Holm I A, Nelson A E, Robinson B G, Mason R S, Marsh D J, Cowell C T, Carpenter T O
Division of Endocrinology, Department of Medicine, Children's Hospital, Boston, Massachusetts 02115, USA.
J Clin Endocrinol Metab. 2001 Aug;86(8):3889-99. doi: 10.1210/jcem.86.8.7761.
PHEX is the gene defective in X-linked hypophosphatemic rickets. In this study, analysis of PHEX revealed mutations in 22 hypophosphatemic rickets patients, including 16 of 28 patients in whom all 22 PHEX exons were studied. In 13 patients, in whom no PHEX mutation had been previously detected in 17 exons, the remaining 5 PHEX exons were analyzed and mutations found in 6 patients. Twenty different mutations were identified, including 16 mutations predicted to truncate PHEX and 4 missense mutations. Phenotype analysis was performed on 31 hypophosphatemic rickets patients with PHEX mutations, including the 22 patients identified in this study, 9 patients previously identified, and affected family members. No correlation was found between the severity of disease and the type or location of the mutation. However, among patients with a family history of hypophosphatemic rickets, there was a trend toward more severe skeletal disease in patients with truncating mutations. Family members in more recent generations had a milder phenotype. Postpubertal males had a more severe dental phenotype. In conclusion, although identifying mutations in PHEX may have limited prognostic value, genetic testing may be useful for the early identification and treatment of affected individuals. Furthermore, this study suggests that other genes and environmental factors affect the severity of hypophosphatemic rickets.
PHEX是X连锁低磷血症性佝偻病中的缺陷基因。在本研究中,对PHEX的分析发现22例低磷血症性佝偻病患者存在突变,其中28例患者中有16例对所有22个PHEX外显子进行了研究。在13例之前对17个外显子未检测到PHEX突变的患者中,对其余5个PHEX外显子进行分析,发现6例患者存在突变。共鉴定出20种不同的突变,包括16种预计会截断PHEX的突变和4种错义突变。对31例携带PHEX突变的低磷血症性佝偻病患者进行了表型分析,包括本研究中鉴定出的22例患者、之前鉴定出的9例患者以及受影响的家庭成员。未发现疾病严重程度与突变类型或位置之间存在相关性。然而,在有低磷血症性佝偻病家族史的患者中,截断突变患者的骨骼疾病有更严重的趋势。较近几代的家庭成员表型较轻。青春期后男性的牙齿表型更严重。总之,虽然鉴定PHEX突变的预后价值可能有限,但基因检测可能有助于早期识别和治疗受影响个体。此外,本研究表明其他基因和环境因素会影响低磷血症性佝偻病的严重程度。