Lundgren E, Rastad J, Thrufjell E, Akerström G, Ljunghall S
Department of Surgery, University Hospital, Uppsala, Sweden.
Surgery. 1997 Mar;121(3):287-94. doi: 10.1016/s0039-6060(97)90357-3.
Population-based screenings for primary hyperparathyroidism have failed to systematically use intact parathyroid hormone (PTH) values for diagnosis, to explore prevalence and diagnostic criteria of normocalcemic hyperparathyroidism, and to attempt surgical verification of the disorder.
A total of 5202 women (ages, 55 to 75 years) attending a population-based mammography screening were investigated for primary hyperparathyroidism. In women lacking a family history of hypercalcemia, significant renal impairment, or low urinary calcium excretion hyperparathyroidism was diagnosed on the basis of predetermined criteria encompassing lower intact serum PTH levels in hypercalcemia (serum PTH 25 ng/L or greater; reference range, 12 to 55 ng/L) than in two intervals of normocalcemia (serum PTH 35 or greater, greater than 55 ng/L).
Prevalence of hyperparathyroidism was 2.1% (n = 109). At diagnosis total serum calcium and serum PTH levels were 2.32 to 3.19 mmol/L and 34 to 300 ng/L, respectively, and 66% of the women exhibited normocalcemia. Repeated examination showed persistent normocalcemia in 30 patients, and all but two of them had normal ionized plasma calcium levels. Significantly higher serum calcium, serum PTH, and urine calcium--but not serum creatinine--levels were found in patients with hyperparathyroidism compared with matched control subjects from the screened population. Within an ongoing stratified treatment program, 59 of 60 patients who underwent operation exhibited pathologic parathyroid tissue (mean weight, 591 mg).
Substantial prevalence of sporadic primary hyperparathyroidism is demonstrated in a risk group. Although criteria for hyperparathyroidism recognition included patients with truly mild biochemical derangement, operative findings suggested underdiagnosis of the disorder.
基于人群的原发性甲状旁腺功能亢进筛查未能系统地使用完整甲状旁腺激素(PTH)值进行诊断,未能探索正常血钙性甲状旁腺功能亢进的患病率和诊断标准,也未尝试对该疾病进行手术验证。
对参加基于人群的乳房X线筛查的5202名女性(年龄55至75岁)进行原发性甲状旁腺功能亢进调查。在没有高钙血症家族史、严重肾功能损害或低尿钙排泄的女性中,根据预定标准诊断甲状旁腺功能亢进,该标准包括高钙血症(血清PTH 25 ng/L或更高;参考范围12至55 ng/L)时的血清完整PTH水平低于两个正常血钙区间(血清PTH 35或更高,大于55 ng/L)。
甲状旁腺功能亢进的患病率为2.1%(n = 109)。诊断时,总血清钙和血清PTH水平分别为2.32至3.19 mmol/L和34至300 ng/L,66%的女性表现为正常血钙。重复检查显示30名患者持续正常血钙,除两人外,其余患者的离子化血浆钙水平均正常。与筛查人群中匹配的对照受试者相比,甲状旁腺功能亢进患者的血清钙、血清PTH和尿钙水平显著更高,但血清肌酐水平无显著差异。在正在进行的分层治疗方案中,60名接受手术的患者中有59名显示有甲状旁腺病理组织(平均重量591 mg)。
在一个风险组中证实了散发性原发性甲状旁腺功能亢进的相当高的患病率。尽管甲状旁腺功能亢进的识别标准包括了生化紊乱真正较轻的患者,但手术结果提示该疾病存在诊断不足的情况。