hematologically normal people, HbF declines from the high levels at birth to mean levels below 1% by 1 year of age. In SS disease, this decline is slower and age related, so comparisons should be matched for age as closely as possible. HbF values in older children and adults in Gujarat[18] and Odisha,[2] in children in Akola,[25] and at the age of 1 year in Nagpur[24] are all significantly higher than for comparable age groups in Jamaica. The observed prevalence of alpha-thalassemia (heterozygous and homozygous combined) was 37% in Jamaica, 16% in Akola,[25] 16% in Nagpur,[24] and 53% in Odisha.[2] Of these two genetic factors associated with the Asian haplotype, the consistently elevated HbF levels seem a more likely candidate influencing splenic natural history than the variable prevalence of alpha-thalassemia.

Splenomegaly does not necessarily imply continued splenic function[4],[5] although low pitted red cell counts consistent with continuing splenic function were found in 17/24 (71%) patients with a mean age of 13.7 years in the Eastern Province of Saudi Arabia.[8] Over half of the Jamaican cohort had abnormal pitted red cell counts by the age of 5 years, but in Odisha patients, abnormal counts began in the 6th year and increased markedly after the age of 15 years.

The persistence of splenic function in Indian patients may have profound implications for clinical management. In SS disease of African origin, the early loss of splenic function renders patients prone to pneumococcal septicemia and ASS, so pneumococcal prophylaxis[26],[27] and parental education on early detection of ASS[28] are now routine in the clinical management. Since the risk of invasive pneumococcal disease falls sharply after the age of 3 years,[19],[20],[21],[22],[23] the persistence of splenic function beyond this age may confer protection against the pneumococcus. This may account for the apparent absence of pneumococcal septicemia in Indian SS disease either in the published literature or from discussions with pediatricians expert in the disease in India. ASS also dominates in the first 3 years of life in disease of African origin,[28] and there is a need to document the natural history of this complication in Indian patients.

Major strengths of the present study are that assessments of spleen size were performed by the same clinician GRS), the pitted red cell counts were performed by the same individual (BES), and that estimations of HbF were performed by the same techniques in the same laboratory. A weakness is the small number of Odisha patients before the age of 4 years, but it seems unlikely that younger patients would manifest earlier loss of splenic function. In view of the more severe disease reported from Central India,[25],[29] it could be argued that lessons from Odisha may not be representative of other areas of India.

   Conclusions Top

Compared to the predominantly Benin haplotype of Jamaica, the Asian haplotype of SS disease in Odisha, India, is associated with the later occurrence of splenomegaly and retention of splenic function beyond the high-risk period for invasive pneumococcal disease. This may account for the absence of this complication in Indian SS disease in the literature and casts doubt on the role of pneumococcal prophylaxis. The persistence of splenic function probably reflects the high HbF levels associated with this haplotype. It is unclear whether these observations may be extrapolated to the more severe disease in Central India. The significance of these observations on other splenic complications such as ASS and hypersplenism remains to be clarified.


The authors are indebted to the late professor BC Kar and the administration of the VSS Medical College Hospital, Burla, Sambalpur, Odisha state, for making this study possible.

Financial support and sponsorship

The Jamaican component of this work was funded by the British Medical Research Council (MRC) through its funding of the MRC Laboratories, University of the West Indies, Kingston, Jamaica. The Indian component was supported by the British Council, Kolkata.

Conflicts of interest

There are no conflicts of interest.

   References Top

Serjeant GR. Irreversibly sickled cells and splenomegaly in sickle-cell anaemia. Br J Haematol 1970;19:635-41.  Back to cited text no. 1
Kar BC, Satapathy RK, Kulozik AE, Kulozik M, Sirr S, Serjeant BE, et al. Sickle cell disease in Orissa State, India. Lancet 1986;2:1198-201.  Back to cited text no. 2
Padmos MA, Roberts GT, Sackey K, Kulozik A, Bail S, Morris JS, et al. Two different forms of homozygous sickle cell disease occur in Saudi Arabia. Br J Haematol 1991;79:93-8.  Back to cited text no. 3
Pearson HA, Spencer RP, Cornelius EA. Functional asplenia in sickle-cell anemia. N Engl J Med 1969;281:923-6.  Back to cited text no. 4
Pearson HA, McIntosh S, Ritchey AK, Lobel JS, Rooks Y, Johnston D. Developmental aspects of splenic function in sickle cell diseases. Blood 1979;53:358-65.  Back to cited text no. 5
Casper JT, Koethe S, Rodey GE, Thatcher LG. A new method for studying splenic reticuloendothelial dysfunction in sickle cell disease patients and its clinical application: A brief report. Blood 1976;47:183-8.  Back to cited text no. 6
Rogers DW, Serjeant BE, Serjeant GR. Early rise in the “pitted” red cell count as a guide to susceptibility to infection in childhood sickle cell anaemia. Arch Dis Child 1982;57:338-42.  Back to cited text no. 7
Al-Awamy B, Wilson WA, Pearson HA. Splenic function in sickle cell disease in the Eastern Province of Saudi Arabia. J Pediatr 1984;104:714-7.  Back to cited text no. 8
Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, et al. The interaction of alpha-thalassemia and homozygous sickle-cell disease. N Engl J Med 1982;306:1441-6.  Back to cited text no. 9
Serjeant GR, Serjeant BE, Forbes M, Hayes RJ, Higgs DR, Lehmann H. Haemoglobin gene frequencies in the Jamaican population: A study in 100,000 newborns. Br J Haematol 1986;64:253-62.  Back to cited text no. 10
Betke K, Marti HR, Schlicht I. Estimation of small percentages of foetal haemoglobin. Nature 1959;184(Suppl 24):1877-8.  Back to cited text no. 11
Mason KP, Grandison Y, Hayes RJ, Serjeant BE, Serjeant GR, Vaidya S, et al. Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: Relationship to parenteral Hb F levels. Br J Haematol 1982;52:455-63.  Back to cited text no. 12
Shriner D, Rotimi CN. Whole-genome-sequence-based haplotypes reveal single origin of the sickle allele during the holocene wet phase. Am J Hum Genet 2018;102:547-56.  Back to cited text no. 13
Kulozik AE, Wainscoat JS, Serjeant GR, Kar BC, Al-Awamy B, Essan GJ, et al. Geographical survey of beta S-globin gene haplotypes: Evidence for an independent Asian origin of the sickle-cell mutation. Am J Hum Genet 1986;39:239-44.  Back to cited text no. 14
Mukherjee MB, Surve RR, Gangakhedkar RR, Ghosh K, Colah RB, Mohanty D. Globin gene cluster haplotypes linked to the S gene in Western India. Hemoglobin 2004;28:157-61.  Back to cited text no. 15
Kulozik AE, Kar BC, Satapathy RK, Serjeant BE, Serjeant GR, Weatherall DJ. Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease. Blood 1987;69:1742-6.  Back to cited text no. 16
Kulozik AE, Kar BC, Serjeant GR, Serjeant BE, Weatherall DJ. The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. Blood 1988;71:467-72.  Back to cited text no. 17
Mukherjee MB, Surve R, Tamankar A, Gangakhedkar RR, Ghosh K, Lu CY, et al. The influence of - Thalassaemia on the haematological and clinical expression of sickle cell disease in western India. Ind J Med Res 1998;107:178-81.  Back to cited text no. 18
Rogers DW, Vaidya S, Serjeant GR. Early splenomegaly in homozygous sickle-cell disease: An indicator of susceptibility to infection. Lancet 1978;2:963-5.  Back to cited text no. 19
Zarkowsky HS, Gallagher D, Gill FM, Wang WC, Falletta JM, Lande WM, et al. Bacteremia in sickle hemoglobinopathies. J Pediatr 1986;109:579-85.  Back to cited text no. 20
Wong WY, Powars DR, Chan L, Hiti A, Johnson C, Overturf G. Polysaccharide encapsulated bacterial infection in sickle cell anemia: A thirty year epidemiologic experience. Am J Hematol 1992;39:176-82.  Back to cited text no. 21
Wong WY, Overturf GD, Powars DR. Infection caused by Streptococcus pneumoniae in children with sickle cell disease: Epidemiology, immunologic mechanisms, prophylaxis, and vaccination. Clin Infect Dis 1992;14:1124-36.  Back to cited text no. 22
Knight-Madden J, Serjeant GR. Invasive pneumococcal disease in homozygous sickle cell disease: Jamaican experience 1973-1997. J Pediatr 2001;138:65-70.  Back to cited text no. 23
Jain D, Tokalwar R, Upadhye D, Colah R, Serjeant GR. Homozygous sickle cell disease in Central India and Jamaica: A comparison of newborn cohorts. Indian J Med Res 2020;151:326-32.  Back to cited text no. 24
[PUBMED]  [Full text]  
Jain D, Warthe V, Dayama P, Sarate D, Colah R, Mehta P, et al. Sickle cell disease in central India: A potentially severe syndrome. Indian J Pediatr 2016;83:1071-6.  Back to cited text no. 25
John AB, Ramlal A, Jackson H, Maude GH, Sharma AW, Serjeant GR. Prevention of pneumococcal infection in children with homozygous sickle cell disease. Br Med J (Clin Res Ed) 1984;288:1567-70.  Back to cited text no. 26
Gaston MH, Verter JI, Woods G, Pegelow C, Kelleher J, Presbury G, et al. Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. N Engl J Med 1986;314:1593-9.  Back to cited text no. 27
Emond AM, Collis R, Darvill D, Higgs DR, Maude GH, Serjeant GR. Acute splenic sequestration in homozygous sickle cell disease: Natural history and management. J Pediatr 1985;107:201-6.  Back to cited text no. 28
Upadhye DS, Jain DL, Trivedi YL, Nadkarni AH, Ghosh K, Colah RB. Neonatal screening and the clinical outcome in children with sickle cell disease in Central India. PLoS One 2016;11:e0147081.  Back to cited text no. 29


  [Figure 1], [Figure 2]

  [Table 1], [Table 2]

This article has been cited by
1 Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassaemia and fetal haemoglobin in HbSS
Graham R Serjeant
Expert Review of Hematology. 2022;
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