Abstract
Nasal nitric oxide (NO) measurement is feasible in infants, potentially allowing earlier diagnosis of primary ciliary dyskinesia http://ow.ly/9K0a30kpcZU
Which infants should be tested for PCD?
Primary ciliary dyskinesia (PCD) generally causes symptoms from the first weeks of life, but diagnosis is usually delayed for years or can be missed altogether. Referral for diagnostic testing is often late because key symptoms, such as wet cough, chronic rhinitis and recurrent upper and lower respiratory tract infection, are non-specific. An international survey of patients reported that 37% had >40 visits to medical professionals due to PCD-related symptoms before being referred for diagnostic testing [1]. Approximately 50% of children with PCD have situs inversus, a rare condition in the general population, and it is therefore not surprising that these patients are investigated earlier. A European survey found that age of diagnosis was at 3.5 years in those with situs inversus and 5.8 years in children with normal situs [2]. Assuming a prevalence of 1 in 10 000 [3], we expect ∼1180 diagnosed children in England (childhood population ∼11.8 million); however, there are currently only ∼340 children in the National Paediatric PCD Service. This highlights a huge proportion of undiagnosed patients even in a country with a national PCD service [4]. This is in stark contrast to cystic fibrosis (CF) where neonatal screening programmes ensure that diagnosis occurs in early infancy in many countries, with positive impact on clinical outcome [5]. Young children with PCD have similarly impaired forced expiratory volume in 1 s to children with CF [6], and require multidisciplinary treatment. Early diagnosis facilitates a management plan, including regular airway clearance physiotherapy, surveillance for airway pathogens with treatment of respiratory exacerbations, genetic counselling for families, audiology monitoring and management of conductive hearing loss [7, 8]. We expect that early diagnosis would delay respiratory decline and ensure specialist treatment of ear, hearing and nasal issues, thereby optimising health, psychological, social and educational outcomes.
There is no single gold standard test for PCD diagnosis. Presently, the diagnosis is made in patients with a compatible medical history following a demanding combination of tests including nasal nitric oxide (nNO), high-speed video microscopy, transmission electron microscopy, genetics, and culture of respiratory epithelial cells [7, 9–12]. These tests are costly and need experienced staff using sophisticated equipment, hence testing is restricted to reference centres which may be geographically distant from the patient. Identifying the correct patients for testing is therefore important and screening tools are needed. Although individual symptoms are non-specific, the pattern of symptoms is often characteristic. A typical history might include neonatal respiratory distress in an infant with no risk factors, a daily wet cough starting in early infancy, recurrent chest infections, persistent rhinitis and serous otitis media. Screening tools (e.g. PICADAR) to identify patients based on their clinical history are helpful but require a history that might not yet have evolved in young infants [13, 14].
nNO as a diagnostic test for PCD in infancy
Lundberg et al. [15] first reported extremely low nNO concentrations in patients with PCD >20 years ago. A more recent meta-analysis of 11 studies reported a mean±sd nNO output of 19±18.6 nL·min−1 in PCD (n=478) and 265±118.9 nL·min−1 in healthy controls (n=338) [16]. Whilst the reason for low nNO remains elusive [17], measurement of nNO has been widely adopted as part of the diagnostic work-up [9, 10, 18–23]. The “gold standard” measurement is made during a velum closure manoeuvre to reduce contamination of nasal gas with lower airway air [24]. This breathing manoeuvre is not possible in young children because it requires patient cooperation to exhale against resistance or to phonate to close the velum during sampling. Hence, this method is not possible in the age group where testing should ideally occur. A number of studies have therefore investigated measurement during tidal mouth breathing and have reported that it provides an acceptable alternative for children who cannot manage velum closure manoeuvres [18, 20, 22, 23, 25]. However, guidelines have previously suggested that nNO cannot be used as a test in infancy because of feasibility issues, and because nNO concentrations are very low in healthy infants. This dogma has been challenged by a cross-sectional study of nNO in infants <1 year [26], and now a study which has longitudinally measured levels throughout infancy from 2 weeks to 2 years [27].
In this issue of the European Respiratory Journal, Marthin et al. [27] report the natural evolution of nNO levels in 44 healthy infants who were followed at six time-points from 2 weeks to 2 years. They additionally use retrospective data from infants with PCD. Theirs is the first manuscript to demonstrate the longitudinal increase in nNO over the first years of life. The authors demonstrated that measurement of nNO during tidal breathing is feasible in healthy infants and those with PCD. Importantly, they report that an extremely good success rate is possible (>99%) [27]. The authors confirmed that success in measuring infant nNO depended on being very patient (personal communication). Newborn infants were apparently easy to measure when fed and asleep. The most challenging ages were 4 to 12-month olds, who often woke and required comforting by pacifier, parents singing to the child, or distracting with a toy. With 1–2 year olds, a smart phone worked well for distraction (personal communication, J.K. Marthin).
Some healthy infants had very low levels of nNO [27], indistinguishable from PCD, and further PCD diagnostic testing, including a repeat nNO measurement after a couple of months, should be conducted. In particular, healthy infants had reduced nNO during upper respiratory tract infections, highlighting that measurements should only be conducted for PCD diagnostics when infection-free.
Notes of caution
The study reported by Marthin et al. [27] has the potential to change practice at our PCD centre, but further research is needed before widespread testing of infants is recommended. Until now we have been reluctant to recommend nNO as a test in this age group because we had concerns that taking measurements would be difficult. Now that we know that measurement is feasible, nNO needs evaluating with infants in a diagnostic setting to see whether it can distinguish PCD cases from children with similar symptoms who do not have PCD.
Importantly, to avoid a large number of false-positive cases, rigorous patient selection is needed before applying diagnostic tests. If the test becomes used as a general screening test, the number of false-positive cases would be very high (poor positive predictive value), overwhelming diagnostic services [28, 29]. Classical clinical features in infancy that should prompt testing for PCD include: unexplained neonatal respiratory distress starting a few hours after delivery, often associated with atelectasis/lobar collapse and prolonged oxygen requirement; persistent rhinitis; daily wet cough; and situs inversus or situs ambiguous, with or without congenital heart disease [18, 30]. However, some infants with PCD may not present as neonates, or their symptoms might be mild; and 50% of infants with PCD have normal situs which should not delay testing in a symptomatic baby.
Additionally, non-specialist centres need training to conduct the measurements and interpret the results. Local testing might utilise portable electrochemical analysers rather than “gold standard” chemoluminescence analysers; a newly “Conformité Européene” (CE)-marked portable nNO analyser is an improvement on previous portable models, with an nNO trace allowing the technician to visualise peak nNO readings [31]. As portable NO analysers become more widespread for use in asthma, the opportunity for nNO measurements of infants at centres without PCD diagnostics is potentially useful, but only if measured by technicians who have received training, in correctly selected patients. Importantly, infants with a strong likelihood should be referred to a specialist centre for further diagnostic tests, even if nNO is within normal limits.
Future perspectives
There are currently no guidelines to standardise tidal breathing measurements of nNO and these are now needed. A study from North America demonstrated that measurement during velum closure could be standardised for testing children >5 years [19]. By this age structural lung damage may already be present and we need tests which target early diagnosis. Marthin et al. [27] have demonstrated that tidal manoeuvres are feasible with potential to contribute to the diagnostic portfolio from the first weeks of life. The tidal breathing method now needs validating in a diagnostic setting because the test might fare less well with disease controls rather than healthy controls [29]. This would need a multicentre approach to include sufficient infants suspected of PCD. Research and consensus will be needed to decide how to take the reading. Marthin et al. [27] used the averaged nNO value from the three highest, distinct, visible peak concentrations measured within 30 to 40 s, and read directly as point values on the screen, whilst other authors have taken the measure from five peaks [25]. Details of quality assessment of the tracings will be an important consideration for standardisation.
Summary
Marthin et al. [27] performed 224 nNO measurements in 44 healthy infants. They reported median (interquartile range) concentrations of 15.0 (9.6 to 22.8) nL·min−1 in newborns, increasing to 93.4 (67.0 to 128.4) nL·min−1 at the age of 24 months. Respiratory tract infections temporarily suppressed nNO by 79% [27]. The success rate of acceptable nNO-sampling was 223/224 (99.6%). With further validation and standardisation, nNO may prove an important diagnostic tool for infants with PCD. This would allow earlier initiation of appropriate management strategies, thereby reducing the risk of early lung damage and respiratory decline.
Footnotes
Conflict of interest: J.S. Lucas is on the PCD advisory board of Aerocrine/Circassia and has received expenses to attend meetings, research monies and honoraria, outside the submitted work.
- Received May 22, 2018.
- Accepted June 7, 2018.
- Copyright ©ERS 2018