A prospective study on the natural course of primary hyperparathyroidism has recently been reported. Since hyperparathyroidism in multiple endocrine neoplasia type 1 (MEN 1) is genetically distinct from most forms of sporadic hyperparathyroidism, it is important to know the natural course of hyperparathyroidism in MEN 1 for better clinical management. For this purpose, we retrospectively reviewed clinical parameters of patients with MEN 1 when they were diagnosed as having hyperparathyroidism, and compared them with those of patients with sporadic primary hyperparathyroidism. In patients with MEN 1: 1) levels of intact PTH (i-PTH) gradually increased with age, which accelerated over 40 years; 2) compared to the steep rise in i-PTH levels in aged patients, increase in serum calcium or decrease of serum inorganic phosphate concentration was relatively mild, and 3) the high concentrations of i-PTH in aged patients were not due to renal insufficiency. These features were not observed in patients with sporadic primary parathyroid adenomas. Clinical features of untreated hyperparathyroidism in MEN 1 may be significantly affected by the age of the patient. The effect, if any, of age-dependent deterioration on recurrence rate after subtotal or total parathyroidectomy requires further elucidation.
Key words:
MEN1 Gene - Mutation - Parathyroid Hormone - Renal Function
References
-
1
Thakker R V.
Multiple endocrine neoplasia - syndromes of the twentieth century.
J Clin Endocrinol Metab .
1998;
83
2617-2620
-
2
van Heerden J A, Kent R B, Sizemore G W, Grant C S, ReMine W H.
Primary hyperparathyroidism in patients with multiple endocrine neoplasia syndromes.
Arch Surg.
1983;
118
533-536
-
3
Thompson N W.
The surgical management of hyperparathyroidism and endocrine disease of the pancreas in the multiple endocrine neoplasia type 1.
J Intern Med.
1995;
238
269-280
-
4
Rizzoli R, Green J III, Marx S J.
Primary hyperparathyroidism in familial multiple endocrine neoplasia type 1. Long-term follow-up of serum calcium levels after parathyroidectomy.
Am J Med.
1985;
78
467-474
-
5
Hellman P, Skogseid B, Öberg K, Juhlin C, Akerström G, Rastad J.
Primary and reoperative parathyroid operations in hyperparathyroidism of multiple endocrine neoplasia type 1.
Surgery.
1998;
124
993-999
-
6
Burgess J R, David R, Parameswaran V, Greenaway T M, Shepherd J J.
The outcome of subtotal parathyroidectomy for the treatment of hyperparathyroidism in multiple endocrine neoplasia type 1.
Arch Surg.
1998;
133
126-129
-
7
Chandrasekharappa S C, Guru S C, Manickam P, Olufemi S -E, Collins F S, Emmert-Buck M R, Debelenko L V, Zhuang Z, Lubensky I A, Liotta L A, Crabtree J S, Wang Y, Roe B A, Weisemann J, Boguski M S, Agarwal S K, Kester M B, Kim Y S, Heppner C, Dong Q, Spiegel A M, Burns AL and Marx S J.
Positional cloning of the gene for multiple endocrine neoplasia-type 1.
Science.
1997;
276
404-407
-
8
Silverberg S J, Shane E, Jacobs T P, Siris E, Bilezikian J P.
A 10-year prospective study of primary hyperparathyroidism with or without parathyroid surgery.
N Engl J Med.
1999;
341
1249-1255
-
9
Katai M, Sakurai A, Itakura Y, Ikeo Y, Nakajima K, Hara M, Iijima S, Kaneko T, Kobayashi M, Ichikawa K, Aizawa T, Hashizume K.
Multiple endocrine neoplasia type 1 is not rare in Japan.
Endocr J.
1997;
44
841-845
-
10
Sakurai A, Shirahama S, Fujimori M, Katai M, Itakura Y, Kobayashi S, Amano J, Fukushima Y, Hashizume K.
Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1.
J Hum Genet.
1998;
43
199-201
-
11
Orwoll E S, Meier D E.
Alterations in calcium, vitamin D, and parathyroid hormone physiology in normal men with aging: relationship to the development of senile osteopenia.
J Clin Endocrinol Metab.
1986;
63
1262-1269
-
12
Sherman S S, Hollis B W, Tobin J D.
Vitamin D status and related parameters in a healthy population: the effects of age, sex and season.
J Clin Endocrinol Metab.
1990;
71
405-413
-
13
Prince R L, Dick I, Devine A, Price R I, Gutteridge D H, Kerr D, Criddle A, Garcia-Webb P, St John A.
The effects of menopause and age on calcitropic hormones: a cross-sectional study of 655 healthy women aged 35 to 90.
J Bone Miner Res.
1995;
10
835-842
-
14
Bassett J HD, Forbes S A, Pannett A AJ, Lloyd S E, Christie P T, Wooding C, Harding B, Besser G M, Edwards C R, Monson J P, Sampson J, Wass J AH, Wheeler M H, Thakker R V.
Characterization of mutations in patients with multiple endocrine neoplasia type 1.<./TI>.
Am J Hum Genet.
1998;
62
232-244
-
15
Smogorzewski M, Tian J, Massry S G.
Down-regulation of PTH-PTHrP receptor of heart in CRF: role of [Ca2+]i.
Kidney Int.
1995;
47
1182-1186
-
16
Morieux Y J, Denne M A, Bouizar Z, Urena P, de Vernejoul M C.
Paridronate corrects the down-regulation of the renal parathyroid hormone (PTH)/PTH-related peptide (PTHrP) receptor mRNA in rats bearing Walker tumors.
Horm Metab Res.
1998;
30
249-255
-
17
Carling T, Rastad J, Ridefelt P, Gobl A, Hellman P, Öberg K, Rask L, Larsson C, Juhlin C, Åkerström G, Skogseid B.
Hyperparathyroidism of multiple endocrine neoplasia type 1: candidate gene and parathyroid calcium sensing protein expression.
Surgery.
1995;
118
924-931
-
18
D’Amour P, Palardy J, Bahsali G, Mallette L E, DeLéan A, Lepage R.
The modulation of circulating parathyroid hormone immunoheterogeneity in man by ionized calcium concentration.
J Clin Endocrinol Metab.
1992;
74
525-532
-
19
Heppner C, Kester M B, Agarwal S K, Debelenko L V, Emmert-Buck M R, Guru S C, Manickam P, Olufemi S -E, Skarulis M C, Doppman J L, Alexander R H, Kim Y S, Saggar S K, Lubensky I A, Zhuang Z, Liotta L A, Chandrasekharappa S C, Collins F S, Spiegel A M, Burns A L, Marx S J.
Somatic mutation of the MEN1 gene in parathyroid tumors.
Nat Genet.
1997;
16
375-378
-
20
Farnebo F, The B T, Kytyölä S, Svensson A, Phelan C, Sandelin K, Thompson N W, Höög A, Weber G, Farnebo L -O, Larsson C.
Alterations of the MEN1 gene in sporadic parathyroid tumors.
J Clin Endocrinol Metab.
1998;
83
2627-2630
-
21
Carling T, Correa P, Hessman O, Hedberg J, Skogseid B, Lindberg D, Rastad J, Westin G, Åkerström G.
Parathyroid MEN 1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism.
J Clin Endocrinol Metab.
1998;
83
2960-2963
-
22
Arnold A, Kim H G, Gaz R D, Eddy R L, Fukushima Y, Byers MG Shows T B, Kronenberg H M.
Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma.
J Clin Invest.
1989;
83
2034-2040
-
23
Cryns V, Yi S M, Tahara E, Gaz R D, Arnold A.
Frequent loss of chromosome arm 1p in parathyroid adenomas.
Genes Chromosome Cancer.
1995;
13
9-17
-
24
Tahara H, Smith A P, Gas R D, Cryns V L, Arnold A.
Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas.
Cancer Res.
1996;
56
599-605
-
25
Teh B T, Farnebo F, Kristoffersson U, Sundelin B, Cardinal J, Axelson R, Yap A, Epstein M, Heath H III, Cameron D, Larsson C.
Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.
J Clin Endocrinol Metab.
1996;
81
4204-4211
A. Sakurai, M.D., Ph.D.
Department of Aging Medicine and Geriatrics
Shinshu University School of Medicine
3-1-1 Asahi
Matsumoto, 390-8621
Japan
Phone: + 81 (263) 37-2686
Fax: + 81 (263) 37-2710
Email: bakabon@hsp.md.shinshu-u.ac.jp