Prevalence of hemoglobinopathies among Malayali tribes of Jawadhu hills, Tiruvannamalai district, Tamil Nadu, India: a community-based cross-sectional study

References

• Williams TN, Weatherall DJ. World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harb Perspect Med. 2012;2:a011692. doi:10.1101/cshperspect.a011692
   PubMed Web of Science ®Google Scholar
• Vachhani NA, Vekariya DJ, Colah RB, et al. Spectrum of β-thalassemia and other hemoglobinopathies in the Saurashtra Region of Gujarat, India: analysis of a large population screening program. Hemoglobin. 2022;46:285–289. doi:10.1080/03630269.2022.2142608
   PubMed Web of Science ®Google Scholar
• Warghade S, Britto J, Haryan R, et al. Prevalence of hemoglobin variants and hemoglobinopathies using cation-exchange high-performance liquid chromatography in central reference laboratory of India: a report of 65779 cases. J Lab Physicians. 2018;10:73–79. doi:10.4103/JLP.JLP_57_17
   PubMed Web of Science ®Google Scholar
• Colah R, Italia K, Gorakshakar A. Burden of thalassemia in India: the road map for control. Pediatr Hematol Oncol J. 2017;2:79–84. doi:10.1016/j.phoj.2017.10.002
   Google Scholar
• Verma IC, Saxena R, Kohli S. Past, present & future scenario of thalassaemic care & control in India. Indian J Med Res. 2011;134:507–521.
   PubMedGoogle Scholar
• Hariharan P, Gorivale M, Sawant P, et al. Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine. Sci Rep. 2021;11:20906. doi:10.1038/s41598-021-00169-x
   PubMed Web of Science ®Google Scholar
• Colah R, Mukherjee M, Ghosh K. Sickle cell disease in India. Curr Opin Hematol. 2014;21:215–223. doi:10.1097/MOH.0000000000000029
   PubMed Web of Science ®Google Scholar
• Serjeant GR, Serjeant BE, editors. Sickle cell disease. 3rd ed. Oxford: Oxford Univ Press; 2001.
   Google Scholar
• Sukumaran PK. Hemoglobinopathies in scheduled castes and tribes of India. Med Gen Ind. 1978;2:81–88.
   Google Scholar
• Kate SL, Mukherjee BN, Malhotra KC, et al. Red cell glucose-6-phosphate dehydrogenase deficiency and haemoglobin variants among ten endogamous groups of Maharshtra and West Bengal. Hum Genet. 1978;44:339–343. doi:10.1007/BF00394299
   PubMed Web of Science ®Google Scholar
• Negi RS. Ethnic component in the distribution of sickle cell trait in India. Bio-anthropological research in India. Calcutta: Anthropol Sur Ind. 1975: 83–85.
   Google Scholar
• Colaco S, Colah R, Nadkarni A. Significance of borderline HbA2 levels in β thalassemia carrier screening. Sci Rep. 2022;12:5414. doi:10.1038/s41598-022-09250-5
   PubMed Web of Science ®Google Scholar
• Colaco S, Nadkarni A. Borderline HbA2 levels: dilemma in diagnosis of beta-thalassemia carriers. Mutat Res Rev Mutat Res. 2021;788:108387. doi:10.1016/j.mrrev.2021.108387
   PubMed Web of Science ®Google Scholar
• Singh MP, Gupta RB, Yadav R, et al. Prevalence of α(+)-thalassemia in the scheduled tribe and scheduled caste populations of Damoh District in Madhya Pradesh, Central India. Hemoglobin. 2016;40:285–288. doi:10.3109/03630269.2016.1170031
   PubMed Web of Science ®Google Scholar
• Chourasia S, Kumar R, Singh MPSS, et al. High prevalence of anemia and inherited hemoglobin disorders in tribal populations of Madhya Pradesh State, India. Hemoglobin. 2020;44:391–396. doi:10.1080/03630269.2020.1848859
   PubMed Web of Science ®Google Scholar
• Census of India. (2011). (https://censusindia.gov.in/census.website/).
   Google Scholar
• Colah RB, Mukherjee MB, Martin S, et al. Sickle cell disease in tribal populations in India. Indian J Med Res. 2015;141:509–515. doi:10.4103/0971-5916.159492
   PubMed Web of Science ®Google Scholar
• Angastiniotis M, Lobitz S. Thalassemias: an overview. Int J Neonatal Screen. 2019;5:16. doi:10.3390/ijns5010016
   PubMed Web of Science ®Google Scholar
• Mohanty D, Colah RB, Gorakshakar AC, et al. Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study. J Community Genet. 2013;4:33–42. doi:10.1007/s12687-012-0114-0
   PubMedGoogle Scholar
• Ghosh K, Colah R, Manglani M, et al. Guidelines for screening, diagnosis and management of hemoglobinopathies. Indian J Hum Genet. 2014;20:101–119. doi:10.4103/0971-6866.142841
   PubMedGoogle Scholar
• Sinha S, Black ML, Agarwal S, et al. Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. Hugo J. 2009;3:51–62. doi:10.1007/s11568-010-9132-3
   PubMedGoogle Scholar
• Mohanty SS, Parihar S, Huda RK, et al. Prevalence of sickle cell anemia, β-thalassemia and glucose-6-phosphate dehydrogenase deficiency among the tribal population residing in the Aravali hills of Sirohi region of Rajasthan state. Clin Epidemiol Glob Health. 2022;13:100916. doi:10.1016/j.cegh.2021.100916
   Web of Science ®Google Scholar
• Ganesh B, Rajakumar T, Acharya SK, et al. Particularly vulnerable tribal groups of Tamil Nadu, India: a sociocultural anthropological review. Indian J Public Health. 2021;65:403–409. doi:10.4103/ijph.IJPH_2_21
   PubMed Web of Science ®Google Scholar
• Ganesh B, Rajakumar T, Acharya SK, et al. Sickle cell anemia/sickle cell disease and pregnancy outcomes among ethnic tribes in India: an integrative mini-review. J Matern Fetal Neonatal Med. 2022;35:4897–4904. doi:10.1080/14767058.2021.1872536
   PubMedGoogle Scholar
• Senthilkumar K, Gobalakrishnan C. Urbanization and social status among irular tribal women: a situation analysis in Dharmapuri district of Tamilnadu. SIPN. 2020;40:161–166.
   Google Scholar
• Vaidyanathan D, Sisubalan N, Ghouse Basha M. Survey of ethnomedicinal plants and folklore studies on malayali tribals of vellakadai village a part of shervaroy range in eastern ghats, Tamil nadu. Int J Recent Sci Res. 2014;5:1368–1380.
   Google Scholar
• Natarajan V, Anbazhagan M, Rajendran R. Studies on ethnomedicinal plants used by the Malayali tribe of Kalrayan hill, Tamil Nadu state. Res Plant Biol. 2012;2:15–21.
   Google Scholar
• Muruganandam S, Kadirvelmurugan V, Selvaraju A, et al. Ethnomedicinal plants used by the Malayali tribals in Jawadhu hills of Thiruvannamalai district, Tamil Nadu, India. J Nat Prod Plant Resour. 2014;4:55–60.
   Google Scholar
• Senthilkumar K, Aravindhan V, Rajendran A. Ethnobotanical survey of medicinal plants used by Malayali tribes in Yercaud hills of Eastern Ghats, India. J Nat Remedies. 2013;13:118–132.
   Google Scholar
• Nigam N, Kushwaha R, Yadav G, et al. A demographic prevalence of β thalassemia carrier and other hemoglobinopathies in adolescent of Tharu population. J Family Med Prim Care. 2020;9:4305–4310. doi:10.4103/jfmpc.jfmpc_879_20
   PubMedGoogle Scholar
• Kar R, Anand J, Kar SS, et al. Haematological screening and its correlation with sociodemographic profile among the indigenous communities in and around Puducherry. J Family Med Prim Care. 2023;12:1629–1635. doi:10.4103/jfmpc.jfmpc_2275_22
   PubMedGoogle Scholar
• Balgir RS. Dimensions of rural tribal health, nutritional status of Kondh tribe and tribal welfare in Orissa: a biotechnological approach. In Proceedings of the UGC Sponsored National Conference on Human Health and Nutrition: A Biotechnological Approach (Lead Lecture); 2004. p. 47–57.
   Google Scholar
• Basu S. Dimensions of tribal health in India. HPPS. 2000;23:61–70.
   Google Scholar
• Gopinath TT, Logaraj M, John KR. Assessment of nutritional status of children aged under five years in tribal population of Jawadhu hills in Tamil Nadu. Int J Community Med Public Heal. 2018;5:1041–1046. doi:10.18203/2394-6040.ijcmph20180758
   Google Scholar
• Dhanappa KB, Hussian KA, Alzoghaibi I, et al. Assessment of factors influencing oral health status and treatment needs among Malayali tribal population at Javadhu Hills, India. J Evol Med Dent Sci. 2014;3:5263–5272. doi:10.14260/jemds/2014/2585
   Google Scholar
• Kumar KS, Natarajan G. A study on utilisation of forest resources in Jawadhu Hills of Tiruvannamalai District. Int J Res Soc Sci. 2017;7:553–566.
   Google Scholar
• Varawalla NY, Old JM, Sarkar R, et al. The spectrum of beta-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis. Br J Haematol. 1991;78:242–247. doi:10.1111/j.1365-2141.1991.tb04423.x
   PubMed Web of Science ®Google Scholar
• Edison ES, Shaji RV, Devi SG, et al. Analysis of beta globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity. Clin Genet. 2008;73:331–337. doi:10.1111/j.1399-0004.2008.00973.x
   PubMed Web of Science ®Google Scholar
• Mistry S, Shah K, Patel J. Prevalence of sickle cell disease in tribal peoples of Valsad district region in Gujarat. India Trop J Path Micro. 2018;4:109–112. doi:10.17511/jopm.2018.i01.19
   Google Scholar
• Balgir RS. The spectrum of haemoglobin variants in two scheduled tribes of Sundargarh district in north-western orissa, India. Ann Hum Biol. 2005;32:560–573. doi:10.1080/03014460500228741
   PubMed Web of Science ®Google Scholar
• 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–LC22. doi:10.7860/JCDR/2016/22010.9002
   PubMed Web of Science ®Google Scholar
• Adamu AL, Crampin A, Kayuni N, et al. Prevalence and risk factors for anemia severity and type in Malawian men and women: urban and rural differences. Popul Health Metr. 2017;15:12. doi:10.1186/s12963-017-0128-2
   PubMed Web of Science ®Google Scholar
• Finkelstein JL, Herman HS, Guetterman HM, et al. Daily iron supplementation for prevention or treatment of iron deficiency anaemia in infants, children, and adolescents. Cochrane Database Syst Rev. 2018;2018:CD013227. doi:10.1002/14651858.CD013227
   Google Scholar
• WHO. Worldwide prevalence of anaemia 1993–2005: WHO global database on anaemia/Edited by Bruno de Benoist, Erin McLean, Ines Egli and Mary Cogswell 2005.
   Google Scholar
• Saravanakumar P, Muthusundari A, Saradha S. Prevalence of anemia among the tribal adolescent girls in Javvadu hills in Thiruvannamalai, Tamil Nadu. Int J Sci Res. 2017;6:25–27.
   Google Scholar