- Research article
- Open Access
- Open Peer Review
Is sweat testing for cystic fibrosis feasible in patients with down syndrome?
© The Author(s). 2018
- Received: 5 June 2017
- Accepted: 9 January 2018
- Published: 16 January 2018
Recurrent airway infections are common in patients with Down’s syndrome (DS). Hence, ruling out Cystic Fibrosis (CF) in these patients is often required. In the past, the value of sweat testing – the gold standard to diagnose CF – has been questioned in DS as false positive results have been reported. However, these reports are based on measurements of sweat osmolality or sodium concentrations, not chloride concentrations. This study analyses sweat secretion rate and chloride concentration in sweat samples of patients with DS in comparison to healthy controls.
We assessed sweat samples in 16 patients with DS and 16 healthy controls regarding sweat secretion rate (SSR) and sweat chloride concentration.
All measured chloride concentrations were within the normal range. The chloride concentrations were slightly, but not significantly lower in patients with DS (15,54 mmol/l (±4,47)) compared to healthy controls (18,31 mmol/l (±10,12)). While no gender gap in chloride concentration could be found, chloride concentration increased with age in both groups.
Insufficient sweat was collected in 2 females with DS (12.5% of the study group) but not in an individual of the control group. A significant lower sweat secretion rate was found in the DS group (27,6 μl/30 min (± 12,18)) compared to the control group (42,7 μl/30 min (± 21,22)). In a sub-analysis, female patients produced significantly less sweat (20,8 ± 10,6 μl/30 min) than male patients with DS (36,4 ± 7,8 μl/30 min), which accounts for the difference between patients and controls. Furthermore, while the sweating secretion rate increased with age in the control group, it did not do so in the DS group. Once again this was due to female patients with DS, who did not show a significant increase of sweat secretion rate with age.
Sweat chloride concentrations were within the normal range in patients with DS and therefore seem to be a reliable tool for testing for CF in these patients. Interestingly, we found a reduced sweat secretion rate in the DS group. Whether the last one has a functional and clinical counterpart, possibly due to a disturbed thermoregulation in DS patients, requires further investigation.
- Sweat secretion rate
- Sweat osmolality
- Gender gap
In patients with Down’s syndrome (DS), infections, especially of the airways, are more common than in the healthy population . Children with frequent infections of the lower airways, though, require assessments to rule out cystic fibrosis (CF). Furthermore, as in patients with CF, children with DS are small of stature . However, only few and old references of results and validity of sweat tests in these children exist [3–6].
An association of DS and CF has been described in the past and is rare but existent and case reports have been published [3–6]. The expected incidence of both conditions co-existing is about 1:2,650,000 in the United Kingdom (UK) (incidence of CF 1:2415, DS 1:1100 live births) . The documented outcome of the combined disease is normally extremely poor, but also moderate courses have been described [4, 5].
An early diagnosis of CF, especially in co-existence with other chronic diseases like DS is crucial for therapy and therefore a reliable diagnostic tool is needed. The gold standard for diagnosing CF is the sweat test ; however, it is unclear, how reliable that tool is for children with DS. Changes in sweat gland anatomy have been described in DS, which could result in alterations of sweating rate and/or sweat electrolyte concentration .
In the past, Symon et al. and Geetha et al. reported an elevated sweat osmolality in children with DS who did not show any signs for CF [9, 10]. In contrast, Chapman et al. reported normal sweat sodium in 13 subjects with DS . Milunsky et al. published three children with DS and CF diagnosed by increased concentration of sweat sodium and chloride  and Vetrella et al. described a child with DS and CF with raised sweat sodium and chloride concentration . The gold standard for the diagnosis of CF nowadays is the measurement of sweat chloride concentration and not sweat osmolality after pilocarpine ionthophoreses .
To our knowledge, data on sweat chloride concentration in people with DS but no signs of CF does not yet exist. Therefore, we aimed to assess such concentrations. Based on the existing literature, we hypothesised that sweat chloride concentrations would be elevated in DS.
The study was approved by the local ethics committee (votum number 17/10; 03.03.2010). 16 patients with DS and 16 healthy controls were included in the study. They were recruited through paediatricians and self-help groups. Written informed consent was obtained from the patients and their legal guardians, if appropriate. Genotyping was not done in this population.
The participants of the study were first familiarized with the equipment. In each participant, sweat collection was performed in duplicate, once on the left and once on the right arm. Pilocarpine-Iontophoresis was performed for 5 min (Wescor Modell 3700; Kreienbaum Neoscience GmbH, Langenfeld, Germany) . Afterwards sweat was collected using a Macroduct Sweat Collection device for 30 min (Wescor Modell 3700; Kreienbaum Neoscience GmbH, Langenfeld, Germany) on each arm. The sweat secretion rate (SSR) was measured. Afterwards sweat chloride concentration (mmol/l) was analysed by using the ChloroChek® Chloridometer® (Kreienbaum Neoscience GmbH, Langenfeld, Germany), if the sweat amount was above 15 μl. If sweat amount was below 15 μl/30 min on both arms, the person was regarded as non-responder .
According to current European guidelines, a sweat test is considered indicative for CF, if the chloride concentration is above 60 mmol/l, a test is interpreted as intermediate if the chloride concentration ranges between 30 and 59 mmol/l. CF is unlikely if the chloride concentration remains below 30 mmol/l .
Statistical analyses were performed by using SPSS Statistics 23 (IBM). Differences between patients with DS and controls as well as between male and female participants were calculated by using Student’s t-test for normally distributed data and Mann-Whitney U test, if data was not normally distributed. For correlations of age and sweat secretion rates, Spearmoan-Rho-correlations were calculated.
Patients with DS
Age < 18 years
47,5 (17–81) n.s.
154 (103–182) n.s.
Children with height below 3rd percentile
Patients with DS
Birth control pills
As Cystic Fibrosis newborn screening via IRT-screening has not been regularly available until October 2016 in Germany, none of the participants underwent this screening, therefore we cannot report on such data.
Sweat chloride concentration
Sweat chloride concentration in relation to sex
Sex did not have any influence on sweat chloride concentration, neither in the control group nor in the DS group (data not shown).
Sweat chloride concentration in relation to age
Sweat secretion rate (SSR)
SSR in relation to sex
When analysing the amount of sweat with regard to sex, it was evident that in the control group, the SSR was more or less equal in male (44,8 ± 30,3 μl) and female participants (41,5 ± 15,4 μl) (Fig. 3b). The patients with DS, however, showed a striking difference: female patients produced significantly less sweat (20,8 ± 10,6 μl) than male patients (36,4 ± 7,8 μl), which accounts for the difference between patients and controls (p < 0.05, see Fig. 3c). Of these female patients, 3 were pre- and 6 post-puberty.
SSR in relation to age
Altered sweat tests have been reported for patients with DS for a long time, especially as the analysis always referred to sweat osmolality [8–10]. Up until now, no data on the measurement of chloride concentration in the sweat of patients with DS without CF has been published. Our data suggests that analysing sweat chloride concentration is a reliable tool to rule out CF in patients with DS, as we did not find any false positive results in our study population. However, this was a pilot study with only a small number of patients.
Some of the data generated on sweat tests in patients with DS have been generated by using the sweat osmolality as a surrogate marker for the sum of sweat electrolytes, especially potassium and sodium. It has been reported that the sweat osmolality is elevated in patients with DS without CF, leading to a false positive results in sweat tests for screening for CF in DS patients . As there are too many influences on osmolality (i.e. hormones, age, sex, concomitant diseases), the analysis of the sweat chloride concentration has become the gold standard in diagnosing CF today . In our study, the sweat amount of the participants was unfortunately too little to also measure sweat osmolality to confirm increased serum osmolality in the DS group, as described before [8, 9]. In contrast, the measured chloride and sodium (data for sweat sodium concentration was not shown, because of too little sweat amount in many participants) concentration in our study was even slightly, but not significant lower in patients with DS compared with the control group. In line with our results, Chapman et al. reported that in 13 children with DS, sweat sodium concentration was normal and not elevated . Therefore, the electrolyte pattern for chloride and sodium seems not to be responsible for the increased sweat osmolality reported in DS.
In a sub-analysis, we further analysed the possible influence of sex and age on sweat chloride concentration in the two groups. While we found no differences between the two groups in relation to sex, the chloride concentration increased with age in both groups. The latter observation is consistent with previous reports, which described a tendency for the sweat chloride to decrease during the first year of life (this age was not included in our study) and then to increase with subsequent aging [14, 15]. In a study of more than 10.000 sweat tests, Traeger et al. also reported about a slightly higher sweat chloride concentration in females compared to males , a finding that was also confirmed by Mishra et al. . This small gender gap could not be represented in our study, probably due to the small study population.
Besides chloride concentration, we studied possible differences in the non-responder rate and the SSR between the two groups. We recognized a higher non-responder rate and lower SSR in patient with DS in our study. A higher non-responder rate to iontophoresis in patients with DS has been described before in the literature (10% in DS group to 3% in normal population) . Also, in the study of Symon et al., 20% (5/25) of patients with DS failed to produce sufficient sweat for osmometry . This could be further confirmed in a study of Geetha et al., in which the proportion of non-responders to pilocarpine was significantly higher in DS patients (> 10%) then in the normal population (3%) . The higher non-responder rate and the difficulty to obtain enough sweat could be due to an abnormal skin commonly found in children with DS . In this context, the anatomy of sweat glands seems to be different in patients with DS. It has been described that the sweat coil size and the ratio of coil volume to duct length are abnormally small in DS patients [18, 19], although it is unclear whether this has any clinical correlate.
In a sub-analysis related to sex, we could show that female patients produced significantly less sweat compared to male patients with DS, which accounts for the difference in SSR between patients and controls. This gender gap could not be found in the control group. This sex difference in SSR specific for DS was not described before. However, a general sex difference of sweat secretion pattern in children with lower median values for SSR for girls than boys has been reported before [16, 20, 21]. In contrast, Rees et al. also found an increased SSR in men than in women, although this difference did not occur in pre-pubertal boys and girls .
In our small study, there was no difference in SSR between pre- and post-pubertal female DS patients. In general, hormone status significantly influences sweat physiology [8, 9]. Androgens as well as growth hormone (GH) seem to play a role here [21–23]. Children with GH deficiency show reduced SSR, while patients with acromegaly have a higher SSR than healthy controls [21, 23]. It is known that DS is associated with growth hormone deficiency . In our albeit small population, children with DS and a height below the 3rd percentile showed no reduced SSR rate compared with the other children (data not shown). However, as we did not draw blood samples, GH levels could not be analysed. It remains mere speculation, whether lower GH levels are responsible for differences in SSR.
Another interesting and new finding was that the SSR did not increase with age in patients with DS, as it did in our control group and in other studies before [16, 25]. The different anatomy of sweat glands in DS, as mentioned before, could be a reason for this difference. When having a closer look, it is especially the female DS patients that account for this difference. Possibly, altered androgens in DS are responsible for this effect. If in a larger population the lower SSR in female patients with DS is confirmed, this may have clinical implications for patients with DS as thermoregulation may not function as well as in patients with a normal SSR. In general, sweating plays an important role for the maintenance of body temperature during exercise or in hot environments . Accordingly, patients lacking sweat glands like in anhidrotic ectodermal dysplasia or patients with impaired sweating like in GH deficiency may be at risk for developing hyperthermia as a consequence of their decreased ability to sweat [27–30]. Especially conditions like fever and physical activity may put these DS patients at risk for hyperthermia and electrolyte derailment. It is certainly worthwhile to analyse this finding and its effects in a larger population.
All our findings were generated in a small sample. As an analysis of validity of chloride concentration in sweat tests in patients with DS has not happened so far, we started with this pilot study in order to have a proof of concept. We were able, though, to cover children as well as adults and male as well as female participants in both groups. Furthermore, we were able to compare patients with DS to healthy controls (without any recurrent lung infections or other CF suspicious symptoms). Due to the small sample, data was analysed using t-Tests and Mann-Whitney-U Tests. In a larger sample univariate analyses of variance or mixed linear models might be worthwhile to evaluate effects of sex and age; in this study, due to the number of participants, the power would have been to weak.
Another limitation is the low amount of sweat that was available for analysis. As we did double analyses (iontophoresis on both arms, analysis, and then calculating means of the results), we only had half of the amount for each test. Therefore, an analysis of osmolality and further electrolytes was possible only in a small group of participants. In further studies, it would be worthwhile to have just one analysis but the double amount of sweat to generate more data (e.g. osmolality, sodium concentration, conductivity). Also, drawing blood samples and having information on hormone status would be worthwhile to further understand differences in SSR.
As no genotyping was done in this study or afterwards in these patients, we cannot speculate, whether changes in sweat chloride levels may have been due to a carrier status, as reported by Ooi et al. .
To our knowledge, this is the first study that shows that measuring chloride concentration in patients with Down’s syndrome without CF is a valid tool to discriminate between patients with CF and those without. Up until now, only osmolality or sodium concentration has been published to analyse the sweat, which lead to difficulty in diagnosis [8–10]. Using chloride concentration though, enables health professionals to not have false-positive sweat test results in patients with DS and is a valid tool to exclude a CF in patients with DS, a knowledge which is of high clinical relevance.
Another interesting finding deserves further analysis; the altered SSR in female patients with DS needs to be confirmed and if this is the case, medical implications of an impaired sweat rate need to be assessed.
Availability of data and materials
The dataset used and analysed during the current study is available on request from the corresponding author.
SK, AD and HH planned and executed the study. KR and AD were responsible for the data analysis. KR drafted the manuscript which was revised by SK, AD and HH. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by the ethics committee of the Medical School of the University of Wuerzburg (votum number 17/10; 03.03.2010). Written informed consent was obtained from the patients and their legal guardians, if appropriate.
Consent for publication
The authors declare that they have no competing interests.
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- Pandit C, Fitzgerald DA. Respiratory problems in children with down syndrome. J Paediatr Child Health. 2012;48(3):E147–52.View ArticlePubMedGoogle Scholar
- Cremers MJ, van der Tweel I, Boersma B, Wit JM, Zonderland M. Growth curves of Dutch children with Down's syndrome. J Intellect Disabil Res. 1996;40(Pt 5):412–20.View ArticlePubMedGoogle Scholar
- Guy EL, Peckham DG, Brownlee KG, Conway SP, Lee TW. Cystic fibrosis co-existing with trisomy 21. J Cyst Fibros. 2010;9(5):330–1.View ArticlePubMedGoogle Scholar
- Milunsky A. Cystic fibrosis and Down's syndrome. Pediatrics. 1968;42(3):501–4.PubMedGoogle Scholar
- Saglani S, Bush A. Cystic fibrosis and Down's syndrome: not always a poor prognosis. Pediatr Pulmonol. 2001;31(4):321–2.View ArticlePubMedGoogle Scholar
- Vetrella M, Barthelmai W, Matsuda H. Down's syndrome and cystic fibrosis. Pediatrics. 1969;43(5):905.PubMedGoogle Scholar
- Farrell PM, Rosenstein BJ, White TB, Accurso FJ, Castellani C, Cutting GR, Durie PR, Legrys VA, Massie J, Parad RB, et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr. 2008;153(2):S4–S14.View ArticlePubMedPubMed CentralGoogle Scholar
- Geetha H, Shetty KT. Sweat osmolality in Down's syndrome and cystic fibrosis in an Indian population. Br Med J (Clin Res Ed). 1987;294(6565):156.View ArticleGoogle Scholar
- Symon DN, Stewart L, Russell G. Abnormally high sweat osmolality in children with Down's syndrome. J Ment Defic Res. 1985;29(Pt 3):257–61.PubMedGoogle Scholar
- Geetha H, Jayakeerthy CM. Sweat osmolality in some of the congenital diseases. Indian J Pathol Microbiol. 1993;36(4):420–4.PubMedGoogle Scholar
- Chapman MJ, Donoghue EC, Saggers BA, Stern J. Parotid saliva sodium in Down's disease. J Ment Defic Res. 1967;11(3):185–93.PubMedGoogle Scholar
- 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(3):545–9.PubMedGoogle Scholar
- Institute CaLS. CLSI. Sweat Testing: Sample Collection and Quantitative Chloride Analysis; Approved Guideline—Third Edition: CLSI document C34-A3; Wayne. 2009.Google Scholar
- Hall SK, Stableforth DE, Green A. Sweat sodium and chloride concentrations--essential criteria for the diagnosis of cystic fibrosis in adults. Ann Clin Biochem. 1990;27(Pt 4):318–20.View ArticlePubMedGoogle Scholar
- Mishra A, Greaves R, Smith K, Carlin JB, Wootton A, Stirling R, Massie J. Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals. J Pediatr. 2008;153(6):758–63.View ArticlePubMedGoogle Scholar
- Traeger N, Shi Q, Dozor AJ. Relationship between sweat chloride, sodium, and age in clinically obtained samples. J Cyst Fibros. 2014;13(1):10–4.View ArticlePubMedGoogle Scholar
- Kersting DW, Rapaport IF. A clinicopathologic study of the skin in mongolism. AMA Arch Derm. 1958;77(3):319–23.View ArticlePubMedGoogle Scholar
- Shankle WR, Azen SP, Landing BH. Comparisons of eccrine sweat gland anatomy in genetic, chromosomal, and other diseases, and a suggested procedure for use of sweat gland measurements in differential diagnosis. Teratology. 1982;25(2):239–45.View ArticlePubMedGoogle Scholar
- Landing BH, Wells TR. Anatomy of eccrine sweat glands in D1, G1 and 18 trisomy syndromes. J Invest Dermatol. 1968;50(6):475–82.View ArticlePubMedGoogle Scholar
- Blakemore C, Zumbroich TJ. Stimulus selectivity and functional organization in the lateral suprasylvian visual cortex of the cat. J Physiol. 1987;389:569–603.View ArticlePubMedPubMed CentralGoogle Scholar
- Main K, Nilsson KO, Skakkebaek NE. Influence of sex and growth hormone deficiency on sweating. Scand J Clin Lab Invest. 1991;51(5):475–80.View ArticlePubMedGoogle Scholar
- Rees J, Shuster S. Pubertal induction of sweat gland activity. Clin Sci (Lond). 1981;60(6):689–92.View ArticleGoogle Scholar
- Sneppen SB, Main KM, Juul A, Pedersen LM, Kristensen LO, Skakkebaek NE, Feldt-Rasmussen U. Sweat secretion rates in growth hormone disorders. Clin Endocrinol. 2000;53(5):601–8.View ArticleGoogle Scholar
- Castells S, Torrado C, Bastian W, Wisniewski KE. Growth hormone deficiency in Down's syndrome children. J Intellect Disabil Res. 1992;36(Pt 1):29–43.PubMedGoogle Scholar
- Ooi CY, Castellani C, Keenan K, Avolio J, Volpi S, Boland M, Kovesi T, Bjornson C, Chilvers MA, Morgan L, et al. Inconclusive diagnosis of cystic fibrosis after newborn screening. Pediatrics. 2015;135(6):e1377–85.View ArticlePubMedGoogle Scholar
- Sato K, Kang WH, Saga K, Sato KT. Biology of sweat glands and their disorders. I. Normal sweat gland function. J Am Acad Dermatol. 1989;20(4):537–63.View ArticlePubMedGoogle Scholar
- Juul A, Hjortskov N, Jepsen LT, Nielsen B, Halkjaer-Kristensen J, Vahl N, Jorgensen JO, Christiansen JS, Skakkebaek NE. Growth hormone deficiency and hyperthermia during exercise: a controlled study of sixteen GH-deficient patients. J Clin Endocrinol Metab. 1995;80(11):3335–40.PubMedGoogle Scholar
- Juul A, Main K, Nielsen B, Skakkebaek NE. Decreased sweating in growth hormone deficiency: does it play a role in thermoregulation? J Pediatr Endocrinol. 1993;6(1):39–44.View ArticlePubMedGoogle Scholar
- Juul A, Skakkebaek NE. Growth hormone deficiency and hyperthermia. Lancet. 1991;338(8771):887.View ArticlePubMedGoogle Scholar
- Basu S, Mitra M, Ghosh A. Evaluation of sweat production by pilocarpine iontophoresis: a noninvasive screening tool for hypohidrosis in ectodermal dysplasia. Indian J Clin Biochem. 2013;28(4):433–5.View ArticlePubMedPubMed CentralGoogle Scholar
- Ooi CY, Dupuis A, Ellis L, Jarvi K, Martin S, Ray PN, Steele L, Kortan P, Gonska T, Dorfman R, et al. Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis? Thorax. 2014;69(3):254–60.View ArticlePubMedGoogle Scholar