Ro Kyung M, Cantor Rita M, Lange Kenneth L, Ahn Samuel S
University of California at Davis School of Medicine, Los Angeles, USA.
J Vasc Surg. 2002 Feb;35(2):382-6. doi: 10.1067/mva.2002.119507.
Primary palmar hyperhidrosis is a condition marked by excessive perspiration and is reported to have an incidence of 1% in the Western population. It is a potentially disabling disorder that interferes with social, psychological, and professional activities. Over the past several years, several investigators have reported a positive family history in their patients treated for hyperhidrosis. To date, the cause is unknown; furthermore, epidemiologic data are scarce and inadequate.
To characterize the genetic contribution to hyperhidrosis, we conducted a prospective study of 58 consecutive patients with palmar, plantar, or axillary hyperhidrosis treated with thoracoscopic sympathectomy from September 1993 to July 1999. Forty-nine of the 58 probands volunteered family history data for these analyses (84% response rate). A standardized questionnaire was administered during the postoperative visit or by phone interview, and a detailed family history was obtained. The same questionnaire was also administered to a set of 20 control patients. The familial aggregation of hyperhidrosis has been quantified by estimating the recurrence risks to the offspring, parents, siblings, aunts, uncles, and cousins of 49 probands and 20 controls. We estimated the penetrance by use of a genetic analysis program.
Thirty-two of 49 (65%) reported a positive family history in our hyperhidrosis group, and 0% reported a positive family history in our control group. A recurrence risk of 0.28 in the offspring of probands compared with frequency of 0.01 in the general population provides strong evidence for vertical transmission of this disorder in pedigrees and is further supported by the 0.14 risk to the parents of the probands. The results indicate that the disease allele is present in about 5% of the population and that one or two copies of the allele will result in hyperhidrosis 25% of the time, whereas the normal allele will result in hyperhidrosis less than 1% of the time.
We conclude that primary palmar hyperhidrosis is a hereditary disorder, with variable penetrance and no proof of sex-linked transmission. However, this does not exclude other possible causes, and we anticipate that genetic confirmation of this disorder may lead to earlier diagnoses and advances in medical and psychosocial interventions.
原发性手掌多汗症是一种以多汗为特征的病症,据报道在西方人群中的发病率为1%。它是一种可能导致功能障碍的疾病,会干扰社交、心理和职业活动。在过去几年中,一些研究者报告称,他们治疗的多汗症患者中有家族病史呈阳性的情况。迄今为止,病因尚不清楚;此外,流行病学数据稀少且不充分。
为了明确多汗症的遗传因素,我们对1993年9月至1999年7月间接受胸腔镜交感神经切除术治疗的58例连续的手掌、足底或腋窝多汗症患者进行了一项前瞻性研究。58例先证者中有49例自愿提供家族病史数据用于这些分析(应答率为84%)。在术后随访期间或通过电话访谈发放标准化问卷,获取详细的家族病史。同样的问卷也发放给了一组20例对照患者。通过估计49例先证者和20例对照的后代、父母、兄弟姐妹、姑姑、叔叔和堂兄弟姐妹的复发风险,对多汗症的家族聚集性进行了量化。我们使用一个遗传分析程序来估计外显率。
在我们的多汗症组中,49例中有32例(65%)报告有家族病史呈阳性,而在我们的对照组中这一比例为0%。先证者后代的复发风险为0.28,而一般人群中的频率为0.01,这为该疾病在谱系中的垂直传播提供了有力证据,先证者父母的风险为0.14进一步支持了这一点。结果表明,疾病等位基因在约5%的人群中存在,一个或两个该等位基因拷贝在25%的情况下会导致多汗症,而正常等位基因导致多汗症的情况少于1%。
我们得出结论,原发性手掌多汗症是一种遗传性疾病,外显率可变,且无性连锁遗传的证据。然而,这并不排除其他可能的病因,我们预计对该疾病的基因确认可能会带来更早的诊断以及医学和心理社会干预方面的进展。