Delayed puberty in girls with cystic fibrosis despite good clinical status

Pediatrics

Volumn 99, Issue 1, 1997, Pages 29-34

  Johannesson, Marie ^a   Gottlieb, Claes ^b   Hjelte, Lena ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b NONE

Author keywords

brain; cystic fibrosis; genotype; nutrition; puberty

Indexed keywords

ADULT; AGE; ARTICLE; CYSTIC FIBROSIS; DELAYED PUBERTY; DISEASE ASSOCIATION; FEMALE; GENETICS; GROWTH RATE; HUMAN; HYPOTHALAMUS HYPOPHYSIS GONAD SYSTEM; MAJOR CLINICAL STUDY; MALNUTRITION; MENARCHE; NUTRITIONAL STATUS; ORAL GLUCOSE TOLERANCE TEST; PRIORITY JOURNAL;

ADOLESCENT; AGE FACTORS; ARACHIDONIC ACID; BODY MASS INDEX; CHILD; CHROMOSOMES, HUMAN, PAIR 7; CYSTIC FIBROSIS; FEMALE; FOLLOW-UP STUDIES; GENOTYPE; HUMANS; MENARCHE; NUTRITIONAL STATUS; PHOSPHOLIPIDS; POINT MUTATION; PUBERTY, DELAYED; RETROSPECTIVE STUDIES;

EID: 0030909068     PISSN: 00314005     EISSN: None     Source Type: Journal    
DOI: 10.1542/peds.99.1.29     Document Type: Article

References (48)

1. Boat TF, Welsh MJ, Beaudet AL. Cystic fibrosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic Basis of Inherited Disease. 6th ed. New York, NY: McGraw-Hill; 1989:2649-2680
2. Dahl N, Grandell U, Martinsson T, et al. Frequency of four cystic fibrosis mutations in a Swedish population. Acta Paediatr. 1993;82:609
3. Rommens JM, Iannuzzi MC, Kerem B-S, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science. 1989;245: 1059-1065
4. Riordan JR, Rommens JM, Kerem B-S, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245:1066-1073
5. Kerem B-S, Rommens JM, Buchanan JA, et al. Identification of the cystic fibrosis gene: genetic analysis. Science. 1989;245:1073-1080
6. Welsh MJ, Smith AE. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell. 1993;73:1251-1254
7. Anderson MP, Gregory RJ, Thompson S, et al. Demonstration that CFTR is a chloride channel by alteration of its anion selectivity. Science. 1991;253:202-205
8. Jackson Stutts M, Canessa CM, Olsen JC, et al. CFTR as a cAMP-dependent regulator of sodium channels. Science. 1995;269:847-850
9. Al-Awqati Q. Regulation of ion channels by ABC transporters that secrete ATP. Science. 1995;269:805-806
10. Dodge JA. Nutritional requirements in cystic fibrosis: a review. J Pediatr Gastroenterol Nutr. 1988;7(suppl 1):S8-S11
11. Galabert C, Filliat M, Chazalette JP. Fatty acid composition of serum-lecithins in cystic fibrosis patients without steatorrea. Lancet. 1978;1:903
12. Rogiers V, Vercruysse A, Dab I, et al. Abnormal fatty acid pattern of the plasma cholesterol ester fraction in cystic fibrosis patients with and without pancreatic insufficiency. Eur J Pediatr. 1983;141:39-42
13. Strandvik B. Nutritional management of cystic fibrosis. Ann Nestlé. 1991;49:38-46
14. Finkelstein SM, Wielinski CL, Elliott GR, et al. Diabetes mellitus associated with cystic fibrosis. J Pediatr. 1988;112:373-377
15. Lanng S, Thorsteinsson B, Erichsen G, et al. Glucose tolerance in cystic fibrosis. Arch Dis Child. 1991;66:612-616
16. Roy CC, Weberg AM, Morin CL, et al. Hepatobiliary disease in cystic fibrosis: a survey of current issues and concepts. J Pediatr Gastroenterol Nutr. 1982;1:69-78
17. Scott-Jupp R, Lama M, Tanner MS. Prevalence of liver disease in cystic fibrosis. Arch Dis Child. 1991;66:698-701
18. Shwachman H, Kulczycki LL, Khaw K-T. Studies in cystic fibrosis: a report on sixty-five patients over 17 years of age. Pediatrics. 1965;36: 689-699
19. Mitchell-Heggs P, Mearns M, Batten JC. Cystic fibrosis in adolescent and adults. Q J Med. XLV. 1976;179:479-504
20. Stern RC, Boat TF, Doershuk CF, et al. Course of cystic fibrosis in 95 patients. J Pediatr. 1976;89:406-411
21. Frisch RE, Revelle R. Height and weight at menarche and a hypothesis of menarche. Arch Dis Child. 1971;46:695-701
22. Frisch R. Fatness of girls from menarche to age 18 years with a nomogram. Hum Biol. 1976;48:353-359
23. Kindstedt-Arfwidson K, Strandvik B. Food intake in patients with cystic fibrosis on an ordinary diet. Scand J Gastroenterol. 1988;123(suppl 143): 160-162
24. Corey M, McLaughlin FJ, Williams M, et al. A comparison of survival, growth and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol. 1988;41:583-591
25. Wood RE. Prognosis. In: Taussig LM, ed. Cystic Fibrosis. New York, NY: Thieme-Stratton; 1984:434
26. Kopito LE, Kosasky HJ, Shwachman H. Water and electrolytes in cervical mucus from patients with cystic fibrosis. Fertil Steril. 1973;24: 512-516
27. Tizzano EF, Silver MM, Chitayat D, et al. Differential cellular expression of cystic fibrosis transmembrane regulator in human reproductive tissues. Clues for the infertility in patients with cystic fibrosis. Am J Pathol. 1994;144:906-914
28. Mulberg AE, Resta LP, Wiedner EB, et al. Expression and localization of the cystic fibrosis transmembrane conductance regulator mRNA and its protein in rat brain. J Clin Invest. 1995;96:646-652
29. Ganong WF. Central regulation of visceral function and neural basis of instinctual behavior and emotions. In: Review of Medical Physiology. Norwalk, CT: Appleton & Lange; 1995:210-242
30. Gibson LE, Cooke RE. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis. Pediatrics. 1959;23:545-549
31. Lindgren G. Height, weight and menarche in Swedish urban school children in relation to socio-economic and regional factors. Ann Hum Biol. 1976;3:501-528
32. Karlberg P, Taranger J, Engström I, et al. The somatic development of children in a Swedish urban community. Acta Paediatr Scand. 1976; (suppl 258)
33. Tanner JM, Whitehouse RH, Takaishi M. Standards from birth to maturity for height, weight, height velocity and weight velocity: British children. Part I. Arch Dis Child. 1966;41:454-471
34. Keys A, Fidanza F, Karvonen MJ, et al. Indices of relative weight and obesity. J Chron Dis. 1972;25:329-343
35. Coates AL, Boyce P, Muller D, et al. The role of nutritional status, airway obstruction, hypoxia and abnormalities in serum lipid composition in limiting exercise tolerance in children with cystic fibrosis. Acta Paediatr Scand. 1989;69:353-358
36. Shwachman H, Kulczycki L. Long-term study of one hundred five patients with cystic fibrosis. Am J Dis Child. 1958;96:6-15
37. Quanjer PhH. Standardized lung function testing. Clin Respir Physiol. 1983;19(suppl 5)
38. Solymar L, Aronson P-H, Bake B, et al. Nitrogen single breath test, flow-volume curves and spirometry in healthy children, 7-18 years of age. Eur J Respir Dis. 1980;61:275-286
39. Damon A, Damon ST, Reed RB, et al. Age at menarche of mothers and daughters with a note on accuracy of recall. Hum Biol. 1969;41:161-175
40. Zacharias L, Rand WM, Wurtman RJ. A prospective study of sexual development and growth in American girls: the statistics of menarche. Obstet Gynecol Surv. 1976;31:325-337
41. Warren MP. The effects of exercise and pubertal progression and reproductive function in girls. J Clin Endocrinol Metab. 1980;51:1150-1157
42. Lindholm C, Hagenfeldt K, Ringerz B-M. Pubertal development in elite juvenile gymnasts. Acta Obstet Gynecol Scand. 1994;73:269-273
43. O'Rawe A, McIntosh I, Dodge JA, et al. Increased energy expenditure in cystic fibrosis is associated with specific mutations. Clin Sci. 1992;82: 71-76
44. Poretsky L, Kalin MF. The gonadotropic function of insulin. Endocr Rev. 1987;8:132-141
45. Reiter EO, Stern RC, Root AW. The reproductive endocrine system in cystic fibrosis. Am J Dis Child. 1981;135:422-426
46. Reiter EO, Stern RC, Root AW. The reproductive endocrine system in cystic fibrosis: 2. Changes in gonadotrophins and sex steroids following LHRH. Clin Endocrinol. 1982;16:127-137
47. Osler DC, Crawford JD. Examination of the hypothesis of a critical weight at menarche in ambulatory and bedridden mentally retarded girls. Pediatrics. 1973;51:675-679
48. Smith SS, Neuringer M, Ojeda SR. Essential fatty acid deficiency delays the onset of puberty in the female rat. Endocrinology. 1989;125:1650-1659