National Consultation on “Benefits and Safety of Iodised Salt”

 

 
 

 

 

 

 


Magnitude of IDD in India

 

 

        In India, Iodine Deficiency Disorders (IDD) are present throughout the country. Out of 275 districts surveyed by Government of India institutions, Indian Council of Medical Research and Central Goitre Survey Teams in different States and Union Territories, 235 have been found to be endemic for iodine deficiency disorders (Table I and II) (1, 2).

 

        Deficiency of iodine, which is among the body’s essential micronutrients, is both easy and inexpensive to prevent. Iodine is an essential element for normal growth and development in animals and humans. It is required for synthesis of the thyroid hormones i.e., thyroxine (T4) and tri-iodothyronine (T3).   Thyroid hormones bring about a wide variety of vital physiological processes such as early growth and develop-ment of the brain and body in man. Scientific studies in India and elsewhere have shown that nutritional iodine deficiency causes deficiency of thyroid hormones during foetal life and childhood.   A normal healthy thyroid gland of an adult human contains 8-12 mg iodine.  This can be reduced to as low as   1 mg or less in iodine deficient endemic areas (3).

 

        Iodine deficiency not only causes goitre; it can also result in impaired brain development in the fetus and infant, and retarded physical and psychomotor development in the child.  It also affects reproductive functions and impairs children’s learning ability.  The cumulative impact of nutritional iodine deficiency results in compromised socio- economic development in the affected communities. Iodine deficiency is the most common cause of preventable mental retardation in  the world today (4).

 

 

Use of Iodised Salt in Prevention of IDD

 

        In the last 50 years, many countries in North America, Asia, Europe and Oceania have successfully eliminated IDD, or made substantial progress in their control, largely as a result of salt iodisation with potassium iodide or potassium iodate and through dietary diversification.  For example, in Switzerland, where salt iodisation began in 1922, cretinism has been eliminated and goitre has disappeared, while there has been negligible evidence of any adverse effects from iodine intake (5, 6, 7, 8).  The status of salt iodisation, iodine compound used and level of iodine in salt in selected countries have been depicted in Table III.

 

        In India, keeping in view the magnitude of the problem and technical, administrative, financial and operational feasibility on the recommendations of  the Central Council of Health, Government of India in 1984, took a policy decision  for USI i.e. all edible salt in the  country would be fortified with iodine (1). 

 

        Substantial progress has been made in the country in the production of iodised salt from 3 Lakh MT in 1983 to nearly 40 Lakh MT in 1997. Similarly, recent IDD surveys conducted by the various institutions have revealed that more than 70% of population is consuming iodised salt (9). Concurrently, the total goitre prevalence and incidence of neonatal hypothy-roidism have also reduced (10). Further, estimation of urinary iodine excretion levels amongst population in different states indicate adequate iodine intake (10,11,12,13,). All these findings have been further substantiated by reports on  iodine content of salt samples analysed and received from differentstates through Monitoring Information System (MIS) of Salt Department and increase in production and supply of Iodised Salt (Table IV). These findings indicate successful implementation of USI programme in India (9). Recently, the scientific journal “Nature Medicine” has commended the Indian salt iodisation programme as one of the most successful preventive public health programme amongst the developing countries (14). 

 

 

Recommended Dietary Allowances of Iodine

 

        Iodine requirements have been calculated based on (a) average daily loss of iodine in the urine which is 100-200 mcg/day and (b) balance studies to attain a  positive balance which is 44-162 mcg/day (3). Based on scientific studies of iodine balance  over a 24 hour period, a safe daily intake of iodine has been estimated to be between a minimum of 50 mcg and a maximum of 1000 mcg (15, 16). A generally accepted desirable adult intake is 100-300 mcg/day. At all intake levels of iodine, a proportionate amount of iodine is excreted in the urine, which is the biochemical basis for assessing iodine status (17).

 

        The Recommended Dietary Allowances (RDA) for various age groups at global level are depicted in the Table VA and VB. The RDA for iodine as recommended by joint consultation of WHO/UNICEF/ICCIDD in 1996 has been given in Table VI (18). The RDA for iodine for Indian population is 150 mcg per day.

 

 

Iodine Toxicity

 

        Iodine has relatively wide margin of safety.  Acute andchronic toxicity studies with sodium iodate have been carried out.  Results of these long-term experiments of administration to man and to animal of doses comparable to those which are used in prophylaxis have failed to produce toxic signs (19). On the basis of toxicological studies it has been confirmed that potassium iodate is very safe  at the level used in salt iodisation (20). This has been confirmed  on the basis of worldwide experience of salt iodisation programme. 

 

 

Iodine intake in USA and Canada

 

        In the United States of America, potassium iodate is used as dough conditioner in bread making.  Under  Food and Drug Administration (FDA) Regulation No. 17, potassium iodate or potassium bromate, calcium iodate and/or calcium peroxide (21) are used in bakery products at a maximal concentration of 0.0075%, that is, 75 parts per million by weight of flour alone.  The FDA regulations (FDA : 121.101) also permit the addition of potassium iodide to table salt for fortification upto a maximum concentration of 0.01%.  As both bakery products and table salt are meant for human consumption, and the maximum permissible limits are 75 parts per million of potassium iodate and 100 parts per million of potassium iodide, it can be concluded that within these specified limits of the FDA, the salts are safe for human consumption (21).

 

        In 1970, the Food and Nutrition Board of the National Academy of Sciences, estimated that a daily intake of 1000 mcg of iodine is safe (22). In 1980 American Medical Association noted that no adverse physiologic reactions were observed with iodine intake up to 1000 mcg per day in healthy adults (23).

 

        Current estimates of daily iodine intakes in Canada and the USA are substantially above physiological need and are in the range of 460 mcg/day among 9-16 years old children, to greater than 1 mg/day among as many as 10-20% of adults (24).  With a level of iodisation that provides these populations approximately 250 mcg/day of iodine from salt, it is thus apparent that much of the intake comes from non salt sources (3). 

 

 

Iodine Intake in Japan    

 

        Average daily intake of iodine in Japan has been reported to be 3000 micrograms which is 20 times more than the RDA value of 150 mcg in  India. Studies carried out in normal Japanese population have shown that they are biochemically and clinically eumetabolic in spite of the consumption of large amounts of iodine.  The values for their thyroid hormone are not different from those in non-endemic areas of other countries indicating their adaptation to excess iodine intake (24, 25).  Existence of this type of adaptation has also been confirmed by animal experiments. There is little indication that iodine in the amounts noted influences the prevalence of any of the thyroid diseases (23).

 

 

Normal population and Iodised Salt

 

        The average daily salt intake in India is  10 g per day. Consumption levels are within the 5-15 g/day range for children and adults. As per Government of India recommendations the level of salt iodisation (quantity of iodine added to salt) should  provide a minimum of 150 mcg of iodine per day at the consumption level (26). This  recommendation  accounts for the usual climatic factors like heat and humidity, whichcan affect retention of iodine in the salt. The use of potassium iodate has  been preferred in India since it is more stable than potassium iodide under our tropical climatic conditions.  Moreover because iodate, on ingestion, is very rapidly reduced to iodide and hence its use in iodised salt is equivalent to  use of potassium iodide.

 

        From the average daily intake of 10 g iodine fortified salt, the estimated availability of iodine would be 150 mcg, of which about 30% is lost during cooking.  The remaining 105 mcg is ingested and from this about 70% is absorbed by the body.  This means approximately only 73.5 mcg is absorbed per day from iodine fortified salt.  This quantity when added to the iodine daily consumed through food will be broadly comparable to the daily physiological need of the body (3). Indeed urinary iodine excretion  studies in the post iodisation phase show that all over the country, the level achieved following salt iodisation is not more than 300 mcg per day. Thus, the level of salt iodisation is  totally safe  in our country.

 

 

Adverse Reactions to Iodised Salt Including Risk of Iodine Induced Hyperthyroidism

 

        Since iodine, when ingested in large amounts, is easily excreted in the urine, iodine intake even at very high levels (milligram amounts) can be safe. It is documented scientifically that through adaptive mechanisms, normal people exposed to excess iodine remain euthyroid and free of goitre.

 

        It is not correct to attribute skin reactions such as  rashes and acne to iodized salt. Physiological levels of iodine intake do not cause “Iodism”. For example, among 20,000 childrenin the USA suffering from allergy during the period 1935-1974, not a single case was reported of allergic hypersensitivity to iodine in food.  Following a publication, in Annals of Allergy, of a request for notification of allergy to iodine, not a single report was recorded between 1974 and 1980 (27).  However, high intakes of dietary iodine may induce hypothyroidism in autoimmune thyroid diseases and may inhibit the effects of thionamide drugs (28).

 

        Iodine-induced hyperthyroidism is an adverse effect which may occur primarily in older people  when severely iodine  deficient populations increase their iodine intake, even when the total amount is within the usually accepted range of 100-200 mcg/day. Epidemiologically  iodine-induced hyperthyroidism represents a transient increase in the incidence of hyperthyroidism, which disappears in due course with the correction of iodine deficiency (29).

 

        Iodine  induced hyperthyroidism occurs in some people who have pre-existing autonomous nodular goitre. It appears likely that some patient with latent Graves  disease are also at risk. The number of people at risk of iodine-induced hyperthyroidism is directly proportional to the number of subjects with nodular goitre. The occurrence of iodine-induced hyperthyroidism is probably related to the relative increase and rapidity of increase of iodine intake, which occurs when iodised salt is introduced in populations that have been severely iodine deficient. There is no level of iodine in salt that offers complete protection against some increase in the incidence of hyperthyroidism in a previously iodine-deficient population.  From a public health point of view, the benefits of correcting iodine deficiency through USI greatly outweigh the risk of iodine-induced hyperthyroidism (29).  A comparativeaccount of various levels of iodine intake to the functional status of the body as a dose response curve is depicted in figure 1.  From this a daily intake in the range of 150-300 g is absolutely safe (30).

 

 

Conclusion

 

        Daily iodine intake of upto 1 mg  i.e. 1000 mcg, appear to be entirely safe.  Iodization of salt at a level that assures an intake of 150-300 mcg/day keeps iodine intakes well within daily physiological needs for all populations, irrespective of their iodine status. In India, daily consumption of 10 g of salt containing 15 parts per million of iodine would add a maximum of only 150 mcg of iodine.  Thus, the likelihood of exceeding an iodine intake of 1 mg/day from iodized salt is remote.

 

        Issues relating to the safety of Universal Salt Iodization were carefully examined by eminent  Scientists, Programme Planners, Managers and Administrators for preparing national consensus document on Benefits and Safety  of Iodised Salt.  Based on hard scientific evidences and  data, it was concluded that USI is the most appropriate and safe public health measure for eliminating IDD in India.

 

 

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References

 

1)      Tiwari BK, Ray I, Malhotra RL. Policy Guidelines on National Iodine Deficiency Disorders Control Programme. Nutrition and IDD Cell. Directorate of Health Services. Ministry of Health and Family Welfare, Government of India, New Delhi, 1998; pp 1-22.

 

2)      ICMR Task Force Study : Epidemiological survey of endemic goiter and endemic cretinism.  Indian Council of Medical Research, New Delhi, 1989.

 

3)      Ranganathan S, Reddy V. Human Requirements of Iodine and safe Use of Iodised Salt. Indian Journal of Medical Research 1995; 102:227-232.

 

4)      Kochupillai N, Pandav CS, Godbole MM, Mehta M, Ahuja MMS. Iodine deficiency and neonatal hypothyroidism. Bull WHO 1986; 64:542-551.

 

5)      Sooch SS, Deo MG, Karmarkar MG, Kochupillai N, Ramachandran K, Ramalingaswami V. Preliminary reports of the experiment in the Kangra Valley for the prevention of Himalayan endemic goitre with iodated salt. Bull WHO 1965; 32:299-315.

 

6)      Sooch SS, Deo MG, Karmarkar MG, Kochupillai N, Ramachandran K, Ramalingaswami V. Prevention of endemic goitre with iodised salt. Bull WHO 1973; 49:307-312.

 

7)      Report of Joint WHO/UNICEF/ICCIDD consultation review of findings from seven country study in Africa on levels of Salt Iodisation in relation to IDD including iodineinduced hyperthyroidism. WHO/AFRO/NUT/97.2, WHO/NUT/97-5 1996 pp 1-29. 

 

8)      Iodine and health:eliminating IDD safely through salt    iodisation.  A statement by WHO, Geneva 1994, pp 1-7.

 

9)      Sundaresan S. Progress achieved in universal salt iodisation programme in India in : Proceeding of symposium on Elimination of IDD through Universal Access to Iodised Salt. Eds. Prakash R, Sunderesan S, Kapil Umesh, Shivansh Computers and Publications, New Delhi 1998, pp 28-42.

 

10)  Kochupillai N. Neonatal Hypothyrodism in India. The Mount Sinai J Medicine 1992;59: 111-115.

 

11)  Kapil U. Current Status of Iodine Deficiency Disorders  Control Programme, Indian Pediatrics 1998; 35:831-836.

 

12)  Sohal KS, Sharma TD, Kapil Umesh. Assessment of iodine deficiency disorders using the 30 cluster approach in the district Hamirpur.  Indian Pediatrics 1998; 65:1008-1011.

 

13)  Kapil Umesh, Sharma TD. Status of iodine deficiency in selected block of Kangra district, Himachal Pradesh.  Indian Pediatrics 1997; 34:338-340.

 

14)  Jayaraman KS.  Iodized salt campaign succeeds in India.  Nature Medicine 1993; 2:55.

 

15)  Evaluation  of certain food additives and contaminants. Thirty seventh report of joint FAO/WHO Expert Committee on Food Additives, Geneva, World Healthinduced hyperthyroidism. WHO/AFRO/NUT/97.2, WHO/NUT/97-5 1996 pp 1-29. 

 

16)  Iodine and health:eliminating IDD safely through salt    iodisation.  A statement by WHO, Geneva 1994, pp 1-7.

 

17)  Sundaresan S. Progress achieved in universal salt iodisation programme in India in : Proceeding of symposium on Elimination of IDD through Universal Access to Iodised Salt. Eds. Prakash R, Sunderesan S, Kapil Umesh, Shivansh Computers and Publications, New Delhi 1998, pp 28-42.

 

18)  Kochupillai N. Neonatal Hypothyrodism in India. The Mount Sinai J Medicine 1992;59: 111-115.

 

19)  Kapil U. Current Status of Iodine Deficiency Disorders  Control Programme, Indian Pediatrics 1998; 35:831-836.

 

20)  Sohal KS, Sharma TD, Kapil Umesh. Assessment of iodine deficiency disorders using the 30 cluster approach in the district Hamirpur.  Indian Pediatrics 1998; 65:1008-1011.

 

21)  Kapil Umesh, Sharma TD. Status of iodine deficiency in selected block of Kangra district, Himachal Pradesh.  Indian Pediatrics 1997; 34:338-340.

 

22)  Jayaraman KS.  Iodized salt campaign succeeds in India.  Nature Medicine 1993; 2:55.

 

23)  Evaluation  of certain food additives and contaminants. Thirty seventh report of joint FAO/WHO Expert Committee on Food Additives, Geneva, World Health24.Barsona CP. Environmental factors altering thyroid function  and their assessment. Environmental Health Perspectives 1981; 38:71-87.

 

24)  Nagataki S. The role of iodine in thyroid disease. In : Programme and Abstracts, Asia and Oceania Thyroid Association, Thyroid Meeting Seoul : Asia and Oceania Thyroid Association 1984, pp 38. 

 

25)  Pandav CS, Karmarkar MG, Kochupillai N. Recommended level of salt iodisation in India. Indian J Pediatr 1984; 51:53-54.

 

26)  Matovinovic J. Complications of goitre prophylaxis. In Endemic goitre and cretinism. Eds Stanbury JB, Hetzel BS, New York, Wiley Medical Publication 1980; 533-549.

 

27)  WHO. Trace elements in human nutrition and health. Prepared in collaboration with the Food and Agriculture Organization of the United Nations and the International Atomic Energy Agency.  WHO, Geneva, 1996, pp 49-68.

 

28)  Recommended iodine levels in salt and guidelines for monitoring  their adequacy and effectiveness, Nutrition Unit, Division of Food and Nutrition. Report of Joint consultation of WHO, UNICEF and ICCIDD. WHO Geneva 1996.

 

29)  Shivakumar B, Madhavan Nair K, Brahmam GNV, Mohanram M.  Control of iodine deficiency through safe use of iodised salt.  ICMR Bulletin 1996; 26:41-46.

 

30)  Barsona CP. Environmental factors altering thyroid function  and their assessment. Environmental Health Perspectives 1981; 38:71-87.

 

31)  Nagataki S. The role of iodine in thyroid disease. In : Programme and Abstracts, Asia and Oceania Thyroid Association, Thyroid Meeting Seoul : Asia and Oceania Thyroid Association 1984, pp 38. 

 

32)  Pandav CS, Karmarkar MG, Kochupillai N. Recommended level of salt iodisation in India. Indian J Pediatr 1984; 51:53-54.

 

33)  Matovinovic J. Complications of goitre prophylaxis. In Endemic goitre and cretinism. Eds Stanbury JB, Hetzel BS, New York, Wiley Medical Publication 1980; 533-549.

 

34)  WHO. Trace elements in human nutrition and health. Prepared in collaboration with the Food and Agriculture Organization of the United Nations and the International Atomic Energy Agency.  WHO, Geneva, 1996, pp 49-68.

 

35)  Recommended iodine levels in salt and guidelines for monitoring  their adequacy and effectiveness, Nutrition Unit, Division of Food and Nutrition. Report of Joint consultation of WHO, UNICEF and ICCIDD. WHO Geneva 1996.

 

36)  Shivakumar B, Madhavan Nair K, Brahmam GNV, Mohanram M.  Control of iodine deficiency through safe use of iodised salt.  ICMR Bulletin 1996; 26:41-46.

 

 

 

APPENDICES

 

Appendix I       

 

Selected Research Papers/ Studies Conducted  in India  on Magnitude of IDD, Health Consequences of Iodine Deficiency  and Impact of Use  of  Iodised  Salt in India.

 

 

*      Click to see details of the TABLES

 

*      Click to see details of the RESEARCH STUDY DATA

 

*      Click to see details of the RESEARCH STUDIES

 

 

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