Study of prevalence and clinical presentation of fibrocalculous pancreatic diabetes in and around Jabalpur (Madhya Pradesh), Central India

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Research Article Study of prevalence and clinical presentation of fibrocalculous pancreatic diabetes in and around Jabalpur (Madhya Pradesh), Central India Hakam Singh Patel, Sandeep Kumar Jain Department of Medicine, Sukh-Sagar Medical College and Hospital, Jabalpur, Madhya Pradesh, India. Correspondence to: Hakam Singh Patel, E-mail: hspatel.india@gmail.com Received May 16, 2016. Accepted May 31, 2016 Abstract Background: Fibrocalculous pancreatic diabetes (FCPD) is an uncommon form of diabetes secondary to nonalcoholic chronic calcific pancreatitis of uncertain etiology predominantly found in tropical regions of the world, characterized by abdominal pain and pancreatic calcification. The term Fibrocalculous Pancreatic Diabetes was introduced by the World Health Organization Report in 1985. Objective: To study prevalence and clinical presentation of FCPD in and around Jabalpur (Madhya Pradesh) Central India. Materials and Methods: A total of 891 cases of diabetes mellitus came from in and around Jabalpur and were presented at the OPD of Department of Medicine, Sukh-Sagar Medical College and Hospital between December 2014 and April 2016 and they were included in the study with informed consent. Subjects were put to detailed history, clinical, and laboratory workup including body mass index, blood sugar level (fasting, postprandial), HbA1c, USG, and plain X-ray abdomen and defined criteria were used for diagnosis of FCPD. Result: Of the total enrolled cases of 891, 94.05% of cases of T2DM, 5.61% of cases of T1DM, and only 0.34% of cases of FCPD were found. All 100% of cases of FCPD belonged to 35 45 years of age group, low socioeconomical status, and consumed high percentage of carbohydrates as a main source of diet. Abdominal pain was one of the main complaints found in all three of FCPD whereas two (66.6%) cases whose plain X-ray abdomen revealed pancreatic calcification were chronic alcoholic. When we investigated further, we found that all the three cases of FCPD had the highest basal, postprandial blood glucose levels, as well as poor glycemic control (HbA1c > 7), and mainly (66.6%) responded to insulin therapy. Conclusion: The prevalence rate of FCPD was found to be 0.34% in and around Jabalpur (Central India) that is lower than Southern India s prevalence rate, probably on account of the economic development, difference in dietary habits, and better levels of malnutrition. Even though the etiology remains unknown more studies need to be conducted to understand the exact nature of the pancreatic pathology in FCPD, what triggers it and if, and how, the process can be arrested, before the development of diabetes. KEY WORDS: Fibrocalculous pancreatic diabetes (FCPD), secondary diabetes, chronic pancreatitis, tropical chronic (calcific) pancreatitis Access this article online Website: http://www.ijmsph.com Quick Response Code: DOI: 10.5455/ijmsph.2016.16052016484 Introduction Fibrocalculous pancreatic diabetes (FCPD) is an uncommon form of diabetes secondary to nonalcoholic chronic calcific pancreatitis of uncertain etiology predominantly found in tropical regions of the world, characterized by abdominal pain and pancreatic calcification. In India, the frequency of FCPD is higher in the South than the North. Several terms International Journal of Medical Science and Public Health Online 2016. 2016 Patel HS. This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license. 2168 International Journal of Medical Science and Public Health 2016 Vol 5 Issue International 10 Journal of Medical Science and Public Health 2016 Vol 5 Issue 11 (Online First) 1

had been earlier proposed for this syndrome including tropical calcific pancreatitis, tropical chronic pancreatitis, tropical pancreatic diabetes, nutritional pancreatitis, endemic pancreatic syndrome, and so on. The term fibrocalculous pancreatic diabetes was introduced by the World Health Organization Report. [1] The term tropical chronic (calcific) pancreatitis (TCP) is used to describe the with this condition before the onset of diabetes. [2] The cardinal triad of FCPD is abdominal pain, pancreatic calculi, and diabetes. Patients with FCPD present with several distinct clinical features. Patients were invariably poor and presented with extreme emaciation, protein energy malnutrition, bilateral parotid enlargement, distension of the abdomen, and rarely, a cyanotic hue of the lips. Recently, there appeared to be a change in the clinical features of with FCPD because of improved nutritional status. Although the etiology of FCPD is still unclear, the role of micronutrient deficiency merits further study. The first report of pancreatic pathology leading to diabetes was published more than 200 years ago by Cawley [3] who described the presence of pancreatic calcification in a patient with diabetes. After that various reports from Indonesia (Zuidema), [4] tropical Africa (Nigeria, Uganda, Zambia), [5,6] South America (Brazil), [7] and Asia (Bangladesh and Sri Lanka, India) [8 11] have suggested that certain type of diabetes may originated from generalized damage to both exocrine portion of pancreas and islets of Langerhans, moreover that this may be a unique form of secondary or pancreatic diabetes in these tropical zone. Our present knowledge suggested that there is not only wide variation in incidence and presentation between European, North American, USA, and South African countries but also a difference in the incidence and presentation between South and North Indian states, which may be due to nutritional and environmental factors. Madhya Pradesh, being the central state of our country, had a variation in environmental and nutritional factors along with inhabitants of different race, cast, and religions. It was thus thought worthwhile to elucidate the incidence and clinical profile of FCPD. Materials and Methods This study was conducted in Department of Medicine, Sukh-Sagar Medical College and Hospital (SSMCH), Mukanwara Jabalpur (Madhya Pradesh, India). A total of 891 cases of diabetes mellitus who were from in and around Jabalpur and who attended the OPD of Department of Medicine, SSMCH between December 2014 and April 2016 took part in the study with informed consent. Subjects were put to detailed history, clinical, and laboratory workup including base metabolic index, blood sugar level (fasting, postprandial), HbA1c, USG abdomen, and plain X-ray Abdomen. The cases which were lost during follow-up or could not be fully investigated were excluded from the study. The standard criteria were used for diagnosis of FCPD. [12] Exocrine ( Tubeless tests) and endocrine (measurement of c-peptide) pancreatic function could not be assessed because of unavailability and high cost of tests. Statistical Analysis Statistical analysis was carried out using SPSS software, version 20.0 (SPSS, Inc., USA). The chi-squared test and independent sample t-test were used to compare categorical and continuous variables, respectively. Data were presented as mean ± standard deviation or proportion as appropriate. The p-value less than 0.05 was considered to be significant. Result The total number of with diabetes enrolled in the study was 891, of these 838 cases were of type 2 DM of which 478 were men and 360 were women, 50 cases were of type 1 DM of which 28 were men and 22 were women, and only 3 cases were of FCPD of which 2 were men and 1 a woman. Table 2 shows increase in FCPD in the third and fourth decade of life (p < 0.001). Two cases whose plain X-ray abdomen revealed pancreatic calcification were due to chronic alcoholism and whether calcification of pancreas was a result of chronic alcoholism or was due to some other factor could not be proved conclusively. Social and economic class of the subjects studied revealed that 100% of the with FCPD belonged to low social and economic status (total family income = Rs.1,001 to 2,000 per month), and 33.3% of the subjects with FCPD consumed 1,500 calories/day whereas 66.6% used to take 1,501 2,000 Table 1: Total diabetic attended OPD of Sukh-Sagar Medical College and Hospital Jabalpur Type of diabetes Male Female Total % of T2DM 478 360 838 94.05 T1DM 28 22 50 5.61 FCPD 2 1 3 0.34 Total 508 383 891 100 FCPD, fibrocalculous pancreatic diabetes; OPD; T1DM; T2DM. Table 2: The age of onset of diabetes mellitus (years) and prevalence of alcoholism in different groups Age (years) T2DM T1DM FCPD Less than 15 0 06 0 16 25 16 37 0 26 35 122 07 0 36 45 266 0 03 46 and above 434 0 0 History of alcoholism Moderate drinker 190 0 1 Abstainers 210 0 1 No information 438 50 1 FCPD, fibrocalculous pancreatic diabetes; T1DM; T2DM. 2 International Journal of Medical Science and Public Health 2016 Vol 5 Issue 11 (Online International First) Journal of Medical Science and Public Health 2016 Vol 5 Issue 10 2169

calories/day. Most of the subjects with FCPD consumed high percentage of carbohydrates and moderate to low quantities of fat and proteins as a source of caloric intake per day. p < 0.001 and p-values preferable suggest significance. In this study, we found that FCPD had the highest basal and postprandial blood glucose levels. Most of our series cases fell in uncontrolled group. In both the subjects with FCPD, HbA1c was found to be > 7%. p < 0.001 and p-values preferable suggest significance. Two of the FCPD cases were insulin dependent, although only one case responded to oral therapy. Discussion T2DM and T1DM are the two major entities of the diabetic syndrome. There are certain types of diabetes, which do not fit into either of these categories. In tropical countries, diabetes associated with malnutrition, such as J type diabetes and tropical pancreatic diabetes and FCPD have been described, and by this study, we were trying to know the prevalence and clinical presentation of FCPD in and around Jabalpur, Central India.Total enrolled cases were 891, of these 94.05% of the cases were of T2DM, 5.61% of the cases were of T1DM, and only 0.34% of the cases were of FCPD. All (100%) cases of FCPD belonged to 35 45 years of age group, low socioeconomical status, and consumed high percentage of carbohydrates as a main source of diet. Abdominal pain was one of the main complaints found in all three with FCPD. Although two (66.6%) cases whose plain X-ray abdomen revealed pancreatic calcification were chronic alcoholic, when we investigated further, we found that all the three cases of FCPD had the highest basal, postprandial blood glucose levels, as well as poor glycemic control (HbA1c > 7), and mainly 66.6% of them responded to insulin therapy. Age and Sex This study was conducted on the entire group with diabetes irrespective of age and sex and it was noticed that FCPD was found in the age group of 35 45 years and calcification was present in men whereas the solitary case of pseudopancreatic cyst was a woman, but no valid conclusion could be drawn. It is likely that condition is more common in men than in women as noted in some previous studies also. [4 6] Table 3: Economical status and caloric intake per day of of different groups Income in rupees (PM) T2DM T1DM FCPD Less than Rs.1,000 414 42 Rs.1,001 Rs.2,000 288 06 03 Rs.2,001 Rs.3,000 34 02 Rs.3,001 to above 42 Calories/day 1500 298 12 01 1501 2000 500 38 02 2001 2500 38 2500 and above 2 Carbohydrates 0 50% 78 08 51% 60% 740 39 60% 75% 20 03 03 Fat 0 20% 120 02 21% 30% 704 33 01 More than 30% 12 11 Proteins 0 10% 178 13 02 10 20% 636 37 01 More than 20% 24 FCPD, fibrocalculous pancreatic diabetes; PM; T1DM; T2DM. Table 4: Blood sugar level, glycemic control, and mode of therapy in of different groups Fasting blood sugar T2DM T1DM FCPD Less than 120 mg% 312 120 140 mg% 168 12 141 160 mg% 76 08 01 161 180 mg% 60 24 181 200 mg% 64 02 Above 200 mg% 158 04 02 Blood sugar (PP) Less than 150 mg% 86 151 200 mg% 230 201 240 mg% 194 26 01 241 280 mg% 108 281 320 mg% 92 14 231 mg% and above 128 10 02 HbA1C% Less than 7% 202 04 01 7% and above 636 46 02 Mode of therapy in of different groups Diet 296 01 OHA + Diet 480 Insulin 40 50 02 OHA + Insulin 22 FCPD, fibrocalculous pancreatic diabetes; HbA1C%; OHA; PP; T1DM; T2DM. 2170 International Journal of Medical Science and Public Health 2016 Vol 5 Issue International 10 Journal of Medical Science and Public Health 2016 Vol 5 Issue 11 (Online First) 3

Nutritional Factors The mean body mass index (BMI) was found to be normal in both men and women but the female cases of FCPD had low BMI when compared with same age and sex. So like other studies by Mohan et al. [12] and Sathiaraj et al., [14] our study also found that malnutrition is not the primary cause of FCPD, although it may well be a promoting factor. Prevalence of Alcoholism in Different Group of Diabetes Mellitus In our series of FCPD, two cases whose plain X-ray abdomen revealed pancreatic calculi were the ones who had chronic alcoholism and whether the calcification of pancreas was as result of chronic alcoholism or some other factor could not be proved conclusively. Howard [15] stated that pancreatic calculi were sequelae of alcoholic pancreatis. Alcoholism is also an important cause of chronic calcific pancreatitis in USA, South Africa, France, Australia, and some part of Europe. Geographic Variations In India, FCPD disease is most prevalent in the states of Kerala, Tamil Nadu, Telangana, Karnataka, and Orissa. Some correlation has been shown between the consumption of Cassava (Tapioca) and the occurrence of FCPD in Kerala (South India). [16] Although in our study, the disease is relatively rare (0.34%), and all were from central India where they do not eat Cassava; thus, the causative factor whether environmental or dietary cannot be ruled out. Blood Sugar Level In our study, we found that all the cases of FCPD had the highest basal, postprandial blood glucose levels, as well as poor glycemic control (HbA1c > 7).but the reason behind this cannot be found. Clinical Features Clinical features of the with FCPD in Kerala, Tamil Nadu, Western Countries, and present study have shown subtle differences in several ways. All of these differences are summarized in the form of Table 5. Mode of Management and Ketone Resistance It was our observation that with FCPD required large dose of insulin for stabilization of the diabetes. One of our was still on diet and oral hypoglycemic drug; however, none of them developed ketosis. Earlier studies to explain the ketosis resistance in MRDM has suggested a number of mechanisms such as low adipose tissue mass and delayed mobilization of free fatty acids from adipose tissue. [18,19] Recent studies have offered other explanations. In one study, it was shown that although the plasma glucagon levels in with IDDM rose after administration of oral glucose, in with malnutrition diabetes (PDDM variety) there was a paradoxical fall in the glucagon levels. [20] Thus, low glucagon levels were suggested as one of the mechanisms for the resistance to ketosis. Conclusion FCPD is a rare form of secondary diabetes that remains confined to tropical parts of Asia, Africa, and South America. The prevalence rate of FCPD was 0.34% in and around Jabalpur (Central India), which was lower than the prevalence rate found in Southern India, probably on account of economic development, difference in dietary habits, and better levels of malnutrition, even though the etiology remains unknown. Also, the management of diabetes in these remains challenging, in spite of the vast strides made in the treatment Table 5: Clinical presentations of FCPD in different studies Criteria Western countries [4 6] Kerala [10] Madras [17] Present study Age of cases > 30 years Most of > 30 90% 100% 100% Sex M:F 03:1 02:1 03:1 02:1 Nutritional status Good 90% Undernourished 80 % Undernourished 66% Undernourished Socioeconomical status Good Poor Poor Poor Abdominal pain 93% 70% 95% 90% 100% Steatorrhea 30% Not recorded Not recorded Not recorded Alcoholism 70% 90% 20% Not recorded 66% Pancreatic calcification 25% 35% 60% 95% 13% 66% Diabetes mellitus 11.8% 50% 90% 90% 100% Insulin requirement 10 50 unit/day 40 60 unit/day 60 100 unit/day > 60 unit/day FCPD, fibrocalculous pancreatic diabetes. 4 International Journal of Medical Science and Public Health 2016 Vol 5 Issue 11 (Online International First) Journal of Medical Science and Public Health 2016 Vol 5 Issue 10 2171

of hyperglycemia over the past few years. More studies need to be conducted to understand the exact nature of the pancreatic pathology in FCPD, what triggers it and if, and how, the process can be arrested, before the development of diabetes. References 1. WHO study group report on diabetes mellitus. WHO Technical Report series No.727. Geneva, Switzerland: WHO, 1985. 2. Mohan V, Premalatha G, Pitchumoni CS. Tropical chronic pancreatitis: an update. J Clin Gastroenterol 2003;36(4): 337 346. 3. Cawley T. A singular case of diabetes consisting entirely in the quality of urine, with an inquiry into the different theories of that disease. Lond Med J 1788;9:286 308. 4. Zuidema PJ. Cirrhosis and disseminated calcification of the pancreas in with malnutrition. Trop Geogr Med 1959;11(1):70 4. 5. Kinnear TWA. Patterns of diabetes in a Nigerian teaching hospital. W Afr Med J 1963;40:228 33. 6. Shaper AG. Chronic pancreatic disease and protein malnutrition. Lancet 1960;1(7136):1223 4. 7. Dani R, Penna FJ, Nogueria CED. Etiology of chronic pancreatitis in Brazil: a report of 329 consecutive cases. Int J Med 1976;1(5 6): 316 20. 8. Azad Khan AK, Banik NG, Mahatab H. Malnutrition related diabetes mellitus in Bangladesh. In: Diabetes 1991, Rifkin H, Colwell JA, Taylor SI (Eds.). Amsterdam: Excerpta Medica, 1991. pp. 944 9. 9. Illangasekara U. Malnutrition related diabetes in Sri Lanka: fact or fiction? J Ceylon College Physicians 1995;28:16 225. 10. Geevarghese PJ. Pancreatic Diabetes. Bombay, India: Popular Prakashan, 1968. pp. 110 105. 11. Mohan V. Fibrocalculous pancreatic diabetes (FCPD) in India. Int J Diab Dev Countries 1993;13:14 21. 12. Mohan V, Mohan R, Susheela L, Snehalatha C, Bharani G, Mahajan VK, et al. Tropical pancreatic diabetes in South India: heterogeneity in clinical and biochemical profile. Diabetologia 1985;28(4):229 32. 13. Pitchumoni CS, Geevarghese PJ. Familial pancreatitis and diabetes mellitus. In: Proceedings of the World Congress on Diabetes in the Tropics, Patel JC, Talwalkar NG, (Eds.). Bombay, India: Diabetic Association of India, 1966. p. 240. 14. Sathiaraj E, Gupta S, Chutke M, Mahurkar S, Mansard MJ, Rao GV, et al. (2010) Malnutrition is not an etiological factor in the development of tropical pancreatitis a case-control study of southern Indian. Trop Gastroenterol 2010;31(3):169 74. 15. Howard JM. Pancreatic calcification (Chapter 16). page 203 In: Surgical Diseases of the Pancreas, Howard JM, Jordan GL, Jr (Eds.). London, UK: Pittman Med Publishing, 1960. p. 203. 16. McMillan DE, Geevarghese PJ. Dietary cyanide and tropical malnutrition diabetes. Diabetes Care 1979;2(2):202 8. 17. Unnikrishnan R, Mohan V. Fibrocalculous pancreatic diabetes. Acta Diabetol 2015;52(1):1 9. 18. Hagroo AA, Verma NPS, Datta P, Ajmani NK, Vaishnava H. Observations on lipolysis in ketosis resistant growth onset diabetes. Diabetes 1974;23(4):268 75. 19. Ahuja MMS, Viswanathan K. Differential mobilization of nonesterified fatty acids and insulin reserve in various types of diabetes mellitus in India. Ind J Med Res 1967;55(8):870 83. 20. Rao RH, Vigg BL, Rao KSJ. Suppressible glucagon secretion in young ketosis resistant, type J diabetic in India. Diabetes 1983;32(12):1168 71. How to cite this article: Patel HS, Jain SK. Study of prevalence and How clinical to cite this presentation article: Patel of fibrocalculous HS, Jain SK. pancreatic Study of prevalence diabetes in and and clinical around presentation Jabalpur of (Madhya fibrocalculous Pradesh), pancreatic Central diabetes India. Int in J and Med around Sci Public Jabalpur Health (Madhya 2016;5 Pradesh), (Online Central First). India. DOI: Int 10.5455/ J Med ijmsph.2016.16052016484 Sci Public Health 2016;5:2168-2172 Source of Support: Nil, Conflict of Interest: None declared. 2172 International Journal of Medical Science and Public Health 2016 Vol 5 Issue International 10 Journal of Medical Science and Public Health 2016 Vol 5 Issue 11 (Online First) 5