key: cord-0742945-iduzpcgd
authors: Usnich, Tatiana; Vollstedt, Eva-Juliane; Schell, Nathalie; Skrahina, Volha; Bogdanovic, Xenia; Gaber, Hanaa; Förster, Toni M.; Heuer, Andreas; Koleva-Alazeh, Natalia; Csoti, Ilona; Basak, Ayse Nazli; Ertan, Sibel; Genc, Gencer; Bauer, Peter; Lohmann, Katja; Grünewald, Anne; Schymanski, Emma L.; Trinh, Joanne; Schaake, Susen; Berg, Daniela; Gruber, Doreen; Isaacson, Stuart H.; Kühn, Andrea A.; Mollenhauer, Brit; Pedrosa, David J.; Reetz, Kathrin; Sammler, Esther M.; Valente, Enza Maria; Valzania, Franco; Volkmann, Jens; Zittel, Simone; Brüggemann, Norbert; Kasten, Meike; Rolfs, Arndt; Klein, Christine
title: LIPAD (LRRK2/Luebeck International Parkinson's Disease) Study Protocol: Deep Phenotyping of an International Genetic Cohort
date: 2021-08-09
journal: Front Neurol
DOI: 10.3389/fneur.2021.710572
sha: d3575c8684007bc3186a8d2c80c1acae813dea56
doc_id: 742945
cord_uid: iduzpcgd

Background: Pathogenic variants in the Leucine-rich repeat kinase 2 (LRRK2) gene are the most common known monogenic cause of Parkinson's disease (PD). LRRK2-linked PD is clinically indistinguishable from idiopathic PD and inherited in an autosomal dominant fashion with reduced penetrance and variable expressivity that differ across ethnicities and geographic regions. Objective: To systematically assess clinical signs and symptoms including non-motor features, comorbidities, medication and environmental factors in PD patients, unaffected LRRK2 pathogenic variant carriers, and controls. A further focus is to enable the investigation of modifiers of penetrance and expressivity of LRRK2 pathogenic variants using genetic and environmental data. Methods: Eligible participants are invited for a personal or online examination which comprises completion of a detailed eCRF and collection of blood samples (to obtain DNA, RNA, serum/plasma, immune cells), urine as well as household dust. We plan to enroll 1,000 participants internationally: 300 with LRRK2-linked PD, 200 with LRRK2 pathogenic variants but without PD, 100 PD patients with pathogenic variants in the GBA or PRKN genes, 200 patients with idiopathic PD, and 200 healthy persons without pathogenic variants. Results: The eCRF consists of an investigator-rated (1 h) and a self-rated (1.5 h) part. The first part includes the Movement Disorder Society Unified Parkinson's Disease Rating, Hoehn &Yahr, and Schwab & England Scales, the Brief Smell Identification Test, and Montreal Cognitive Assessment. The self-rating part consists of a PD risk factor, food frequency, autonomic dysfunction, and quality of life questionnaires, the Pittsburgh Sleep Quality Inventory, and the Epworth Sleepiness as well as the Hospital Anxiety and Depression Scales. The first 15 centers have been initiated and the first 150 participants enrolled (as of March 25th, 2021). Conclusions: LIPAD is a large-scale international scientific effort focusing on deep phenotyping of LRRK2-linked PD and healthy pathogenic variant carriers, including the comparison with additional relatively frequent genetic forms of PD, with a future perspective to identify genetic and environmental modifiers of penetrance and expressivity Clinical Trial Registration:ClinicalTrials.gov, NCT04214509.

Pathogenic variants in the Leucine-rich repeat kinase 2 (LRRK2) gene are the most common known monogenic cause of Parkinson's disease (PD). First identified in 2004, LRRK2 pathogenic variants account for up to ∼40% of all PD cases in selected populations, e.g., North African Berber (1) . In the PD phenotype-genotype database MDSGene (www.mdsgene.org), ∼700 individual LRRK2 pathogenic variant carriers are listed, but clinical information apart from cardinal signs of PD is overall scarce (1) .

The majority of the reported LRRK2 pathogenic variantpositive PD patients are of European descent (63%), whereas all other ethnicities comprise ∼10% or fewer patients of described pathogenic variant carriers despite clusters in the Ashkenazi Jewish (AJ) and Arab Berber populations (1, 2) . Definitely pathogenic variants identified in LRRK2 include p.G2019S, p.R1441C/G/H, p.N1437H, p.Y1699C, and, p.I2020T. Of these, the p.G2019S pathogenic variant is the most common with an estimated frequency of 1% in sporadic and 4% in hereditary PD cases worldwide (3) . However, data on many populations are still missing.

LRRK2-linked PD is inherited in an autosomal dominant fashion with reduced, age-dependent penetrance and variable expressivity that differ across ethnicities and geographic regions, indicating that ancestral background or environmental factors contribute to the manifestation and expressivity of pathogenic LRRK2 variants. For example, at the age of 60 years, 60% of Tunisian p.G2019S pathogenic variant carriers manifest PD, compared with only 20% of the Norwegian carriers of the same pathogenic variant (4) . Recent studies have suggested mitochondrial involvement in the penetrance of LRRK2-linked PD (5, 6) . Environmental factors can also influence penetrance, as recently found in the Tunisian Arab Berber population, where tobacco and black tea use delayed age at onset in LRRK2 pathogenic variant carriers (7) .

LRRK2-linked PD is clinically indistinguishable from idiopathic PD, i.e., PD of unknown cause, although the disease course appears to be milder with regard to motor and cognitive functions (8) . In this comparatively small subgroup of PD patients with a known etiology, valuable clues can be garnered toward pathophysiological mechanisms and targeted treatments, which may be generalized to idiopathic PD. Currently, there are three substances in clinical trial specifically targeting LRRK2: the LRRK2 kinase inhibitors DNL151 (NCT04557800) and DNL201 (NCT04551534) from Denali and the antisense oligonucleotide BIIB094 (NCT03976349) from Biogen (2) . However, no genetic testing guidelines and no clinical trial-ready cohorts exist to date.

To identify LRRK2 pathogenic variant carriers among 10,000 PD patients from 15 countries and to establish a clinical trialready cohort, the ROPAD study was initiated (9) . The ROPAD study performs genetic testing of pathogenic variants in the LRRK2 and GBA genes and, if negative, carries out genetic screening of 68 genes linked to PD or related movement disorders. Out of the first 1,288 participants who underwent genetic testing in ROPAD, 40 (3.1%) harbored pathogenic or likely pathogenic LRRK2 variants, 109 (8.5%) harbored GBA variants, three (0.2%) had alterations in both genes (9) . The ROPAD study is still ongoing and continues to identify LRRK2 pathogenic variant carriers internationally. It gathers only basic clinical data: age at examination, age at onset, cardinal PD symptoms, and 12/33 items of MDS-UPDRS Part III and, thus, does not allow a systematic in-depth characterization of LRRK2 pathogenic variant carriers. Recently published data from the currently largest multinational prospective study that includes LRRK2 pathogenic variant carriers, i.e., the Parkinson's Progression Markers Initiative (PPMI), provide more phenotypic details on LRRK2 pathogenic variant carriers across international sites (6) . However, as the focus of the PPMI study is predominantly on biomarkers, it does not cover environmental factors in-depth, and only includes participants with a PD diagnosis 2 years or less before enrolment who are untreated with PD medication. There remains a gap in combining phenotypic, genetic, and environmental data on LRRK2 pathogenic variant carriers internationally, regardless of the onset of signs and symptoms and their medication status, that LIPAD is aiming to close. The objectives of the LIPAD study are (1) to provide a systematic characterization of PD patients and unaffected carriers with pathogenic variants in the LRRK2 gene; and (2) to enable the investigation of modifiers of penetrance of LRRK2 pathogenic variants using genetic and environmental data.

Here, we describe a protocol and a feasibility study of the first 150 participants and give a brief overview of nested studies within LIPAD. Of note, the LIPAD protocol has also been adapted to take place online due to COVID19 contact restriction measures.

We aim to build the LIPAD cohort consisting of 1,000 participants internationally: 300 of them with LRRK2-PD (LRRK2+/PD+), 200 with pathogenic LRRK2 variants but without PD (LRRK2+/PD-), 100 PD patients with pathogenic variants in PD genes other than LRRK2 (genPD), 200 patients with idiopathic PD from the same populations (iPD; LRRK2-/PD+), and 200 healthy persons without pathogenic variants (HC). The majority of participants will be enrolled after genetic analysis within ROPAD (Figure 1) . Extrapolating from the ROPAD findings, we expect to have a sufficient number of participants in the LRRK2+/ PD+, iPD, and genPD groups. Further, family members of pathogenic LRRK2 variant carriers will be asked to participate in the LIPAD study and will be genetically tested for the familial pathogenic LRRK2 variant. Depending on the results, they will be assigned either to LRRK2+/PD-or HC group. Healthy persons without pathogenic variants will be recruited from spouses of study participants or the general population. Within an anticipated 24-month recruitment period per site, ∼25 centers in 10 countries on three continents will be established. Each center will have 24 months for recruitment after initiation. The majority of the centers will be those already participating in ROPAD, however, additional centers that do not participate in ROPAD but follow LRRK2 pathogenic variant carriers will be invited to become LIPAD sites.

Recruited participants have to meet one of the following criteria: (i) clinical diagnosis of PD according to the Movement disorder Society (MDS) diagnostic criteria, (ii) first-or second-degree relative of a participant that is positive for a pathogenetic LRRK2 variant, (iii) healthy participants with or without a family history of PD in a control group. All participants have to be above 18 years of age and have to sign an informed consent form.

Participants with the following LRRK2 variants will be included in the LRRK2+ group: p.Gly2019Ser (c.6055G>A), p.Arg1441His (c.4322G>A), p.Arg1441Cys (c.4321C>T), p.Arg1441Gly (c.4321C>G), p.Asn1437His (c.4309A>C), p.Ile2020Thr (c.6059T>C), p.Tyr1699Cys (c.5096A>G).

Upon completion of genetic screening (e.g., in ROPAD), participants are invited for a personal examination using the three-level biomaterial protocol. During a single visit, an electronic Case Report Form (eCRF) is administered and blood samples for DNA, RNA, serum/plasma, immune cell isolation, urine, and household dust for toxicological analyses are collected.

The three-level protocol was designed to accommodate available laboratory facilities at the different sites. The details of the three levels for biomaterial sampling are listed in Supporting Information Methods S2 in Supplementary Material.

In case genetic testing has not been performed before, a dried blood spot card will be sent for DNA extraction and genetic screening, as specified in ROPAD.

There are no serious safety concerns associated with the study. Participants may experience temporary discomfort during venous blood sampling and while answering the questions. However, they are instructed that they are free to omit questions they would rather not answer. There are no health risks associated with the collection of urine and house dust.

Data analysis will be performed at the Institute of Neurogenetics (University of Luebeck, Germany). To cover the first objective, which is the systematic characterization of PD patients and unaffected carriers with pathogenic variants in the LRRK2 gene, we will describe the frequency of all clinical signs and symptoms including non-motor signs and the most important influencing factors such as sex, disease duration, and medication. This will result in raw and corrected frequencies with 95% confidence intervals. We will use t-tests for numerical and continuous variables and chi-square tests for categorical variables at a significance level of 0.05 for the comparisons of the clinical signs and symptoms across the groups.

For aim 2, which is to investigate the modifiers of penetrance of pathogenic LRRK2 variants using genetic and environmental data, we will examine penetrance in logistic regression models to quantify the influence of different factors impacting penetrance.

All LIPAD centers can suggest nested projects, which will be coordinated by a Scientific Advisory Board. These projects can apply for external funding, will have individual ethics approvals, and can use the ROPAD/LIPAD network. The following nested studies are planned or have started at the Institute of Neurogenetics (University of Luebeck):

Penetrance of LRRK2-linked PD depends on the age of a given individual subject. Asymptomatic carriers may, however, already demonstrate neurodegenerative changes including hyposmia, abnormal midbrain hyperechogenicity upon transcranial sonography, pathologic dopaminergic neurotransmission, structural changes of the gray and white matter, and functional reorganization of neural networks. Although first morphological and functional brain changes in pathogenic LRRK2 variant carriers have already been identified, the overall picture is still elusive due to the relatively low number of included subjects in most studies, ascertainment biases, and variable imaging protocols. Multimodal high-quality MRI, however, is a promising secondary endpoint for clinical trials given its wide availability, cost-effectiveness, and lack of radiation.

To reveal an MRI-based biomarker for LRRK2+/PD+ and prodromal LRRK2+/PD+, we aim to acquire the following MRI modalities:

1. Multiparameter mapping (R1, PD * , MT, and R2 * ) to reveal physical tissue properties. 2. Diffusion-weighted imaging for multicompartment diffusion models to reveal neuroinflammation and microstructural alterations. 3. Neuromelanin imaging to reveal substantia nigra and locus coeruleus degeneration. 4. Blood-oxygen-level-dependent functional MRI to identify changes in functional connectivity. 5. Magnetic resonance spectroscopy to depict the mechanisms of neurodegeneration, such as involvement of energy metabolism due to mitochondrial dysfunction, which may be subject to faster change than other aspects of MR-based imaging (e.g., changes in gray matter).

To investigate whether metabolic changes in LRRK2 carriers already exist before the motor manifestation or are secondary to it, we conduct the following studies:

1. Energy consumption at rest using indirect calorimetry, where energy consumption is determined by measuring the air the subject breathes. 2. Measurement of body composition, i.e., the proportion of body fat mass and lean mass, employing air displacement plethysmography. In addition, body circumference (e.g., waist and hips) and body skin folds (e.g., on the arm and waist) are measured. 3. Measurement of physical activity and sleep behavior under everyday conditions using accelerometry. The study participants are asked to wear the accelerometer in the form of a wristwatch continuously for 7 days.

We will perform a genome-wide association study analysis in manifesting vs. non-manifesting carriers aimed at discovering genetic modifiers of penetrance of LRRK2 pathogenic variants.

A broad non-target liquid chromatography high-resolution mass spectrometry (LC-HR-MS) screening will be performed on household dust samples collected by participants in vacuum bags [see (10) ], with identification of potential toxicants of interest via the in silico fragmenter MetFrag (11) coupled with open chemical databases such as PubChem (12) and CompTox (13), The self-rating part PD risk factor questionnaire (PD-RFQ-U) Food frequency questionnaire Autonomic dysfunction (SCOPA-AUT) WHO Quality of life questionnaire (WHO-QoL) Pittsburgh Sleep Quality Inventory Epworth Sleepiness Scale Hospital Anxiety and Depression Scales plus specific neurotoxicity-related candidate lists and end-point information (14) .

A comprehensive eCRF has been developed, consisting of an investigator-rated (1 h) and a self-rated (1.5-h) part. The questionnaires are listed in Table 1 . We used validated versions of questionnaires and scales in the local languages. The first 10 centers across Germany and five international sites have been initiated with further centers currently undergoing ethical review (Figure 2 ). The first 150 participants have been enrolled (as of March 25th, 2021); Table 2 .

LIPAD is a large-scale international scientific effort focusing on deep phenotyping of LRRK2-linked PD and healthy pathogenic variant carriers, including a comparison with additional relatively frequent genetic forms of PD, and with a future perspective to identify genetic and environmental modifiers of penetrance and expressivity.

The clinical assessment in LIPAD is close to the one used in the currently largest multinational cohort of genetic PD (PPMI), except for lack of collection of cerebrospinal fluid, but with the addition of an extensive questionnaire on environmental factors (15) . Further, there are no restrictions on the age at diagnosis or medication for inclusion in the LIPAD study. Several other multinational prospective studies focusing on pathogenic LRRK2 variants included only a small number of populations (4, 16, 17) , revealing an important knowledge gap in multinational, standardized, genetic prospective studies, which LIPAD is aiming to close.

A comprehensive investigation of modifiers of penetrance and expressivity requires assessment of a considerable number of pathogenic variant carriers. Due to the direct enrolment of family members at an international scale, the LIPAD study will enable the analysis of modifiers of penetrance in different populations in one setting. Our recruitment strategy, mainly through the international multicenter ROPAD study, will ensure participation of a large number of LRRK2+/PD+ patients.

With the nested studies, which will be conducted on a subset of participants, we are aiming to provide a more in-depth phenotypic characterization especially of non-affected carriers of LRRK2 pathogenic variants.

Currently, a complication affecting many patient studies across the world are measures imposed on personal visits to contain SARS-CoV-2 in many countries, limiting the possibility for the collection of data and biomaterials. To allow the study to proceed under these circumstances, we adjusted the protocol and procedures to collect the necessary data online. After making an online appointment, patients receive a package with patient information, informed consent forms, and a smell test by post. Then an online appointment with the study team takes place, during which the study is explained, the data is collected and the examination is performed. Study participants send signed informed consent forms and a household dust sample back to the study center by post. Biomaterials will be taken at a general practitioner's office or the study center at a later time point when study visits become possible again. The study will revert to the on-site recruitment as soon as possible after the pandemic restrictions are lifted.

LIPAD aims for a longitudinal follow-up of its study participants over a 10-15-year time period. The exact protocol is currently being developed and potential funding opportunities are being explored.

The studies involving human participants were reviewed and approved by Ethics Committee (EC) of the 

The LIPAD study has been supported by institutional funds (Institute of Neurogenetics, University of Lübeck), and partly supported by Centogene GmbH. AB (NDAL) was funded by 

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