|Year : 2018 | Volume
| Issue : 4 | Page : 734-738
Prevalence of anemia among the women of childbearing age belonging to the tea garden community of Assam, India: A community-based study
Rita Panyang1, Anju Barhai Teli2, Sidhartha Protim Saikia3
1 Department of Paediatrics, Assam Medical College and Hospital, Dibrugarh, Assam, India
2 Department of Biochemistry, Jorhat Medical College and Hospital, Assam, India
3 Department of Microbiology, Assam Medical College and Hospital, Dibrugarh, Assam, India
|Date of Web Publication||4-Sep-2018|
Dr. Anju Barhai Teli
Department of Biochemistry, Jorhat Medical College and Hospital, Jorhat - 785 001, Assam
Source of Support: None, Conflict of Interest: None
Background: Anemia is a condition in which the number of red blood cells becomes insufficient to meet the body's physiologic needs. Anemia is one of the major public health problems in India. The aim of this study was to find the prevalence and determinants of anemia among the adult females of tea garden community of Assam. Materials and Methods: A community-based cross-sectional study was conducted among 770 numbers of adult females belonging to the tea garden community. For all the samples, complete blood count, abnormal hemoglobin variants screening by high-performance liquid chromatography (HPLC), serum iron level, total iron binding capacity (TIBC), and serum ferritin concentrations were determined. Results: Out of 770 patients, 19.7% were severely anemic. Hb S and β-thalassemia were the only hemoglobin types detected in the study. Hemoglobin type, mean corpuscular volume, TIBC, and serum ferritin level were the important determinants of anemia in the present study. Conclusion: To reduce the burden of anemia among the adult females of tea garden community, the females should be screened periodically, and appropriate measures should be taken.
Keywords: Cross-sectional study, high-performance liquid chromatography, prevalence, public health
|How to cite this article:|
Panyang R, Teli AB, Saikia SP. Prevalence of anemia among the women of childbearing age belonging to the tea garden community of Assam, India: A community-based study. J Family Med Prim Care 2018;7:734-8
|How to cite this URL:|
Panyang R, Teli AB, Saikia SP. Prevalence of anemia among the women of childbearing age belonging to the tea garden community of Assam, India: A community-based study. J Family Med Prim Care [serial online] 2018 [cited 2019 Aug 22];7:734-8. Available from: http://www.jfmpc.com/text.asp?2018/7/4/734/240406
| Introduction|| |
Anemia is a major health problem among the females of reproductive age in developing countries. The World Health Organization global estimates of anemia prevalence averaged 56%, with a range of 35%–75% depending on geographic location. In India, the prevalence of anemia is 52%. Assam also reflects a similar scenario of the national average in the prevalence of anemia. Previous studies conducted among tea garden workers of Assam show a high prevalence of anemia.,, As per SRS 2007–2009 data, Assam is having the highest maternal mortality (380) of which tea garden community constitute the most. Women of reproductive age are the most at risk for anemia. The data of National Family Health Survey-3 shows that anemia is particularly high 55.3% in all women (15–49 years). Therefore, it is important to assess anemia which is a risk for pregnancy-related complications, including greater risk for having a preterm delivery or low-birth-weight baby and also burdens the mother by increasing the risk of blood loss during labor and making it more difficult to fight infections.
The present study was carried out to get a clear idea of the different degree of anemia among the women of childbearing age of tea garden community of Assam and to find the role of different variables in the development of anemia.
| Materials and Methods|| |
This was cross-sectional study.
The study population included women of childbearing age (15–44 years) from 7 randomly selected tea gardens of Dibrugarh, Assam who consent to participate in the study and fulfilled the inclusion criteria.
The study was conducted during 2015–2016.
Considering 70% of women of childbearing age as anemic, with 3.5% margin of error and 95% confidence interval the required minimum sample size was 655. Taking 30% non-response rate and rounding up the sample size becomes 770.
- Women of childbearing age (15–44 years) belonging to the tea garden population of Assam.
- The individuals who did not give consent to participate in the study
- The individuals who have blood transfusion history in last 3 months.
Data collection technique and tools
For sample collection, health camps were organized in the respective tea gardens. Before the survey, information and objectives of the survey were circulated in the selected tea gardens. All the study participants were made aware about the study before the collection of samples. During sample collection, details about the age, gender, educational status, ethnic origin, class in which studying, the name of the head of the family, information about the residential address, etc., were recorded by the study team in a predesigned questionnaire. Qualified government medical practitioner (Allopathic) has supervised sanctity of data collection. The study has been approved by the Institutional Ethical Committee. Prior permission was obtained from the authorities of the respective tea gardens, and a written informed consent was obtained from all the participants before sample collection.
For the study of complete blood count, hemoglobinopathies, β-thalassemia (beta-thalassemia), serum ferritin, serum iron, and total iron binding capacity (TIBC) venous blood (3 ml) was collected from every participant in K3EDTA vials as well as in plain clot activator vials under aseptic condition. After collection, all the samples were transported to the laboratory in insulated packaging by maintaining refrigerated (+2°C to +8°C) condition with the help of gel packs. In the laboratory, serum was separated from the samples collected in clot activator vials by following standard laboratory procedure. A complete blood count of the individual blood samples was done in automated cell counter (SYSMEX XS-800i, Japan) using the standard procedure. For screening of β-thalassemia and hemoglobinopathies cation exchanger high-performance liquid chromatography (HPLC)-based D10 Hemoglobin Testing System (BioRad Laboratories, USA) was used. A calibrated Dimension ® RxL Max ® integrated chemistry system (Siemens Healthcare, Germany) was used to measure serum iron and TIBC concentrations. Transferrin saturation was calculated by dividing the serum iron level by total iron-binding capacity and multiplied by 100. Ferritin concentrations were determined by using IMMULITE ® 1000 Immunoassay system (chemiluminescence method) (Siemens Healthcare, Germany).
The data generated were computed and analyzed using SPSS 21 (IBM Corporation, U.S). The mean hemoglobin level across the study group, based on hemoglobin types, i.e., HbAA (normal hemoglobin), sickle cell homozygous (HbSS), HbAS (Sickle cell trait), β-thalassemia trait, β-thalassemia major was compared by analysis of variance. Multiple regression analysis was used to determine factors influencing hemoglobin level in a subset of women of childbearing age. The factors (independent variables), hemoglobin type, serum iron, TIBC, serum ferritin were entered, and the hemoglobin level (dependent variable) was entered as a continuous variable. We used “Enter” option for regression analysis.
| Results|| |
During the study, 770 individuals were screened. The mean (± standard deviation [SD]) age of the study individuals was 24.8 ± 7.3 years. The mean (± SD) hemoglobin level of the participants enrolled in the study was 9.6 ± 2.6 g/dl. Screening of the blood samples by cation exchanger HPLC-based D10 Hemoglobin Testing System (BioRad Laboratories, USA) indicates HbS was the widely prevalent variant hemoglobin in the present study. HbS and β-thalassemia were highly prevalent in the present study [Table 1]. Mean ± (SD) of Hb%, serum iron level, TIBC level, serum ferritin level, and mean corpuscular volume (MCV) levels are shown in [Table 1]. Within the studied population, 23.9% of samples had hemoglobinopathies and β-thalassemia. Severe anemia (Hb <8 g/dl) was observed in 8.4% of the study population. However, moderate (Hb 8–10.9 g/dl) anemia was detected in 91.6% of participants. Multiple regression analysis revealed that hemoglobin type, MCV, serum ferritin, and TIBC level were the important determinants of anemia among the tea garden community of Assam in the present study [Table 2]. The effect of various hemoglobin types on the levels of Hb is shown in [Figure 1]. In the present study, 7.9% of individuals had high levels of ferritin and 6.4% of individuals had low levels of ferritin. In the studied population, 31.8% of individuals were illiterate.
|Table 2: Determinants of hemoglobin level based on multiple linear regressionsa|
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|Figure 1: Box and Whisker plot showing hemoglobin level among the study population according to their hemoglobin type|
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| Discussion|| |
Anemia is a major public health problem in India. The present study revealed that anemia is one of the major health problems among the childbearing women of tea garden community of Assam. Among numerous factors, nutritional (such as vitamin and mineral deficiency) and nonnutritional (such as infections and hemoglobinopathies) factors contribute to the onset of anemia which leads to iron deficiency. Among the hemoglobin variants, sickle cell hemoglobin (HbS) is mostly confined to the tea garden communities of Assam., β-thalassemia is also prevalent in this community. In this study, 18.9% of the population were severely anemic. To classify anemia WHO cutoff had been applied.
One of the major findings of this study was the role of HbS and β-thalassemia as an important nonnutritional determinant of anemia among the study population. Earlier studies showed the prevalence of β-thalassemia in Assam.,
HbAA (normal hemoglobin) – In the present study, 76.1% of the participants were with normal hemoglobin variants. All the participants had moderate anemia. Some of the participants of this group had iron deficiency anemia. Lower serum ferritin level indicates iron deficiency as the main cause of anemia. There was wide variation in the range of serum ferritin values among this group varying from 4.2 to 350 ng/ml.
Anemia among the women with normal hemoglobin may be influenced by nutritional deficiencies. Another study done in adolescent girls living in slums of Ahmedabad shows a significant association between fathers occupation, the habit of tea consumption with food, the habit of green leafy vegetable consumption, and body mass index.
Nutritional anemia is one of the major public health problems in India affecting almost 70% of children and 56% among ever-married women. The ICMR study also revealed the high magnitude of undernutrition and infectious diseases among tea garden population of Assam.
HbS (sickle hemoglobin) – in this study, 2.7% of the population suffered from sickle cell homozygous (HbSS). All the participants of this group had severe anemia. An increase in ferritin levels combined with an increase in transferrin saturation usually is a sign of iron overload.,, Chronically transfused iron overloaded patients with sickle cell homozygous (HbSS) have significantly higher mortality than less transfused HbSS patients without iron overload, as well as age and race-matched normal controls., Normal ferritin concentrations vary by age and sex. Concentrations are high at birth, rise during the first 2 months of life, and then fall throughout later infancy. However, normal or elevated levels of serum ferritin do not indicate adequate iron stores necessarily, particularly in populations exposed to recurrent infections., Nearly 14.2% of the studied population had HbAS (Sickle cell trait). All of them had moderate anemia. Nearly 1.1% of the studied population had HbS/β-thalassemia (Sickle cell-beta thalassemia). All of them had moderate anemia.
β-thalassemia – β-thalassemia syndromes are the result of insufficient (β+) or absent (β0) production of β-globin chains. Their molecular causes are β-globin gene mutations. In this study, 3.2% of the population had β-thalassemia major and 2.4% had β-thalassemia trait. All of them had severe anemia. β-thalassemia major is hereditary hemolytic anemia which is treated with multiple blood transfusions. However, iron overload is a major complication suffered by β-thalassemia major patients due to multiple blood transfusions. Studies suggested that greater iron absorption and lower utilization in β-thalassemia major resulted in large increases in body iron that exceeds iron-binding capacity.,,
In India, 8.19% population distributed in different states has tribal population. The tribal population is vulnerable population, in terms of social development, isolating dwelling places in difficult terrain, rigid customs and beliefs, illiteracy, and separation from non-tribal population exposes them to many health and social issues. In this group of the population, anemia has a number of consequences which includes reducing in working capacity and impaired immunity., It has also a direct impact during pregnancy since 50% of anemic cases during pregnancy starts at the time of conception. This study indicated the importance to improve the iron status of this population and the need for planning intervention programs that would increase the health condition of these women.
Anemia is one of the most common nutritional deficiency disorders., The high prevalence of mild, moderate and severe anemia demands a due emphasis on iron and folic acid supplementation and health education on the consumption of iron-rich foods, to bring down the prevalence of anemia among the women of the reproductive age group of this particular population.
As the prevalence of anemia among this population was found higher than the national average more focused attention and better coverage is needed.
Limitation of the study
The sampling was done from the women of childbearing age from 15 to 44 years.
Future directions of the study
In this community-based study, we can further explore the other nutritional factors and infections that might be related to anemia.
| Conclusion|| |
This kind of the study shows the clear picture of the health of the general population. The present study indicates the need for a further comprehensive study to determine the role of hemoglobin type as an associating determinant of anemia in this part of India. The study also shows that before starting treatment all anemic patients should be properly investigated for the cause and type of anemia. Anemia is a major problem among the women of childbearing age belonging to the tea garden community. To overcome these problems, new innovative and cost-effective methods should be developed for the fortification of food of these populations. Awareness programs should be organized for these people about the fortification of food as well as the importance of iron for females.
Financial support and sponsorship
The study was funded by the Department of Biotechnology (DBT), Ministry of Science & Technology, Government of India
Conflicts of interest
There are no conflicts of interest.
| References|| |
Bentley ME, Griffiths PL. The burden of anemia among women in India. Eur J Clin Nutr 2003;57:52-60.
World Health Organization. The Prevalence of Anemia in Women: A Tabulation of Available Information, Tech. Rep. WHO/NUT/MCM/92.2. Geneva, Switzerland: World Health Organization; 1992.
Medhi GK, Hazarika NC, Shah B, Mahanta J. Study of health problems and nutritional status of tea garden population of Assam. Indian J Med Sci 2006;60:496-505.
] [Full text]
Saikia SP, Teli AB, Pathak K. Assessment of thyroid function among the individuals of tea garden community of Assam: A hospital based study. Int J Adv Res 2016;4:1443-7.
Deori R, Teli AB, Saikia SP. Prevalence of anaemia and role of haemoglobinopathy as an associating factor among the children belonging to the tea garden community of Assam, India. Int J Health Sci Res 2016;6:196-200.
McLean E, Cogswell M, Egli I, Wojdyla D, de Benoist B. Worldwide prevalence of anaemia, WHO vitamin and mineral nutrition information system, 1993-2005. Public Health Nutr 2009;12:444-54.
National Nutrition Monitoring Bureau, Diet and Nutritional Status of Rural Population and Prevalence of Hypertension Among Adults in Rural Areas, NNMB Technical Report No. 24, NNMB, NIN, Hyderabad; 2006.
Teli AB, Deori R, Saikia SP. Haemoglobinopathies and β-thalassaemia among the tribals working in the tea gardens of Assam, India. J Clin Diagn Res 2016;10:LC19-22.
Sharma D, Mathur R, Singh P. Iron metabolism: A review. Int J Comput Biol 1993;8:80-101.
McLean E, Egli I, de Benoist B, Wojdyla D. Kraemer K, Zimmermann MB, editors. Nutritional Anemia. Basel: Sight and Life Press; 2007. p. 1-12.
Balgir RS, Sharma SK. Distribution of sickle cell haemoglobin in India. Ind J Hemat 1988;6:1-14.
Batabyal JN, Wilson JM. Sickle cell anaemia in Assam. J Indian Med Assoc 1958;30:8-11.
World Health Organization. Haemoglobin Concentrations for the Diagnosis of Anaemia and Assessment of Severity. Vitamin and Mineral Nutrition Information System. Geneva: World Health Organization; 2011.
Teli AB, Deori R, Saikia SP, Pathak K, Panyang R, Rajkakati R, et al.
B-thalassaemia and its co-existence with haemoglobin E and haemoglobin S in upper Assam region of North Eastern India: A Hospital based study. J Clin Diagn Res 2016;10:GC01-4.
Baruah MK, Saikia M, Baruah A. Pattern of hemoglobinopathies and thalassemias in upper Assam region of North Eastern India: High performance liquid chromatography studies in 9000 patients. Indian J Pathol Microbiol 2014;57:236-43.
] [Full text]
Mondal NC, Biswas R, Manna A. Risk factors of diarrhoea among flood victims: A controlled epidemiological study. Indian J Public Health 2001;45:122-7.
Jayashree S, Naik RK. Iodine losses in iodised salt following different storage methods. Indian J Pediatr 2000;67:559-61.
Toteja GS, Singh P, Dhillon BS, Saxena BN, Ahmed FU, Singh RP, et al.
Prevalence of anemia among pregnant women and adolescent girls in 16 districts of India. Food Nutr Bull 2006;27:311-5.
Camaschella C. Understanding iron homeostasis through genetic analysis of hemochromatosis and related disorders. Blood 2005;106:3710-7.
Brissot P, Troadec MB, Bardou-Jacquet E, Le Lan C, Jouanolle AM, Deugnier Y, et al.
Current approach to hemochromatosis. Blood Rev 2008;22:195-210.
Camaschella C, Poggiali E. Towards explaining “unexplained hyperferritinemia”. Haematologica 2009;94:307-9.
Fung EB, Harmatz P, Milet M, Ballas SK, De Castro L, Hagar W, et al.
Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: A report from the multi-center study of Iron overload. Am J Hematol 2007;82:255-65.
Ballas SK. Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease. Semin Hematol 2001;38:30-6.
Domellöf M, Dewey KG, Lönnerdal B, Cohen RJ, Hernell O. The diagnostic criteria for iron deficiency in infants should be reevaluated. J Nutr 2002;132:3680-6.
Kohgo Y, Nishisato T, Kondo H, Tsushima N, Niitsu Y, Urushizaki I. Circulating transferrin receptor in human serum. Br J Haematol 1986;64:277-81.
Kohgo Y, Niitsu Y, Nishisato T, Kato J, Kondo H, Sasaki K, et al.
Quantitation and characterization of serum transferrin receptor in patients with anemias and polycythemias. Jpn J Med 1988;27:64-70.
Argyropoulou MI, Astrakas L. MRI evaluation of tissue iron burden in patients with beta-thalassaemia major. Pediatr Radiol 2007;37:1191-200.
Fiorelli G, Fargion S, Piperno A, Battafarano N, Cappellini MD. Iron metabolism in thalassemia intermedia. Haematologica 1990;75 Suppl 5:89-95.
Walter PB, Fung EB, Killilea DW, Jiang Q, Hudes M, Madden J, et al.
Oxidative stress and inflammation in iron-overloaded patients with beta-thalassaemia or sickle cell disease. Br J Haematol 2006;135:254-63.
Esposito BP, Breuer W, Sirankapracha P, Pootrakul P, Hershko C, Cabantchik ZI. Labile plasma iron in iron overload: Redox activity and susceptibility to chelation. Blood 2003;102:2670-7.
The Ministry of Tribal Affairs, Govt. of India, Introduction; Scheduled Tribes; Statistics, December 2011; Registrar General of India. Percentage of Scheduled Caste and Scheduled Tribe Population in District, Villages and UAs/Towns-India; Primary Census Abstract, Census of India; 2011.
Mahanta TG, Mahanta BN, Gogoi P, Dixit P, Joshi V, Ghosh S. Anaemia, its determinants and effect of different interventions amongst tea tribe adolescent girls living in Dibrugarh district of Assam. Indian J Comm Health 2014;26:300-9.
World Health Report, Reducing Risks, Promoting Healthy Life, Geneva, Switzerland: World Health Organization; 2002.
Bharati P, Som S, Chakrabarty S, Bharati S, Pal M. Prevalence of anemia and its determinants among nonpregnant and pregnant women in India. Asia Pac J Public Health 2008;20:347-59.
[Table 1], [Table 2]