Skip to main content
Gut logoLink to Gut
. 1996 Aug;39(2):210–213. doi: 10.1136/gut.39.2.210

Lactose absorption in patients with glucose 6-phosphate dehydrogenase deficiency with and without favism.

T Meloni 1, C Colombo 1, A Ogana 1, M C Mannazzu 1, G F Meloni 1
PMCID: PMC1383300  PMID: 8991858

Abstract

BACKGROUND: It has recently been suggested that primary lactase deficiency might have been selected for by malaria, as has been previously shown to occur for thalasaemia and glucose 6-phosphate dehydrogenase (G6PD) deficiency. AIMS: To test this hypothesis, the prevalence of primary lactase deficiency in G6PD deficient subjects and in controls from the area of Sassari (Northern Sardinia) was determined, which in the past was characterised by an intermediate malarial endemicity. SUBJECTS: 70 adult subjects with G6PD deficiency, 34 of whom had a past history of favism, and 50 age matched control subjects. METHODS: The capacity to absorb lactose was assessed by measuring breath hydrogen production after oral administration of lactose (50 g) by a gas chromatographic method. RESULTS: Twenty per cent of G6PD deficient subjects with a positive history of favism and 22% of G6PD deficient subjects without a positive history of favism were lactose absorbers compared with 14% lactose absorbers in the control group. The differences were not statistically significant. CONCLUSIONS: These data show that the prevalence of primary lactase deficiency in the area of Sassari is relatively high, but comparable to that seen in the adult population from another area of southern Italy (Naples) where malaria was less endemic.

Full text

PDF
210

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anderson B., Vullo C. Did malaria select for primary adult lactase deficiency? Gut. 1994 Oct;35(10):1487–1489. doi: 10.1136/gut.35.10.1487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Battistuzzi G., Esan G. J., Fasuan F. A., Modiano G., Luzzatto L. Comparison of GdA and GdB activities in Nigerians. A study of the variation of the G6PD activity. Am J Hum Genet. 1977 Jan;29(1):31–36. [PMC free article] [PubMed] [Google Scholar]
  3. Burgio G. R., Flatz G., Barbera C., Patané R., Boner A., Cajozzo C., Flatz S. D. Prevalence of primary adult lactose malabsorption and awareness of milk intolerance in Italy. Am J Clin Nutr. 1984 Jan;39(1):100–104. doi: 10.1093/ajcn/39.1.100. [DOI] [PubMed] [Google Scholar]
  4. Das B. S., Das D. B., Satpathy R. N., Patnaik J. K., Bose T. K. Riboflavin deficiency and severity of malaria. Eur J Clin Nutr. 1988 Apr;42(4):277–283. [PubMed] [Google Scholar]
  5. Flatz G., Kühnau W., Naftali D. Breath hydrogen test for lactose absorption capacity: importance of timing of hydrogen excretion and of high fasting hydrogen concentration. Am J Clin Nutr. 1984 May;39(5):752–755. doi: 10.1093/ajcn/39.5.752. [DOI] [PubMed] [Google Scholar]
  6. Mareni C., Repetto L., Forteleoni G., Meloni T., Gaetani G. F. Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiency. J Med Genet. 1984 Aug;21(4):278–280. doi: 10.1136/jmg.21.4.278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Meloni T., Forteleoni G., Ena F., Meloni G. F. Glucose-6-phosphate dehydrogenase deficiency and bacterial infections in northern Sardinia. J Pediatr. 1991 Jun;118(6):909–911. doi: 10.1016/s0022-3476(05)82206-1. [DOI] [PubMed] [Google Scholar]
  8. Nagel R. L., Roth E. F., Jr Malaria and red cell genetic defects. Blood. 1989 Sep;74(4):1213–1221. [PubMed] [Google Scholar]
  9. Rinaldi E., Albini L., Costagliola C., De Rosa G., Auricchio G., De Vizia B., Auricchio S. High frequency of lactose absorbers among adults with idiopathic senile and presenile cataract in a population with a high prevalence of primary adult lactose malabsorption. Lancet. 1984 Feb 18;1(8373):355–357. doi: 10.1016/s0140-6736(84)90409-4. [DOI] [PubMed] [Google Scholar]
  10. Seddon H. R., Green A., Gray R. G., Leonard J. V., Pollitt R. J. Regional variations in medium-chain acyl-CoA dehydrogenase deficiency. Lancet. 1995 Jan 14;345(8942):135–136. doi: 10.1016/s0140-6736(95)90105-1. [DOI] [PubMed] [Google Scholar]
  11. Simoons F. J. The geographic hypothesis and lactose malabsorption. A weighing of the evidence. Am J Dig Dis. 1978 Nov;23(11):963–980. doi: 10.1007/BF01263095. [DOI] [PubMed] [Google Scholar]
  12. Spinelli D., Vota M. G., Formenti F., Accetta S., Careddu P., Roggero P., Imbriano A., Volpe C. Idiopathic presenile and senile cataract formation and changes in lactase activity. Fortschr Ophthalmol. 1987;84(6):666–668. [PubMed] [Google Scholar]
  13. Stamatoyannopoulos G., Fraser G. R., Motulsky A. C., Fessas P., Akrivakis A., Papayannopoulou T. On the familial predisposition to favism. Am J Hum Genet. 1966 May;18(3):253–263. [PMC free article] [PubMed] [Google Scholar]
  14. Zhang Y., König I., Schirmer R. H. Glutathione reductase-deficient erythrocytes as host cells of malarial parasites. Biochem Pharmacol. 1988 Mar 1;37(5):861–865. doi: 10.1016/0006-2952(88)90173-6. [DOI] [PubMed] [Google Scholar]

Articles from Gut are provided here courtesy of BMJ Publishing Group

RESOURCES